CROMOLYN

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C23H16O11
Molecular Weight	468.3665
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of CROMOLYN

Structure Search

SMILES

OC(COC1=CC=CC2=C1C(=O)C=C(O2)C(O)=O)COC3=CC=CC4=C3C(=O)C=C(O4)C(O)=O

InChI

InChIKey=IMZMKUWMOSJXDT-UHFFFAOYSA-N

InChI=1S/C23H16O11/c24-11(9-31-14-3-1-5-16-20(14)12(25)7-18(33-16)22(27)28)10-32-15-4-2-6-17-21(15)13(26)8-19(34-17)23(29)30/h1-8,11,24H,9-10H2,(H,27,28)(H,29,30)

HIDE SMILES / InChI

Molecular Formula	C23H16O11
Molecular Weight	468.3665
Charge	0
Count

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

Approval Year

Substance Class	Chemical Created by `admin` on `Sat Dec 16 17:37:56 UTC 2023` Edited by `admin` on `Sat Dec 16 17:37:56 UTC 2023`
Record UNII	Y0TK0FS77W
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

CROMOLYN

Common Name

English

Cromoglicic acid [WHO-DD]

Common Name

English

4H-1-BENZOPYRAN-2-CARBOXYLIC ACID, 5,5'-((2-HYDROXY-1,3-PROPANEDIYL)BIS(OXY))BIS(4-OXO-)

Common Name

English

CROMO-COMOD

Brand Name

English

CROMOGLICATE

Common Name

English

CROMOGLYCIC ACID

Common Name

English

5,5'-((2-HYDROXYTRIMETHYLENE)DIOXY)BIS(4-OXO-4H-1-BENZOPYRAN-2-CARBOXYLATE)

Systematic Name

English

CROMOGLICIC ACID

Official Name

English

CROMOLYN [HSDB]

Common Name

English

R03BC01

Code

English

cromoglicic acid [INN]

Common Name

English

CROMOGLYCATE

Common Name

English

CROMOLYN [VANDF]

Common Name

English

CROMOLYN [MI]

Common Name

English

Classification Tree Code System Code

WHO-ATC

R01AC01

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

WHO-VATC

QS01GX51

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

NDF-RT

N0000175630

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

WHO-ATC

R01AC51

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

WHO-ATC

S01GX01

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

NCI_THESAURUS

C29714

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

NDF-RT

N0000175628

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

WHO-VATC

QS01GX01

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

WHO-ATC

A07EB01

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

WHO-ATC

D11AH03

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

WHO-VATC

QR01AC01

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

WHO-VATC

QA07EB01

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

WHO-VATC

QD11AH03

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

LIVERTOX

243

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

WHO-ATC

S01GX51

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

FDA ORPHAN DRUG

602817

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

WHO-ATC

R03BC01

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

WHO-VATC

QR03BC01

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

Code System Code Type Description

SMS_ID

100000083740

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

EPA CompTox

DTXSID4022860

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

INN

2427

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

DAILYMED

Y0TK0FS77W

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

MERCK INDEX

m3851

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

Merck Index

EVMPD

SUB06825MIG

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

NCI_THESAURUS

C61691

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

CHEBI

59773

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

HSDB

3308

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

CHEBI

59039

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

RXCUI

2921

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

ALTERNATIVE

ECHA (EC/EINECS)

240-279-8

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

DRUG CENTRAL

741

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

IUPHAR

7608

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

DRUG BANK

DB01003

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

CAS

16110-51-3

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

WIKIPEDIA

CROMOGLICIC ACID

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

FDA UNII

Y0TK0FS77W

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

ChEMBL

CHEMBL428880

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

LACTMED

Cromolyn

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

PUBCHEM

2882

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

RXCUI

42612

Created by admin on Sat Dec 16 17:37:57 UTC 2023 , Edited by admin on Sat Dec 16 17:37:57 UTC 2023

PRIMARY

Related Record Type Details


					D5EHL8V2EH

Human Mast Cell

TARGET->STABILIZER

Amount:


					Q2WXR1I0PK

CROMOLYN SODIUM

SALT/SOLVATE -> PARENT

Amount:

Related Record Type Details


					VOZ07VZP8G

CROMOGLICATE LISETIL

PRODRUG -> METABOLITE ACTIVE

Amount:

Related Record Type Details


					Y0TK0FS77W

CROMOLYN

ACTIVE MOIETY

Comments:

inhibit mast cells-mediated adverse effects on brain pathology and neuronal loss as well as interfere with Aβ oligomerization and accumulation.

Amount: