General Information of Drug (ID: DMARZHU)

Drug Name
N4-(4-chlorobenzyl)-2,4-diaminobutanoylpiperidine Drug Info
Synonyms
DNVZYSMOLXCOLY-HNNXBMFYSA-N; UAMC00039; CHEMBL98869; SCHEMBL6824340; GTPL6538; ZINC13561228; BDBM50146972; NCGC00379239-01; 1-[(S)-2-Amino-4-[(4-chlorobenzyl)amino]butyryl]piperidine; (S)-4-(4-chlorobenzylamino)-2-amino-1-(piperidin-1-yl)butan-1-one; (2S)-2-amino-4-[(4-chlorophenyl)methylamino]-1-piperidin-1-ylbutan-1-one; 2-(S)-Amino-4-(4-chloro-benzylamino)-1-piperidin-1-yl-butan-1-one
Indication
Disease Entry ICD 11 Status REF
Discovery agent N.A. Investigative [1]
Cross-matching ID
PubChem CID
11232124
ChEBI ID
CHEMBL98869
TTD Drug ID
DMARZHU

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Patented Agent(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Saxagliptin DMGXENV Type-2 diabetes 5A11 Approved [4]
Sitagliptin DMGDKXN Cystic fibrosis CA25 Approved [5]
Alogliptin DM8WI3R Type-2 diabetes 5A11 Approved [6]
Linagliptin DMWFJTR Non-insulin dependent diabetes 5A11 Approved [7]
Vildagliptin DMYN59P Type-2 diabetes 5A11 Approved [8]
Dapagliflozin Propanediol; Saxagliptin Hydrochloride DM34TXO Type-2 diabetes 5A11 Approved [9]
Anagliptin DMJXIC9 Type-2 diabetes 5A11 Approved [10]
SaxaDapa FDC DMAPRWV Diabetic complication 5A2Y Phase 3 [11]
LC-150444 DM09RKB Type-2 diabetes 5A11 Phase 3 [12]
Dutogliptin DMM5VTA Type-2 diabetes 5A11 Phase 3 [13]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
BDBM50382283 DMQJ5S8 N. A. N. A. Patented [14]
BDBM50434165 DMDTYJ9 N. A. N. A. Patented [14]
BDBM50434164 DM6DFTX N. A. N. A. Patented [14]
US8470836, 5 DMYR10P N. A. N. A. Patented [15]
US8470836, 8 DMM4GLH N. A. N. A. Patented [15]
CRWCYVOHVXAEMF-LBPRGKRZSA-N DMBV5Z0 N. A. N. A. Patented [14]
US8470836, 2 DMH7JVA N. A. N. A. Patented [15]
US8470836, 6 DMVYQXH N. A. N. A. Patented [15]
⏷ Show the Full List of 8 Drug(s)

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Dipeptidyl peptidase 4 (DPP-4) TTDIGC1 DPP4_HUMAN Inhibitor [2]
Dipeptidyl-peptidase 7 (DPP7) TTOYT5L DPP2_HUMAN Inhibitor [3]

References

1 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 6538).
2 Synthesis and dipeptidyl peptidase inhibition of N-(4-substituted-2,4-diaminobutanoyl)piperidines. Bioorg Med Chem Lett. 2006 Sep 15;16(18):4777-9.
3 Dipeptidyl peptidase II and leukocyte cell death. Biochem Pharmacol. 2006 Jun 28;72(1):70-9.
4 Hughes B: 2009 FDA drug approvals. Nat Rev Drug Discov. 2010 Feb;9(2):89-92.
5 Novel therapeutics for type 2 diabetes: incretin hormone mimetics (glucagon-like peptide-1 receptor agonists) and dipeptidyl peptidase-4 inhibitors. Pharmacol Ther. 2009 Oct;124(1):113-38.
6 Clinical pipeline report, company report or official report of Takeda (2009).
7 Boehringer Ingelheim. Product Development Pipeline. June 2 2009.
8 Emerging drug candidates of dipeptidyl peptidase IV (DPP IV) inhibitor class for the treatment of Type 2 Diabetes. Curr Drug Targets. 2009 Jan;10(1):71-87.
9 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services.
10 Diabetes Treatment. Diabetes Care. 2009 March; 32(3): e25-e30.
11 Saxagliptin: a new dipeptidyl peptidase-4 inhibitor for type 2 diabetes. Cardiol Rev. 2010 Jul-Aug;18(4):213-7.
12 Clinical pipeline report, company report or official report of ShangHai APIs Chemical.
13 Dutogliptin, a selective DPP4 inhibitor, improves glycaemic control in patients with type 2 diabetes: a 12-week, double-blind, randomized, placebo-controlled, multicentre trial. Diabetes Obes Metab. 2010 Apr;12(4):348-55.
14 FAP inhibitors. US9346814.
15 Dipeptidyl peptidase-IV inhibiting compounds, methods of preparing the same, and pharmaceutical compositions containing the same as active agent. US8470836.