GCR

GALLICHROME

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is present as a standalone ligand in 1 entries

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Chemical Component Summary
Name	GALLICHROME
Formula	C₂₈ H₄₄ Ga N₉ O₁₃
Molecular Weight	784.424
Type	NON-POLYMER
Isomeric SMILES	CC1=O[Ga]2345O=C(N(O2)CCC[C@H]6C(=O)NCC(=O)N[C@H](C(=O)NCC(=O)N[C@@H](CCCN1O3)C(=O)N[C@@H](CCCN(O4)C(=O5)C)C(=O)N6)CO)C
InChI	InChI=1S/C28H44N9O13.Ga/c1-16(39)35(48)10-4-7-19-25(44)29-14-24(43)32-22(15-38)26(45)30-13-23(42)31-20(8-5-11-36(49)17(2)40)27(46)34-21(28(47)33-19)9-6-12-37(50)18(3)41;/h19-22,38H,4-15H2,1-3H3,(H,29,44)(H,30,45)(H,31,42)(H,32,43)(H,33,47)(H,34,46);/q-3;+3/t19-,20-,21-,22?;/m0./s1
InChIKey	BEDMDXBTNSVNGS-GSJIPYROSA-N

Chemical Details
Formal Charge	0
Atom Count	95
Chiral Atom Count	7
Bond Count	100
Aromatic Bond Count	0

Drug Info: DrugBank

DrugBank ID	DB03436
Name	Gallichrome
Groups	experimental
Synonyms	Gallichrome
Categories	Amines Amino Acids, Peptides, and Proteins Gallium Hydroxamic Acids Hydroxy Acids Hydroxylamines Peptides Peptides, Cyclic

Drug Targets

Name	Target Sequence	Pharmacological Action	Actions
Iron(3+)-hydroxamate-binding protein FhuD	MSGLPLISRRRLLTAMALSPLLWQMNTAHAAAIDPNRIVALEWLPVELLL...	unknown	antagonist

Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS. Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682