Bioactive Small Molecules
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Filtered Search Results
Cayman Chemical ANTIBODY SpInorphIn 500ug
A peptide inhibitor of enkephalin-degrading enzymes; inhibits aminopeptidase, dipeptidyl aminopeptidase, ACE, and enkephalinase (IC50s = 3.3, 1.4, 2.4, and 10 UG/ml, respectively, for the monkey brain enzymes); selective for these enzymes over human serum aminopeptidase A (IC50 = >100 UG/ml), as well as porcine kidney aminopeptidase B, aminopeptidase M, and DPP-1, -2, -3, and -4 (IC50s = >55 UG/ml for all); inhibits chemotaxis, production of ROS, and exocytosis of glucuronidase and collagenase in PMNs; potentiates enkephalin-induced action potentials in rat hippocampal slices; enhances the antinociceptive effects of Leu-enkephalin in mice at 5 UG/animal
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Cayman Chemical CVT-6883, Purity: ≥98%, CAS: 752222-83-6, 1 mg
An adenosine A2B receptor antagonist (Ki = 22 nM); selective for adenosine A2B over adenosine A1, A2A, and A3 receptors (Kis = 1,940, 3,280, and 1,070 nM, respectively), as well as a panel of 84 proteins at 10 µM; decreases allergen challenge-induced BALF eosinophil and lymphocyte infiltration and airway reactivity in a mouse model of allergic asthma at 6 mg/kg; decreases fibrosis in the non-infarct zone, improves ejection fractions, and reduces ventricular tachycardia in a rat model of myocardial infarction
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Medchemexpress LLC GPNMB/Osteoactivin 5ug
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Recombinant human GPNMB (Osteoactivin), expressed in HEK293 cells with a C-terminal His tag, is supplied as a lyophilized, glycosylated protein of >95% purity and is functionally active in cell-based assays. It is intended for in vitro receptor binding, signaling studies, and assay development; aliquot and store frozen after reconstitution to preserve activity.
- High purity glycosylated protein suitable for functional assays.
- Expressed in mammalian cells for native post-translational modifications.
- Lyophilized format for long-term storage and transport.
- Validated activity in cell proliferation assays.
- Stable when aliquoted and stored at -20°C or -80°C for extended storage.
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Cayman Chemical YVAD-CHO (trifluoroacetate salt), Purity: ≥95%, 5 mg
A caspase-1/ICE inhibitor; prevents ICE-like and CPP32-like proteinase activity and inhibits apoptosis induced by ceramide or irinotecan in 4B1 cells at 600 µM; prevents chromogranin A-induced cell death of primary rat microglia at 100 µM
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Cayman Chemical Tauro-Obeticholic Acid (sodium salt), Purity: ≥98%, CAS: 2278141-79-8, 5 mg
An active metabolite of obeticholic acid
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Medchemexpress LLC Oncrasin-72 | 92407-90-4 | 97.6% | 271.74 | C16H14ClNO | 5 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Oncrasin-72 is a synthetic small-molecule research compound reported to inhibit RNA polymerase II and to induce cell death in susceptible human cancer cell lines. It is offered in milligram-scale quantities for laboratory use and is characterized by its published chemical identifiers and analytical purity.
- Provides well-characterized small-molecule activity for mechanistic studies.
- High chemical purity suitable for in vitro research applications.
- Available in multiple milligram pack sizes for flexible dosing.
- Appropriate for cellular assays and transcriptional regulation studies.
- Documented chemical identifiers simplify database referencing.
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Cayman Chemical 3,5,6,7,8,3',4'-Heptamethoxyflavone, Purity: ≥98%, CAS: 1178-24-1, 5 mg
A polymethoxyflavone; inhibits the efflux of Hoechst 33342 by BCRP and rhodamine 123 by P-gp in MDCK cells expressing the human transporters (IC50s = 1.4 and 31 µM, respectively); prevents UVB-induced decreases in type I procollagen in HDFn cells at 50, 100, and 200 µg/ml; inhibits the proliferation of B16 melanoma 4A5, CCRF-HSB-2 leukemia, and TGBC11TKB gastric cancer cells (IC50s = 38, 29, and 9 µM, respectively); prevents corticosterone-induced increases in immobility time in the forced swim test in mice at 50 mg/kg
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Medchemexpress LLC 3'-((3-hydroxy-2,4-dioxo-3,4-dihydrothieno[3,2-d]pyrimidin-1(2H)-yl)methyl)-biphenyl-4-carboxamide | 824983-94-0 | 99.9% | 25 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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FEN1-IN-2 is a small-molecule inhibitor of flap endonuclease 1 (FEN1) used for biochemical and cellular research. It potently inhibits FEN1 (IC50 3 nM) and shows activity against XPG (IC50 226 nM).
- Potent FEN1 inhibitor with an IC50 of 3 nM.
- Shows measurable activity against XPG (IC50 226 nM).
- High purity suitable for research use (99.94%).
- Molecular weight 393.42 g/mol, formula C20H15N3O4S.
- Available in 25 MG quantities for laboratory experiments.
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Cayman Chemical M2I-1, Purity: ≥98%, CAS: 312271-03-7, 5 mg
An inhibitor of the Mad2-Cdc20 interaction; inhibits Mad2 binding to Cdc20111-138 from 6.25-100 μM; reduces paclitaxel-induced increases in mitotic duration in HeLa cells at 25 μM; reduces 4-cell embryo and blastocyst formation in hydrogen peroxide-exposed mouse zygotes from 20-120 μM, as well as increases the rate of sex chromosome mosaicism in male mouse in vitro fertilization-derived embryos
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Cayman Chemical CHM-1, Purity: ≥98%, CAS: 154554-41-3, 1 mg
An inhibitor of tubulin polymerization (IC50 = 0.68 µM); inhibits chochicine tubulin binding at 5 µM; inhibits the growth of K562, NCI H226, HCT116, OVCAR-3, RXF 393L, SK-MEL-5, SF-268, and SF-295 cancer cells (mean GI50 = 130 nM); induces apoptosis in HA22T hepatocellular carcinoma cells; reduces tumor volume and increases survival in an HA22T mouse xenograft model at 10 mg/kg
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Cayman Chemical Lidocaine-d10, Purity: ≥99% deuterated forms (d1-d10), CAS: 851528-09-1, 5 mg
An internal standard for the quantification of lidocaine by GC- or LC-MS
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Cayman Chemical Lotusine, Purity: ≥98%, CAS: 6871-67-6, 5 mg
An alkaloid with diverse biological activities; increases cAMP levels in rat myocardium at 0.1-3 µM and cGMP levels in rabbit corpus cavernosum in a concentration-dependent manner; prevents doxorubicin-induced lipid peroxidation in H9c2 embryonic rat cardiomyocytes; increases LVP, LVEDP, and SAP in anesthetized rats at 5 mg/kg
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Cayman Chemical BB-22 7-hydroxyisoquinoline isomer, Purity: ≥98%, CAS: 2365471-55-0, 5 mg
BB-22 7-hydroxyisoquinoline isomer differs from BB-22 structurally by having the quinoline group replaced with an isoquinoline group attached at its seven position; intended for forensic and research applications
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Cayman Chemical PRT060318, Purity: ≥98%, CAS: 1194961-19-7, 5 mg
A potent and selective Syk inhibitor (IC50 = 4 nM); inhibits 92% of Syk activity, while other kinases retain >70% activity, at a concentration of 50 nM in a panel of 270 kinases; inhibits convulxin-induced aggregation of human platelet-rich plasma (IC50 = 2.5 μM); prevents thrombosis in a transgenic mouse model of heparin-induced thrombocytopenia; induces CLL B cell apoptosis and inhibits the secretion of chemokines CCL3, CCL4, and CXCL13; inhibits CLL B cell chemotaxis and pseudoemperipolesis
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Cayman Chemical Folitixorin, Purity: ≥75% (mixture of diastereomers), CAS: 3432-99-3, 5 mg
A reduced form of folate and cofactor for thymidylate synthetase; forms a ternary complex with thymidylate synthetase and FdUMP that inhibits thymidylate synthetase activity and DNA synthesis; has synergistic or additive cytotoxic effects against LS 174 or HT-29 human colon cancer cells, respectively, when used in combination with 5-fluorouracil; increases survival and reduces tumor growth in an HT-29 mouse xenograft model at 0.6 mg/animal when administered in combination with 5-fluorouracil
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