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Reserpine

  Cat. No.:  DC82022   Featured
Chemical Structure
50-55-5
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More than 5000 active chemicals with high quality for research!
Field of application
Reserpine is an inhibitor of the vesicular monoamine transporter 2 (VMAT2).
Chemicals PropertiesBiological activity COA & MSDSRelated productsDatasheet
Cas No.: 50-55-5
Chemical Name: methyl (1S,2R,3R,4aS,13bR,14aS)-2,11-dimethoxy-3-((3,4,5-trimethoxybenzoyl)oxy)-1,2,3,4,4a,5,7,8,13,13b,14,14a-dodecahydroindolo[2',3':3,4]pyrido[1,2-b]isoquinoline-1-carboxylate
Synonyms: Reserpine, Reserpine phosphate, Raudixin, Serpalan, Serpasil
SMILES: O=C(OC)[C@H]1[C@@]2([H])C[C@](N(CC3)C[C@@]2([H])C[C@@H](OC(C4=CC(OC)=C(OC)C(OC)=C4)=O)[C@@H]1OC)([H])C5=C3C(C=CC(OC)=C6)=C6N5
Formula: C33H40N2O9
M.Wt: 608.688
Purity: >98%
Sotrage: 4°C for 1 year, -20°C for more than 2 years
Description: Reserpine is an inhibitor of the vesicular monoamine transporter 2 (VMAT2).
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
Cat. No. Product name Field of application
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DC74557 PREX-in1 PREX-in1 is a specific small-molecule inhibitor of P-Rex1 and P-Rex2 Rac-GEF activity with IC50 of 4.5 uM (P-Rex1 DHPH Rac-GEF activity) in liposome-based GEF assay, inhibits P-Rex1 and P-Rex2 through their catalytic DH domain.
DC74555 GYS32661 GYS32661 (GYS 32661) is a potent Rac inhibitor capable of inhibiting both Rac1 and Rac1b, inhibited activated Rac1 with IC50 of 1.18 uM in in vitro pull-down assays.
DC74539 L557-0155 L557-0155 is a small molecule inhibitor of VSIG-8, prevents VSIG-8 binding to VISTA, promotes cytokine production and cell proliferation in PBMCs and suppresses melanoma growth.
DC74528 K284 K284 is a selective small molecule inhibitor of chitinase 3 like1 (CHI3L1) with strong binding affinity (Kd=-9.7 kcal·mol-1), inhibits lung metastasis by blocking IL-13Rα2-mediated JNK-AP-1 signals.
DC74225 YB-537 YB-537 (YB537) is a potent, highly specific quinone reductase 2 (QR2) inhibitor with IC50 of 3 nM, shows no activity against QR1 (IC50>10 uM).
DC74218 UT-59 UT-59 is a specific inhibitor of cholesterol-sensing membrane protein Scap, binds to Scap's cholesterol-binding site, blocks SREBP activation and inhibits lipid synthesis.
DC74205 Tryptolinamide Tryptolinamide (TLAM) is a small-molecule compound that activates mitochondrial respiration in cybrids generated from patient-derived mitochondria and fibroblasts from patient-derived iPSCs, inhibits phosphofructokinase-1 (PFK1) with an ATP-uncompetitive
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