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Filtered Search Results
eMolecules 2804732-78-1 | 4-Amino-5-methyl-hexanoic acid ethyl ester hydrochloride | J&W PharmLab LLC209.710 | C9H20ClNO2 | 96.000 | Cl.CCOC(=O)CCC(N)C(C)C | 1g | 592890195
4-Amino-5-methyl-hexanoic acid ethyl ester hydrochloride | J&W PharmLab LLC | 2804732-78-1209.710 | C9H20ClNO2 | 96.000 | Cl.CCOC(=O)CCC(N)C(C)C | 1g | 592890195
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Chemscene ChemScene | 9-Bromononanoic acid | 5G | CS-W007587 | 0.98 | 41059-02-3| MFCD00046564 | 237.13
ChemScene | 9-Bromononanoic acid | 5G | CS-W007587 | 0.98 | 41059-02-3| MFCD00046564 | 237.13
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Medchemexpress LLC 5-hexynoic acid | 53293-00-8 | MFCD00066346 | ≥97.0% | 112.13 | C6H8O2 | 5g
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5-Hexynoic acid (Hex-5-ynoic acid) is a biochemical reagent that can be used as a biological material or organic compound for life science related research
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Medchemexpress LLC Octanoic acid (caprylic acid) | 124-07-2 | 99.85% | 144.21 | 10 G
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Octanoic acid, also known as Caprylic acid, is an oily liquid utilized in commercial applications such as the production of esters for perfumery and dyes. It is classified as a human endogenous metabolite and has demonstrated various biological activities, including acting as a tremor-suppressing agent.
- Used in commercial production of esters for perfumery and dyes.
- Functions as a tremor-suppressing agent.
- Potentiates glucose-stimulated insulin secretion in MIN6 cells.
- Induces neurite outgrowth in PC12 cells.
- Inhibits harmaline tremor in mouse models.
- Shows protective effects in Parkinson's disease models.
- Promotes branched-chain amino acid catabolism.
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Medchemexpress LLC 7-OCTYNOIC ACID 25G
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7-OCTYNOIC ACID 25G
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Medchemexpress LLC 6-METHYLHEPTANOIC AC 1G
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5000205613 6-METHYLHEPTANOIC AC 1G
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Chemscene CHEMSCENE
5000578153 2E -2-HEXENOIC ACID METHY 500G
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Medchemexpress LLC 8-HYDROXYOCTANOIC AC 100 mg
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8-HYDROXYOCTANOIC AC 100MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000741859 6-BROMOHEXANOIC ACID 10G
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Ambeed AMBEED
5000882127 BOC-7-AMINOHEPTANOIC ACI 10G
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Medchemexpress LLC 8-HYDROXYOCTANOIC AC 500 mg
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8-HYDROXYOCTANOIC AC 500MG
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Medchemexpress LLC Nonanoic acid (pelargonic acid) | 112-05-0 | 50 G
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Nonanoic acid is a naturally-occurring saturated fatty acid with nine carbon atoms. It significantly reduces bacterial translocation, enhances antibacterial activity, and remarkably increases the secretion of porcine β-defensins 1 (pBD-1) and pBD-2.
- Naturally-occurring saturated fatty acid
- Reduces bacterial translocation
- Enhances antibacterial activity
- Increases secretion of porcine β-defensins 1 (pBD-1) and pBD-2
- Upregulates endogenous host defense peptides
- Enhances intestinal epithelial immunological barrier function via histone deacetylase inhibition
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Medchemexpress LLC 2-methylheptanoic acid | 1188-02-9 | MFCD00142944 | 99.3% | 144.21 g/mol | C8H16O2 | 25 G
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2-Methylheptanoic acid is a branched C8 carboxylic acid (CAS 1188-02-9) supplied as a high-purity liquid and used as a flavoring ingredient isolated from honey. It is useful for flavor research and small-scale formulation work.
- Chemical formula C8H16O2.
- Molecular weight 144.21 g/mol.
- CAS number 1188-02-9.
- Purity 99.3%.
- Physical form liquid; density 0.906 g/cm3.
- Used as a flavoring ingredient isolated from honey.
- Available in pack sizes including 25 g.
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Matrix Scientific 5-METHYLHEXANOIC ACID-5G
5-Methylhexanoic acid, 97%; 5g,C7H14O2, MFCD00036494, mw 130.19, [628-46-6]
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Apexbio Technology LLC Ko 143 461054-93-3 5mg
Ko 143 (CAS 461054-93-3) is a selective inhibitor of the breast cancer resistance protein (BCRP/ABCG2) an ATP-binding cassette transporter implicated in multidrug resistance in cancer cells By targeting BCRP Ko 143 effectively blocks BCRP-mediated drug efflux as demonstrated by an EC90 of 26 nM in cell-based assays This compound exhibits over 200-fold selectivity for BCRP compared to P-glycoprotein and MRP1 In vitro Ko 143 reverses BCRP-mediated resistance to chemotherapeutics such as topotecan and mitoxantrone enhancing their potency up to tenfold in relevant cancer cell lines Ko 143 has been used in murine models to increase systemic exposure of BCRP substrates supporting its utility in studying drug resistance mechanisms and improving chemotherapeutic efficacy in preclinical research
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