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Details

Stereochemistry ABSOLUTE
Molecular Formula C23H31NO5
Molecular Weight 401.4959
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RITOBEGRON ETHYL

SMILES

CCOC(=O)COC1=C(C)C=C(CCN[C@@H](C)[C@H](O)C2=CC=C(O)C=C2)C(C)=C1

InChI

InChIKey=SLXOKVKOBXCWCK-SBUREZEXSA-N
InChI=1S/C23H31NO5/c1-5-28-22(26)14-29-21-13-15(2)19(12-16(21)3)10-11-24-17(4)23(27)18-6-8-20(25)9-7-18/h6-9,12-13,17,23-25,27H,5,10-11,14H2,1-4H3/t17-,23-/m0/s1

HIDE SMILES / InChI

Molecular Formula C23H31NO5
Molecular Weight 401.4959
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Ritobegron (KUC 7483) is a selective β3-adrenoceptor agonist that was developed for oral treatment of overactive bladder. It is the prodrug of the active compound KUC-7322. Phase I studies have investigated the pharmacodynamic and pharmacokinetic effects of ritobegron in healthy individuals and patients with spinal cord injury. Ritobegron exhibits a high selectivity for the bladder versus other organs, and decreased intravesical pressure with minimal effects on the cardiovascular system in rats. When administered in combination with organic anion transporter (OAT) inhibitors such as probenecid (primarily used in treating gout and hyperuricemia), the plasma concentration of the active compound KUC-7322 may increase.

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 05:31:09 GMT 2023
Edited
by admin
on Sat Dec 16 05:31:09 GMT 2023
Record UNII
E89L9L8KFH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RITOBEGRON ETHYL
Common Name English
ACETIC ACID, 2-(4-(2-(((1S,2R)-2-HYDROXY-2-(4-HYDROXYPHENYL)-1-METHYLETHYL)AMINO)ETHYL)-2,5-DIMETHYLPHENOXY)-, ETHYL ESTER
Common Name English
RITOBEGRON ETHYL, (-)-
Common Name English
(-)-RITOBEGRON ETHYL
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID30180263
Created by admin on Sat Dec 16 05:31:10 GMT 2023 , Edited by admin on Sat Dec 16 05:31:10 GMT 2023
PRIMARY
FDA UNII
E89L9L8KFH
Created by admin on Sat Dec 16 05:31:10 GMT 2023 , Edited by admin on Sat Dec 16 05:31:10 GMT 2023
PRIMARY
PUBCHEM
9810282
Created by admin on Sat Dec 16 05:31:10 GMT 2023 , Edited by admin on Sat Dec 16 05:31:10 GMT 2023
PRIMARY
CAS
255733-81-4
Created by admin on Sat Dec 16 05:31:10 GMT 2023 , Edited by admin on Sat Dec 16 05:31:10 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
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METABOLITE ACTIVE -> PRODRUG
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ACTIVE MOIETY