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Details

Stereochemistry ACHIRAL
Molecular Formula C4H9NO
Molecular Weight 87.1204
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTANAMIDE

SMILES

CCCC(N)=O

InChI

InChIKey=DNSISZSEWVHGLH-UHFFFAOYSA-N
InChI=1S/C4H9NO/c1-2-3-4(5)6/h2-3H2,1H3,(H2,5,6)

HIDE SMILES / InChI

Molecular Formula C4H9NO
Molecular Weight 87.1204
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis and phosphodiesterase 5 inhibitory activity of new 5-phenyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one derivatives containing an N-acylamido group phenyl ring.
2001 Jul
Preparation of chiral 4-benzyloxymethyldihydrofuran-2-one using lipase-catalyzed kinetic resolution: synthesis of (-)-virginiae butanolide C (VB C).
2002 Sep 2
Synthesis of the butanamide derivative S 19812, a new dual inhibitor of cyclooxygenase and lipoxygenase pathways.
2003
Sterically and guest-controlled self-assembly of calix[4]arene derivatives.
2004 May 3
Neuroprotective effects of ONO-1924H, an inhibitor of poly ADP-ribose polymerase (PARP), on cytotoxicity of PC12 cells and ischemic cerebral damage.
2004 Nov 26
Amide derivatives of 9,11-seco-estra-1,3,5(10)-trien-11-oic acid as modified orally active estrogen agonists with moderate antagonistic activity.
2005 Jan 3
Synthesis of uniform protein-polymer conjugates.
2005 Nov-Dec
Gastroprotective activity and cytotoxic effect of cyperenoic acid derivatives.
2006 Nov
Future therapeutic treatment of COPD: struggle between oxidants and cytokines.
2007
[Preprocessing of collagenous sources with the aim of extracting minimally denatured collagen].
2007 Apr-Jun
Comparative transport efficiencies of urea analogues through urea transporter UT-B.
2007 Jul
Bioconversion of butyronitrile to butyramide using whole cells of Rhodococcus rhodochrous PA-34.
2007 Mar
Reduction of site-specific CYP3A-mediated metabolism for dual angiotensin and endothelin receptor antagonists in various in vitro systems and in cynomolgus monkeys.
2007 May
Selective androgen receptor modulators in preclinical and clinical development.
2008
Synthesis of DL-fluorobenzenamides as anticonvulsants.
2008
2-(4-Chloro-phen-yl)-3-methyl-N-(5-methyl-thia-zol-2-yl)butanamide.
2008 Dec 20
Advances in marine microbial symbionts in the china sea and related pharmaceutical metabolites.
2009 Apr 20
N-(3,4-Dichloro-phen-yl)-3-oxo-butanamide.
2009 Dec 4
An analytic potential energy function for the amide-amide and amide-water intermolecular hydrogen bonds in peptides.
2009 Nov 30
A new acylamidase from Rhodococcus erythropolis TA37 can hydrolyze N-substituted amides.
2010 Aug
Direct assay of delta-aminolevulinic acid dehydratase in heme biosynthesis for the detection of porphyrias by tandem mass spectrometry.
2010 Aug 1
Gallium(III) complexes of DOTA and DOTA-monoamide: kinetic and thermodynamic studies.
2010 Dec 6
1-(4-Bromo-phen-yl)-3-butano-ylthio-urea.
2010 Dec 8
Structure-activity relationships of 33 carboxamides as toxicants against female Aedes aegypti (Diptera: Culicidae).
2010 Mar
Dimeric supramolecular motifs of two carboxylate-guanidinium compounds.
2010 Sep
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:53:59 GMT 2023
Edited
by admin
on Fri Dec 15 18:53:59 GMT 2023
Record UNII
9J6OR937VR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BUTANAMIDE
Systematic Name English
BUTYRAMIDE
FHFI  
Systematic Name English
N-BUTYRAMIDE
MI  
Common Name English
N-BUTYLAMIDE
HSDB  
Systematic Name English
BUTYRAMIDE [FHFI]
Common Name English
NSC-8424
Code English
N-BUTYLAMIDE [HSDB]
Common Name English
BUTANOIC ACID, AMIDE
Common Name English
BUTANIMIDIC ACID
Systematic Name English
FEMA NO. 4252
Code English
N-BUTYRAMIDE [MI]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION BUTYRAMIDE
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
Code System Code Type Description
MESH
C006866
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY
CHEBI
50724
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY
PUBCHEM
10927
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY
DRUG BANK
DB02121
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY
RXCUI
1653515
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY RxNorm
WIKIPEDIA
BUTYRAMIDE
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY
JECFA MONOGRAPH
1582
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-776-4
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY
MERCK INDEX
m2866
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY Merck Index
NSC
8424
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY
HSDB
5684
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY
CAS
541-35-5
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY
SMS_ID
100000163191
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY
EVMPD
SUB177334
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY
FDA UNII
9J6OR937VR
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY
EPA CompTox
DTXSID8060248
Created by admin on Fri Dec 15 18:53:59 GMT 2023 , Edited by admin on Fri Dec 15 18:53:59 GMT 2023
PRIMARY