U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C7H18NO2P
Molecular Weight 179.1971
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTAFOSFAN

SMILES

CCCCNC(C)(C)P(O)=O

InChI

InChIKey=WCXWARPXYQCRPP-UHFFFAOYSA-N
InChI=1S/C7H18NO2P/c1-4-5-6-8-7(2,3)11(9)10/h8,11H,4-6H2,1-3H3,(H,9,10)

HIDE SMILES / InChI
Butafosfan is a phosphororganic supplement that is given, most commonly with cyanocobalamin, to cattle, swine, horses, and poultry for the prevention or treatment of phosphorus deficiencies. Butafosfan also plays a vital role in hepatic carbohydrate metabolism. In addition, butafosfan has been regarded as an antistress agent in combination with vitamin B12. Studies with butafosfan in different animals have shown that it improved general health status by stimulating feed intake, immune system, and digestive function. Butafosfan has been reported for the treatment of metabolic disorders caused by stress or nutrition problems in various species.

Originator

Sources: Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft (1967), 300, (10), 868-74.

Approval Year

PubMed

PubMed

TitleDatePubMed
Effects of butafosfan with or without cyanocobalamin on the metabolism of early lactating cows with subclinical ketosis.
2016 Feb
Pharmacokinetics of butafosfan after intravenous and intramuscular administration in piglets.
2017 Apr
Patents

Patents

Sample Use Guides

Cows: 10 ml/100 kg
Route of Administration: Intravenous
Name Type Language
BUTAFOSFAN
INN  
INN  
Official Name English
butafosfan [INN]
Common Name English
BUTAPHOSPHAN
Common Name English
(1-(BUTYLAMINO)-1-METHYLETHYL)PHOSPHINIC ACID
Systematic Name English
1-( N-BUTYLAMINO)-1-METHYLETHYL PHOSPHONOUS ACID
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29730
Created by admin on Fri Dec 15 16:26:39 GMT 2023 , Edited by admin on Fri Dec 15 16:26:39 GMT 2023
WHO-VATC QA12CX91
Created by admin on Fri Dec 15 16:26:39 GMT 2023 , Edited by admin on Fri Dec 15 16:26:39 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
241-341-7
Created by admin on Fri Dec 15 16:26:39 GMT 2023 , Edited by admin on Fri Dec 15 16:26:39 GMT 2023
PRIMARY
ChEMBL
CHEMBL1979022
Created by admin on Fri Dec 15 16:26:39 GMT 2023 , Edited by admin on Fri Dec 15 16:26:39 GMT 2023
PRIMARY
EVMPD
SUB05997MIG
Created by admin on Fri Dec 15 16:26:39 GMT 2023 , Edited by admin on Fri Dec 15 16:26:39 GMT 2023
PRIMARY
INN
4312
Created by admin on Fri Dec 15 16:26:39 GMT 2023 , Edited by admin on Fri Dec 15 16:26:39 GMT 2023
PRIMARY
EPA CompTox
DTXSID5048681
Created by admin on Fri Dec 15 16:26:39 GMT 2023 , Edited by admin on Fri Dec 15 16:26:39 GMT 2023
PRIMARY
PUBCHEM
72084
Created by admin on Fri Dec 15 16:26:39 GMT 2023 , Edited by admin on Fri Dec 15 16:26:39 GMT 2023
PRIMARY
NCI_THESAURUS
C73233
Created by admin on Fri Dec 15 16:26:39 GMT 2023 , Edited by admin on Fri Dec 15 16:26:39 GMT 2023
PRIMARY
DAILYMED
3Q2LQ1149L
Created by admin on Fri Dec 15 16:26:39 GMT 2023 , Edited by admin on Fri Dec 15 16:26:39 GMT 2023
PRIMARY
RXCUI
819929
Created by admin on Fri Dec 15 16:26:39 GMT 2023 , Edited by admin on Fri Dec 15 16:26:39 GMT 2023
PRIMARY RxNorm
SMS_ID
100000088475
Created by admin on Fri Dec 15 16:26:39 GMT 2023 , Edited by admin on Fri Dec 15 16:26:39 GMT 2023
PRIMARY
FDA UNII
3Q2LQ1149L
Created by admin on Fri Dec 15 16:26:39 GMT 2023 , Edited by admin on Fri Dec 15 16:26:39 GMT 2023
PRIMARY
CAS
17316-67-5
Created by admin on Fri Dec 15 16:26:39 GMT 2023 , Edited by admin on Fri Dec 15 16:26:39 GMT 2023
PRIMARY