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11004-30-1

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11004-30-1 Usage

Description

(22S,25R)-5α-Solanidan-3β-ol is a complex chemical compound belonging to the solanidane alkaloid class, derived from Solanum species plants. It has demonstrated intriguing biological activities, such as antitumor, anti-inflammatory, and antifungal effects, making it a promising candidate for pharmaceutical research and development.

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

11004-30-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 22(S),25(R)-demissidine

1.2 Other means of identification

Product number -
Other names 5α,22β25αH-solanidan-3β-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:11004-30-1 SDS

11004-30-1Downstream Products

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.

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