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Details

Stereochemistry RACEMIC
Molecular Formula C20H33NO
Molecular Weight 303.4821
Optical Activity ( + / - )
Defined Stereocenters 2 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENPROPIMORPH

SMILES

CC(CN1C[C@H](C)O[C@H](C)C1)CC2=CC=C(C=C2)C(C)(C)C

InChI

InChIKey=RYAUSSKQMZRMAI-ALOPSCKCSA-N
InChI=1S/C20H33NO/c1-15(12-21-13-16(2)22-17(3)14-21)11-18-7-9-19(10-8-18)20(4,5)6/h7-10,15-17H,11-14H2,1-6H3/t15?,16-,17+

HIDE SMILES / InChI

Molecular Formula C20H33NO
Molecular Weight 303.4821
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 2 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Synergism between demethylation inhibitor fungicides or gibberellin inhibitor plant growth regulators and bifenthrin in a pyrethroid-resistant population of Listronotus maculicollis (Coleoptera: Curculionidae).
2010-10
Azole drugs are imported by facilitated diffusion in Candida albicans and other pathogenic fungi.
2010-09-30
Candida albicans virulence and drug-resistance requires the O-acyltransferase Gup1p.
2010-09-15
PKC signaling regulates drug resistance of the fungal pathogen Candida albicans via circuitry comprised of Mkc1, calcineurin, and Hsp90.
2010-08-26
Synthesis and characterization of N,N-dialkyl and N-alkyl-N-aralkyl fenpropimorph-derived compounds as high affinity ligands for sigma receptors.
2010-06-15
Chemical combinations elucidate pathway interactions and regulation relevant to Hepatitis C replication.
2010-06-08
Requirement for ergosterol in V-ATPase function underlies antifungal activity of azole drugs.
2010-06-03
Characterization of a CuZn superoxide dismutase gene in the arbuscular mycorrhizal fungus Glomus intraradices.
2010-06
Pesticide cocktails can interact synergistically on aquatic crustaceans.
2010-05
High-content, image-based screening for drug targets in yeast.
2010-04-14
Arbuscular mycorrhiza partially protect chicory roots against oxidative stress induced by two fungicides, fenpropimorph and fenhexamid.
2010-03
Endocytosis restricts Arabidopsis KNOLLE syntaxin to the cell division plane during late cytokinesis.
2010-02-03
Toxicity of fungicides to natural bacterial communities in wetland water and sediment measured using leucine incorporation and potential denitrification.
2010-02
A phenotypic profile of the Candida albicans regulatory network.
2009-12
Baseline sensitivity to proquinazid in Blumeria graminis f. sp. tritici and Erysiphe necator and cross-resistance with other fungicides.
2009-08
Fenpropimorph slows down the sterol pathway and the development of the arbuscular mycorrhizal fungus Glomus intraradices.
2009-08
Chemogenomic profiling predicts antifungal synergies.
2009
Functional characterization of a C-4 sterol methyl oxidase from the endomycorrhizal fungus Glomus intraradices.
2008-12-23
Differential effects of fenpropimorph and fenhexamid, two sterol biosynthesis inhibitor fungicides, on arbuscular mycorrhizal development and sterol metabolism in carrot roots.
2008-12
Chemogenetic fingerprinting by analysis of cellular growth dynamics.
2008-08-22
Novel chamber to measure equilibrium soil-air partitioning coefficients of low-volatility organic chemicals under conditions of varying temperature and soil moisture.
2008-07-01
Effects of two sterol biosynthesis inhibitor fungicides (fenpropimorph and fenhexamid) on the development of an arbuscular mycorrhizal fungus.
2008-05
Survival in the presence of antifungals: genome-wide expression profiling of Aspergillus niger in response to sublethal concentrations of caspofungin and fenpropimorph.
2007-11-09
Identification of regions of the sigma-1 receptor ligand binding site using a novel photoprobe.
2007-10
Factors influencing degradation of pesticides in soil.
2007-05-30
Lipids: architects and regulators of membrane dynamics and trafficking.
2007-05
Sterol demethylation inhibitor fungicides as disruptors of insect development and inducers of glutathione S-transferase activities in Mamestra brassicae.
2007-04
Comparison of wind tunnel and field experiments to measure potential deposition of fenpropimorph following volatilisation from treated crops.
2007-02
Insights into the role of specific lipids in the formation and delivery of lipid microdomains to the plasma membrane of plant cells.
2007-01
Antifungals: need to search for a new molecular target.
2006-04-17
Volatilization of the pesticides chlorpyrifos and fenpropimorph from a potato crop.
2006-01-01
Common pesticide increases costs of antipredator defenses in Rana temporaria tadpoles.
