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11026-01-0

(24R)-20,24-Epoxy-5α-lanost-9(11)-ene-3β,6α,16β,25-tetrol is a complex chemical compound derived from lanostane triterpenoids, which are natural steroids found in various plant sources. It is characterized by its unique structure, with an epoxy group at the 20th and 24th positions, and hydroxyl groups at the 3rd, 6th, 16th, and 25th positions. The 24R stereochemistry indicates the configuration of the molecule at the 24th carbon atom. These structural features give this compound potential medicinal properties, including anti-inflammatory, anti-cancer, and anti-viral activities. Its structure also suggests that it may have applications in the development of new pharmaceuticals or as a potential lead compound for drug discovery.

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  • 11026-01-0 Structure

  • Basic information

    1. Product Name: (24R)-20,24-Epoxy-5α-lanost-9(11)-ene-3β,6α,16β,25-tetrol
    2. Synonyms: (24R)-20,24-Epoxy-5α-lanost-9(11)-ene-3β,6α,16β,25-tetrol;Sapogenin A
    3. CAS NO:11026-01-0
    4. Molecular Formula: C30H50O5
    5. Molecular Weight: 490.715
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 11026-01-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 607.2±55.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.16±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 14.57±0.29(Predicted)
    10. CAS DataBase Reference: (24R)-20,24-Epoxy-5α-lanost-9(11)-ene-3β,6α,16β,25-tetrol(CAS DataBase Reference)
    11. NIST Chemistry Reference: (24R)-20,24-Epoxy-5α-lanost-9(11)-ene-3β,6α,16β,25-tetrol(11026-01-0)
    12. EPA Substance Registry System: (24R)-20,24-Epoxy-5α-lanost-9(11)-ene-3β,6α,16β,25-tetrol(11026-01-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 11026-01-0(Hazardous Substances Data)

11026-01-0 Usage

Uses

Used in Pharmaceutical Industry:
(24R)-20,24-Epoxy-5α-lanost-9(11)-ene-3β,6α,16β,25-tetrol is used as a potential lead compound for drug discovery due to its unique structure and potential medicinal properties, including anti-inflammatory, anti-cancer, and anti-viral activities.
Used in Drug Development:
(24R)-20,24-Epoxy-5α-lanost-9(11)-ene-3β,6α,16β,25-tetrol is used in the development of new pharmaceuticals, as its structural features and potential medicinal properties make it a promising candidate for creating novel therapeutic agents.
Further research is needed to fully understand the chemical and biological properties of (24R)-20,24-Epoxy-5α-lanost-9(11)-ene-3β,6α,16β,25-tetrol and to explore its potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 11026-01-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,1,0,2 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 11026-01:
(7*1)+(6*1)+(5*0)+(4*2)+(3*6)+(2*0)+(1*1)=40
40 % 10 = 0
So 11026-01-0 is a valid CAS Registry Number.
InChI:InChI=1/C27H44O2.C15H16Cl3N3O2/c1-17-10-14-27(28-16-17)18(2)24-23(29-27)15-22-20-9-8-19-7-5-6-12-25(19,3)21(20)11-13-26(22,24)4;1-2-4-20(15(22)21-5-3-19-10-21)6-7-23-14-12(17)8-11(16)9-13(14)18/h17-24H,5-16H2,1-4H3;3,5,8-10H,2,4,6-7H2,1H3/t17-,18-,19?,20+,21-,22-,23-,24-,25-,26-,27+;/m0./s1

11026-01-0SDS

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 sieversigenin

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:11026-01-0 SDS

11026-01-0Upstream product

11026-01-0Relevant articles and documents

TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS. II. THE STRUCTURE OF CYCLOSIEVERSIGENIN

Svechnikova, A. N.,Umarova, R. U.,Gorovits, M. B.,Seitanudi, K. L.,Rashkes, Ya. V.,et al

, p. 60 - 67 (2007/10/02)

The bitter plant Astragalus sieversianus has yielded a new isoprenoid cyclosieversigenin the structure of which has been established on the basis of spectral characteristics and chemical transformations as 20(S),24(R)-epoxycycloartane-3β,6α,16β,25-tetraol.

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