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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

Molecular Formula C18H15Sn
Molecular Weight 350.022
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Effects of pretreatment with cytochrome P-450 inducers, especially phenobarbital on triphenyltin metabolism and toxicity in hamsters.
1999 Oct 1
Degradation of triphenyltin by a fluorescent pseudomonad.
2000 Aug
Triphenyltin enhances the neutrophilic differentiation of promyelocytic HL-60 cells.
2003 Jun 20
Triphenyltin as a potential human endocrine disruptor.
2004 Jul-Aug
Inhibitory effect of organotin compounds on rat neuronal nitric oxide synthase through interaction with calmodulin.
2004 Nov 5
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
Effects of various pesticides on human 5alpha-reductase activity in prostate and LNCaP cells.
2007 Apr
Tributyltin and triphenyltin inhibit osteoclast differentiation through a retinoic acid receptor-dependent signaling pathway.
2007 Mar 30
Reproductive inhibition and transgenerational toxicity of triphenyltin on medaka (Oiyzias latipes) at environmentally relevant levels.
2008 Nov 1
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
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 Jul 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
Substance Class Chemical
Created
by admin
on Sat Dec 16 05:03:34 GMT 2023
Edited
by admin
on Sat Dec 16 05:03:34 GMT 2023
Record UNII
95T92AGN0V
Record Status Validated (UNII)
Record Version
  • Download
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
PRIMARY
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
PRIMARY
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
PRIMARY
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
PRIMARY
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
PRIMARY
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
PRIMARY
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