Kryptogenin
Code | Size | Price |
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TAR-T32420-5mg | 5mg | £850.00 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here. |
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Overview
Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃
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Further Information
Bioactivity:
Kryptogenin, derived from carp bile, can be used to synthesize C27-intermediates in bile acid biosynthesis.
CAS:
468-99-5
Formula:
C27H42O4
Molecular Weight:
430.629
Purity:
0.98
SMILES:
[H][C@@]12CC(=O)[C@H]([C@H](C)C(=O)CCC(C)CO)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@@H](O)CC[C@]12C
References
1. Alessandrini L, Ciuffreda P, Santaniello E, Terraneo G. Clemmensen reduction of diosgenin and kryptogenin: synthesis of [16,16,22,22,23,23-(2)H(6)]-(25R)-26-hydroxycholesterol. Steroids. 2004 Dec;69(13-14):789-94. PubMed PMID: 15582533.
2. KAUFMANN S, ROSENKRANZ G. Steroidal sapogenins; transformation of kryptogenin into diosgenin and pseudodiosgenin. J Am Chem Soc. 1948 Oct;70(10):3502-5. PubMed PMID: 18891907.
3. ROSENKRANZ G, KAUFMANN S, et al. Steroidal sapogenins; new derivatives of kryptogenin. J Am Chem Soc. 1948 Oct;70(10):3518-20. PubMed PMID: 18933565.
4. Smith AG, Gilbert JD, Harland WA, Brooks CJ. The isolation of cholest-5-ene-3beta,26-diol from human brain. Biochem J. 1974 Jun;139(3):793-5. PubMed PMID: 4854921; PubMed Central PMCID: PMC1166347.