Bioactive Small Molecules
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Filtered Search Results
Creative Biomart Recombinant Protein 377.43 Inquiry Inquiry 10 MG 1/EA
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p38 Inhibitor
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Cayman Chemical F2201, Purity: ≥98%, CAS: 1391485-39-4, 10 mg
F2201 is an analog of AM2201 with a fluorine at the 4 position of the naphthyl group. The physiological and toxicological properties of this compound have not been delineated. This product is intended for research and forensic purposes.
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Cayman Chemical CMP8, Purity: ≥98%, CAS: 851107-28-3, 1 mg
A mutant ERα antagonist and ligand used for bump and hole; is selective for ERα containing three substitutions, ErαL384M, ErαM421G, and ErαG521R, over the wild-type ERα and ERβ (IC50s= 29, 1,085, and 2,232 nM, respectively); reduces reporter gene expression in HeLa cells expressing the triple mutant ERα (EC50 = 41 nM).
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Medchemexpress LLC N-(3-{[5-chloro-4-(1H-indol-3-yl)pyrimidin-2-yl]amino}phenyl)-3-[4-(dimethylamino)but-2-enamido]... | 1604810-84-5 | 98.0% | 5 MG
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THZ2 is a potent, selective covalent inhibitor of cyclin-dependent kinase 7 (CDK7) with low-nanomolar inhibitory activity (IC50 ≈ 13.9 nM). It is used in vitro and in vivo to study transcriptional regulation and oncogenic proliferation, particularly in triple-negative breast cancer models.
- Potent CDK7 inhibition with IC50 of ~13.9 nM.
- Selective activity in the low-nanomolar range for cellular and biochemical assays.
- Demonstrated anti-proliferative and pro-apoptotic effects in triple-negative breast cancer models.
- Supplied as a solid; soluble in DMSO and available in multiple pack sizes for research use.
- Molecular formula C31H28ClN7O2, molecular weight 566.05 g/mol.
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Cayman Chemical Octodrine (hydrochloride), Purity: ≥95%, CAS: 5984-59-8, 5 mg
An analytical reference standard categorized as a stimulant; intended for research and forensic applications
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Cayman Chemical SPA70, Purity: ≥90%, CAS: 931314-31-7, 10 mg
A PXR antagonist (IC50 = 0.51 µM); selective for PXR over 10 additional nuclear receptors at >5 µM, as well as over a panel of 384 kinases at 10 µM; inhibits rifampicin-induced PXR activation from 0.1-10 µM; inhibits rifampicin-induced CYP3A4 activity in primary human hepatocytes; inhibits PXR agonist-induced CYP3A4-mediated metabolism of midazolam and paclitaxel in hPXR-tg mice at 200 mg/kg
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Cayman Chemical 6-Deoxypenciclovir, Purity: ≥95%, CAS: 104227-86-3, 5 mg
An inactive metabolite of famciclovir; a precursor metabolite to penciclovir; has been used in the synthesis of prodrug forms of penciclovir
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Medchemexpress LLC Iso-VQA-ACC acetate | 99.5% | 625.63 | 5 MG
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Iso-VQA-ACC acetate is a substrate for constitutive proteasome, typically appearing as a white to off-white solid.
- Functions as a substrate for constitutive proteasome
- Targets proteasome activity
- Involved in the metabolic enzyme/protease pathway
- Molecular sequence: iso-Val-Gln-Ala-{ACC}
- Achieves a purity of 99.5% by HPLC
- Structure confirmed by MS analysis
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eMolecules 522649-59-8 | Medchem Express | Malic enzyme inhibitor ME1 | 1mg | 495800183 | HY-124861 | 351.406 | C20H21N3O3
Medchem Express | Malic enzyme inhibitor ME1 | 1mg | 495800183 | HY-124861 | 522649-59-8 | 351.406 | C20H21N3O3
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Cayman Chemical GBT-440, Purity: ≥98%, CAS: 1446321-46-5, 5 mg
A modulator of sickle hemoglobin; increases HbS affinity for oxygen (EC50s = 8.2 and 415 μM for purified HbS and whole blood from sickle cell anemia patients, respectively); delays oxygen release from and polymerization of HbS in a concentration-dependent manner; increases red blood cell half-life and reduces sickling ex vivo in whole blood isolated from a murine model of sickle cell anemia
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Medchemexpress LLC 3-isobutyl-1-methylxanthine | 28822-58-4 | MFCD00005584 | 222.24 g/mol | C10H14N4O2 | 5MG
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IBMX (3-isobutyl-1-methylxanthine) is a broad-spectrum phosphodiesterase (PDE) inhibitor used as a research reagent and analytical standard. It raises intracellular cyclic AMP and cyclic GMP by inhibiting multiple PDE isoforms and is commonly used in biochemical and cell-based assays. Reported IC50 values reflect activity against several PDE families.
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Medchemexpress LLC EMT inhibitor-2 | 2232228-60-1 | 98.8% | 25 MG
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EMT inhibitor-2 (Compound 1) inhibits epithelial-mesenchymal transition (EMT) induced by substances such as IL-1β and TGF-β released from immunocytes. It also inhibits CYP3A4 testosterone and CYP2C9 with IC50s of 49.72 and 5.54 μM, respectively.
- Inhibits epithelial-mesenchymal transition (EMT)
- Inhibits CYP3A4 testosterone
- Inhibits CYP2C9
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Cayman Chemical Darusentan, Purity: ≥98%, CAS: 171714-84-4, 1 mg
An ETA receptor antagonist (Ki = 13 nM in rat aortic vascular smooth muscle cells); inhibits ET-1-induced contractions in isolated rat aortic rings and mesenteric microvessels (pA2s = 8.1 and 7.97, respectively); decreases systolic blood pressure in DOCA-salt hypertensive rats at 50 mg/kg; decreases MAP and LVDP in normotensive pigs at 1 and 5 mg/kg; reduces myocardial infarct size as a percentage of the area at risk in a porcine model of LAD coronary artery ligation-induced ischemia-reperfusion injury
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Cayman Chemical 4-Methyl-7-(4-nitrophenoxy)-2H-chromen-2-one, Purity: ≥98%, CAS: 1644277-00-8, 5 mg
A fluorescent coumarin derivative; ex/em = 323/445 nm, respectively
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Cayman Chemical Cypermethrin-d9, Purity: ≥99% deuterated forms (d1-d9), 5 mg
An internal standard for the quantification of cypermethrin by GC- or LC-MS
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