CHEBI:73175 - 2,3,5-triiodobenzoic acid

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ChEBI Name 2,3,5-triiodobenzoic acid
ChEBI ID CHEBI:73175
Definition A member of the class of benzoic acids that is benzoic acid in which the hydrogens at positions 2, 3 and 5 are replaced by iodine atoms. It is an auxin polar transport inhibitor.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Johnny Lloyd
Secondary ChEBI IDs CHEBI:40944
Supplier Information
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Formula C7H3I3O2
Net Charge 0
Average Mass 499.81090
Monoisotopic Mass 499.72671
InChI InChI=1S/C7H3I3O2/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2H,(H,11,12)
InChIKey ZMZGFLUUZLELNE-UHFFFAOYSA-N
SMILES OC(=O)c1cc(I)cc(I)c1I
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): antiauxins

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ChEBI Ontology
Outgoing 2,3,5-triiodobenzoic acid (CHEBI:73175) has role antiauxins (CHEBI:22581)
2,3,5-triiodobenzoic acid (CHEBI:73175) is a benzoic acids (CHEBI:22723)
2,3,5-triiodobenzoic acid (CHEBI:73175) is a organoiodine compound (CHEBI:37142)
IUPAC Name
2,3,5-triiodobenzoic acid
Synonyms Sources
2,3,5-TIBA ChemIDplus
2,3,5-tri-iodobenzoic acid ChEBI
acide 2,3,5-triiodobenzoique ChEBI
NSC 2582 NIST Chemistry WebBook
TIBA ChemIDplus
Triiodobenzoic acid ChemIDplus
Brand Names Sources
Floraltone ChemIDplus
Regim-8 ChEBI
Manual Xrefs Databases
2941 PPDB
B3I PDBeChem
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Registry Numbers Types Sources
1955088 Reaxys Registry Number Reaxys
88-82-4 CAS Registry Number NIST Chemistry WebBook
88-82-4 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
11337075 PubMed citation Europe PMC
16654211 PubMed citation Europe PMC
16661364 PubMed citation Europe PMC
16661662 PubMed citation Europe PMC
19689397 PubMed citation Europe PMC
5035796 PubMed citation Europe PMC
5125766 PubMed citation Europe PMC
5134653 PubMed citation Europe PMC
5373716 PubMed citation Europe PMC
5411351 PubMed citation Europe PMC
IND44469853 Agricola citation Europe PMC
Last Modified
12 April 2013