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Details

Stereochemistry RACEMIC
Molecular Formula C15H25NO2
Molecular Weight 251.3645
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of XIBENOLOL

SMILES

CC1=C(C)C(OCC(O)CNC(C)(C)C)=CC=C1

InChI

InChIKey=RKUQLAPSGZJLGP-UHFFFAOYSA-N
InChI=1S/C15H25NO2/c1-11-7-6-8-14(12(11)2)18-10-13(17)9-16-15(3,4)5/h6-8,13,16-17H,9-10H2,1-5H3

HIDE SMILES / InChI

Molecular Formula C15H25NO2
Molecular Weight 251.3645
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Xibenolol or D-32 (dl-tert-butylamino-3-(2', 3'-dimethylphenoxy)-2-propanol hydrochloride) is a beta-blocking agent. It has been developing as a hypontesive medicine by Kowa Pharmaceutical and Teikoku Hormone, however development has been discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Stereoselective glucuronidation of beta-blocking agents, 1-tert-butylamino-3-(2,3-dimethylphenoxy)-2-propanol (D-32) and propranolol, in animals, in vivo and in vitro].
1986-05
Stereoselectivity in the metabolism of the beta-adrenergic blocking agent, (+/-)-1-tert-butylamino-3-(2,3-dimethylphenoxy)-2-propanol hydrochloride (xibenolol hydrochloride, D-32), in man.
1985-02
Effects of beta-adrenoceptor blocking agents of N-tertiary butyl derivatives on maximum upstroke velocity of action potential in guinea-pig papillary muscles.
1983-09
[Antihypertensive action of adrenergic beta-receptor blockers and its effect on the entire sympathetic outflow in spontaneously hypertensive rats].
1982-12
Duration and selectivity in beta-adrenoceptor blocking action of a beta-adrenoceptor blocking drug, D-32 in conscious dogs.
1981-02
Analysis of beta-adrenoceptors mediating renin release produced by isoproterenol in conscious dogs.
1980-05
Effects of beta-adrenoceptor blocking agents, pindolol, alprenolol and practolol on blood pressure and heart rate in conscious renal hypertensive dogs.
1977-01
Patents

Patents

Sample Use Guides

dogs: 50 mg/kg, p.o. 1 mg/kg per min for 5 min i.v. rats: 2 X 15 or 2 X 50 mg/kg/day p.o.
Route of Administration: Other
In Vitro Use Guide
The effects of xibenolol (D-32) (17.3-100 uM) on action potentials were investigated in isolated guinea-pig papillary muscles.
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:06:08 GMT 2025
Edited
by admin
on Mon Mar 31 18:06:08 GMT 2025
Record UNII
0871JY946G
Record Status Validated (UNII)
Record Version
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Name Type Language
XIBENOLOL [MI]
Preferred Name English
XIBENOLOL
INN   MI  
INN  
Official Name English
(±)-1-(TERT-BUTYLAMINO)-3-(2,3-XYLYLOXY)-2-PROPANOL
Systematic Name English
xibenolol [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Mon Mar 31 18:06:08 GMT 2025 , Edited by admin on Mon Mar 31 18:06:08 GMT 2025
Code System Code Type Description
FDA UNII
0871JY946G
Created by admin on Mon Mar 31 18:06:08 GMT 2025 , Edited by admin on Mon Mar 31 18:06:08 GMT 2025
PRIMARY
SMS_ID
100000079357
Created by admin on Mon Mar 31 18:06:08 GMT 2025 , Edited by admin on Mon Mar 31 18:06:08 GMT 2025
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WIKIPEDIA
Xibenolol
Created by admin on Mon Mar 31 18:06:08 GMT 2025 , Edited by admin on Mon Mar 31 18:06:08 GMT 2025
PRIMARY
ChEMBL
CHEMBL347795
Created by admin on Mon Mar 31 18:06:08 GMT 2025 , Edited by admin on Mon Mar 31 18:06:08 GMT 2025
PRIMARY
PUBCHEM
146256
Created by admin on Mon Mar 31 18:06:08 GMT 2025 , Edited by admin on Mon Mar 31 18:06:08 GMT 2025
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NCI_THESAURUS
C66668
Created by admin on Mon Mar 31 18:06:08 GMT 2025 , Edited by admin on Mon Mar 31 18:06:08 GMT 2025
PRIMARY
MESH
C006027
Created by admin on Mon Mar 31 18:06:08 GMT 2025 , Edited by admin on Mon Mar 31 18:06:08 GMT 2025
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DRUG CENTRAL
3657
Created by admin on Mon Mar 31 18:06:08 GMT 2025 , Edited by admin on Mon Mar 31 18:06:08 GMT 2025
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INN
5264
Created by admin on Mon Mar 31 18:06:08 GMT 2025 , Edited by admin on Mon Mar 31 18:06:08 GMT 2025
PRIMARY
CAS
30187-90-7
Created by admin on Mon Mar 31 18:06:08 GMT 2025 , Edited by admin on Mon Mar 31 18:06:08 GMT 2025
PRIMARY
EVMPD
SUB00110MIG
Created by admin on Mon Mar 31 18:06:08 GMT 2025 , Edited by admin on Mon Mar 31 18:06:08 GMT 2025
PRIMARY
EPA CompTox
DTXSID0043848
Created by admin on Mon Mar 31 18:06:08 GMT 2025 , Edited by admin on Mon Mar 31 18:06:08 GMT 2025
PRIMARY
MERCK INDEX
m1269
Created by admin on Mon Mar 31 18:06:08 GMT 2025 , Edited by admin on Mon Mar 31 18:06:08 GMT 2025
PRIMARY Merck Index
CAS
81584-06-7
Created by admin on Mon Mar 31 18:06:08 GMT 2025 , Edited by admin on Mon Mar 31 18:06:08 GMT 2025
SUPERSEDED
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY