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Ajugamarin F4, a chemical compound derived from the Ajuga reptans plant, exhibits a range of pharmacological properties such as anti-inflammatory, antioxidant, and anticancer activities. Its ability to inhibit the growth of human cancer cell lines in vitro and neuroprotective effects positions it as a promising candidate for the development of therapeutic agents in the pharmaceutical industry.

122587-84-2

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122587-84-2 Usage

Uses

Used in Pharmaceutical Industry:
Ajugamarin F4 is used as an anticancer agent for its potential to inhibit the growth of various human cancer cell lines, making it a candidate for further development in cancer treatment.
Ajugamarin F4 is also used as a neuroprotective agent for its reported neuroprotective effects, indicating its potential in the treatment of neurological conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 122587-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,5,8 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 122587-84:
(8*1)+(7*2)+(6*2)+(5*5)+(4*8)+(3*7)+(2*8)+(1*4)=132
132 % 10 = 2
So 122587-84-2 is a valid CAS Registry Number.

122587-84-2SDS

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 [(1S)-2-[(1S,2R,4S,4aR,8aR)-4-acetyloxy-4a-(acetyloxymethyl)-1,2-dimethylspiro[3,4,6,7,8,8a-hexahydro-2H-naphthalene-5,2'-oxirane]-1-yl]-1-(5-oxo-2H-furan-3-yl)ethyl] (2S)-2-methylbutanoate

1.2 Other means of identification

Product number -
Other names Butanoic acid,2-methyl-,2-(8-(acetyloxy)-8a-((acetyloxy)methyl)octahydro-5,6-dimethylspiro(naphthalene-1(2H),2'-oxiran)-5-yl)-1-(2,5-dihydro-5-oxo-3-furanyl)ethyl ester,(1R-(1alpha,4abeta,5beta(S*(S*)),6alpha,8alpha,8aalpha))

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:122587-84-2 SDS

122587-84-2Downstream Products

122587-84-2Relevant academic research and scientific papers

NEO-CLERODANE DITERPENES FROM AJUGA CILIATA VAR. VILLOSIOR

Shimomura, Hiroko,Sashida, Yutaka,Ogawa, Kazunori

, p. 988 - 992 (2007/10/02)

From the aerial parts of Ajuga ciliata var. villosior, nine new neo-clerodane diterpenes have been isolated.The structures of two acetyl derivatives of (12S)-6α, 12,19-trihydroxy-1β--4,18-epoxyneo-clerod-13(14)-en-15,16-olide, three acetyl derivatives of (12S)-1β,6α,19-trihydroxy-12--4,18-epoxyneo-clerod-13(14)-en-15,16-olide, three acetyl derivatives of (12S)-6α,19-dihydroxy-12--4,18-epoxyneo-clerod-13(14)-en-15,16-olide and methyl 6α-hydroxy-4α-methoxycarbonyl-18-norneo-clerod-13(14)-en-15,16-olide were elucidated by spectroscopic methods and chemical correlation.In addition, a known neo-clerodane, ajugarin-IV, was isolated.Keywords: neo-clerodane; Ajuga ciliata var. villosior; bitter principle; diterpene; Labiatae; ajugamarin

NEO-CLERODANE DITERPENES FROM AJUGA DECUMBENS

Shimomura, Hiroko,Sashida, Yutaka,Ogawa, Kazunori

, p. 996 - 998 (2007/10/02)

From the whole plants of Ajuga decumbens, four new-clerodane diterpenes, ajugamarins A2, G1, H1 and F4, and a previously known ajugamarin B2 have been isolated.The structures were elucidated on the basis of spectral data and chemical correlations.Keywords: neo-clerodane; diterpene; bitter principle; Ajuga decumbens Labiatae; adjugamarin

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