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Substrate Report for: Fenobucarb

General
Type Insecticide, Carbamate
Chemical_Nomenclature (2-butan-2-ylphenyl) N-methylcarbamate
Canonical SMILES CCC(C)C1=CC=CC=C1OC(=O)NC
InChI InChI=1S/C12H17NO2/c1-4-9(2)10-7-5-6-8-11(10)15-12(14)13-3/h5-9H,4H2,1-3H3,(H,13,14)
InChIKey DIRFUJHNVNOBMY-UHFFFAOYSA-N
Other name(s) BPMC ; Baycarb ; Bassa ; Barizon ; Fenobcarb ; Carvil ; Hopcin ; Osbac ; Bayer 41367C ; Bayer 41637 ; Geocarb 50EC ; BAY 41637 ; CHEBI:34304 ; EINECS 223-188-8 ; BRN 2052332 ; AI3-27212 ; AC1L2EFJ ; PS1046_SUPELCO ; SCHEMBL73674 ; 45488_RIEDEL ; CHEMBL226650 ; 45488_FLUKA ; CTK8E4127 ; MolPort-003-931-168 ; AKOS015960925 ; AK129225 ; LS-50077 ; TR-015292 ; FT-0603649 ; C14425
________________________________________________________________________________________________
MW|207.26
Formula|C12H17NO2
CAS_number|3766-81-2, 34681-10-2
PubChem|19588
UniChem|DIRFUJHNVNOBMY-UHFFFAOYSA-N
IUPHAR|
Wikipedia|Fenobucarb

Target
Families | Fenobucarb ligand of proteins in family: ACHE, Hormone-sensitive_lipase_like
Protein | 9bact-CEUbrb

References:
Search PubMed for references concerning: Fenobucarb

9 more
    Title: Comprehensive Enantioselectivity Evaluation of Insecticidal Activity and Mammalian Toxicity of Fenobucarb
    He Z, Li C, Xia W, Wang Z, Li R, Zhang Y, Wang M
    Ref: Journal of Agricultural and Food Chemistry, :, 2022 : PubMed

            

    Title: Discovery of carbamate degrading enzymes by functional metagenomics
    Ufarte L, Laville E, Duquesne S, Morgavi D, Robe P, Klopp C, Rizzo A, Pizzut-Serin S, Potocki-Veronese G
    Ref: PLoS ONE, 12:e0189201, 2017 : PubMed

            

    Title: Identification of two acetylcholinesterases in Pardosa pseudoannulata and the sensitivity to insecticides
    Zhang Y, Shao Y, Jiang F, Li J, Liu Z
    Ref: Insect Biochemistry & Molecular Biology, 46C:25, 2014 : PubMed