4356-25-6 Usage
Molecular Structure
A complex structure consisting of a cholestane backbone fused to an indole ring.
Compound Type
An uncommon steroid derivative.
Potential Activities
Pharmacological and biological activities, though limited research has been conducted.
Biological Effects of Cholestane Derivatives
Anti-inflammatory, antitumor, and neuroprotective properties.
Uniqueness
The fusion of cholestane and indole structures may result in unique biological activities.
Research Interest
An interesting target for further exploration in drug development and medical research.
Check Digit Verification of cas no
The CAS Registry Mumber 4356-25-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,5 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4356-25:
(6*4)+(5*3)+(4*5)+(3*6)+(2*2)+(1*5)=86
86 % 10 = 6
So 4356-25-6 is a valid CAS Registry Number.
InChI:InChI=1/C33H49N/c1-21(2)9-8-10-22(3)27-15-16-28-25-14-13-23-19-31-26(24-11-6-7-12-30(24)34-31)20-33(23,5)29(25)17-18-32(27,28)4/h6-7,11-12,21-23,25,27-29,34H,8-10,13-20H2,1-5H3/t22-,23+,25+,27-,28+,29+,32-,33+/m1/s1
4356-25-6Relevant academic research and scientific papers
Cholesteno-Indoles, I. Preparation of 1'H-5α-Cholest-2-enoindoles
Samu, Janos,Botyanszki, Janos,Duddeck, Helmut,Snatzke, Guenther
, p. 1225 - 1228 (2007/10/02)
1'H-5α-Cholest-2-enoindole (1a), the corresponding N-methyl, N-acetyl, and N-formyl compounds 1b-d, as well as the respective methoxy derivatives 2b-5d have been synthesized as model compounds for intended CD investigations.Application of the Fischer indole synthesis afforded the compounds 1a-5a which were N-methylated to 1b-5b, N-acetylated to 1c-5c, and N-formylated to 1d-5d. - Key Words: Fischer indole synthesis / Cholestenoindoles / Cholestenes / Steroids