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892869-55-5

(3beta)-3-Hydroxy-2-(hydroxyimino)olean-12-en-28-oic acid phenylmethyl ester is a chemical compound derived from oleanolic acid, a naturally occurring triterpenoid found in many plants. It possesses potential medicinal properties, including anti-inflammatory, anti-cancer, and anti-diabetic effects. Its phenylmethyl ester form is a modified derivative of oleanolic acid, which may increase its stability and bioavailability.
Used in Pharmaceutical Industry:
(3beta)-3-Hydroxy-2-(hydroxyimino)olean-12-en-28-oic acid phenylmethyl ester is used as a potential pharmaceutical drug for various health conditions due to its anti-inflammatory, anti-cancer, and anti-diabetic effects. Its phenylmethyl ester form may enhance its stability and bioavailability, making it a promising candidate for the development of new medications.
However, further study is needed to fully understand its biological activities and therapeutic potential.

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  • (3beta)-3-Hydroxy-2-(hydroxyimino)olean-12-en-28-oic acid phenylmethyl ester

    Cas No: 892869-55-5

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  • (3beta)-3-Hydroxy-2-(hydroxyimino)olean-12-en-28-oic acid phenylmethyl ester

    Cas No: 892869-55-5

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  • (3beta)-3-Hydroxy-2-(hydroxyimino)olean-12-en-28-oic acid phenylmethyl ester

    Cas No: 892869-55-5

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  • 892869-55-5 Structure

  • Basic information

    1. Product Name: (3beta)-3-Hydroxy-2-(hydroxyimino)olean-12-en-28-oic acid phenylmethyl ester
    2. Synonyms: (3β)-3-Hydroxy-2- (hydroxyimino)- olean- 12-en-28-oic acid phenylmethyl ester;(3BETA)-3-HYDROXY-2-(HYDROXYIMINO)OLEAN-12-EN-28-OIC ACID PHENYLMETHYL ESTER
    3. CAS NO:892869-55-5
    4. Molecular Formula: C37H53NO4
    5. Molecular Weight: 575.82
    6. EINECS: N/A
    7. Product Categories: Pentacyclic Triterpenes
    8. Mol File: 892869-55-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: 1.602
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (3beta)-3-Hydroxy-2-(hydroxyimino)olean-12-en-28-oic acid phenylmethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3beta)-3-Hydroxy-2-(hydroxyimino)olean-12-en-28-oic acid phenylmethyl ester(892869-55-5)
    11. EPA Substance Registry System: (3beta)-3-Hydroxy-2-(hydroxyimino)olean-12-en-28-oic acid phenylmethyl ester(892869-55-5)

  • 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: 892869-55-5(Hazardous Substances Data)

892869-55-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 892869-55-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,2,8,6 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 892869-55:
(8*8)+(7*9)+(6*2)+(5*8)+(4*6)+(3*9)+(2*5)+(1*5)=245
245 % 10 = 5
So 892869-55-5 is a valid CAS Registry Number.
InChI:InChI=1/C37H53NO4/c1-32(2)17-19-37(31(40)42-23-24-11-9-8-10-12-24)20-18-35(6)25(26(37)21-32)13-14-29-34(5)22-27(38-41)30(39)33(3,4)28(34)15-16-36(29,35)7/h8-13,26,28-30,39,41H,14-23H2,1-7H3/b38-27-/t26-,28-,29+,30-,34-,35+,36+,37-/m0/s1

892869-55-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzyl (2Z,3β)-3-hydroxy-2-(hydroxyimino)olean-12-en-28-oate

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

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More Details:892869-55-5 SDS

892869-55-5Downstream Products

892869-55-5Relevant articles and documents

Pentacyclic triterpenes. Part 3: Synthesis and biological evaluation of oleanolic acid derivatives as novel inhibitors of glycogen phosphorylase

Chen, Jun,Liu, Jun,Zhang, Luyong,Wu, Guanzhong,Hua, Weiyi,Wu, Xiaoming,Sun, Hongbin

, p. 2915 - 2919 (2007/10/03)

Oleanolic acid and its synthetic derivatives have been identified as novel inhibitors of glycogen phosphorylase. Within this series of compounds, 4 (IC50 = 3.3 μM) is the most potent GPa inhibitor. Preliminary structure-activity relationships of the oleanolic acid derivatives are discussed.

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