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Metabolome analysis and chemical profiling of Indonesian royal jellies as the raw material for cosmetic and bio-supplement products

Metabolome analysis and chemical profiling of Indonesian royal jellies as the raw material for cosmetic and bio-supplement products

Posted on September 11, 2021October 7, 2021 by Lindsey

Royal jellies (RJs) possess moisturizing, emulsifying, and stabilizing properties, and a number of pharmacological actions have additionally been discovered to be current, which make them a perfect element for cosmetic and skincare products. Nevertheless, regardless of the considerable efficacies, there’s a lack of research that discover the chemical composition of RJ utilizing metabolome analysis.

Moreover, an analysis of the chemical composition of Indonesian RJs collected from completely different areas has but to be carried out. Due to this fact, the fundamental goal of this examine was to determine any variations in the chemical composition of such RJs. Chemical profiling was additionally carried out to allow extra focused utilization primarily based on the precise compositions.

Chemical profiling can be essential given the wealthy Indonesian biodiversity and the excessive dependence of the RJ compositions on the botanical supply. On this analysis, ultra-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry was used as half of an untargeted metabolomics method.

From the chemical profiling, >30 compounds have been recognized throughout 4 RJ samples. The key constituents of the samples have been discovered to be oligosaccharides, fatty acids, and adenosine monophosphate derivatives. In the meantime, sucrose and planteose have been discovered to be highest in the samples from Banjarnegara and Kediri, whereas dimethyloctanoic acid was discovered to be distinctive to the pattern from Banjarnegara.

It was additionally found that the RJs from Demak and Tuban contained extra natural fatty acids and oligosaccharides than the different samples. Though the pattern from Demak demonstrated good potential for use in the cosmetic, skincare, and bio-supplement industries, the larger abundance of fatty acids and oligosaccharides in the pattern from Tuban indicated that it’s maybe the best suited RJ for use on this discipline.

Information Mining Approaches for Assessing Chemical Coexposures Utilizing Shopper Product Buy Information

The use of shopper products presents a possible for chemical exposures to people. Toxicity testing and publicity fashions are routinely employed to estimate dangers from their use; nevertheless, a key problem is the sparseness of info regarding who makes use of products and which products are used contemporaneously.

Our objective was to display a way to deduce use patterns by method of buy knowledge. We examined buy patterns for three varieties of private care products (cosmetics, hair care, and skincare) and two family care products (family cleaners and laundry provides) utilizing knowledge from 60,000 households collected over a one-year interval in 2012.

The market basket analysis methodology frequent itemset mining (FIM) was used to determine co-occurring units of product purchases for all households and demographic teams primarily based on revenue, training, race/ethnicity, and household composition. Our methodology captured strong co-occurrence patterns for private and family products, globally and for completely different demographic teams.

FIM recognized cosmetic co-occurrence patterns captured in prior surveys of cosmetic use, as properly as a pattern of elevated variety of cosmetic purchases as youngsters mature to teenage years. We suggest that shopper product buy knowledge may be mined to tell person-oriented use patterns for high-throughput chemical screening purposes, for mixture and mixed chemical danger evaluations.

Chemical Elimination of Lead Corrosion Products

Restoration therapy, specimen preparation or mass loss measurements on coupons made of lead require a dependable course of of dissolution of corrosion products. On this examine, a number of varieties of mannequin corrosion products with compositions consultant of these discovered on actual objects have been ready and characterised.

Ten options have been then totally examined in interval cleansing experiments, relating to the effectivity of removing of the corrosion products, corrosivity in the direction of naked lead, and remnants left on the floor. The answer advisable in the present model of the ISO 8470 customary was discovered to be improper for the cleansing of each historic artefacts and corrosion coupons attributable to its incapability to take away sulfide corrosion products and the danger of floor contamination and staining.

An answer of 20% hydrochloric acid is the best option for the preparation of lead coupons earlier than publicity or for analysis of mass loss of uncovered samples as a result of its considerably larger corrosivity in the direction of metallic lead is tolerable for these purposes.

Metabolome analysis and chemical profiling of AGTC bioproducts with electrophoresis
Accugel gel electrophoresis

Rochelle salt answer was discovered to be optimum for the cleansing of historic artefacts free of sulfide corrosion products attributable to the lowest corrosivity. None of these various options depart remnants on the floor and they’re environment friendly at laboratory temperature.

Figuring out Risky Chemical Product Tracer Compounds in U.S. Cities

With visitors emissions of risky natural compounds (VOCs) reducing quickly over the final a long time, the contributions of the emissions from different supply classes, such as risky chemical products (VCPs), have turn out to be extra obvious in city air. On this work, in situ measurements of numerous VOCs are reported for New York Metropolis, Pittsburgh, Chicago, and Denver.

The magnitude of completely different emission sources relative to visitors is set by measuring the city enhancement of particular person compounds relative to the enhancement of benzene, a recognized tracer of fossil gas in the United States. The enhancement ratios of a number of VCP compounds to benzene correlate properly with inhabitants density (R2 ∼ 0.6-0.8).

These observations are in keeping with the expectation that some human exercise ought to correlate higher with the inhabitants density than transportation emissions, attributable to the decrease per capita fee of driving in denser cities. Utilizing these knowledge, along with a bottom-up fuel-based stock of car emissions and risky chemical products (FIVE-VCP) stock, we determine tracer compounds for completely different VCP classes: decamethylcyclopentasiloxane (D5-siloxane) for private care products, monoterpenes for fragrances, p-dichlorobenzene for pesticides, D4-siloxane for adhesives, para-chlorobenzotrifluoride (PCBTF) for solvent-based coatings, and Texanol for water-based coatings.

Methacycline HCl

B1971-S ApexBio Evaluation Sample 97.2 EUR
Description: Methacycline HCl is a tetracycline antibiotic.

Methapyrilene HCl

S-2450 Scientific Laboratory Supplies 1ML 85.2 EUR

METHYL HYDRAZINE HCL

913019 Survival Technologies each Ask for price

3-Methoxytyramine · HCl

Q-1330.0001 Bachem 1.0g 181.2 EUR
Description: Sum Formula: C9H13NO2·HCl; CAS# [1477-68-5]

3-Methoxytyramine · HCl

Q-1330.0005 Bachem 5.0g 618 EUR
Description: Sum Formula: C9H13NO2·HCl; CAS# [1477-68-5]

(R)-2-Methylcysteine HCl

A8912-10 ApexBio 10 mg 259.2 EUR
Description: (R)-2-Methylcysteine HCl

(R)-2-Methylcysteine HCl

A8912-50 ApexBio 50 mg 861.6 EUR
Description: (R)-2-Methylcysteine HCl

HCl Dilution Matrix (10g/l HCl)

HADM1 Scientific Laboratory Supplies 1L 134.4 EUR

HCl Dilution Matrix 10g/L HCl

HADM1A Scientific Laboratory Supplies 2ML 122.73 EUR

ZM 323881 HCl

B2302-10 ApexBio 10 mg 325.2 EUR
Description: ZM323881 is a novel VEGF-R2 selective inhibitor with IC50 of <2nM.

