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Details

Stereochemistry ACHIRAL
Molecular Formula C7H15N3O2S2
Molecular Weight 237.343
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARTAP

SMILES

CN(C)C(CSC(N)=O)CSC(N)=O

InChI

InChIKey=IRUJZVNXZWPBMU-UHFFFAOYSA-N
InChI=1S/C7H15N3O2S2/c1-10(2)5(3-13-6(8)11)4-14-7(9)12/h5H,3-4H2,1-2H3,(H2,8,11)(H2,9,12)

HIDE SMILES / InChI

Molecular Formula C7H15N3O2S2
Molecular Weight 237.343
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 various insecticides on the development of the egg parasitoid Trichogramma dendrolimi (Hymenoptera: Trichogrammatidae).
2001 Dec
Optimum timing of insecticide applications against diamondback moth Plutella xylostella in cole crops using threshold catches in sex pheromone traps.
2001 Jan
Nereistoxin and cartap neurotoxicity attributable to direct block of the insect nicotinic receptor/channel.
2003 Apr 23
Action of nereistoxin on recombinant neuronal nicotinic acetylcholine receptors expressed in Xenopus laevis oocytes.
2003 Nov
Susceptibility to cartap-induced lethal effect and diaphragmatic injury via ocular exposure in rabbits.
2003 Nov 5
The effect of operational parameters on the photocatalytic degradation of pesticide.
2004 Jan
Cartap hydrolysis relative to its action at the insect nicotinic channel.
2004 Jan 14
Rapid report acetamiprid resistance and cross-resistance in the diamondback moth, Plutella xylostella.
2004 Sep
Influence of insecticidal derivative (cartap hydrochloride) from the marine polycheate on certain enzyme systems of the fresh water fish Oreochromis mossambicus.
2005 Apr
Ion channels: molecular targets of neuroactive insecticides.
2005 Nov
Cartap-induced cytotoxicity in mouse C2C12 myoblast cell line and the roles of calcium ion and oxidative stress on the toxic effects.
2006 Feb 15
Toxicity of insecticides to the sweetpotato whitefly (Hemiptera: Aleyrodidae) and its natural enemies.
2007 Jul
[Determination of cartap residues in tea by GC/micro-ECD].
2007 Mar
Impact of some selected insecticides application on soil microbial respiration.
2008 Aug 15
Aquatic toxicity of cartap and cypermethrin to different life stages of Daphnia magna and Oryzias latipes.
2008 Jan
Crystal structures of Lymnaea stagnalis AChBP in complex with neonicotinoid insecticides imidacloprid and clothianidin.
2008 Jun
Effect of sublethal exposure of Cartap on hypothalamo-neurosecretory system of the freshwater spotted murrel, Channa punctatus (Bloch).
2008 Nov
Developmental toxicity of cartap on zebrafish embryos.
2009 Dec 13
Cross-resistance, inheritance and biochemical mechanisms of imidacloprid resistance in B-biotype Bemisia tabaci.
2009 Nov
Responses of striped stem borer, Chilo suppressalis (Lepidoptera: Pyralidae), from Taiwan to a range of insecticides.
2010 Jul
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:52:15 UTC 2023
Edited
by admin
on Fri Dec 15 19:52:15 UTC 2023
Record UNII
Z45YUY784H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARTAP
ISO   MI  
Common Name English
CARTAP [ISO]
Common Name English
CARBAMIC ACID, THIO-, S,S'-(2-(DIMETHYLAMINO)TRIMETHYLENE) ESTER
Common Name English
CARBAMOTHIOIC ACID, S,S'-(2-(DIMETHYLAMINO)-1,3-PROPANEDIYL) ESTER
Common Name English
CARTAP [MI]
Common Name English
CARBAMOTHIOIC ACID SC,SC'-(2-(DIMETHYLAMINO)-1,3-PROPANEDIYL) ESTER
Common Name English
1,3-BIS(CARBAMOYLTHIO)-2-N,N-(DIMETHYLAMINO)PROPANE
Common Name English
Code System Code Type Description
WIKIPEDIA
CARTAP
Created by admin on Fri Dec 15 19:52:15 UTC 2023 , Edited by admin on Fri Dec 15 19:52:15 UTC 2023
PRIMARY
CAS
15263-53-3
Created by admin on Fri Dec 15 19:52:15 UTC 2023 , Edited by admin on Fri Dec 15 19:52:15 UTC 2023
PRIMARY
MERCK INDEX
m3135
Created by admin on Fri Dec 15 19:52:15 UTC 2023 , Edited by admin on Fri Dec 15 19:52:15 UTC 2023
PRIMARY Merck Index
ALANWOOD
cartap
Created by admin on Fri Dec 15 19:52:15 UTC 2023 , Edited by admin on Fri Dec 15 19:52:15 UTC 2023
PRIMARY
CHEBI
3436
Created by admin on Fri Dec 15 19:52:15 UTC 2023 , Edited by admin on Fri Dec 15 19:52:15 UTC 2023
PRIMARY
FDA UNII
Z45YUY784H
Created by admin on Fri Dec 15 19:52:15 UTC 2023 , Edited by admin on Fri Dec 15 19:52:15 UTC 2023
PRIMARY
EPA CompTox
DTXSID4044165
Created by admin on Fri Dec 15 19:52:15 UTC 2023 , Edited by admin on Fri Dec 15 19:52:15 UTC 2023
PRIMARY
PUBCHEM
27159
Created by admin on Fri Dec 15 19:52:15 UTC 2023 , Edited by admin on Fri Dec 15 19:52:15 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT