Ophiocarpine
| Code | Size | Price |
|---|
| TAR-T33811-5mg | 5mg | £850.00 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃
Documents
Further Information
Bioactivity:
Ophiocarpine is a protoberberine alkaloid.
CAS:
478-13-7
Formula:
C20H21NO5
Molecular Weight:
355.39
Purity:
0.98
SMILES:
COc1ccc2C(O)C3N(CCc4cc5OCOc5cc34)Cc2c1OC
References
OHTA M, TANI H, MOROZUMI S. THE STEREOCHEMISTRY OF HYDRASTINE, NARCOTINE, OPHIOCARPINE, AND THEIR DERIVATIVES. I. ABSOLUTE CONFIGURATION OF HYDRASTINE AND OPHIOCARPINE. Chem Pharm Bull (Tokyo). 1964 Sep;12:1072-80. PubMed PMID: 14245904.
Kametani T, Matsumoto H, Satoh Y, Nemoto H, Fukumoto K. Studies on the syntheses of heterocyclic compounds. Part 679. A stereoselective total synthesis of (+/-)-ophiocarpine; a simple route to 13-hydroxyberbines. J Chem Soc Perkin 1. 1977;4:376-82. PubMed PMID: 557491.
OHTA M, TANI H, MOROZUMI S, KODAIRA S. THE STEREOCHEMISTRY OF HYDRASTINE, NARCOTINE, OPHIOCARPINE, AND THEIR DERIVATIVES. II. ABSOLUTE CONFIGURATION OF NARCOTINE AND THEIR DERIVATIVES. Chem Pharm Bull (Tokyo). 1964 Sep;12:1080-9. PubMed PMID: 14245270.
Jeffs PW, Scharver JD. Biosynthesis of ophiocarpine. Introduction of a stereospecific label through transannular cyclization. J Am Chem Soc. 1976 Jul 7;98(14):4301-10. PubMed PMID: 932362.