General Information of the Compound
Compound ID
CP0035896
Compound Name
GM6001
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Synonyms
(R)-N(sup 1)-Hydroxy-N-((S)-2-indol-3-yl-1-(methylcarbamoyl)ethyl)-2-isobutylsuccinamide
(R)-N4-Hydroxy-N1-[(S)-2-(1H-indol-3-yl)-1-methylcarbamoyl-ethyl]-2-isobutyl-succinamide
(S-(R*,S*))-N(sup 4)-Hydroxy-N(sup
142880-36-2
3-(N-HYDROXYCARBOXAMIDO)-2-ISOBUTYLPROPANOYL-TRP-METHYLAMIDE
CHEMBL19611
CS 610
GM 6001
GM-6001
GM6001
Galardin
I0403ML141
ILOMASTAT
Illomastat
Ilomastat
Ilomastat (GM6001, Galardin)
N-[(2R)-2-(Hydroxamidocarbonylmethyl)-4-methylpentanoyl]-L-tryptophan Methylamide
NCGC00163450-02
UNII-I0403ML141
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Structure
Formula
C20H28N4O4
Molecular Weight
388.468
Canonical SMILES
CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(C)C)CC(=O)NO
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InChI
InChI=1S/C20H28N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-7,11-13,17,22,28H,8-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/t13-,17+/m1/s1
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InChIKey
NITYDPDXAAFEIT-DYVFJYSZSA-N
CAS
142880-36-2
Physicochemical Property
logP
1.499
Rotatable Bonds
9
Heavy Atom Count
28
Polar Areas
123.32
Hydrogen Bond Donor Count
5
Hydrogen Bond Acceptor Count
4
Complexity
28

"RO5" indicates the cutoff set by lipinski's rule of five:

(1) Molecular weight less than 500 Dalton;

(2) xlogp less than 5;

(3) No more than 5 hbonddonor (Hydrogen Bond Donor Count);

(4) No more than 10 hbondacc (Hydrogen Bond Acceptor Count);

(5) No more than 10 rotbonds (Rotatable Bond Count).

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PubChem ID
CID: 132519
SID: 14902905
ChEMBL ID
CHEMBL19611
DrugBank ID
DB02255
Map of Molecular Bioactivity Related to the Compound
Map of Molecular Bioactivity Related to the Compound

Compound
Cell Line
Protein

Bioactivity Value:

<= 0.1 μM
> 0.1 μM and <= 10 μM
> 10 μM
Imprecise Activity
Table of Molecular Bioactivities Related to the Compound
Protein ID: PT01178, A disintegrin and metalloproteinase with thrombospondin motifs 4
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
IC50 = 480 nM
   TI
   LI
   LO
   TS
Protein ID: PT01250, A disintegrin and metalloproteinase with thrombospondin motifs 5
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
IC50 = 500 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( GM6001 )
Drug Name GM6001
Indication
Corneal ulcer
Discontinued in Phase 2
Target(s)
Matrix metalloproteinase-12 (MMP-12)
Inhibitor
Matrix metalloproteinase-13 (MMP-13)
Inhibitor
Matrix metalloproteinase-1 (MMP-1)
Inhibitor
Matrix metalloproteinase-14 (MMP-14)
Inhibitor
Matrix metalloproteinase-2 (MMP-2)
Inhibitor
Matrix metalloproteinase-9 (MMP-9)
Inhibitor
Matrix metalloproteinase-8 (MMP-8)
Inhibitor
Bacterial Lethal factor (Bact lef)
Inhibitor
Matrix metalloproteinase-3 (MMP-3)
Inhibitor