Iopromide - 10mM in DMSO , Diagnostic agent, CAS No.73334-07-3, Diagnostic agent

CAS: 73334-07-3 Cat. No.: I425729 Molecular Weight: 791.11 EC Number: 277-385-9

GRADE & PURITY 10mM in DMSO

Synonyms

AKOS025402129 | IOPROMIDE [WHO-DD] | 1,3-Benzenedicarboxamide, N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-5-((methoxyacetyl)amino)-N-methyl- | DB09156 | Iopromida | Iopromidum (INN-Latin) | lopromid | BRN 7085608 | Iopromide, analytical standard | Ioprom

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

Synonyms

AKOS025402129 | IOPROMIDE [WHO-DD] | 1, 3-Benzenedicarboxamide, N, N'-bis(2, 3-dihydroxypropyl)-2, 4, 6-triiodo-5-((methoxyacetyl)amino)-N-methyl- | DB09156 | Iopromida | Iopromidum (INN-Latin) | lopromid | BRN 7085608 | Iopromide, analytical standard | Ioprom

Specifications & Purity

10mM in DMSO

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

This product requires cold chain shipping. Ground and other economy services are not available.

Mechanism of action

Diagnostic agent

Product Properties

• ALogP: -2.1

Names and Identifiers

• Canonical Smiles: CN(CC(CO)O)C(=O)C1=C(C(=C(C(=C1I)C(=O)NCC(CO)O)I)NC(=O)COC)I
• IUPAC Name: 1-N,3-N-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-5-[(2-methoxyacetyl)amino]-3-N-methylbenzene-1,3-dicarboxamide
• InChIKey: DGAIEPBNLOQYER-UHFFFAOYSA-N
• INCHI: 1S/C18H24I3N3O8/c1-24(4-9(28)6-26)18(31)12-13(19)11(17(30)22-3-8(27)5-25)14(20)16(15(12)21)23-10(29)7-32-2/h8-9,25-28H,3-7H2,1-2H3,(H,22,30)(H,23,29)
• Isomeric SMILES: CN(CC(CO)O)C(=O)C1=C(C(=C(C(=C1I)C(=O)NCC(CO)O)I)NC(=O)COC)I
• Molecular Weight: 791.11
• Reaxy-Rn: 7085608
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7085608&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Benzene and substituted derivatives
      • Subclass Benzoic acids and derivatives
        • Level5 Halobenzoic acids and derivatives
          • Level6 4-halobenzoic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Benzoic acids and derivatives
• Intermediate Tree Nodes: Halobenzoic acids and derivatives
• Direct Parent: 4-halobenzoic acids and derivatives
• Alternative Parents: 2-halobenzoic acids and derivatives Benzamides Benzoyl derivatives Iodobenzenes Aryl iodides Vinylogous halides Tertiary carboxylic acid amides Secondary alcohols Propargyl-type 1,3-dipolar organic compounds Carboximidic acids Dialkyl ethers Hydrocarbon derivatives Organic oxides Organoiodides Organonitrogen compounds Organopnictogen compounds Primary alcohols
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: 4-halobenzoic acid or derivatives - 2-halobenzoic acid or derivatives - Benzamide - Benzoyl - Halobenzene - Iodobenzene - Aryl halide - Aryl iodide - Vinylogous halide - Tertiary carboxylic acid amide - Carboxamide group - Secondary alcohol - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid derivative - Dialkyl ether - Ether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organohalogen compound - Organoiodide - Organonitrogen compound - Organooxygen compound - Primary alcohol - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as 4-halobenzoic acids and derivatives. These are benzoic acids or derivatives carrying a halogen atom at the 4-position of the benzene ring.
• External Descriptors: dicarboxylic acid diamide - organoiodine compound

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

Homo sapiens (32628 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)

Discover Target: USP1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RAN Tchem GTP-binding nuclear protein Ran/Importin subunit beta-1/Snurportin-1 (21853 Activities)

Discover Target: RAN

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Sensitivity: Moisture sensitive.
• Melt Point(°C): 145-149°C
• Molecular Weight: 791.100 g/mol
• XLogP3: -2.100
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 11
• Exact Mass: 790.87 Da
• Monoisotopic Mass: 790.87 Da
• Topological Polar Surface Area: 169.000 Ų
• Heavy Atom Count: 32
• Formal Charge: 0
• Complexity: 647.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 2
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Naying Qi, Jia Dong, Xiaoyang Cai, Hongtao Fan, Ying Zhang, Chang Liu, Hongguo Wang, Siqi Zhang.  (2024)  Graphene-based nanomaterials for adsorption of iodinated X-ray contrast media from contaminated water: A comparative study.  CHEMOSPHERE,      [PMID:39038712] [10.1016/j.chemosphere.2024.142915]

2. Wen Xu, Shiwen Dong, Haijun Cheng, Stefanos Giannakis, Xiaohui Lu, Zhiqiao He, Da Wang, Shuang Song, Jun Ma.  (2025)  Nanoparticle contrast agent Mn3O4/SiO2/C as an ozonation catalyst with unexpected synergy in degrading organic contrast agent iopamidol: an effective “treat-waste-with-waste” strategy for medical wastewater.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.162624]