2005-08-15
A latent variable model for chemogenomic profiling.
2005-08-01
Specific patterns of changes in wheat gene expression after treatment with three antifungal compounds.
2005-03
Measured and computed volatilisation of the fungicide fenpropimorph from a sugar beet crop.
2005-02
Pesticide retention in the watershed and in a small constructed wetland treating diffuse pollution.
2005
Cold-climate vegetative buffer zones as pesticide-filters for surface runoff.
2005
Pesticide volatilization from plants: improvement of the PEC model PELMO based on a boundary-layer concept.
2004-05-15
A link between sterol biosynthesis, the cell wall, and cellulose in Arabidopsis.
2004-04
Chemical genomics in yeast.
2004
Subsurface tile drainage loss of modern pesticides: field experiment results.
2004
Pesticide volatilization from soil: lysimeter measurements versus predictions of European registration models.
2003-08-23
Sterols regulate development and gene expression in Arabidopsis.
2003-03
Ergosterol biosynthesis inhibitors become fungicidal when combined with calcineurin inhibitors against Candida albicans, Candida glabrata, and Candida krusei.
2003-03
Screening the retention of thirteen pesticides in a small constructed wetland.
2003
Effects of three fungicides alone and in combination on glutathione S-transferase activity (GST) and cytochrome P-450 (CYP 1A1) in the liver and gill of brown trout (Salmo trutta).
2002-11-01
Inhibition of the sterol pathway in leek seedlings impairs phosphatidylserine and glucosylceramide synthesis but triggers an accumulation of triacylglycerols.
2002-08-08
Semi-volatile organic compounds at the leaf/atmosphere interface: numerical simulation of dispersal and foliar uptake.
2002-08
Measurement of xylem translocation of weak electrolytes with the pressure chamber technique.
2002-05
Impact of strobilurins on physiology and yield formation of wheat.
2002
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 22:04:43 GMT 2025
Edited
by admin
on Mon Mar 31 22:04:43 GMT 2025
Record UNII
4548UM725F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENPROPIMORPH
ISO   MI  
Common Name English
CORBEL
Preferred Name English
(2R,6S)-FENPROPIMORPH
Common Name English
CIS-4-(3-(4-TERT-BUTYLPHENYL)-2-METHYLPROPYL)-2,6-DIMETHYLMORPHOLINE
Systematic Name English
RO-14-3169/000
Code English
MORPHOLINE, 4-(3-(4-(1,1-DIMETHYLETHYL)PHENYL)-2- METHYLPROPYL)-2,6-DIMETHYL-
Systematic Name English
4-(3-(4-(1,1-DIMETHYLETHYL)PHENYL)-2-METHYLPROPYL)-2,6- DIMETHYLMORPHOLINE
Systematic Name English
FENPROPIMORPH [MI]
Common Name English
FENPROPIMORPH [ISO]
Common Name English
BAS-42100F
Code English
MORPHOLINE, 4-(3-(4-(1,1-DIMETHYLETHYL)PHENYL)-2-METHYLPROPYL)-2,6-DIMETHYL-, CIS-
Systematic Name English
MORPHOLINE, 4-(3-(4-(1,1-DIMETHYLETHYL)PHENYL)-2-METHYLPROPYL)-2,6-DIMETHYL-, (2R,6S)-REL-
Systematic Name English
MISTRAL
Brand Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 121402
Created by admin on Mon Mar 31 22:04:43 GMT 2025 , Edited by admin on Mon Mar 31 22:04:43 GMT 2025
Code System Code Type Description
FDA UNII
4548UM725F
Created by admin on Mon Mar 31 22:04:43 GMT 2025 , Edited by admin on Mon Mar 31 22:04:43 GMT 2025
PRIMARY
MERCK INDEX
m5291
Created by admin on Mon Mar 31 22:04:43 GMT 2025 , Edited by admin on Mon Mar 31 22:04:43 GMT 2025
PRIMARY Merck Index
ECHA (EC/EINECS)
266-719-9
Created by admin on Mon Mar 31 22:04:43 GMT 2025 , Edited by admin on Mon Mar 31 22:04:43 GMT 2025
PRIMARY
CAS
67306-03-0
Created by admin on Mon Mar 31 22:04:43 GMT 2025 , Edited by admin on Mon Mar 31 22:04:43 GMT 2025
ALTERNATIVE
ALANWOOD
fenpropimorph
Created by admin on Mon Mar 31 22:04:43 GMT 2025 , Edited by admin on Mon Mar 31 22:04:43 GMT 2025
PRIMARY
CAS
67564-91-4
Created by admin on Mon Mar 31 22:04:43 GMT 2025 , Edited by admin on Mon Mar 31 22:04:43 GMT 2025
PRIMARY
PUBCHEM
93365
Created by admin on Mon Mar 31 22:04:43 GMT 2025 , Edited by admin on Mon Mar 31 22:04:43 GMT 2025
PRIMARY
ECHA (EC/EINECS)
266-639-4
Created by admin on Mon Mar 31 22:04:43 GMT 2025 , Edited by admin on Mon Mar 31 22:04:43 GMT 2025
ALTERNATIVE
WIKIPEDIA
Fenpropimorph
Created by admin on Mon Mar 31 22:04:43 GMT 2025 , Edited by admin on Mon Mar 31 22:04:43 GMT 2025
PRIMARY
CHEBI
50145
Created by admin on Mon Mar 31 22:04:43 GMT 2025 , Edited by admin on Mon Mar 31 22:04:43 GMT 2025
PRIMARY
EPA CompTox
DTXSID4034601
Created by admin on Mon Mar 31 22:04:43 GMT 2025 , Edited by admin on Mon Mar 31 22:04:43 GMT 2025
PRIMARY