3650-30-4 Usage
Diterpenoid compound
A type of organic compound that is derived from the diterpene class of terpenoids.
Found in Bacopa monnieri
A Chinese medicinal herb that is known for its cognitive-enhancing and neuroprotective properties.
Neuroprotective properties
The ability to protect the brain and nervous system from damage or degeneration.
Anti-inflammatory properties
The ability to reduce inflammation in the body, which can be beneficial for treating conditions such as arthritis and other inflammatory diseases.
Inhibits production of pro-inflammatory cytokines
Cytokines are proteins that are involved in cell signaling and can contribute to inflammation. 13-epitorulosol has been shown to inhibit the production of these cytokines, which can help reduce inflammation.
Potential treatment for neurodegenerative diseases
Due to its neuroprotective and anti-inflammatory properties, 13-epitorulosol has been identified as a promising candidate for the treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's.
Anti-cancer effects
Studies have shown that 13-epitorulosol can induce apoptosis (programmed cell death) in cancer cells, which could potentially be used as a treatment for cancer.
Further research needed
While 13-epitorulosol has shown promise in preclinical studies, more research is needed to fully understand its therapeutic potential and mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 3650-30-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,5 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3650-30:
(6*3)+(5*6)+(4*5)+(3*0)+(2*3)+(1*0)=74
74 % 10 = 4
So 3650-30-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H34O2/c1-6-19(4,22)13-10-16-15(2)8-9-17-18(3,14-21)11-7-12-20(16,17)5/h6,16-17,21-22H,1-2,7-14H2,3-5H3/t16?,17?,18-,19-,20-/m1/s1
3650-30-4Relevant articles and documents
Microbial Transformation of Manool and (12Z)-Labda-8(17),12,14-triene by Rhodococcus erythropolis JTS-131
Hieda, Tadaharu,Mikami, Yoichi,Obi, Yukiteru
, p. 787 - 794 (2007/10/02)
Rhodococcus erythropolis JTS-131, a cis-abienol and sclareol transformable bacterium, converted manool and accumulated manoyl oxide in the culture broth.In the presence of metabolic inhibitors, 13β-hydroxylabda-8(17),14-dien-18-oic acid and its methylester (a new compound) were accumulated as the transformation products.This strain also transformed (12Z)-labda-8(17),12,14-triene and accumulated (12Z)-labda-8(17),12,14-trien-18-al in the culture broth.In the presence of metabolic inhibitors, two compounds, (12Z)-labda-8(17),12,14-trien-18-ol and 4,18,19-trinor-3,4-seco-5-oxo-(12Z)-labda-8(17),12,14-trien-3-oic acid were accumulated.Based on the experiments on the degradation sequence, transformation pathways for these two labdanes by the bacterium are proposed.
