6168-59-8 Usage
General Description
(±)-Intermedeol is a naturally occurring chemical compound found in various plants and is classified as a sesquiterpene alcohol. It has a complex and unique chemical structure, consisting of multiple carbon atoms and functional groups. (±)-Intermedeol has been found to possess potent biological activities, including anti-inflammatory, antimicrobial, and antifungal properties. Additionally, (±)-Intermedeol has been studied for its potential in cancer therapy due to its ability to induce apoptosis (programmed cell death) in cancer cells. Its diverse range of activities and its natural origin makes (±)-Intermedeol an interesting target for further research and potential applications in pharmaceutical and medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 6168-59-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,6 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6168-59:
(6*6)+(5*1)+(4*6)+(3*8)+(2*5)+(1*9)=108
108 % 10 = 8
So 6168-59-8 is a valid CAS Registry Number.
6168-59-8Relevant articles and documents
Mechanistic characterization of three sesquiterpene synthases from the termite-associated fungus: Termitomyces
Burkhardt, Immo,Kreuzenbeck, Nina B.,Beemelmanns, Christine,Dickschat, Jeroen S.
supporting information, p. 3348 - 3355 (2019/04/01)
Three terpene synthases from the termite associated fungus Termitomyces were functionally characterized as (+)-intermedeol synthase, (-)-γ-cadinene synthase and (+)-germacrene D-4-ol synthase, with the germacrene D-4-ol synthase as the first reported enzyme that produces the (+)-enantiomer. The enzymatic mechanisms were thoroughly investigated by incubation with isotopically labeled precursors to follow the stereochemical courses of single reaction steps in catalysis. The role of putative active site residues was tested by site directed mutagenesis of a highly conserved tryptophan in all three enzymes and additional residues in (-)-γ-cadinene synthase that were identified by homology model analysis.
Synthetic approaches to 10 epieudesmane sesquiterpenes. A synthesis of intermedeol
Huffman,Miller,Pinder
, p. 3705 - 3710 (2007/10/10)
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