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(25R)-3β-Hydroxy-5α-spirost-9(11)-en-12-one is a naturally occurring steroidal saponin, which belongs to the spirostane family of compounds. It is characterized by its unique chemical structure, featuring a 3β-hydroxyl group, a 5α-spirostane skeleton, and a 9(11)-en-12-one functional group. (25R)-3β-Hydroxy-5α-spirost-9(11)-en-12-one is typically found in various plant species, particularly in the genus Solanum, and has been studied for its potential biological activities, such as anti-inflammatory, anti-cancer, and immunomodulatory effects. The specific stereochemistry at the 25th carbon position (25R) is crucial for its biological properties, and the compound's structure plays a significant role in its interactions with target proteins and receptors. Research on this chemical and its derivatives continues to explore their potential applications in medicine and pharmacology.

3514-26-9

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3514-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3514-26-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3514-26:
(6*3)+(5*5)+(4*1)+(3*4)+(2*2)+(1*6)=69
69 % 10 = 9
So 3514-26-9 is a valid CAS Registry Number.
InChI:InChI=1/C27H40O4/c1-15-7-10-27(30-14-15)16(2)24-22(31-27)12-21-19-6-5-17-11-18(28)8-9-25(17,3)20(19)13-23(29)26(21,24)4/h13,15-19,21-22,24,28H,5-12,14H2,1-4H3/t15-,16+,17+,18+,19-,21+,22+,24+,25+,26-,27?/m1/s1

3514-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-Dehydrohecogenin

1.2 Other means of identification

Product number -
Other names -

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:3514-26-9 SDS

3514-26-9Relevant academic research and scientific papers

Two new steroidal saponins with antifungal activity from Hosta plantaginea rhizomes

Wang, Mengyue,Xu, Zihan,Peng, Ying,Zhong, Guoyue,Li, Xiaobo

, p. 1047 - 1051 (2018/03/21)

Two new steroidal saponins, (25R)-3β-hydroxy-5α-spirost-9-en-12-one 3-O-β-D-galactopyranoside (hostasaponin A, 1), and (25R)-2α,3β-dihydroxy-5α-spirost-12-one 3-O-β-D-galactopyranoside (hostasaponin B, 2), together with a new natural product, 2α,3β-dihydroxy-5α-pregn-16-en-20-one (3), were isolated from the rhizomes of Hosta plantaginea, a perennial herb used mainly as an ornamental plant and folk medicine for fungal infection and various inflammations. The active evaluation results showed that 1 and 2 possess potent inhibition activity against Candida albicans, with MIC values less than 20 μg/mL.

Simple and convenient method for the synthesis of Δ9(11)-3-hydroxy, Δ1,4- and Δ1,4,9(11)-3-ketosteroids by selective dehydrogenation of 3-hydroxy-12-ketosteroids

Kongkathip, Boonsong,Kongkathip, Ngampong,Khunnavutimanotum, Ponsak,Sakee, Uthai

, p. 1207 - 1208 (2007/10/03)

Hecogenin can be selectively dehydrogenated to the corresponding Δ9(11)-3-hydroxysteroid, Δ1,4- and Δ1,4,9(11)-ketosteroids by the treatment of 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) with a variety of solvents.

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