88034-27-9 Usage
General Description
Lantadene C is a toxic chemical compound found in the leaves and seeds of the Lantana plant. It belongs to the class of triterpenoid compounds, which have been shown to have cytotoxic, anti-inflammatory, and antimicrobial properties. Lantadene C has been identified as one of the main toxic components responsible for the poisoning of livestock and humans that ingest the plant. It acts as an inhibitor of the enzyme 3-beta-hydroxysteroid dehydrogenase, leading to the disruption of adrenal steroidogenesis and ultimately causing symptoms such as gastrointestinal distress, liver damage, and neurological effects. Due to its toxicity, lantadene C is considered a potential hazard and should be handled with caution.
Check Digit Verification of cas no
The CAS Registry Mumber 88034-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,3 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88034-27:
(7*8)+(6*8)+(5*0)+(4*3)+(3*4)+(2*2)+(1*7)=139
139 % 10 = 9
So 88034-27-9 is a valid CAS Registry Number.
InChI:InChI=1/C35H54O5/c1-10-21(2)28(37)40-27-20-30(3,4)19-23-22-11-12-25-32(7)15-14-26(36)31(5,6)24(32)13-16-34(25,9)33(22,8)17-18-35(23,27)29(38)39/h11,21,23-25,27H,10,12-20H2,1-9H3,(H,38,39)/t21-,23+,24?,25+,27+,32-,33+,34+,35-/m0/s1
88034-27-9Relevant articles and documents
22β--3-oxoolean-12-en-28-oic Acid, a New Constituent of Lantana camara
Johns, Stanley R.,Lamberton, John A.,Morton, Trevor C.,Suares, Hector,Willing, Richard I.
, p. 1895 - 1902 (2007/10/02)
22β--3-oxoolean-12-en-28-oic acid, a new constituent of Lantana camara L. is closely related to lantadene A and lantadene B.Although hydrolysis gives 2-methylbutanoic acid as a partial racemate, it has been shown by n.m.r. spectroscopy that the natural ester is the optically pure (S)-isomer.Catalytic hydrogenation of lantadene A gives a mixture of diastereoisomeric esters in which the (S)-2-methylbutanoate predominates, and a 1:1 mixture of the (R)- and (S)-esters was obtained by esterification with (RS)-2-methylbutanoyl chloride of 22β-hydroxy- 3-oxoolean-12-en-28-oic acid protected as the diphenylmethyl ester.
