Details
Stereochemistry | ACHIRAL |
Molecular Formula | C14H30O2S2 |
Molecular Weight | 294.517 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OCCSCCCCCCCCCCSCCO
InChI
InChIKey=WRCITXQNXAIKLR-UHFFFAOYSA-N
InChI=1S/C14H30O2S2/c15-9-13-17-11-7-5-3-1-2-4-6-8-12-18-14-10-16/h15-16H,1-14H2
Molecular Formula | C14H30O2S2 |
Molecular Weight | 294.517 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
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[Tolerability and side-effects of bis-(hydroxy-2-ethylthio)-1,10-decane (BS 530) as compared with clofibrate in the therapy of hyperlipemia]. | 1979 Oct 31 |
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Peroxisome proliferation in primary cultures of rat hepatocytes. | 1983 Jan |
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Morphological transformation and catalase activity of Syrian hamster embryo cells treated with hepatic peroxisome proliferators, TPA and nickel sulphate. | 1990 Jan |
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Peroxisome proliferators attenuate free arachidonic acid pool in the kidney through inducing lysophospholipid acyltransferases. | 2009 Oct |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2864317
The enhancement of palmitoyl-CoA hydrolase, carnitine acetyl-transferase and catalase activities in cultured C3H/10T1/2 cells was dose-related over a concentration range of 2 to 20 microM tiadenol, depending on the enzyme assayed.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:48:28 GMT 2023
by
admin
on
Sat Dec 16 17:48:28 GMT 2023
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Record UNII |
22251270CX
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Record Status |
Validated (UNII)
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Record Version |
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29703
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WHO-VATC |
QC10AX03
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WHO-ATC |
C10AX03
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Code System | Code | Type | Description | ||
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CHEMBL1697775
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SUB10998MIG
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DTXSID50219903
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66316
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6964-20-1
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TIADENOL
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230-165-6
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23403
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DB13348
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C152597
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22251270CX
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C004568
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m10841
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38248
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2647
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100000082154
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3253
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Related Record | Type | Details | ||
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ACTIVE MOIETY |