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Details

Stereochemistry ACHIRAL
Molecular Formula C18H15Sn
Molecular Weight 351.03
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

Molecular Formula C18H15Sn
Molecular Weight 351.03
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
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.
2015-06
Structurally-diverse, PPARγ-activating environmental toxicants induce adipogenesis and suppress osteogenesis in bone marrow mesenchymal stromal cells.
2015-05-04
Characterizing the peroxisome proliferator-activated receptor (PPARγ) ligand binding potential of several major flame retardants, their metabolites, and chemical mixtures in house dust.
2015-02
In vitro assessment of human nuclear hormone receptor activity and cytotoxicity of the flame retardant mixture FM 550 and its triarylphosphate and brominated components.
2014-07-15
Effects of triphenyltin on growth and development of the wood frog (Lithobates sylvaticus).
2013-11-15
Species-specific differences in the inhibition of human and zebrafish 11β-hydroxysteroid dehydrogenase 2 by thiram and organotins.
2012-11-15
Sex-dependent aromatase activity in rat offspring after pre- and postnatal exposure to triphenyltin chloride.
2010-10-29
Reproductive inhibition and transgenerational toxicity of triphenyltin on medaka (Oiyzias latipes) at environmentally relevant levels.
2008-11-01
Effects of various pesticides on human 5alpha-reductase activity in prostate and LNCaP cells.
2007-04
Tributyltin and triphenyltin inhibit osteoclast differentiation through a retinoic acid receptor-dependent signaling pathway.
2007-03-30
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
Inhibitory effect of organotin compounds on rat neuronal nitric oxide synthase through interaction with calmodulin.
2004-11-05
Triphenyltin as a potential human endocrine disruptor.
2004-06-19
Triphenyltin enhances the neutrophilic differentiation of promyelocytic HL-60 cells.
2003-06-20
Degradation of triphenyltin by a fluorescent pseudomonad.
2000-08
Effects of pretreatment with cytochrome P-450 inducers, especially phenobarbital on triphenyltin metabolism and toxicity in hamsters.
1999-10-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:26:07 GMT 2025
Edited
by admin
on Mon Mar 31 21:26:07 GMT 2025
Record UNII
95T92AGN0V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRIPHENYLTIN HYDRIDE
MI  
Systematic Name English
TRIPHENYLTIN HYDRIDE [MI]
Preferred Name English
TRIPHENYLTIN
Systematic Name English
TIN, TRIPHENYL-, HYDRIDE
Systematic 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 Mon Mar 31 21:26:07 GMT 2025 , Edited by admin on Mon Mar 31 21:26:07 GMT 2025
PRIMARY
WIKIPEDIA
TRIPHENYLTIN HYDRIDE
Created by admin on Mon Mar 31 21:26:07 GMT 2025 , Edited by admin on Mon Mar 31 21:26:07 GMT 2025
PRIMARY
PUBCHEM
6460
Created by admin on Mon Mar 31 21:26:07 GMT 2025 , Edited by admin on Mon Mar 31 21:26:07 GMT 2025
PRIMARY
ECHA (EC/EINECS)
212-967-8
Created by admin on Mon Mar 31 21:26:07 GMT 2025 , Edited by admin on Mon Mar 31 21:26:07 GMT 2025
PRIMARY
EPA CompTox
DTXSID40893312
Created by admin on Mon Mar 31 21:26:07 GMT 2025 , Edited by admin on Mon Mar 31 21:26:07 GMT 2025
PRIMARY
MERCK INDEX
m11189
Created by admin on Mon Mar 31 21:26:07 GMT 2025 , Edited by admin on Mon Mar 31 21:26:07 GMT 2025
PRIMARY Merck Index
MESH
C030665
Created by admin on Mon Mar 31 21:26:07 GMT 2025 , Edited by admin on Mon Mar 31 21:26:07 GMT 2025
PRIMARY
FDA UNII
95T92AGN0V
Created by admin on Mon Mar 31 21:26:07 GMT 2025 , Edited by admin on Mon Mar 31 21:26:07 GMT 2025
PRIMARY
CAS
892-20-6
Created by admin on Mon Mar 31 21:26:07 GMT 2025 , Edited by admin on Mon Mar 31 21:26:07 GMT 2025
PRIMARY
CHEBI
27139
Created by admin on Mon Mar 31 21:26:07 GMT 2025 , Edited by admin on Mon Mar 31 21:26:07 GMT 2025
PRIMARY