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Details

Stereochemistry ABSOLUTE
Molecular Formula C19H23Cl2N3O4
Molecular Weight 428.31
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ORE-1001

SMILES

CC(C)C[C@H](N[C@@H](CC1=CN=CN1CC2=CC(Cl)=CC(Cl)=C2)C(O)=O)C(O)=O

InChI

InChIKey=NTCCRGGIJNDEAB-IRXDYDNUSA-N
InChI=1S/C19H23Cl2N3O4/c1-11(2)3-16(18(25)26)23-17(19(27)28)7-15-8-22-10-24(15)9-12-4-13(20)6-14(21)5-12/h4-6,8,10-11,16-17,23H,3,7,9H2,1-2H3,(H,25,26)(H,27,28)/t16-,17-/m0/s1

HIDE SMILES / InChI
Ore Pharmaceuticals developed ORE1001 previously known as MLN-4760 as an orally administered, small molecule compound, for the treatment of inflammatory bowel diseases. ORE1001 is a specific angiotensin-converting enzyme 2 inhibitor. It was shown that ORE1001 markedly decreased tissue myeloperoxidase activity, a well-known marker of inflammation. As a result, ORE1001 was studied as a treatment of gastrointestinal inflammatory conditions. ORE1001 was involved in phase I clinical trial to investigate its safety and activity in subjects with ulcerative colitis. In addition, the drug was studied for NSAID-induced ulcer and obesity. However, all these studies were discontinued.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q9BYF1
Gene ID: 59272.0
Gene Symbol: ACE2
Target Organism: Homo sapiens (Human)
PubMed

PubMed

TitleDatePubMed
Murine recombinant angiotensin-converting enzyme 2: effect on angiotensin II-dependent hypertension and distinctive angiotensin-converting enzyme 2 inhibitor characteristics on rodent and human angiotensin-converting enzyme 2.
2012 Sep

Sample Use Guides

Oral capsules containing 300 mg of the active, study drug
Route of Administration: Oral
Name Type Language
ORE-1001
Common Name English
ORE-1001 FREE ACID
Code English
GL1001
Code English
MLN-4760
Code English
L-HISTIDINE, N-((1S)-1-CARBOXY-3-METHYLBUTYL)-3-((3,5-DICHLOROPHENYL)METHYL)-
Systematic Name English
ORE1001
Code English
GL-1001
Common Name English
Code System Code Type Description
FDA UNII
4LD0ZHV25K
Created by admin on Sat Dec 16 05:40:19 GMT 2023 , Edited by admin on Sat Dec 16 05:40:19 GMT 2023
PRIMARY
EPA CompTox
DTXSID70184609
Created by admin on Sat Dec 16 05:40:19 GMT 2023 , Edited by admin on Sat Dec 16 05:40:19 GMT 2023
PRIMARY
CAS
305335-31-3
Created by admin on Sat Dec 16 05:40:19 GMT 2023 , Edited by admin on Sat Dec 16 05:40:19 GMT 2023
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CHEBI
166834
Created by admin on Sat Dec 16 05:40:19 GMT 2023 , Edited by admin on Sat Dec 16 05:40:19 GMT 2023
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DRUG BANK
DB12271
Created by admin on Sat Dec 16 05:40:19 GMT 2023 , Edited by admin on Sat Dec 16 05:40:19 GMT 2023
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PUBCHEM
448281
Created by admin on Sat Dec 16 05:40:19 GMT 2023 , Edited by admin on Sat Dec 16 05:40:19 GMT 2023
PRIMARY