UROLITHIN A

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C13H8O4
Molecular Weight	228.2002
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of UROLITHIN A

Structure Search

SMILES

OC1=CC2=C(C=C1)C3=C(C=C(O)C=C3)C(=O)O2

InChI

InChIKey=RIUPLDUFZCXCHM-UHFFFAOYSA-N

InChI=1S/C13H8O4/c14-7-1-3-9-10-4-2-8(15)6-12(10)17-13(16)11(9)5-7/h1-6,14-15H

HIDE SMILES / InChI

Molecular Formula	C13H8O4
Molecular Weight	228.2002
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

Targets

Targets

Primary Target	Pharmacology	Condition	Potency
autophagy 17 Target ID: GO:0006914 Sources: https://www.ncbi.nlm.nih.gov/pubmed/28976622	Activator 1447

Substance Class	Chemical Created by `admin` on `Wed Apr 02 00:15:28 GMT 2025` Edited by `admin` on `Wed Apr 02 00:15:28 GMT 2025`
Record UNII	ILJ8NEF6DT
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

Mitopure

Preferred Name

English

UROLITHIN A

Official Name

English

6H-DIBENZO(B,D)PYRAN-6-ONE, 3,8-DIHYDROXY-

Systematic Name

English

Urolithin A [WHO-DD]

Common Name

English

URO-A

Common Name

English

3,8-DIHYDROXYUROLITHIN

Common Name

English

3,8-DIHYDROXYBENZO(C)CHROMEN-6-ONE

Systematic Name

English

Code System Code Type Description

EPA CompTox

DTXSID40150694

Created by admin on Wed Apr 02 00:15:28 GMT 2025 , Edited by admin on Wed Apr 02 00:15:28 GMT 2025

PRIMARY

DAILYMED

ILJ8NEF6DT

Created by admin on Wed Apr 02 00:15:28 GMT 2025 , Edited by admin on Wed Apr 02 00:15:28 GMT 2025

PRIMARY

WIKIPEDIA

Urolithin_A

Created by admin on Wed Apr 02 00:15:28 GMT 2025 , Edited by admin on Wed Apr 02 00:15:28 GMT 2025

PRIMARY

CAS

1143-70-0

Created by admin on Wed Apr 02 00:15:28 GMT 2025 , Edited by admin on Wed Apr 02 00:15:28 GMT 2025

PRIMARY

PUBCHEM

5488186

Created by admin on Wed Apr 02 00:15:28 GMT 2025 , Edited by admin on Wed Apr 02 00:15:28 GMT 2025

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GRAS Notification (GRN No.)

791

Created by admin on Wed Apr 02 00:15:28 GMT 2025 , Edited by admin on Wed Apr 02 00:15:28 GMT 2025

PRIMARY

DRUG BANK

DB15464

Created by admin on Wed Apr 02 00:15:28 GMT 2025 , Edited by admin on Wed Apr 02 00:15:28 GMT 2025

PRIMARY

FDA UNII

ILJ8NEF6DT

Created by admin on Wed Apr 02 00:15:28 GMT 2025 , Edited by admin on Wed Apr 02 00:15:28 GMT 2025

PRIMARY

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FORMED BY MICROFLORA

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					ILJ8NEF6DT

ACTIVE MOIETY

Comments:

induce mitophagy, which is a selective recycling of mitochondria by autophagy,

Amount: