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| Catharanthine Basic information |
Product Name: | Catharanthine | Synonyms: | (+)-3,4-didehydrocoronaridine;18-beta)-lph;catharanthin;ibogamine-18-carboxylicacid,3,4-didehydro-,methylester,(2-alpha,5-beta,6-a;7-Ethyl-9,10,12,13-tetrahydro-6,9-methano-5H-pyrido[1′,2′:1,2]azepino[4,5-b]indole-6(6aH)-carboxylic acid methyl ester;Catharanthine, 98%, from Catharanthus roseus (L.) G. Don;4-Didehydrocoronaridine;methyl(2-alpha,5-beta,6-alpha,18-beta)-3,4-didehydroibogamine-18-carboxylate | CAS: | 2468-21-5 | MF: | C21H24N2O2 | MW: | 336.43 | EINECS: | 219-586-6 | Product Categories: | chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Inhibitors;Heterocycles;Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals | Mol File: | 2468-21-5.mol | |
| Catharanthine Chemical Properties |
Melting point | 138-1400C | alpha | D27 +29.8° (CHCl3) | Boiling point | 472.9°C (rough estimate) | density | 1.1367 (rough estimate) | refractive index | 1.6500 (estimate) | storage temp. | Sealed in dry,Store in freezer, under -20°C | solubility | DMSO: soluble5mg/mL (clear solution; warmed) | form | powder | pka | 6.8(at 25℃) | color | white to beige | optical activity | [α]/D +30 to +38° (c=0.5, CDCl3) |
| Catharanthine Usage And Synthesis |
Chemical Properties | Off-White to Pale Beige Solid | Uses | Precursor of Vinblastine-type alkaloids | Uses | Anticancer | Uses | Catharanthine is an indole alkaloid analog and an inhibitor of TRPM8. | Definition | ChEBI: Catharanthine is an organic heteropentacyclic compound and monoterpenoid indole alkaloid produced by the medicinal plant Catharanthus roseus via strictosidine. It is a bridged compound, an organic heteropentacyclic compound, a methyl ester, a monoterpenoid indole alkaloid, a tertiary amino compound and an alkaloid ester. It is a conjugate base of a catharanthine(1+). | target | NO | Calcium Channel | Nicotinic receptor |
| Catharanthine Preparation Products And Raw materials |
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