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

Details

Stereochemistry RACEMIC
Molecular Formula C10H14N4O3
Molecular Weight 238.2432
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROTHEOBROMINE

SMILES

CC(O)CN1C(=O)N(C)C2=C(N(C)C=N2)C1=O

InChI

InChIKey=MXRGZXBFSKSZPH-UHFFFAOYSA-N
InChI=1S/C10H14N4O3/c1-6(15)4-14-9(16)7-8(11-5-12(7)2)13(3)10(14)17/h5-6,15H,4H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C10H14N4O3
Molecular Weight 238.2432
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Protheobromine is a derivative of the xanthine alkaloid theobromine with diuretic and vasodilating activity.

Originator

Sources: Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft (1930), 268, 567-72.

Approval Year

PubMed

PubMed

TitleDatePubMed
Low-dose acetylsalicylic acid therapy monitored with ultra high performance liquid chromatography.
2013 Aug
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:44:44 GMT 2023
Edited
by admin
on Sat Dec 16 16:44:44 GMT 2023
Record UNII
8067S1388X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROTHEOBROMINE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
protheobromine [INN]
Common Name English
CORODIL
Brand Name English
TEBE
Brand Name English
Protheobromine [WHO-DD]
Common Name English
BONICOR
Brand Name English
PROTHEOBROMINE [MI]
Common Name English
VASCOPIL
Brand Name English
1-(2-HYDROXYPROPYL)-3,7-DIMETHYLXANTHINE
Systematic Name English
PANTOBROMINA
Common Name English
PRO-COR
Brand Name English
THEOBROMINE, 1-(2-HYDROXYPROPYL)-
Systematic Name English
PROTHEOBROMINE [MART.]
Common Name English
CORDABROMIN
Brand Name English
1H-PURINE-2,6-DIONE, 3,7-DIHYDRO-1-(2-HYDROXYPROPYL)-3,7-DIMETHYL-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C448
Created by admin on Sat Dec 16 16:44:45 GMT 2023 , Edited by admin on Sat Dec 16 16:44:45 GMT 2023
Code System Code Type Description
CAS
50-39-5
Created by admin on Sat Dec 16 16:44:45 GMT 2023 , Edited by admin on Sat Dec 16 16:44:45 GMT 2023
PRIMARY
ChEMBL
CHEMBL85140
Created by admin on Sat Dec 16 16:44:45 GMT 2023 , Edited by admin on Sat Dec 16 16:44:45 GMT 2023
PRIMARY
SMS_ID
100000080854
Created by admin on Sat Dec 16 16:44:45 GMT 2023 , Edited by admin on Sat Dec 16 16:44:45 GMT 2023
PRIMARY
EVMPD
SUB10137MIG
Created by admin on Sat Dec 16 16:44:45 GMT 2023 , Edited by admin on Sat Dec 16 16:44:45 GMT 2023
PRIMARY
INN
1666
Created by admin on Sat Dec 16 16:44:45 GMT 2023 , Edited by admin on Sat Dec 16 16:44:45 GMT 2023
PRIMARY
DRUG CENTRAL
3497
Created by admin on Sat Dec 16 16:44:45 GMT 2023 , Edited by admin on Sat Dec 16 16:44:45 GMT 2023
PRIMARY
NCI_THESAURUS
C76647
Created by admin on Sat Dec 16 16:44:45 GMT 2023 , Edited by admin on Sat Dec 16 16:44:45 GMT 2023
PRIMARY
PUBCHEM
66120
Created by admin on Sat Dec 16 16:44:45 GMT 2023 , Edited by admin on Sat Dec 16 16:44:45 GMT 2023
PRIMARY
EPA CompTox
DTXSID00861572
Created by admin on Sat Dec 16 16:44:45 GMT 2023 , Edited by admin on Sat Dec 16 16:44:45 GMT 2023
PRIMARY
FDA UNII
8067S1388X
Created by admin on Sat Dec 16 16:44:45 GMT 2023 , Edited by admin on Sat Dec 16 16:44:45 GMT 2023
PRIMARY
MERCK INDEX
m1242
Created by admin on Sat Dec 16 16:44:45 GMT 2023 , Edited by admin on Sat Dec 16 16:44:45 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
200-034-8
Created by admin on Sat Dec 16 16:44:45 GMT 2023 , Edited by admin on Sat Dec 16 16:44:45 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY