General Information of Drug (ID: DMLDUJ1)

Drug Name
KURAIDIN Drug Info
Synonyms KURAIDIN; kuraridin; CHEMBL243362; PIAPWPAWQGDOMN-SXAWMYDMSA-N; ZINC13817033
Indication
Disease Entry ICD 11 Status REF
Discovery agent N.A. Investigative [1]
Cross-matching ID
PubChem CID
44428631
CAS Number
CAS 34981-25-4
TTD Drug ID
DMLDUJ1
VARIDT Drug ID
DR00952

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Discontinued Drug(s)
Investigative Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Tadalafil DMJZHT1 Benign prostatic hyperplasia GA90 Approved [3]
Udenafil DM1IQRP Erectile dysfunction HA01.1 Approved [4]
Vardenafil DMTBGW8 Cystic fibrosis CA25 Approved [5]
Dipyridamole DMXY30O Atrial fibrillation BC81.3 Approved [6]
Papaverine DMCA9QP Brain ischaemia 8B1Z Approved [7]
Avanafil DM75CXN Erectile dysfunction HA01.1 Approved [8]
Rhucin DM3ADGP Erectile dysfunction HA01.1 Approved [9]
ICARIIN DMOJQGT N. A. N. A. Phase 3 [10]
EXISULIND DMBY56U Colorectal cancer 2B91.Z Phase 3 [11]
PF-489791 DM3C8GQ Chronic obstructive pulmonary disease CA22 Phase 2 [12]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
DENBUFYLLINE DM2R15Q Cognitive impairment 6D71 Phase 3 [13]
SOTB07 DMIG4OX Asthma CA23 Phase 3 [14]
BI 1015550 DM6DO2P Idiopathic pulmonary fibrosis CB03.4 Phase 3 [15]
AN-2898 DMDK7CL Atopic dermatitis EA80 Phase 2 [16]
GPD-1116 DMOQ7YI Asthma CA23 Phase 2 [17]
TA-7906 DMZTAJL Atopic dermatitis EA80 Phase 2 [18]
HT-0712 DM2WP8F Cognitive impairment 6D71 Phase 2 [14]
TOFIMILAST DMLCUAS Chronic obstructive pulmonary disease CA22 Phase 2 [19]
AWD-12-281 DMVADGZ Rhinitis FA20 Phase 2 [20]
LIRIMILAST DMD4KAU Chronic obstructive pulmonary disease CA22 Phase 2 [19]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Sotagliflozin DMMLXA9 Heart failure BD10-BD13 Approved [21]
LIK-066 DM32NWD Heart failure BD10-BD13 Phase 2 [22]
YG1699 DM1NR1J Type-1 diabetes 5A10 Phase 2 [23]
1614235 + 2330672 DMD751X Type-2 diabetes 5A11 Phase 1 [22]
GSK1614235 DM7I1AQ Type-2 diabetes 5A11 Phase 1 [24]
LX2761 DM8ZS7T Type 2 diabetes 5A11 Phase 1 [25]
T-1095 DMGFS51 Diabetic complication 5A2Y Discontinued in Phase 2 [26]
KURARINONE DMH0G8W Discovery agent N.A. Investigative [2]
10-methoxy-N(1)-methylburnamine-17-O-veratrate DMJW25X Discovery agent N.A. Investigative [27]
Alstiphyllanine F DMKRAEW Discovery agent N.A. Investigative [27]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Dyphylline DM8DZC1 Acute bronchial asthma CA23 Approved [28]
Enprofylline DMFYZKN Asthma CA23 Approved [29]
DENBUFYLLINE DM2R15Q Cognitive impairment 6D71 Phase 3 [13]
SOTB07 DMIG4OX Asthma CA23 Phase 3 [30]
Tofisopam DMTGNWU Hyperuricaemia 5C55.Y Phase 2 [31]
AN-2898 DMDK7CL Atopic dermatitis EA80 Phase 2 [16]
GPD-1116 DMOQ7YI Asthma CA23 Phase 2 [17]
TA-7906 DMZTAJL Atopic dermatitis EA80 Phase 2 [18]
HT-0712 DM2WP8F Cognitive impairment 6D71 Phase 2 [30]
TOFIMILAST DMLCUAS Chronic obstructive pulmonary disease CA22 Phase 2 [32]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Bexagliflozin DMK56G0 Type 2 diabetes 5A11 Approved [33]
ISIS-SGLT2 DMDKAIC Type-2 diabetes 5A11 Phase 1 [34]
KURARINONE DMH0G8W Discovery agent N.A. Investigative [2]
10-methoxy-N(1)-methylburnamine-17-O-veratrate DMJW25X Discovery agent N.A. Investigative [27]
Alstiphyllanine F DMKRAEW Discovery agent N.A. Investigative [27]
Kushenol N DMY13UR Discovery agent N.A. Investigative [2]
Alstiphyllanine E DMTNQ5E Discovery agent N.A. Investigative [27]
Burnamine-17-O-3',4',5'-trimethoxybenzoate DMBO0WI Discovery agent N.A. Investigative [27]
Alstiphyllanine D DM2FLDJ Discovery agent N.A. Investigative [27]
O-spiroketal glucoside DM3FS62 Discovery agent N.A. Investigative [35]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Cilostazol DMZMSCT Intermittent claudication BD40.00 Approved [36]
Aminophylline DML2NIB Bronchial asthma CA23 Approved [37]
Anagrelide DMSQ8MD Thrombocythemia 3B63 Approved [38]
Enoximone DMQVZJD Congestive heart failure BD10 Approved [39]
VESNARINONE DMBKX3C Cardiac failure BD10-BD13 Approved [40]
BEMORADAN DMUL6GY Heart failure BD10-BD13 Phase 2 [8]
CI-930 DMADPQX N. A. N. A. Discontinued in Phase 2 [41]
EMD-53998 DMVS8IE Cardiovascular disease BA00-BE2Z Discontinued in Phase 1 [8]
IMAZODAN DMWTFO3 N. A. N. A. Terminated [42]
LAS-31180 DMW2K1L Heart failure BD10-BD13 Terminated [43]
⏷ 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
Phosphodiesterase 3A (PDE3A) TT06AWU PDE3A_HUMAN Inhibitor [1]
Phosphodiesterase 4A (PDE4A) TTZ97H5 PDE4A_HUMAN Inhibitor [1]
Phosphodiesterase 4B (PDE4B) TTVIAT9 PDE4B_HUMAN Inhibitor [1]
Phosphodiesterase 5A (PDE5A) TTJ0IQB PDE5A_HUMAN Inhibitor [1]
SLC5A2 messenger RNA (SLC5A2 mRNA) TTF8JAT SC5A2_HUMAN Inhibitor [2]
Sodium/glucose cotransporter 1 (SGLT1) TT2UE56 SC5A1_HUMAN Inhibitor [2]

References

1 A prenylated flavonol, sophoflavescenol: a potent and selective inhibitor of cGMP phosphodiesterase 5. Bioorg Med Chem Lett. 2002 Sep 2;12(17):2313-6.
2 Na+-glucose cotransporter (SGLT) inhibitory flavonoids from the roots of Sophora flavescens. Bioorg Med Chem. 2007 May 15;15(10):3445-9.
3 Pulmonary arterial hypertension: the most devastating vascular complication of systemic sclerosis. Rheumatology (Oxford). 2009 Jun;48 Suppl 3:iii25-31.
4 Increased expression of the nitric oxide synthase gene and protein in corpus cavernosum by repeated dosing of udenafil in a rat model of chemical d... Asian J Androl. 2009 Jul;11(4):435-42.
5 The effect of vardenafil, a potent and highly selective phosphodiesterase-5 inhibitor for the treatment of erectile dysfunction, on the cardiovascular response to exercise in patients with coronary artery disease. J Am Coll Cardiol. 2002 Dec 4;40(11):2006-12.
6 Anti-platelet therapy: phosphodiesterase inhibitors.Br J Clin Pharmacol.2011 Oct;72(4):634-46.
7 Effects of icariin on cGMP-specific PDE5 and cAMP-specific PDE4 activities. Asian J Androl. 2003 Mar;5(1):15-8.
8 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services. 2015
9 cGMP-hydrolytic activity and its inhibition by sildenafil in normal and failing human and mouse myocardium. J Pharmacol Exp Ther. 2009 Sep;330(3):884-91.
10 Potent inhibition of human phosphodiesterase-5 by icariin derivatives. J Nat Prod. 2008 Sep;71(9):1513-7.
11 Exisulind induction of apoptosis involves guanosine 3',5'-cyclic monophosphate phosphodiesterase inhibition, protein kinase G activation, and attenuated beta-catenin. Cancer Res. 2000 Jul 1;60(13):3338-42.
12 Highlights of the society for medicinesresearch symposium held december 10th 2009 at the national heart and lung institute, London, UK. Drugs of the Future 2010, 35(4): 349-358.
13 Pyrazolopyrimidine-2,4-dione sulfonamides: novel and selective calcitonin inducers. J Med Chem. 2002 May 23;45(11):2342-5.
14 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. (Target id: 1301).
15 BI 1015550 is a PDE4B Inhibitor and a Clinical Drug Candidate for the Oral Treatment of Idiopathic Pulmonary Fibrosis. Front Pharmacol. 2022 Apr 20;13:838449.
16 An assessment of the genetic toxicology of novel boron-containing therapeutic agents. Environ Mol Mutagen. 2013 Jun;54(5):338-46.
17 Phosphodiesterase 4 inhibitor GPD-1116 markedly attenuates the development of cigarette smoke-induced emphysema in senescence-accelerated mice P1 s... Am J Physiol Lung Cell Mol Physiol. 2008 Feb;294(2):L196-204.
18 Potential role of phosphodiesterase 7 in human T cell function: comparative effects of two phosphodiesterase inhibitors. Clin Exp Immunol. 2002 Jun;128(3):460-6.
19 Therapeutic target database update 2012: a resource for facilitating target-oriented drug discovery. Nucleic Acids Res. 2012 Jan;40(Database issue):D1128-36.
20 The phosphodiesterase 4 inhibitor AWD 12-281 is active in a new guinea-pig model of allergic skin inflammation predictive of human skin penetration and suppresses both Th1 and Th2 cytokines in mice. J Pharm Pharmacol. 2005 Dec;57(12):1609-17.
21 LX4211, a dual SGLT1/SGLT2 inhibitor, improved glycemic control in patients with type 2 diabetes in a randomized, placebo-controlled trial. Clin Pharmacol Ther. 2012 Aug;92(2):158-69.
22 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. (Target id: 915).
23 ClinicalTrials.gov (NCT04956263) A Comparison of Postprandial Glucose After a Mixed Meal Tolerance Test, and the Metabolic Effects of Insulin Withdrawal in a Crossover Study of the Dual Systemic SGLT1 and SGLT2 Inhibitor YG1699, and the Selective SGLT2 Inhibitor Dapagliflozin in Subjects With Type 1 Diabetes. U.S.National Institutes of Health.
24 Clinical pipeline report, company report or official report of GlaxoSmithKline (2009).
25 Clinical pipeline report, company report or official report of Lexicon Pharmaceuticals.
26 T-1095, an inhibitor of renal Na+-glucose cotransporters, may provide a novel approach to treating diabetes. Diabetes. 1999 Sep;48(9):1794-800.
27 Alstiphyllanines E-H, picraline and ajmaline-type alkaloids from Alstonia macrophylla inhibiting sodium glucose cotransporter. Bioorg Med Chem. 2010 Mar 15;18(6):2152-2158.
28 Ocular hypotension induced by topical dopaminergic drugs and phosphodiesterase inhibitors. Eur J Pharmacol. 1994 Jun 2;258(1-2):85-94.
29 Effects of enprofylline, a new xanthine derivate, on human pregnant myometrium. Am J Obstet Gynecol. 1987 Apr;156(4):958-62.
30 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. (Target id: 1300).
31 The atypical anxiolytic drug, tofisopam, selectively blocks phosphodiesterase isoenzymes and is active in the mouse model of negative symptoms of psychosis. J Neural Transm (Vienna). 2010 Nov;117(11):1319-25.
32 GSK256066, an exceptionally high-affinity and selective inhibitor of phosphodiesterase 4 suitable for administration by inhalation: in vitro, kinetic, and in vivo characterization. J Pharmacol Exp Ther. 2011 Apr;337(1):145-54.
33 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
34 Clinical pipeline report, company report or official report of ISIS Pharmaceuticals (2011).
35 ortho-Substituted C-aryl glucosides as highly potent and selective renal sodium-dependent glucose co-transporter 2 (SGLT2) inhibitors. Bioorg Med Chem. 2010 Jun 15;18(12):4422-32.
36 A new generation of phosphodiesterase inhibitors: multiple molecular forms of phosphodiesterase and the potential for drug selectivity. J Med Chem. 1985 May;28(5):537-45.
37 Topical fat reduction from the waist. Diabetes Obes Metab. 2007 May;9(3):300-3.
38 Hydroxyurea compared with anagrelide in high-risk essential thrombocythemia. N Engl J Med. 2005 Jul 7;353(1):33-45.
39 Inhibitors of cyclic AMP phosphodiesterase. 2. Structural variations of N-cyclohexyl-N-methyl-4-[(1,2,3,5-tetrahydro- 2-oxoimidazo[2,1-b]quinazolin... J Med Chem. 1987 Feb;30(2):303-18.
40 Design, synthesis and biological evaluation of 6-(benzyloxy)-4-methylquinolin-2(1H)-one derivatives as PDE3 inhibitors. Bioorg Med Chem. 2010 Jan 15;18(2):855-62.
41 Cardiotonic agents. 9. Synthesis and biological evaluation of a series of (E)-4,5-dihydro-6-[2-[4-(1H-imidazol-1-yl)phenyl]ethenyl]-3 (2H)-pyridazi... J Med Chem. 1989 Feb;32(2):342-50.
42 3,4-Dihydroquinolin-2(1H)-ones as combined inhibitors of thromboxane A2 synthase and cAMP phosphodiesterase. J Med Chem. 1992 Feb 21;35(4):620-8.
43 Pharmacological profile of LAS 31180, a new inotropic/vasodilator quinolone derivative. Arzneimittelforschung. 2000 Nov;50(11):980-6.