Bioactive Small Molecules
A vast array of small, non-peptide, organic compounds that are biologically active. Products include receptor antagonists, molecular probes, metabolites, GPCR ligands, neurotransmitters, ion channel modulators, and signaling activators and inhibitors.
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7,141
Medchemexpress LLC CADHERIN-1/CD324 MO 50UG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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5000178338 CADHERIN-1/CD324 MO 50UG
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7,142
Medchemexpress LLC ANTICANCER AGENT 7 10MG
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5000210124 ANTICANCER AGENT 7 10MG
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7,143
Medchemexpress LLC 1- PYRIMIDIN-5-YL ET 1G
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5000210177 1- PYRIMIDIN-5-YL ET 1G
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7,144
Medchemexpress LLC BOC-D-ARG PBF -OH 5G
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5000210178 BOC-D-ARG PBF -OH 5G
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7,145
Medchemexpress LLC 2-METHYLPYRAZINE-D6 5MG
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5000210524 2-METHYLPYRAZINE-D6 5MG
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7,146
Medchemexpress LLC 3-CYANOBICYCLO 1.1.1 100MG
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5000210525 3-CYANOBICYCLO 1.1.1 100MG
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7,147
![Medchemexpress LLC 1-[(9H-Fluoren-2-yl)methyl]-1-cycloheptyl-3-mesitylurea | 138046-43-2 | MFCD00905424 | >98.0% | 452.63 g·mol⁻¹ | C31H36N2O | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000239905.png-250.jpg)
Medchemexpress LLC 1-[(9H-Fluoren-2-yl)methyl]-1-cycloheptyl-3-mesitylurea | 138046-43-2 | MFCD00905424 | >98.0% | 452.63 g·mol⁻¹ | C31H36N2O | 25 MG
Small and Specialty Supplier Partner
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Small and Specialty Supplier Partner
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YM-750 is a research-grade acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor with reported in vitro potency (IC50 = 0.18 μM). It is used in biochemical and cellular studies to probe cholesterol esterification and lipid metabolism. Key chemical identifiers include CAS 138046-43-2, formula C31H36N2O, and molecular weight 452.63 g·mol⁻¹.
- Potent ACAT inhibitor (IC50 0.18 μM).
- Suitable for biochemical and cellular assays.
- High purity suitable for research (>98% by HPLC).
- Available as solids and as a DMSO solution in multiple package sizes.
- Consistent chemical identity: CAS 138046-43-2 and formula C31H36N2O.
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7,148
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000288512 MYC-IN-3 10MG
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7,149
REAGENTS DIRECT
NC3923172 PD0325901 MEK INHIBITOR 99.7
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7,150
Medchemexpress LLC MEDCHEMEXPRESS LLC
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NC3970870 CANERTINIB-READY FOR RECONSTIT
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7,151
HARRIS PRODUCTS GROUP
NC3981122 702-050-320BE
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7,152
Medchemexpress LLC MYC-IN-3 | 3042878-82-7 | 98.7% | 543.89 | 100 MG
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MYC-IN-3 (compound 37) is a potent MYC inhibitor that demonstrates antiproliferative and anticancer activity. It shows potential for research related to prostate cancer.
- Potent MYC inhibitor.
- Shows antiproliferative activity.
- Shows anticancer activity.
- Has potential for the research of prostate cancer.
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7,153
Medchemexpress LLC L-galactono-1,4-lactone | 1668-08-2 | MFCD00066466 | 98.0% | 178.14 g/mol | C6H10O6 | 100 MG
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L-galactono-1,4-lactone is a white to off-white solid biochemical reagent used in laboratory research, notably as an intermediate in ascorbate (vitamin C) biosynthesis and in enzymatic assays. For research use only; not for human therapeutic use.
- Purity 98.0%.
- Molecular weight 178.14 g/mol.
- Available in multiple pack sizes (5 mg, 10 mg, 50 mg, 100 mg, 200 mg, 500 mg).
- Storage: room temperature stability for 3 years; in solvent -80°C for 2 years, -20°C for 1 year.
- Appearance white to off-white solid.
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7,154
Medchemexpress LLC IACS-8803 disodium | 2243079-36-7 | 99.97% | 1 ML
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IACS-8803 disodium is a highly potent cyclic dinucleotide STING agonist that exhibits robust systemic antitumor efficacy.
- Highly potent cyclic dinucleotide STING agonist
- Exhibits robust systemic antitumor efficacy
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7,155
Medchemexpress LLC MMG-11 | 313254-94-3 | 306.27 | 100 MG
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MMG-11 is a potent and selective human TLR2 antagonist with low cytotoxicity. It inhibits both TLR2/1 and TLR2/6 signaling with IC50s of 1.7 μM for Pam3CSK4-induced hTLR2/1 and 5.7 μM for Pam2CSK4-induced hTLR2/6 responses.
- Potent and selective human TLR2 antagonist.
- Low cytotoxicity.
- Inhibits both TLR2/1 and TLR2/6 signaling with IC50s of 1.7 μM for Pam3CSK4-induced hTLR2/1 and 5.7 μM for Pam2CSK4-induced hTLR2/6 responses.
- Does not show cellular toxicity or interference with signaling induced by other TLR agonists, IL-1β or TNF.
- Exhibits no cytotoxic effects up to 100 μM in peripheral blood mononuclear cells (PBMCs).
- Effective inhibition of TLR2/1 and TLR2/6 signaling.
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