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Molecule
ID:105993
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₁₅KOS₂
Molecular Mass
266.4645
Exact Mass
266.02013878
Charge
0
InChI
InChI=1S/C11H16OS2.K/c13-11(14)12-10-5-6-4-9(10)8-3-1-2-7(6)8;/h6-10H,1-5H2,(H,13,14);/q;+1/p-1
InChIKey
IGULCCCBGBDZKQ-UHFFFAOYSA-M
Canonic Smiles
[K]SC(=S)OC1CC2CC1C1C2CCC1
Isomeric Smiles
[K]SC(=S)OC1CC2CC1C1CCCC21
Calculated Properties
JChem
H Acceptors
0
H Donor
0
LogD (pH = 5.5)
2.1175
LogD (pH = 7.4)
2.1175
Log P
2.1175
Molar Refractivity
63.301098
Polarizability
28.196167
Polar Surface Area
9.23
Rotatable Bonds
3
Lipinski's Rule of Five
true
Data Source
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Registration numbers
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Properties
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Related Proteins
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
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RDKit
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IUPAC name
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IUPAC Traditional name
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PubChem CID
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PubChem SID
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Molecular Spectra
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MP Biomedicals
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02195683
Academic Data
PubChem
4234241
Names and Identifiers
Synonyms
TRICYCLODECAN-9-YL XANTHOGENATE POTASSIUM SALT
D609
IUPAC name
(potassiosulfanyl)({tricyclo[5.2.1.0^{2,6}]decan-8-yloxy})methanethione
IUPAC Traditional name
(potassiosulfanyl)({tricyclo[5.2.1.0^{2,6}]decan-8-yloxy})methanethione
Registration numbers
EC Number
280-379-9
CAS Number
83373-60-8
PubChem CID
4234241
PubChem SID
162092878
Properties
Safety Information
MSDS Link
Download link
Source
Storage Condition
-20°C
Source
Product Information
Certificate of Analysis
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Source
Purity
98%
Source
Molecule Details
MP Biomedicals
02195683
Purity: 98%
Potassium Salt
A selective inhibitor of phosphatidylcholine-specific PLC. Possesses antitumor and antiviral activity.
Bioactivity
PubChem BioAssay
References
PubChem Literature
No Data Available
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