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(25R)-5α-Spirostane-2α,3β,5-triol is a naturally occurring spirostane-type steroid compound found in plants, particularly in species of the Cucurbitaceae family. It features a spirostane backbone with hydroxyl groups at the 2nd, 3rd, and 5th positions, which may allow it to interact with specific receptors in the body and exhibit biological activity. (25R)-5α-Spirostane-2α,3β,5-triol has been studied for its potential pharmacological properties, such as anti-inflammatory and immunomodulatory effects, and is being investigated as a natural alternative for the treatment of various health conditions.

546-37-2

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546-37-2 Usage

Uses

Used in Pharmaceutical Industry:
(25R)-5α-Spirostane-2α,3β,5-triol is used as a potential therapeutic agent for its anti-inflammatory and immunomodulatory effects. It is being explored as a natural alternative for the treatment of various health conditions due to its ability to interact with specific receptors in the body and exhibit biological activity.
Used in Research and Development:
(25R)-5α-Spirostane-2α,3β,5-triol serves as a subject of study for its potential pharmacological properties. Further research on (25R)-5α-Spirostane-2α,3β,5-triol may contribute to the development of new pharmaceuticals by uncovering its therapeutic potential and understanding its interactions with biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 546-37-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 546-37:
(5*5)+(4*4)+(3*6)+(2*3)+(1*7)=72
72 % 10 = 2
So 546-37-2 is a valid CAS Registry Number.

546-37-2SDS

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 agapanthagenin

1.2 Other means of identification

Product number -
Other names Agapanthagenin

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:546-37-2 SDS

546-37-2Downstream Products

546-37-2Relevant academic research and scientific papers

Agapanthussaponins A-D, new potent cAMP phosphodiesterase inhibitors from the underground parts of Agapanthus inapertus

Nakamura,Mimaki,Sashida,Nikaido,Ohmoto

, p. 1784 - 1789 (1993)

The saponin fraction prepared from the methanolic extract of the underground parts of Agapanthus inapertus was found to exhibit inhibitory activity on cAMP phosphodiesterase (55.2%) at a concentration of 100 μg/ml. From this fraction, four new steroidal saponins, designated as agapanthussaponin A (1), B (2), C (3) and D (4), were isolated as the active principles, along with an inactive new furostanol saponin (5). The structures of 1-5 were determined by spectroscopic data and hydrolysis. The IC50 of 1- 4 on cAMP phosphodiesterase were 0.7, 1.2, 1.1 and 2.0 (x 10-5 M), respectively, which are more potent than that of papaverine (IC50 3.0 x 10-5 M).

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