General Information of Drug (ID: DMHINE0)

Drug Name
N(6)-cyclohexyladenosine Drug Info
Synonyms
N6-Cyclohexyladenosine; 36396-99-3; (2R,3R,4S,5R)-2-(6-(Cyclohexylamino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol; N(6)-Cyclohexyladenosine; C16H23N5O4; Adenosine, N-cyclohexyl-; CHEMBL45891; (2R,3R,4S,5R)-2-[6-(cyclohexylamino)purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol; n-cyclohexyladenosine; N6 -cyclohexyladenosine; N-6-cyclohexyladenosine; N6-Cyclohexylado (CHA); n6-cyclohexyl[3h]adenosine; Lopac0_000331; GTPL423; SCHEMBL145856; SZBULDQSDUXAPJ-XNIJJKJLSA-N; MolPort-027-835-536; HMS3261C03; ZINC4217017
Indication
Disease Entry ICD 11 Status REF
Discovery agent N.A. Investigative [1]
Cross-matching ID
PubChem CID
9841284
TTD Drug ID
DMHINE0

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Clinical Trial Drug(s)
Discontinued Drug(s)
Preclinical Drug(s)
Approved Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
IB-MECA DM9G5XD Psoriasis vulgaris EA90 Phase 3 [5]
Tonapofylline DMBH316 Acute and chronic heart failure BD1Z Phase 2 [6]
NITD609 DMQHBSX Malaria 1F40-1F45 Phase 2 [7]
CF102 DMP56WJ Hepatocellular carcinoma 2C12.02 Phase 2 [8]
SCH-442416 DMQ2K1V N. A. N. A. Phase 1 [9]
AST-004 DM5WMG7 Stroke 8B20 Phase 1 [10]
BEMESETRON DMSPJX9 N. A. N. A. Discontinued in Phase 3 [11]
BAY 60-6583 DMTEJV1 Myocardial ischemia BA6Z Preclinical [12]
CF602 DM0ULO2 Inflammation 1A00-CA43.1 Preclinical [8]
CF502 DMQSJ20 Inflammation 1A00-CA43.1 Preclinical [8]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Adenosine DMM2NSK Paroxysmal supraventricular tachycardia BC81.Z Approved [13]
Vidarabine DM0N85H Hepatosplenic T-cell lymphoma Approved [13]
A295 DM55GO2 Aggressive cancer 2A00-2F9Z IND submitted [14]
Tonapofylline DMBH316 Acute and chronic heart failure BD1Z Phase 2 [6]
YT-146 DM3YVKQ Hypertension BA00-BA04 Phase 2 [15]
AB928 DMDOXMN Metastatic colorectal cancer 2B91 Phase 1/2 [16]
KF-17837 DMQ6DLZ Parkinson disease 8A00.0 Phase 1 [17]
Xanthine DMFBOQ7 Apnea MD11.0 Phase 1 [18]
CVT-6883 DMY84TW Asthma CA23 Phase 1 [19]
PBF-1129 DMOPGXM Non-small-cell lung cancer 2C25.Y Phase 1 [16]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Caffeine DMKBJWP Allergic rhinitis CA08.0 Approved [20]
Rolofylline DMSZPR3 Heart failure BD10-BD13 Phase 3 [21]
Tonapofylline DMBH316 Acute and chronic heart failure BD1Z Phase 2 [6]
AMP-579 DMJ4GPR Hyperlipidaemia 5C80 Phase 2 [22]
SELODENOSON DMQM3IX Cardiac arrhythmias BC9Z Phase 2 [23]
Apaxifylline DMQMV9F Cognitive impairment 6D71 Phase 2 [24]
SLV320 DM867BJ Heart failure BD10-BD13 Phase 2 [25]
DTI-0009 DMV84OK Atrial fibrillation BC81.3 Phase 2 [23]
Capadenoson DMYWO62 Atrial fibrillation BC81.3 Phase 2 [26]
BAY 1067197 DM4JGNH Heart failure BD10-BD13 Phase 2 [27]
⏷ Show the Full List of 10 Drug(s)

