75567-37-2

  • Product Name:Ingenol-3-angelate
  • Molecular Formula:C25H34O6
  • Molecular Weight:430.541
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Purity:99%

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1.What is the Ingenol-3-angelate ?

ChEBI: A tetracyclic diterpenoid ester obtained by formal condensation of the carboxy group of (2Z)-2-methylbut-2-enoic (angelic) acid with the 3-hydroxy group of ingenol. Used for the topical treatment of actinic keratosis.

Ingenol mebutate (also known as PEP005) was approved in January 2012 by the US FDA for the topical treatment of actinic keratoses (AK). Ingenol mebutate also received approval in 2012 in the European Union, Australia, and Brazil for the same indication. Ingenol mebutate, a diterpene ester natural product, is the active agent in the sap of the plant Euphorbia peplus, which has long been used as a traditional remedy for skin lesions. Ingenol mebutate has a novel mechanism of action involving initial plasma membrane disruption, rapid loss of mitochondrial membrane potential, and cell death by primary necrosis within 1 h; a subsequent tumor-specific immune response results in antibodydependent cellular toxicity that eliminates residual cells. Ingenol mebutate is obtained by extraction from the dried, milled aerial parts of Euphorbia peplus followed by a series of purification steps.

2.What is the CAS number for Ingenol-3-angelate ?

The CAS number of Ingenol-3-angelate is 75567-37-2.

3.What are another words for Ingenol-3-angelate ?

Synonyms for Ingenol-3-angelate 75567-37-2:Ingenol-3-angelate;3-Indolyl-b-D-galactopyranoside;(1S,4S,5S,6R,9R,10R,12R,14R)-5,6-Dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.01,5.010,12]pentadeca-2,7-dien-4-yl (2Z)-2-methyl-2-butenoate;indican (glucoside);Ingenol mebutate;Indoxyl |A-D-galactopyranoside;3-O-angeloylingenol;ingenol 3-angelate;

4.What is Ingenol-3-angelate (75567-37-2) used for?

Ingenol 3-Angelate is known to exhibit antitumor activities which induces plasma membrane and mitochondrial disruption and necrotic cell death.

Relevant articles related to Ingenol-3-angelate:

Article

Source

Identification, structural modification, and dichotomous effects on human immunodeficiency virus type 1 (HIV-1) replication of ingenane esters from Euphorbia kansui

Liu, Qingbo,Li, Wei,Huang, Li,Asada, Yoshihisa,Morris-Natschke, Susan L.,Chen, Chin-Ho,Lee, Kuo-Hsiung,Koike, Kazuo

, p. 618 - 627 (2018/07/29)

A CONTINUOUS FLOW PROCESS FOR THE PREPARATION OF INGENOL-3-MEBUTATE

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Paragraph 0072-0077, (2015/12/08)

PROCESS FOR THE PREPARATION OF INGENOL-3-ANGELATE FROM 20-DEOXY-INGENOL

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Page/Page column 4; 5; 7, (2014/02/15)

5.Buy Ingenol-3-angelate with the best price .

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