ChemicalBook > CAS DataBase List > Ursolic acid acetate

Ursolic acid acetate

Product Name: Ursolic acid acetate
CAS No.: 7372-30-7
Chemical Name: Ursolic acid acetate
Synonyms: Aids070315;Aids-070315;Acetylursolicaci;3-Acetylursolic acid;URSOLIC ACID ACETATE;Acetylursolic acid、Ursolic acetate;3β-(Acetyloxy)urs-12-en-28-oic acid;Ursolic acid acetate, 10 mM in DMSO;(3β)-3-(Acetyloxy)-urs-12-en-28-oic acid;URSOLIC ACID ACETATE (ACETYLURSOLIC ACID)
CBNumber: CB91463427
Molecular Formula: C32H50O4
Formula Weight: 498.74
MOL File: 7372-30-7.mol

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Ursolic acid acetate Property

Melting point:: 279-280 °C
Boiling point:: 567.6±50.0 °C(Predicted)
Density: 1.09±0.1 g/cm3(Predicted)
storage temp.: 2-8°C
solubility: Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form: Powder
pka: 4.67±0.70(Predicted)
color: White to off-white

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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical

Product number: 30220
Product name: 3-Acetylursolic Acid
Packaging: 25mg
Price: $684
Updated: 2024/03/01

Cayman Chemical

Product number: 30220
Product name: 3-Acetylursolic Acid
Packaging: 50mg
Price: $1139
Updated: 2024/03/01

Cayman Chemical

Product number: 30220
Product name: 3-Acetylursolic Acid
Packaging: 5mg
Price: $153
Updated: 2024/03/01

Cayman Chemical

Product number: 30220
Product name: 3-Acetylursolic Acid
Packaging: 10mg
Price: $290
Updated: 2024/03/01

TRC

Product number: U850115
Product name: UrsolicAcidAcetate
Packaging: 1mg
Price: $65
Updated: 2021/12/16

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Ursolic acid acetate Chemical Properties,Usage,Production

Uses

Ursolic acid acetate (Acetylursolic acid), isolated from the aerial roots of Ficus microcarpa, exhibits cytotoxicity against KB cells with IC50 of 8.4 μM[1].

Definition

ChEBI: Acetylursolic acid is a triterpenoid.

Synthesis

77-52-1

108-24-7

915-79-7

Acetylation of ursolic acid (5.00 g, 10.96 mmol) with acetic anhydride (2.60 mL, 26.00 mmol) in pyridine (80 mL) was carried out by adding triethylamine (3.00 mL, 21.68 mmol) and a catalytic amount of DMAP for a 12 h reaction at 25°C. The reaction was carried out by aqueous post-treatment. Upon completion of the reaction, an aqueous post-treatment and purification by silica gel column chromatography (SiO2, eluent: hexane/ethyl acetate, 8:2) afforded the target compound 14 (5.30 g, 97% yield) as a colorless solid. Thin layer chromatography (TLC) showed Rf = 0.71 (SiO2, eluent: hexane/ethyl acetate, 7:3). The melting point of the compound is 235-238°C (literature value:[8] 242-244°C). Specific optical rotation [α]D = +64.89° (c = 0.86, CHCl3) (literature value:[8] [α]D = +71.2° (c = 1.0, CHCl3)). Mass spectra (ESI, MeOH) showed m/z = 499.1 (15%, [M + H]+), 521.3 (30%, [M + Na]+), 1019.3 (100%, [2M + Na]+).

References

[1] Chiang YM, et al. Cytotoxic triterpenes from the aerial roots of Ficus microcarpa. Phytochemistry. 2005 Feb;66(4):495-501. DOI:10.1016/j.phytochem.2004.12.026

Ursolic acid acetate Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from Ursolic acid acetate manufacturers

Career Henan Chemical Co

Product: Ursolic acid acetate 7372-30-7
Price: US $6.00/KG
Min. Order: 1KG
Purity: 98%
Supply Ability: 1kg, 10kg ,50kg
Release date: 2020-03-09

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(1S,2R,6aS,6aS,6bR,8aS,12aS)-10-acetyloxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid

(3β)-3-(Acetyloxy)-urs-12-en-28-oic acid

URSOLIC ACID ACETATE

(3beta)-3-(Acetyloxy)-urs-12-en-28-oic acid

3-Acetylursolic acid

3β-(Acetyloxy)urs-12-en-28-oic acid

Aids070315

Aids-070315

Urs-12-en-28-oic acid, 3-(acetyloxy)-, (3beta)-

URSOLIC ACID ACETATE (ACETYLURSOLIC ACID)

Urs-12-en-28-oic acid, 3-(acetyloxy)-, (3β)-

Acetylursolicaci

(1S,2R,4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-acetoxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid

Acetylursolic acid、Ursolic acetate

Ursolic acid,inhibit,Ursolic acid acetate,Inhibitor

Ursolic acid acetate, 10 mM in DMSO

(1S,2R,4AS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-acetoxy-1,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-octadecahydropicene-4a(2H)-carboxylic acid

7372-30-7

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