11004-30-1 Usage
Uses
Used in Pharmaceutical Industry:
(22S,25R)-5α-Solanidan-3β-ol is used as a potential therapeutic agent for its antitumor properties, offering a novel approach to cancer treatment by targeting and inhibiting tumor growth and progression.
(22S,25R)-5α-Solanidan-3β-ol is also used as an anti-inflammatory agent, leveraging its ability to reduce inflammation and alleviate symptoms associated with various inflammatory conditions.
Furthermore, (22S,25R)-5α-Solanidan-3β-ol is utilized as an antifungal agent, providing an alternative treatment option for combating fungal infections and their associated complications.
Check Digit Verification of cas no
The CAS Registry Mumber 11004-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,1,0,0 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 11004-30:
(7*1)+(6*1)+(5*0)+(4*0)+(3*4)+(2*3)+(1*0)=31
31 % 10 = 1
So 11004-30-1 is a valid CAS Registry Number.
InChI:InChI=1/C27H45NO/c1-16-5-8-23-17(2)25-24(28(23)15-16)14-22-20-7-6-18-13-19(29)9-11-26(18,3)21(20)10-12-27(22,25)4/h16-25,29H,5-15H2,1-4H3/t16-,17-,18+,19+,20-,21+,22+,23+,24+,25+,26+,27+/m1/s1
11004-30-1Relevant articles and documents
Confirmation of Structure of Isosolacapine: Stereochemistry at Ring Juncture of Indolizidine Moiety of 22βH Solanidanes by 13C and 1H NMR Spectroscopy
Chakravarty, Ajit K.,Pakrashi, Satyesh C.
, p. 311 - 313 (2007/10/02)
Isosolacapine, a minor steroidal alkaloid of Solanum pseudocapsicum, earlier assigned structure 3, possesses a novel 22β N stereochemistry in a 22,26-epiminocholestane skeleton.This alkaloid has now been isolated from Solanum capsicastrum and its structure confirmed by its conversion to solanogantamine (8), a 22αH solanidane derivative ex Solanum giganteum.The ring-juncture stereochemistry of the indolizidine moiety of 22β H solanidanes, in general, has been elucidated on 13C and 1H NMR spectral evidences.
