IOXAGLIC ACID

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C24H21I6N5O8
Molecular Weight	1268.8791
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of IOXAGLIC ACID

Structure Search

SMILES

CNC(=O)C1=C(I)C(C(=O)NCC(=O)NC2=C(I)C(C(=O)NCCO)=C(I)C(C(O)=O)=C2I)=C(I)C(N(C)C(C)=O)=C1I

InChI

InChIKey=TYYBFXNZMFNZJT-UHFFFAOYSA-N

InChI=1S/C24H21I6N5O8/c1-7(37)35(3)20-17(29)10(21(39)31-2)13(25)11(18(20)30)23(41)33-6-8(38)34-19-15(27)9(22(40)32-4-5-36)14(26)12(16(19)28)24(42)43/h36H,4-6H2,1-3H3,(H,31,39)(H,32,40)(H,33,41)(H,34,38)(H,42,43)

HIDE SMILES / InChI

Molecular Formula	C24H21I6N5O8
Molecular Weight	1268.8791
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 `Fri Dec 15 15:23:35 UTC 2023` Edited by `admin` on `Fri Dec 15 15:23:35 UTC 2023`
Record UNII	Z40X7EI2AF
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

IOXAGLIC ACID

Official Name

English

Ioxaglic acid [WHO-DD]

Common Name

English

IOXAGLIC ACID [MI]

Common Name

English

IOXAGLIC ACID [USP-RS]

Common Name

English

N-(2-Hydroxyethyl)-2,4,6-triiodo-5-[2-[2,4,6-triiodo-3-(N-methylacetamido)-5-(methylcarbamoyl)benzamido]acetamido]isophthalamic acid

Systematic Name

English

P-286

Code

English

ioxaglic acid [INN]

Common Name

English

IOXAGLIC ACID [USAN]

Common Name

English

HEXABRIX 320

Brand Name

English

IOXAGLATE

Common Name

English

IOXAGLIC ACID [MART.]

Common Name

English

IOXAGLIC ACID [EP MONOGRAPH]

Common Name

English

IOXAGLIC ACID [JAN]

Common Name

English

BENZOIC ACID, 3-((((3-(ACETYLMETHYLAMINO)-2,4,6-TRIIODO-5-9((METHYLAMINO)CARBONYL)BENZOYL)AMINO)ACETYL)AMINO)-5-(((2-HYDROXYETHYL)AMINO)CARBONYL)-2,4,6-TRIIODO-

Common Name

English

IOXAGLIC ACID [USP MONOGRAPH]

Common Name

English

IOXAGLATE [VANDF]

Common Name

English

Classification Tree Code System Code

NDF-RT

N0000180185

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

NCI_THESAURUS

C28500

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

WHO-ATC

V08AB03

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

WHO-VATC

QV08AB03

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

NDF-RT

N0000010258

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

Code System Code Type Description

INN

4217

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

LACTMED

Ioxaglate

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

ECHA (EC/EINECS)

261-560-1

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

EVMPD

SUB08264MIG

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

RS_ITEM_NUM

1345159

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

CHEBI

31718

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

EPA CompTox

DTXSID5023166

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

RXCUI

1426458

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

HSDB

8077

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

PUBCHEM

3742

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

USAN

T081

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

SMS_ID

100000083116

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

WIKIPEDIA

Ioxaglic acid

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

DRUG BANK

DB09313

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

MESH

D007485

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

FDA UNII

Z40X7EI2AF

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

DRUG CENTRAL

1472

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

NCI_THESAURUS

C61793

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

CAS

59017-64-0

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

MERCK INDEX

m6380

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

PRIMARY

Merck Index

RXCUI

5973

Created by admin on Fri Dec 15 15:23:35 UTC 2023 , Edited by admin on Fri Dec 15 15:23:35 UTC 2023

ALTERNATIVE

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IOXAGLATE SODIUM

SALT/SOLVATE -> PARENT

Related Record Type Details


					N39M6PDW7W

3-[[[[3-(Acetylmethylamino)-5-(dimethylcarbamoyl)-2,4,6-triiodobenzoyl]amino]acetyl]amino]-5-[(2-hydroxyethyl)carbamoyl]-2,4,6-triiodobenzoic acid

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					TK97ZSN5NZ

3-[[[[3-(Acetylmethylamino)-2,6-diiodo-5-(methylcarbamoyl)benzoyl]amino]acetyl]amino]-5-[(2-hydroxyethyl)carbamoyl]-2,4,6-triiodobenzoic acid

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					Y7G54UT2XG

3-((((3-(ACETYLMETHYLAMINO)-2,4,6-TRIIODO-5-(METHYLCARBAMOYL)BENZOYL)AMINO)ACETYL)AMINO)-5-((2-(ACETYLOXY)ETHYL)CARBAMOYL)-2,4,6-TRIIODOBENZOIC ACID

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					P2DB4YR43F

3-AMINO-5-(((2-HYDROXYETHYL)AMINO)CARBONYL)-2,4,6-TRIIODOBENZOIC ACID

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					KV86B47DA2

3,3′-[[5-(Acetylmethylamino)-2,4,6-triiodo-1,3-phenylene]bis(carbonyliminomethylenecarbonylimino)]bis[5-[(2-hydroxyethyl)carbamoyl]-2,4,6-triiodobenzoic] acid

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					63UF2TJ4TT

3-[[[[3-[[[[3-(Acetylmethylamino)-2,4,6-triiodo-5-(methylcarbamoyl)benzoyl]amino]acetyl]amino]-5-[(2-hydroxyethyl)carbamoyl]-2,4,6-triiodobenzoyl]amino]acetyl]amino]-5-[(2-hydroxyethyl)carbamoyl]-2,4,6-triiodobenzoic acid

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:

Related Record Type Details


					Z40X7EI2AF

ACTIVE MOIETY