ZM 323881 HCl

B2302-5.1 ApexBio 10 mM (in 1mL DMSO) 404.4 EUR
Description: ZM323881 is a novel VEGF-R2 selective inhibitor with IC50 of <2nM.

ZM 323881 HCl

B2302-50 ApexBio 50 mg 1090.8 EUR
Description: ZM323881 is a novel VEGF-R2 selective inhibitor with IC50 of <2nM.

CGS 21680 HCl

B1324-10 ApexBio 10 mg 235.2 EUR
Description: CGS 21680 HCl is a selective agonist of A2 adenosine receptor with IC50 value of 22nM [1].In rat striatal membranes, CGS 21680 potently prevents ligands from binding to A2 adenosine receptors with IC50 value of 22nM.

CGS 21680 HCl

B1324-100 ApexBio 100 mg 1312.8 EUR
Description: CGS 21680 HCl is a selective agonist of A2 adenosine receptor with IC50 value of 22nM [1].In rat striatal membranes, CGS 21680 potently prevents ligands from binding to A2 adenosine receptors with IC50 value of 22nM.

CGS 21680 HCl

B1324-5 ApexBio 5 mg 189.6 EUR
Description: CGS 21680 HCl is a selective agonist of A2 adenosine receptor with IC50 value of 22nM [1].In rat striatal membranes, CGS 21680 potently prevents ligands from binding to A2 adenosine receptors with IC50 value of 22nM.

CGS 21680 HCl

B1324-50 ApexBio 50 mg 783.6 EUR
Description: CGS 21680 HCl is a selective agonist of A2 adenosine receptor with IC50 value of 22nM [1].In rat striatal membranes, CGS 21680 potently prevents ligands from binding to A2 adenosine receptors with IC50 value of 22nM.

RS 127445 HCl

B7848-10 ApexBio 10 mg 170.4 EUR
Description: RS-127445 is a selective, high affinity 5-HT2B receptor antagonist.The 5-HT2B receptor is a G-protein coupled receptor. 5-HT2B receptors are widely expressed in peripheral tissues of various species.

RS 127445 HCl

B7848-5 ApexBio 5 mg 129.6 EUR
Description: RS-127445 is a selective, high affinity 5-HT2B receptor antagonist.The 5-HT2B receptor is a G-protein coupled receptor. 5-HT2B receptors are widely expressed in peripheral tissues of various species.

RS 127445 HCl

B7848-5.1 ApexBio 10 mM (in 1mL DMSO) 135.6 EUR
Description: RS-127445 is a selective, high affinity 5-HT2B receptor antagonist.The 5-HT2B receptor is a G-protein coupled receptor. 5-HT2B receptors are widely expressed in peripheral tissues of various species.

RS 127445 HCl

B7848-50 ApexBio 50 mg 505.2 EUR
Description: RS-127445 is a selective, high affinity 5-HT2B receptor antagonist.The 5-HT2B receptor is a G-protein coupled receptor. 5-HT2B receptors are widely expressed in peripheral tissues of various species.

WAY 316606 HCl

B8302-10 ApexBio 10 mg 703.2 EUR
Description: WAY 316606 is a selective small-molecule inhibitor of secreted frizzled-related protein-1 (sFRP-1) with EC50 value of 0.65 ?M [1].The Wnt signaling has been proved to be a drug target of treatment for metabolic bone diseases such as osteoporosis.

WAY 316606 HCl

B8302-100 ApexBio 100 mg 2349.6 EUR
Description: WAY 316606 is a selective small-molecule inhibitor of secreted frizzled-related protein-1 (sFRP-1) with EC50 value of 0.65 ?M [1].The Wnt signaling has been proved to be a drug target of treatment for metabolic bone diseases such as osteoporosis.

WAY 316606 HCl

B8302-5 ApexBio 5 mg 487.2 EUR
Description: WAY 316606 is a selective small-molecule inhibitor of secreted frizzled-related protein-1 (sFRP-1) with EC50 value of 0.65 ?M [1].The Wnt signaling has been proved to be a drug target of treatment for metabolic bone diseases such as osteoporosis.

WAY 316606 HCl

B8302-50 ApexBio 50 mg 1489.2 EUR
Description: WAY 316606 is a selective small-molecule inhibitor of secreted frizzled-related protein-1 (sFRP-1) with EC50 value of 0.65 ?M [1].The Wnt signaling has been proved to be a drug target of treatment for metabolic bone diseases such as osteoporosis.

ZM 39923 HCl

A4151-10 ApexBio 10 mg 184.8 EUR
Description: ZM 39923 is a selective inhibitor of JAK1 and JAK3 with pIC50 value of 4.4 and 7.1, respectively [1] [2].

ZM 39923 HCl

A4151-5.1 ApexBio 10 mM (in 1mL DMSO) 196.8 EUR
Description: ZM 39923 is a selective inhibitor of JAK1 and JAK3 with pIC50 value of 4.4 and 7.1, respectively [1] [2].

ZM 39923 HCl

A4151-50 ApexBio 50 mg 463.2 EUR
Description: ZM 39923 is a selective inhibitor of JAK1 and JAK3 with pIC50 value of 4.4 and 7.1, respectively [1] [2].

ML133 HCl

B2199-10 ApexBio 10 mg 150 EUR
Description: ML133 is a selective potassium channel inhibitor for Kir2.1 with IC50 of 1.8 ?M (pH 7.4) and 290 nM (pH 8.5), has no effect on Kir1.1 and weak activity for Kir4.1 and Kir7.1.

ML133 HCl

B2199-25 ApexBio 25 mg 274.8 EUR
Description: ML133 is a selective potassium channel inhibitor for Kir2.1 with IC50 of 1.8 ?M (pH 7.4) and 290 nM (pH 8.5), has no effect on Kir1.1 and weak activity for Kir4.1 and Kir7.1.

ML133 HCl

B2199-5 ApexBio 5 mg 129.6 EUR
Description: ML133 is a selective potassium channel inhibitor for Kir2.1 with IC50 of 1.8 ?M (pH 7.4) and 290 nM (pH 8.5), has no effect on Kir1.1 and weak activity for Kir4.1 and Kir7.1.

ML133 HCl

B2199-50 ApexBio 50 mg 420 EUR
Description: ML133 is a selective potassium channel inhibitor for Kir2.1 with IC50 of 1.8 ?M (pH 7.4) and 290 nM (pH 8.5), has no effect on Kir1.1 and weak activity for Kir4.1 and Kir7.1.

ML133 HCl

B2199-S ApexBio Evaluation Sample 97.2 EUR
Description: ML133 is a selective potassium channel inhibitor for Kir2.1 with IC50 of 1.8 ?M (pH 7.4) and 290 nM (pH 8.5), has no effect on Kir1.1 and weak activity for Kir4.1 and Kir7.1.

LX7101 HCL

B5863-10 ApexBio 10 mg 927.6 EUR
Description: Description:IC50: 4.3, 32, 69 and 32 nM for LIMK2, KIMK1, ROCK1 and ROCK2, respectivleyLIM-kinases 1 and 2 (LIMK1 and LIMK2) regulate cytoskeletal dynamics by phosphorylating and deactivating cofilin, a protein that depolymerizes actin filaments.

LX7101 HCL

B5863-100 ApexBio 100 mg 4837.2 EUR
Description: Description:IC50: 4.3, 32, 69 and 32 nM for LIMK2, KIMK1, ROCK1 and ROCK2, respectivleyLIM-kinases 1 and 2 (LIMK1 and LIMK2) regulate cytoskeletal dynamics by phosphorylating and deactivating cofilin, a protein that depolymerizes actin filaments.

LX7101 HCL

B5863-5 ApexBio 5 mg 582 EUR
Description: Description:IC50: 4.3, 32, 69 and 32 nM for LIMK2, KIMK1, ROCK1 and ROCK2, respectivleyLIM-kinases 1 and 2 (LIMK1 and LIMK2) regulate cytoskeletal dynamics by phosphorylating and deactivating cofilin, a protein that depolymerizes actin filaments.

LX7101 HCL

B5863-5.1 ApexBio 10 mM (in 1mL DMSO) 576 EUR
Description: Description:IC50: 4.3, 32, 69 and 32 nM for LIMK2, KIMK1, ROCK1 and ROCK2, respectivleyLIM-kinases 1 and 2 (LIMK1 and LIMK2) regulate cytoskeletal dynamics by phosphorylating and deactivating cofilin, a protein that depolymerizes actin filaments.

LX7101 HCL

B5863-50 ApexBio 50 mg 3099.6 EUR
Description: Description:IC50: 4.3, 32, 69 and 32 nM for LIMK2, KIMK1, ROCK1 and ROCK2, respectivleyLIM-kinases 1 and 2 (LIMK1 and LIMK2) regulate cytoskeletal dynamics by phosphorylating and deactivating cofilin, a protein that depolymerizes actin filaments.

GW3965 HCl

A8444-10 ApexBio 10 mg 205.2 EUR
Description: GW3965 HCl is a selective, orally active non-steroidal agonist for the liver X receptor (LXR) [1].Nuclear receptors LXR? and LXR? have an important role in control of cholesterol and fatty acid metabolism in multiple cell types.

GW3965 HCl

A8444-5 ApexBio 5 mg 154.8 EUR
Description: GW3965 HCl is a selective, orally active non-steroidal agonist for the liver X receptor (LXR) [1].Nuclear receptors LXR? and LXR? have an important role in control of cholesterol and fatty acid metabolism in multiple cell types.

GW3965 HCl

A8444-5.1 ApexBio 10 mM (in 1mL DMSO) 199.2 EUR
Description: GW3965 HCl is a selective, orally active non-steroidal agonist for the liver X receptor (LXR) [1].Nuclear receptors LXR? and LXR? have an important role in control of cholesterol and fatty acid metabolism in multiple cell types.

GW3965 HCl

A8444-50 ApexBio 50 mg 614.4 EUR
Description: GW3965 HCl is a selective, orally active non-steroidal agonist for the liver X receptor (LXR) [1].Nuclear receptors LXR? and LXR? have an important role in control of cholesterol and fatty acid metabolism in multiple cell types.

LX7101 HCL

B5863-2 ApexBio 2mg 215 EUR
Description: Dual LIM-kinase and ROCK inhibitor

Doxepin HCl

20-abx184015 Abbexa
  • 1328.40 EUR
  • 243.60 EUR
  • 610.80 EUR
  • 343.20 EUR
  • 100 g
  • 1 g
  • 25 g
  • 5 g

Ozagrel HCl

B2116-10 ApexBio 10 mg 153.6 EUR
Description: Ozagrel HCl

Ozagrel HCl

B2116-5.1 ApexBio 10 mM (in 1mL DMSO) 129.6 EUR
Description: Ozagrel HCl

Ozagrel HCl

B2116-50 ApexBio 50 mg 265.2 EUR
Description: Ozagrel HCl

Ozagrel HCl

B2116-S ApexBio Evaluation Sample 97.2 EUR
Description: Ozagrel HCl

Scopine HCl

B2130-100 ApexBio 100 mg 517.2 EUR
Description: Scopine HCl

Scopine HCl

B2130-25 ApexBio 25 mg 201.6 EUR
Description: Scopine HCl

Scopine HCl

B2130-S ApexBio Evaluation Sample 97.2 EUR
Description: Scopine HCl

Adenine HCl

B1471-5.1 ApexBio 10 mM (in 1mL DMSO) 170.4 EUR
Description: Adenine HCl, a purine derivative and a nucleobase, plays crucial roles in substantial biochemistry processes in vivo, including cellular respiration, formation of the energy-rich adenosine triphosphate (ATP), the cofactors nicotinamide adenine dinucleotide (NAD) and flavin adenine dinucleotide.

Adenine HCl

B1471-50 ApexBio 50 mg 153.6 EUR
Description: Adenine HCl, a purine derivative and a nucleobase, plays crucial roles in substantial biochemistry processes in vivo, including cellular respiration, formation of the energy-rich adenosine triphosphate (ATP), the cofactors nicotinamide adenine dinucleotide (NAD) and flavin adenine dinucleotide.

Adenine HCl

B1471-S ApexBio Evaluation Sample 97.2 EUR
Description: Adenine HCl, a purine derivative and a nucleobase, plays crucial roles in substantial biochemistry processes in vivo, including cellular respiration, formation of the energy-rich adenosine triphosphate (ATP), the cofactors nicotinamide adenine dinucleotide (NAD) and flavin adenine dinucleotide.

SRT1720 HCl

A4180-10 ApexBio 10 mg 309.6 EUR
Description: SRT1720 is a small-molecule compound which has the ability of activating the sirtuin subtype SIRT1 in vitro. The activity of SRT1720 as a SIRT1 activator is stronger than that of resveratrol.

SRT1720 HCl

A4180-200 ApexBio 200 mg 1730.4 EUR
Description: SRT1720 is a small-molecule compound which has the ability of activating the sirtuin subtype SIRT1 in vitro. The activity of SRT1720 as a SIRT1 activator is stronger than that of resveratrol.

SRT1720 HCl

A4180-5 ApexBio 5 mg 212.4 EUR
Description: SRT1720 is a small-molecule compound which has the ability of activating the sirtuin subtype SIRT1 in vitro. The activity of SRT1720 as a SIRT1 activator is stronger than that of resveratrol.

SRT1720 HCl

A4180-5.1 ApexBio 10 mM (in 1mL DMSO) 226.8 EUR
Description: SRT1720 is a small-molecule compound which has the ability of activating the sirtuin subtype SIRT1 in vitro. The activity of SRT1720 as a SIRT1 activator is stronger than that of resveratrol.

SRT1720 HCl

A4180-50 ApexBio 50 mg 825.6 EUR
Description: SRT1720 is a small-molecule compound which has the ability of activating the sirtuin subtype SIRT1 in vitro. The activity of SRT1720 as a SIRT1 activator is stronger than that of resveratrol.

SRT1720 HCl

A4180-S ApexBio Evaluation Sample 97.2 EUR
Description: SRT1720 is a small-molecule compound which has the ability of activating the sirtuin subtype SIRT1 in vitro. The activity of SRT1720 as a SIRT1 activator is stronger than that of resveratrol.

ADL5859 HCl

A2986-100 ApexBio 100 mg 1423.2 EUR
Description: Selective ? opioid receptor agonists are promising potential therapeutic agents for the treatment of various types of pain conditions. A spirocyclic derivative was identified as a promising hit through screening.

ADL5859 HCl

A2986-25 ApexBio 25 mg 588 EUR
Description: Selective ? opioid receptor agonists are promising potential therapeutic agents for the treatment of various types of pain conditions. A spirocyclic derivative was identified as a promising hit through screening.

ADL5859 HCl

A2986-5 ApexBio 5 mg 226.8 EUR
Description: Selective ? opioid receptor agonists are promising potential therapeutic agents for the treatment of various types of pain conditions. A spirocyclic derivative was identified as a promising hit through screening.

ADL5859 HCl

A2986-5.1 ApexBio 10 mM (in 1mL DMSO) 261.6 EUR
Description: Selective ? opioid receptor agonists are promising potential therapeutic agents for the treatment of various types of pain conditions. A spirocyclic derivative was identified as a promising hit through screening.

Esmolol HCl

B1748-5.1 ApexBio 10 mM (in 1mL DMSO) 129.6 EUR
Description: Esmolol is a cardioselective b-blocker, used to control rapid heartbeats or abnormal heart rhythms.

Esmolol HCl

B1748-50 ApexBio 50 mg 153.6 EUR
Description: Esmolol is a cardioselective b-blocker, used to control rapid heartbeats or abnormal heart rhythms.

Nefopam HCl

B1794-10 ApexBio 10 mg 142.8 EUR
Description: Nefopam HCl is an centrally-acting but non-opioid analgesic drug by blocking voltage-gated sodium channel and inhibition of serotonin, dopamine and noradrenaline reuptake.

Nefopam HCl

B1794-5.1 ApexBio 10 mM (in 1mL H2O) 158.4 EUR
Description: Nefopam HCl is an centrally-acting but non-opioid analgesic drug by blocking voltage-gated sodium channel and inhibition of serotonin, dopamine and noradrenaline reuptake.

Nefopam HCl

B1794-50 ApexBio 50 mg 208.8 EUR
Description: Nefopam HCl is an centrally-acting but non-opioid analgesic drug by blocking voltage-gated sodium channel and inhibition of serotonin, dopamine and noradrenaline reuptake.

Arbidol HCl

A8362-10 ApexBio 10 mg 129.6 EUR
Description: Arbidol (Umifenovir) hydrochloride is an broad-spectrum antiviral chemical agent which can inhibit cell entry of enveloped viruses by blocking viral fusion with host cell membrane.

Arbidol HCl

A8362-100 ApexBio 100 mg 421.2 EUR
Description: Arbidol (Umifenovir) hydrochloride is an broad-spectrum antiviral chemical agent which can inhibit cell entry of enveloped viruses by blocking viral fusion with host cell membrane.

Arbidol HCl

A8362-5.1 ApexBio 10 mM (in 1mL DMSO) 135.6 EUR
Description: Arbidol (Umifenovir) hydrochloride is an broad-spectrum antiviral chemical agent which can inhibit cell entry of enveloped viruses by blocking viral fusion with host cell membrane.

Quinine HCl

Q011-10G TOKU-E 10 g 27.99 EUR
Description: C20H24N2O2 ∙ HCl

Quinine HCl

Q011-50G TOKU-E 50 g 84.63 EUR
Description: C20H24N2O2 ∙ HCl

Adenine HCl

B1471-1000 ApexBio 1g 37 EUR
Description: Adenine receptor agonist

Adenine HCl

B1471-5000 ApexBio 5g 48 EUR
Description: Adenine receptor agonist

Ambroxol Hcl

abx188586-250g Abbexa 250 g 309.6 EUR

Pd128907 Hcl

20-abx184299 Abbexa
  • 543.60 EUR
  • 393.60 EUR
  • 10 mg
  • 5 mg

Procaine HCl

20-abx184762 Abbexa
  • 292.80 EUR
  • 577.20 EUR
  • 100 g
  • 500 g

Thiamine HCl

20-abx184786 Abbexa
  • 292.80 EUR
  • 526.80 EUR
  • 100 g
  • 500 g

Prazosin HCl

20-abx185996 Abbexa
  • 292.80 EUR
  • 543.60 EUR
  • 100 mg
  • 1 g

GW791343 HCl

B2165-10 ApexBio 10 mg 320.4 EUR
Description: GW791343 is a P2X7 allosteric modulator. Exhibits species-specific activity and acts as a negative allosteric modulator of human P2X7 (pIC50 = 6.9 - 7.2). A positive allosteric modulator of rat P2X7.

GW791343 HCl

B2165-5 ApexBio 5 mg 211.2 EUR
Description: GW791343 is a P2X7 allosteric modulator. Exhibits species-specific activity and acts as a negative allosteric modulator of human P2X7 (pIC50 = 6.9 - 7.2). A positive allosteric modulator of rat P2X7.

GW791343 HCl

B2165-50 ApexBio 50 mg 884.4 EUR
Description: GW791343 is a P2X7 allosteric modulator. Exhibits species-specific activity and acts as a negative allosteric modulator of human P2X7 (pIC50 = 6.9 - 7.2). A positive allosteric modulator of rat P2X7.

Urapidil HCl

B2242-50 ApexBio 50 mg 153.6 EUR
Description: Urapidil HCl is an ?1-adrenoceptor antagonist and 5-HT1A receptor agonist.

Urapidil HCl

B2242-S ApexBio Evaluation Sample 97.2 EUR
Description: Urapidil HCl is an ?1-adrenoceptor antagonist and 5-HT1A receptor agonist.

SB269970 HCl

B2254-10 ApexBio 10 mg 297.6 EUR
Description: SB269970 HCl is a potent and selective antagonist of 5-HT7 receptor with pKi value of 8.3 [1].SB269970 is a selective antagonist of 5-HT7 receptor. It shows at least 100-fold selective against 5-HT7 over a variety of receptors and enzymes

SB269970 HCl

B2254-25 ApexBio 25 mg 591.6 EUR
Description: SB269970 HCl is a potent and selective antagonist of 5-HT7 receptor with pKi value of 8.3 [1].SB269970 is a selective antagonist of 5-HT7 receptor. It shows at least 100-fold selective against 5-HT7 over a variety of receptors and enzymes

SB269970 HCl

B2254-5 ApexBio 5 mg 184.8 EUR
Description: SB269970 HCl is a potent and selective antagonist of 5-HT7 receptor with pKi value of 8.3 [1].SB269970 is a selective antagonist of 5-HT7 receptor. It shows at least 100-fold selective against 5-HT7 over a variety of receptors and enzymes

SB269970 HCl

B2254-50 ApexBio 50 mg 999.6 EUR
Description: SB269970 HCl is a potent and selective antagonist of 5-HT7 receptor with pKi value of 8.3 [1].SB269970 is a selective antagonist of 5-HT7 receptor. It shows at least 100-fold selective against 5-HT7 over a variety of receptors and enzymes

Ambroxol HCl

B2267-50 ApexBio 50 mg 129.6 EUR
Description: AmbroxolHCl is a potent inhibitor of the neuronal Na+ channels, inhibits TTX-resistant Na+ currents with IC50 of 35.2 ?M and 22.5 ?M for tonic and phasic block, inhibits TTX-sensitive Na+ currents with IC50 of 100 ?M. Phase 3.

Ambroxol HCl

B2267-S ApexBio Evaluation Sample 97.2 EUR
Description: AmbroxolHCl is a potent inhibitor of the neuronal Na+ channels, inhibits TTX-resistant Na+ currents with IC50 of 35.2 ?M and 22.5 ?M for tonic and phasic block, inhibits TTX-sensitive Na+ currents with IC50 of 100 ?M. Phase 3.

Procaine HCl

B2273-50 ApexBio 50 mg 153.6 EUR
Description: Procaine is an inhibitor of sodium channel, NMDA receptor and nAChR with IC50 of 60 ?M, 0.296 mM and 45.5 ?M, which is also an inhibitor of 5-HT3 with KD of 1.7 ?M.

Procaine HCl

B2273-S ApexBio Evaluation Sample 97.2 EUR
Description: Procaine is an inhibitor of sodium channel, NMDA receptor and nAChR with IC50 of 60 ?M, 0.296 mM and 45.5 ?M, which is also an inhibitor of 5-HT3 with KD of 1.7 ?M.

Xylazine HCl

B1351-100 ApexBio 100 mg 129.6 EUR
Description: Xylazine HCl is a strong agonist of ?2-adrenoceptor [1]. Xylazine HCl has been reported to stimulate the proliferation of rat thymocytes in vivo (at doses of 2.5 mg/kg and 5 mg/kg) and in vitro (at concentration of 5 mM) [2].

Xylazine HCl

B1351-5.1 ApexBio 10 mM (in 1mL DMSO) 135.6 EUR
Description: Xylazine HCl is a strong agonist of ?2-adrenoceptor [1]. Xylazine HCl has been reported to stimulate the proliferation of rat thymocytes in vivo (at doses of 2.5 mg/kg and 5 mg/kg) and in vitro (at concentration of 5 mM) [2].

Xylazine HCl

B1351-500 ApexBio 500 mg 184.8 EUR
Description: Xylazine HCl is a strong agonist of ?2-adrenoceptor [1]. Xylazine HCl has been reported to stimulate the proliferation of rat thymocytes in vivo (at doses of 2.5 mg/kg and 5 mg/kg) and in vitro (at concentration of 5 mM) [2].

Xylazine HCl

B1351-S ApexBio Evaluation Sample 97.2 EUR
Description: Xylazine HCl is a strong agonist of ?2-adrenoceptor [1]. Xylazine HCl has been reported to stimulate the proliferation of rat thymocytes in vivo (at doses of 2.5 mg/kg and 5 mg/kg) and in vitro (at concentration of 5 mM) [2].

Dopamine HCl

B1482-5.1 ApexBio 10 mM (in 1mL DMSO) 170.4 EUR
Description: Dopamine HCl is a catecholamine neurotransmitter present in a wide variety of animals,And a dopamine D1-5 receptors agonist.

Dopamine HCl

B1482-50 ApexBio 50 mg 153.6 EUR
Description: Dopamine HCl is a catecholamine neurotransmitter present in a wide variety of animals,And a dopamine D1-5 receptors agonist.

Dopamine HCl

B1482-S ApexBio Evaluation Sample 97.2 EUR
Description: Dopamine HCl is a catecholamine neurotransmitter present in a wide variety of animals,And a dopamine D1-5 receptors agonist.

PD128907 HCl

B1491-10 ApexBio 10 mg 351.6 EUR
Description: PD 128907 HCl is a potent and selective dopamine D3 receptor agonist, with EC50 of 0.64 nM, exhibits 53-fold selectivity over dopamine D2 receptor.

PD128907 HCl

B1491-25 ApexBio 25 mg 633.6 EUR
Description: PD 128907 HCl is a potent and selective dopamine D3 receptor agonist, with EC50 of 0.64 nM, exhibits 53-fold selectivity over dopamine D2 receptor.

PD128907 HCl

B1491-5 ApexBio 5 mg 247.2 EUR
Description: PD 128907 HCl is a potent and selective dopamine D3 receptor agonist, with EC50 of 0.64 nM, exhibits 53-fold selectivity over dopamine D2 receptor.

LP533401 hcl

B5823-25 ApexBio 25 mg 1312.8 EUR
Description: LP533401 hcl is an inhibitor of Tph-1 [1]. Tryptophan hydroxylase-1 (Tph-1) is an isoenzyme of tryptophan hydroxylase and the initial enzyme in gut- and lung-derived serotonin biosynthesis. Tph-1 is mainly expressed in the gut and lung [2].

LP533401 hcl

B5823-5 ApexBio 5 mg 547.2 EUR
Description: LP533401 hcl is an inhibitor of Tph-1 [1]. Tryptophan hydroxylase-1 (Tph-1) is an isoenzyme of tryptophan hydroxylase and the initial enzyme in gut- and lung-derived serotonin biosynthesis. Tph-1 is mainly expressed in the gut and lung [2].

Ambroxol HCl

20-abx076696 Abbexa
  • 376.80 EUR
  • 309.60 EUR
  • 500 mg
  • 50 mg

SKF38393 HCl

B6030-100 ApexBio 100 mg 192 EUR
Description: SKF38393 HCl (SKF38393) is a selective dopamine D1 receptor agonist [1], with an IC50 value of 110 nM [2].There are two functional types of dopamine receptors, D1 and D2 receptors [3]. The stimulation of the D1 receptor (D1R) in prefrontal cortex (PFC) results in an ?inverted-U? dose-response.

SKF38393 HCl

B6030-200 ApexBio 200 mg 282 EUR
Description: SKF38393 HCl (SKF38393) is a selective dopamine D1 receptor agonist [1], with an IC50 value of 110 nM [2].There are two functional types of dopamine receptors, D1 and D2 receptors [3]. The stimulation of the D1 receptor (D1R) in prefrontal cortex (PFC) results in an ?inverted-U? dose-response.

SKF38393 HCl

B6030-500 ApexBio 500 mg 547.2 EUR
Description: SKF38393 HCl (SKF38393) is a selective dopamine D1 receptor agonist [1], with an IC50 value of 110 nM [2].There are two functional types of dopamine receptors, D1 and D2 receptors [3]. The stimulation of the D1 receptor (D1R) in prefrontal cortex (PFC) results in an ?inverted-U? dose-response.

Doxapram HCl

A8419-5.1 ApexBio 10 mM (in 1mL DMSO) 170.4 EUR
Description: Doxapram HCl is a respiratory stimulant.

Doxapram HCl

A8419-50 ApexBio 50 mg 157.2 EUR
Description: Doxapram HCl is a respiratory stimulant.

Prazosin HCl

A5318-100 ApexBio 100 mg 199.2 EUR
Description: ?1 and ?2B-adrenoceptor antagonist. Also a potent antagonist at the melatonin MT3 receptor (Ki = 10.2 nM). Also available as part of the ?1-Adrenoceptor Tocriset? and Mixed Adre

Prazosin HCl

A5318-5.1 ApexBio 10 mM (in 1mL DMSO) 129.6 EUR
Description: ?1 and ?2B-adrenoceptor antagonist. Also a potent antagonist at the melatonin MT3 receptor (Ki = 10.2 nM). Also available as part of the ?1-Adrenoceptor Tocriset? and Mixed Adre

Xylazine · HCl

Q-1440.0025 Bachem 25.0g 385.2 EUR
Description: Sum Formula: C12H16N2S·HCl; CAS# [23076-35-9]

Dopamine HCl

B1482-100 ApexBio 100mg 37 EUR
Description: Dopamine D1-5 receptors agonist

Dopamine HCl

B1482-500 ApexBio 500mg 62 EUR
Description: Dopamine D1-5 receptors agonist

Procaine HCl

B2273-1000 ApexBio 1g 55 EUR
Description: inhibitor of sodium channel, NMDA receptor and nAChR

Procaine HCl

B2273-5000 ApexBio 5g 96 EUR
Description: inhibitor of sodium channel, NMDA receptor and nAChR

Dyclonine HCl

B1936-5.1 ApexBio 10 mM (in 1mL DMSO) 129.6 EUR
Description: Dyclonine is an oral anaesthetic found in Sucrets, an over the counter throat lozenge.

Dyclonine HCl

B1936-50 ApexBio 50 mg 153.6 EUR
Description: Dyclonine is an oral anaesthetic found in Sucrets, an over the counter throat lozenge.

Dyclonine HCl

B1936-S ApexBio Evaluation Sample 97.2 EUR
Description: Dyclonine is an oral anaesthetic found in Sucrets, an over the counter throat lozenge.

Guanidine HCl

B1949-5.1 ApexBio 10 mM (in 1mL DMSO) 129.6 EUR
Description: Guanidine HCl, the crystalline compound of strong alkalinity formed by the oxidation of guanine, is a normal product of protein metabolism and a protein denaturant.

Guanidine HCl

B1949-50 ApexBio 50 mg 153.6 EUR
Description: Guanidine HCl, the crystalline compound of strong alkalinity formed by the oxidation of guanine, is a normal product of protein metabolism and a protein denaturant.

Naftifine HCl

B1984-50 ApexBio 50 mg 166.8 EUR
Description: Naftifine is an allylamine antifungal drug for the topical treatment of tinea pedis, tinea cruris, and tinea corporis, probably involves selectively blocking sterol biosynthesis via inhibition of the squalene 2,3-epoxidase enzyme.

Naftifine HCl

B1984-500 ApexBio 500 mg 711.6 EUR
Description: Naftifine is an allylamine antifungal drug for the topical treatment of tinea pedis, tinea cruris, and tinea corporis, probably involves selectively blocking sterol biosynthesis via inhibition of the squalene 2,3-epoxidase enzyme.

Diltiazem HCl

B2089-10 ApexBio 10 mg 129.6 EUR
Description: Diltiazem HCl

Diltiazem HCl

B2089-5.1 ApexBio 10 mM (in 1mL DMSO) 135.6 EUR
Description: Diltiazem HCl

Diltiazem HCl

B2089-50 ApexBio 50 mg 268.8 EUR
Description: Diltiazem HCl

Diltiazem HCl

B2089-S ApexBio Evaluation Sample 97.2 EUR
Description: Diltiazem HCl

Quinapril HCl

B2207-5.1 ApexBio 10 mM (in 1mL DMSO) 129.6 EUR
Description: Quinapril is a prodrug that belongs to the angiotensin-converting enzyme (ACE) inhibitor class of medications.

Quinapril HCl

B2207-50 ApexBio 50 mg 153.6 EUR
Description: Quinapril is a prodrug that belongs to the angiotensin-converting enzyme (ACE) inhibitor class of medications.

Quinapril HCl

B2207-S ApexBio Evaluation Sample 97.2 EUR
Description: Quinapril is a prodrug that belongs to the angiotensin-converting enzyme (ACE) inhibitor class of medications.

Moexipril HCl

B2212-100 ApexBio 100 mg 381.6 EUR
Description: Moexipril HCl is a potent orally active non-sulfhydryl angiotensin converting enzyme(ACE) inhibitor, which is used for the treatment of hypertension and congestive heart failure.

Moexipril HCl

B2212-25 ApexBio 25 mg 176.4 EUR
Description: Moexipril HCl is a potent orally active non-sulfhydryl angiotensin converting enzyme(ACE) inhibitor, which is used for the treatment of hypertension and congestive heart failure.

Moexipril HCl

B2212-50 ApexBio 50 mg 235.2 EUR
Description: Moexipril HCl is a potent orally active non-sulfhydryl angiotensin converting enzyme(ACE) inhibitor, which is used for the treatment of hypertension and congestive heart failure.

Trazodone HCl

B2230-5.1 ApexBio 10 mM (in 1mL DMSO) 129.6 EUR
Description: Trazodone HCl is an antidepressant belonging to the class of serotonin receptor antagonists and reuptake inhibitors for treatment of anxiety disorders.Trazodone is a triazolopyridine derivative, chemically and pharmacologically unrelated to other currentl

Trazodone HCl

B2230-50 ApexBio 50 mg 153.6 EUR
Description: Trazodone HCl is an antidepressant belonging to the class of serotonin receptor antagonists and reuptake inhibitors for treatment of anxiety disorders.Trazodone is a triazolopyridine derivative, chemically and pharmacologically unrelated to other currentl

Azasetron HCl

B2233-10 ApexBio 10 mg 236.4 EUR
Description: Azasetron Hydrochloride is a 5-HT3 receptor antagonist which is used as an anti-emetic.Azasetron inhibited the specific binding of [3H]quipazine to 5-HT3 receptors at the synaptic membranes of the rat cerebral cortex with a Ki value of 2.9 nM. Azasetron

Azasetron HCl

B2233-100 ApexBio 100 mg 1261.2 EUR
Description: Azasetron Hydrochloride is a 5-HT3 receptor antagonist which is used as an anti-emetic.Azasetron inhibited the specific binding of [3H]quipazine to 5-HT3 receptors at the synaptic membranes of the rat cerebral cortex with a Ki value of 2.9 nM. Azasetron

Azasetron HCl

B2233-200 ApexBio 200 mg 1663.2 EUR
Description: Azasetron Hydrochloride is a 5-HT3 receptor antagonist which is used as an anti-emetic.Azasetron inhibited the specific binding of [3H]quipazine to 5-HT3 receptors at the synaptic membranes of the rat cerebral cortex with a Ki value of 2.9 nM. Azasetron

Azasetron HCl

B2233-5.1 ApexBio 10 mM (in 1mL H2O) 271.2 EUR
Description: Azasetron Hydrochloride is a 5-HT3 receptor antagonist which is used as an anti-emetic.Azasetron inhibited the specific binding of [3H]quipazine to 5-HT3 receptors at the synaptic membranes of the rat cerebral cortex with a Ki value of 2.9 nM. Azasetron

Azasetron HCl

B2233-50 ApexBio 50 mg 702 EUR
Description: Azasetron Hydrochloride is a 5-HT3 receptor antagonist which is used as an anti-emetic.Azasetron inhibited the specific binding of [3H]quipazine to 5-HT3 receptors at the synaptic membranes of the rat cerebral cortex with a Ki value of 2.9 nM. Azasetron

Topotecan HCl

B2296-10 ApexBio 10 mg 115.2 EUR
Description: Topotecan HCl?SKF104864?is an inhibitor of topoisomerase 1 and semisynthetic analogue of camptothecin [1].Topotecan HCl?SKF104864?has been reported to have a potent antitumor activity against tumors in murine models.

Topotecan HCl

B2296-100 ApexBio 100 mg 268.8 EUR
Description: Topotecan HCl?SKF104864?is an inhibitor of topoisomerase 1 and semisynthetic analogue of camptothecin [1].Topotecan HCl?SKF104864?has been reported to have a potent antitumor activity against tumors in murine models.

Topotecan HCl

B2296-5.1 ApexBio 10 mM (in 1mL DMSO) 135.6 EUR
Description: Topotecan HCl?SKF104864?is an inhibitor of topoisomerase 1 and semisynthetic analogue of camptothecin [1].Topotecan HCl?SKF104864?has been reported to have a potent antitumor activity against tumors in murine models.

Topotecan HCl

B2296-50 ApexBio 50 mg 240 EUR
Description: Topotecan HCl?SKF104864?is an inhibitor of topoisomerase 1 and semisynthetic analogue of camptothecin [1].Topotecan HCl?SKF104864?has been reported to have a potent antitumor activity against tumors in murine models.

Amprolium HCl

B1663-5.1 ApexBio 10 mM (in 1mL DMSO) 129.6 EUR
Description: Amprolium chloride is a thiamin antagonist, which prevents carbohydrate synthesis by blocking thiamine uptake.

Amprolium HCl

B1663-50 ApexBio 50 mg 153.6 EUR
Description: Amprolium chloride is a thiamin antagonist, which prevents carbohydrate synthesis by blocking thiamine uptake.

Buspirone HCl

B1687-5.1 ApexBio 10 mM (in 1mL DMSO) 129.6 EUR
Description: Buspirone HCl

Buspirone HCl

B1687-50 ApexBio 50 mg 153.6 EUR
Description: Buspirone HCl

Clonidine HCl

B1333-5.1 ApexBio 10 mM (in 1mL DMSO) 129.6 EUR
Description: Clonidine Hydrochloride is a centrally acting alpha-agonist hypotensive agent.

Clonidine HCl

B1333-50 ApexBio 50 mg 153.6 EUR
Description: Clonidine Hydrochloride is a centrally acting alpha-agonist hypotensive agent.

Clonidine HCl

B1333-S ApexBio Evaluation Sample 97.2 EUR
Description: Clonidine Hydrochloride is a centrally acting alpha-agonist hypotensive agent.

