63785-19-3 Usage
Uses
Used in Pharmaceutical Industry:
(22β,25β)-3β-Amino-5α-solanidan-23β-ol is used as a pharmaceutical compound for its potential therapeutic applications. (22β,25β)-3β-Amino-5α-solanidan-23β-ol's unique structure and properties make it a promising candidate for the development of new drugs targeting various health conditions.
Used in Research and Development:
(22β,25β)-3β-Amino-5α-solanidan-23β-ol is used as a research compound for studying its chemical properties, structural characteristics, and potential interactions with biological systems. This research can lead to a better understanding of the compound's applications and its role in the development of new pharmaceuticals and therapies.
Used in Drug Delivery Systems:
(22β,25β)-3β-Amino-5α-solanidan-23β-ol can be used as a component in drug delivery systems, potentially enhancing the delivery, bioavailability, and therapeutic outcomes of other drugs. Its unique properties may allow for the development of novel drug carriers and formulations, improving the efficacy of existing treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 63785-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,8 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63785-19:
(7*6)+(6*3)+(5*7)+(4*8)+(3*5)+(2*1)+(1*9)=153
153 % 10 = 3
So 63785-19-3 is a valid CAS Registry Number.
InChI:InChI=1/C27H46N2O/c1-15-11-23(30)25-16(2)24-22(29(25)14-15)13-21-19-6-5-17-12-18(28)7-9-26(17,3)20(19)8-10-27(21,24)4/h15-25,30H,5-14,28H2,1-4H3/t15-,16+,17+,18+,19-,20+,21+,22+,23+,24+,25-,26+,27+/m1/s1
63785-19-3Relevant academic research and scientific papers
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.
