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Details

Stereochemistry ACHIRAL
Molecular Formula C18H15Sn
Molecular Weight 350.022
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRIPHENYLTIN HYDRIDE

SMILES

C1=CC=C(C=C1)[SnH](C2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=NFHRNKANAAGQOH-UHFFFAOYSA-N
InChI=1S/3C6H5.Sn.H/c3*1-2-4-6-5-3-1;;/h3*1-5H;;

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Degradation of triphenyltin by a fluorescent pseudomonad.
2000 Aug
Triphenyltin as a potential human endocrine disruptor.
2004 Jul-Aug
Inhibitory effects of some possible endocrine-disrupting chemicals on the isozymes of human 11beta-hydroxysteroid dehydrogenase and expression of their mRNA in gonads and adrenal glands.
2005
Sex-dependent aromatase activity in rat offspring after pre- and postnatal exposure to triphenyltin chloride.
2010 Oct 29
Species-specific differences in the inhibition of human and zebrafish 11β-hydroxysteroid dehydrogenase 2 by thiram and organotins.
2012 Nov 15
Effects of triphenyltin on growth and development of the wood frog (Lithobates sylvaticus).
2013 Nov 15
Characterizing the peroxisome proliferator-activated receptor (PPARγ) ligand binding potential of several major flame retardants, their metabolites, and chemical mixtures in house dust.
2015 Feb
A comparison of the effects of tributyltin chloride and triphenyltin chloride on cell proliferation, proapoptotic p53, Bax, and antiapoptotic Bcl-2 protein levels in human breast cancer MCF-7 cell line.
2015 Jun
Structurally-diverse, PPARγ-activating environmental toxicants induce adipogenesis and suppress osteogenesis in bone marrow mesenchymal stromal cells.
2015 May 4
Patents
Name Type Language
TRIPHENYLTIN HYDRIDE
MI  
Systematic Name English
TRIPHENYLTIN
Systematic Name English
TIN, TRIPHENYL-, HYDRIDE
Systematic Name English
TRIPHENYLTIN HYDRIDE [MI]
Common Name English
TRIPHENYLSTANNYL HYDRIDE
Systematic Name English
TRIPHENYLSTANNANE
Systematic Name English
STANNANE, TRIPHENYL-
Systematic Name English
Code System Code Type Description
CHEBI
30537
Created by admin on Sat Dec 16 05:03:34 GMT 2023 , Edited by admin on Sat Dec 16 05:03:34 GMT 2023
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WIKIPEDIA
TRIPHENYLTIN HYDRIDE
Created by admin on Sat Dec 16 05:03:34 GMT 2023 , Edited by admin on Sat Dec 16 05:03:34 GMT 2023
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PUBCHEM
6460
Created by admin on Sat Dec 16 05:03:34 GMT 2023 , Edited by admin on Sat Dec 16 05:03:34 GMT 2023
PRIMARY
ECHA (EC/EINECS)
212-967-8
Created by admin on Sat Dec 16 05:03:34 GMT 2023 , Edited by admin on Sat Dec 16 05:03:34 GMT 2023
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EPA CompTox
DTXSID40893312
Created by admin on Sat Dec 16 05:03:34 GMT 2023 , Edited by admin on Sat Dec 16 05:03:34 GMT 2023
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MERCK INDEX
m11189
Created by admin on Sat Dec 16 05:03:34 GMT 2023 , Edited by admin on Sat Dec 16 05:03:34 GMT 2023
PRIMARY Merck Index
MESH
C030665
Created by admin on Sat Dec 16 05:03:34 GMT 2023 , Edited by admin on Sat Dec 16 05:03:34 GMT 2023
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FDA UNII
95T92AGN0V
Created by admin on Sat Dec 16 05:03:34 GMT 2023 , Edited by admin on Sat Dec 16 05:03:34 GMT 2023
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CAS
892-20-6
Created by admin on Sat Dec 16 05:03:34 GMT 2023 , Edited by admin on Sat Dec 16 05:03:34 GMT 2023
PRIMARY
CHEBI
27139
Created by admin on Sat Dec 16 05:03:34 GMT 2023 , Edited by admin on Sat Dec 16 05:03:34 GMT 2023
PRIMARY