Ritodrine HCl

B1347-5.1 ApexBio 10 mM (in 1mL DMSO) 129.6 EUR
Description: Ritodrine HCl is a ?-2 adrenergic receptor agonist.Ritodrine is a tocolytic drug, used to stop premature labor. Ritodrine can significantly prolong a short interval more quickly but with relatively more side effects than magnesium sulphate. Stratified RCT

Ritodrine HCl

B1347-50 ApexBio 50 mg 153.6 EUR
Description: Ritodrine HCl is a ?-2 adrenergic receptor agonist.Ritodrine is a tocolytic drug, used to stop premature labor. Ritodrine can significantly prolong a short interval more quickly but with relatively more side effects than magnesium sulphate. Stratified RCT

Ritodrine HCl

B1347-S ApexBio Evaluation Sample 97.2 EUR
Description: Ritodrine HCl is a ?-2 adrenergic receptor agonist.Ritodrine is a tocolytic drug, used to stop premature labor. Ritodrine can significantly prolong a short interval more quickly but with relatively more side effects than magnesium sulphate. Stratified RCT

Betaxolol HCl

B1353-10 ApexBio 10 mg 129.6 EUR
Description: Betaxolol is a ?1 adrenergic receptor blocker with IC50 of 6 ?M.

Betaxolol HCl

B1353-5.1 ApexBio 10 mM (in 1mL DMSO) 129.6 EUR
Description: Betaxolol is a ?1 adrenergic receptor blocker with IC50 of 6 ?M.

Betaxolol HCl

B1353-50 ApexBio 50 mg 226.8 EUR
Description: Betaxolol is a ?1 adrenergic receptor blocker with IC50 of 6 ?M.

Betaxolol HCl

B1353-S ApexBio Evaluation Sample 97.2 EUR
Description: Betaxolol is a ?1 adrenergic receptor blocker with IC50 of 6 ?M.

Terazosin HCl

B1365-250 ApexBio 250 mg 268.8 EUR
Description: Terazosin HCl dihydrate is a selective alpha1-antagonist used for treatment of symptoms of benign prostatic hyperplasia (BPH).

Terazosin HCl

B1365-5.1 ApexBio 10 mM (in 1mL DMSO) 129.6 EUR
Description: Terazosin HCl dihydrate is a selective alpha1-antagonist used for treatment of symptoms of benign prostatic hyperplasia (BPH).

Terazosin HCl

B1365-50 ApexBio 50 mg 129.6 EUR
Description: Terazosin HCl dihydrate is a selective alpha1-antagonist used for treatment of symptoms of benign prostatic hyperplasia (BPH).

Terazosin HCl

B1365-S ApexBio Evaluation Sample 97.2 EUR
Description: Terazosin HCl dihydrate is a selective alpha1-antagonist used for treatment of symptoms of benign prostatic hyperplasia (BPH).

Buclizine HCl

B1546-50 ApexBio 50 mg 153.6 EUR
Description: Buclizine HCL is an antihistamine and anticholinergic of the piperazine derivative family.

EPZ004777 HCl

B1581-5 ApexBio 5 mg 212.4 EUR
Description: EPZ004777 is a potent and selective inhibitor of DOT1L, a protein methyltransferase catalyzing the methylation of lysine 4 of histone H3 (H3K4), with the half maximal inhibition concentration IC50 value of 400 pM [1].

EPZ004777 HCl

B1581-50 ApexBio 50 mg 825.6 EUR
Description: EPZ004777 is a potent and selective inhibitor of DOT1L, a protein methyltransferase catalyzing the methylation of lysine 4 of histone H3 (H3K4), with the half maximal inhibition concentration IC50 value of 400 pM [1].

Biperiden HCl

B1598-100 ApexBio 100 mg 495.6 EUR
Description: Biperiden HCl is an anticholinergic drug [1].As an anticholinergic drug, biperiden is first used in the treatment of Parkinson's disease. It is a competitive antagonist of muscarinic receptor.

Biperiden HCl

B1598-25 ApexBio 25 mg 176.4 EUR
Description: Biperiden HCl is an anticholinergic drug [1].As an anticholinergic drug, biperiden is first used in the treatment of Parkinson's disease. It is a competitive antagonist of muscarinic receptor.

Biperiden HCl

B1598-5.1 ApexBio 10 mM (in 1mL DMSO) 184.8 EUR
Description: Biperiden HCl is an anticholinergic drug [1].As an anticholinergic drug, biperiden is first used in the treatment of Parkinson's disease. It is a competitive antagonist of muscarinic receptor.

Biperiden HCl

B1598-500 ApexBio 500 mg 860.4 EUR
Description: Biperiden HCl is an anticholinergic drug [1].As an anticholinergic drug, biperiden is first used in the treatment of Parkinson's disease. It is a competitive antagonist of muscarinic receptor.

Donepezil HCl

B1602-1000 ApexBio 1 g 162 EUR
Description: Donepezil Hydrochloride (Donepezil HCL) is a novel, potent and selective inhibitor of acetylcholinesterase (AChE), an enzyme possibly involved in cognitive dysfunction of patients suffering Alzheimer?s disease (AD), with the half maximal inhibition concentration IC50 value of 6.7 nM [1].

Donepezil HCl

B1602-5.1 ApexBio 10 mM (in 1mL DMSO) 135.6 EUR
Description: Donepezil Hydrochloride (Donepezil HCL) is a novel, potent and selective inhibitor of acetylcholinesterase (AChE), an enzyme possibly involved in cognitive dysfunction of patients suffering Alzheimer?s disease (AD), with the half maximal inhibition concentration IC50 value of 6.7 nM [1].

Donepezil HCl

B1602-5000 ApexBio 5 g 370.8 EUR
Description: Donepezil Hydrochloride (Donepezil HCL) is a novel, potent and selective inhibitor of acetylcholinesterase (AChE), an enzyme possibly involved in cognitive dysfunction of patients suffering Alzheimer?s disease (AD), with the half maximal inhibition concentration IC50 value of 6.7 nM [1].

Labetalol HCl

B4795-100 ApexBio 100 mg 142.8 EUR

Labetalol HCl

B4795-200 ApexBio 200 mg 199.2 EUR

Labetalol HCl

B4795-5.1 ApexBio 10 mM (in 1mL DMSO) 142.8 EUR
×

Moreover, a number of different compounds are recognized (e.g., ethanol) that correlate with inhabitants density and originate from a number of VCP sources. Ethanol and fragrances are amongst the most considerable and reactive VOCs related to VCP emissions.

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