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Adenosine A1 receptor (ADORA1) TTK25J1 AA1R_HUMAN Agonist [2]
Adenosine A2b receptor (ADORA2B) TTNE7KG AA2BR_HUMAN Agonist [3]
Adenosine A3 receptor (ADORA3) TTJFY5U AA3R_HUMAN Agonist [4]

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: 423).
2 Structure-activity relationships for 2-substituted adenosines at A1 and A2 adenosine receptors. Pharmacology. 1993;46(2):91-100.
3 Adenosine receptor activation in human fibroblasts: nucleoside agonists and antagonists. Can J Physiol Pharmacol. 1980 Jun;58(6):673-91.
4 Inhibition of TNF-alpha expression by adenosine: role of A3 adenosine receptors. J Immunol. 1996 May 1;156(9):3435-42.
5 A role for central A3-adenosine receptors. Mediation of behavioral depressant effects. FEBS Lett. 1993 Dec 20;336(1):57-60.
6 2-Amino-5-benzoyl-4-phenylthiazoles: Development of potent and selective adenosine A1 receptor antagonists. Bioorg Med Chem. 2010 Mar 15;18(6):2195-2203.
7 Spiroindolones, a potent compound class for the treatment of malaria. Science. 2010 Sep 3;329(5996):1175-80.
8 2011 Pipeline of Can-Fite BioPharm.
9 Synthesis and evaluation of 1,2,4-triazolo[1,5-c]pyrimidine derivatives as A2A receptor-selective antagonists. Bioorg Med Chem Lett. 2010 Oct 1;20(19):5690-4.
10 Adenosine A1R/A3R (Adenosine A1 and A3 Receptor) Agonist AST-004 Reduces Brain Infarction in a Nonhuman Primate Model of Stroke. Stroke. 2022 Jan;53(1):238-248.
11 2-n-Butyl-9-methyl-8-[1,2,3]triazol-2-yl-9H-purin-6-ylamine and analogues as A2A adenosine receptor antagonists. Design, synthesis, and pharmacolog... J Med Chem. 2005 Nov 3;48(22):6887-96.
12 Protein kinase C protects preconditioned rabbit hearts by increasing sensitivity of adenosine A2b-dependent signaling during early reperfusion. J Mol Cell Cardiol. 2007 Sep;43(3):262-71.
13 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services.
14 Clinical pipeline report, company report or official report of Klus Pharma
15 Identification of adenosine A2 receptor-cAMP system in human aortic endothelial cells. Biochem Biophys Res Commun. 1994 Mar 15;199(2):905-10.
16 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
17 Photoisomerization of a potent and selective adenosine A2 antagonist, (E)-1,3-Dipropyl-8-(3,4-dimethoxystyryl)-7-methylxanthine. J Med Chem. 1993 Nov 12;36(23):3731-3.
18 Role of adenosine in asthma. Drug Dev Res. 1996;39:333-6.
19 GS-6201, a selective blocker of the A2B adenosine receptor, attenuates cardiac remodeling after acute myocardial infarction in the mouse. J Pharmacol Exp Ther. 2012 Dec;343(3):587-95.
20 Caffeine as a psychomotor stimulant: mechanism of action. Cell Mol Life Sci. 2004 Apr;61(7-8):857-72.
21 Association between the PDE4D gene and ischaemic stroke in the Chinese Han population. Clin Sci (Lond). 2009 Aug 17;117(7):265-72.
22 Adenosine A1/A2a receptor agonist AMP-579 induces acute and delayed preconditioning against in vivo myocardial stunning. Am J Physiol Heart Circ Physiol. 2004 Dec;287(6):H2746-53.
23 Recent developments in adenosine receptor ligands and their potential as novel drugs. Biochim Biophys Acta. 2011 May;1808(5):1290-308.
24 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800004779)
25 Role of matrix metalloproteinases and their tissue inhibitors as potential biomarkers of left ventricular remodelling in the athlete's heart. Clin Sci (Lond). 2009 Jul 16;117(4):157-64.
26 A1 adenosine receptor agonists and their potential therapeutic applications. Expert Opin Investig Drugs. 2008 Dec;17(12):1901-10.
27 Separation of on-target efficacy from adverse effects through rational design of a bitopic adenosine receptor agonist. Current Issue vol. 111 no. 12 Celine Valant, 4614-4619.