General Information of DTT (ID: TT0PG8F)

DTT Name Cyclin-dependent kinase 4 (CDK4) DTT Info
Gene Name CDK4

Molecule-Related Drug & Molecule List

Molecule-Related Drug List
Molecule Type:
DTT
DTP
DME
Drug Status:
Discontinued Drug(s)
Approved Drug(s)
Clinical Trial Drug(s)
Preclinical Drug(s)
Patented Agent(s)
Investigative Drug(s)
5 Approved Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
Apremilast DMTWS9E Psoriasis vulgaris EA90 Approved [1]
LY2835219 DM93VBZ Breast cancer 2C60-2C65 Approved [2]
Palbociclib DMD7L94 Breast cancer 2C60-2C65 Approved [3]
Ribociclib Succinate DM9CIUW Breast cancer 2C60-2C65 Approved [4]
Trilaciclib DMP5A4T Small-cell lung cancer 2C25.Y Approved [5]
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16 Clinical Trial Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
LEE011 DMMX75K Breast cancer 2C60-2C65 Phase 3 [6]
G1T38 DMQO2IT Breast cancer 2C60-2C65 Phase 2 [7]
P-276 DMMJUHD Breast cancer 2C60-2C65 Phase 2 [8]
P276-00 DM9DJL2 Mantle cell lymphoma 2A85.5 Phase 2 [9]
Ro 31-7453 DM83QCL Solid tumour/cancer 2A00-2F9Z Phase 2 [10]
FCN-437 DMQ8VUW Breast cancer 2C60-2C65 Phase 1/2 [11]
GLR2007 DM7DWLY Glioblastoma of brain 2A00.00 Phase 1/2 [12]
NUV-422 DMQJQNT Malignant glioma 2A00.0 Phase 1/2 [13]
AG-024322 DMY4WVK Solid tumour/cancer 2A00-2F9Z Phase 1 [9]
FN-1501 DM7BMD6 Solid tumour/cancer 2A00-2F9Z Phase 1 [14]
G1T28-1 DML028U Solid tumour/cancer 2A00-2F9Z Phase 1 [2]
P1446A-05 DMXHKYJ Solid tumour/cancer 2A00-2F9Z Phase 1 [9]
PF-07220060 DMPKO84 Liposarcoma 2B59 Phase 1 [15]
PHA-793887 DM2Y4FG Solid tumour/cancer 2A00-2F9Z Phase 1 [8]
RGB-286638 DMEGOQP Haematological malignancy 2B33.Y Phase 1 [8]
RGT-419B DMD2MND Breast cancer 2C60-2C65 Phase 1 [16]
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⏷ Show the Full List of 16 Clinical Trial Drug(s)
13 Patented Agent(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
Imidazo pyridine derivative 3 DMPCLZB N. A. N. A. Patented [17]
Indole-based analog 13 DMV7DFM N. A. N. A. Patented [17]
Isoquinoline 1,3-dione derivative 1 DMIYUAN N. A. N. A. Patented [17]
Oxazolyl methylthiothiazole derivative 1 DMZM6FW N. A. N. A. Patented [17]
PMID25726713-Compound-47 DMXE5KM N. A. N. A. Patented [18]
PMID25726713-Compound-48 DMSIOUA N. A. N. A. Patented [18]
PMID25726713-Compound-49 DM2CT4G N. A. N. A. Patented [18]
PMID25726713-Compound-50 DM3BDFV N. A. N. A. Patented [18]
PMID25726713-Compound-51 DMF0OW4 N. A. N. A. Patented [18]
PMID25991433-Compound-A1 DM89LF0 N. A. N. A. Patented [19]
PMID26161698-Compound-17 DMB92RA N. A. N. A. Patented [17]
Pyrrolo[2,3-d]pyrimidine derivative 10 DMRWG2E N. A. N. A. Patented [17]
Pyrrolo[2,3-d]pyrimidine derivative 9 DM0HU5O N. A. N. A. Patented [17]
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⏷ Show the Full List of 13 Patented Agent(s)
5 Discontinued Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
BAY 10-00394 DMV2DIW Small-cell lung cancer 2C25.Y Discontinued in Phase 2 [8]
R547 DMK25FU Advanced solid tumour 2A00-2F9Z Discontinued in Phase 1 [9]
ZK 304709 DMJ9R4A Advanced solid tumour 2A00-2F9Z Discontinued in Phase 1 [9]
CYC-103 DM17NYA Solid tumour/cancer 2A00-2F9Z Terminated [8]
PD-0183812 DMWYP86 Retinoblastoma 2D02.2 Terminated [20]
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1 Preclinical Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
INOC-005 DMBQGZ9 Solid tumour/cancer 2A00-2F9Z Preclinical [8]
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21 Investigative Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
1-(1H-Indazol-6-yl)-3-pyridin-2-yl-urea DM9MCAU Discovery agent N.A. Investigative [21]
1-(7-Hydroxy-naphthalen-1-yl)-3-pyridin-2-yl-urea DM7OGLI Discovery agent N.A. Investigative [21]
1-(9-Oxo-9H-fluoren-4-yl)-3-pyridin-2-yl-urea DM30FNL Discovery agent N.A. Investigative [21]
1-Pyridin-2-yl-3-quinolin-5-yl-urea DMTMXN4 Discovery agent N.A. Investigative [21]
10-hydroxy-18-methoxybetaenone DM4R7X8 Discovery agent N.A. Investigative [22]
3,4-di-(4-methoxyphenyl)-1H-pyrrole-2,5-dione DMDO175 Discovery agent N.A. Investigative [23]
3,4-diphenyl-1H-pyrrole-2,5-dione DMPK6YT Discovery agent N.A. Investigative [23]
3-(4-methoxyphenyl)-4-phenyl-1H-pyrrole-2,5-dione DMGC7RY Discovery agent N.A. Investigative [23]
3-(indole-3-yl)-4-phenyl-1H-pyrrole-2,5-dione DM3EV9N Discovery agent N.A. Investigative [23]
4-[(3,5-diamino-1H-pyrazol-4-yl)diazenyl]phenol DMSKJ1X Discovery agent N.A. Investigative [24]
Cdk4 inhibitor III DMNZJAX Discovery agent N.A. Investigative [25]
Fascaplysin DMG5OZP Discovery agent N.A. Investigative [20]
K00024 DMP8M9Q Discovery agent N.A. Investigative [26]
N-(2-(1H-Indol-3-yl)ethyl)biphenyl-4-carboxamide DM6NC8G Discovery agent N.A. Investigative [27]
NSC-625987 DMLG05U Discovery agent N.A. Investigative [28]
NU-6102 DMMOFKD Discovery agent N.A. Investigative [29]
NU6140 DMCUSG3 Discovery agent N.A. Investigative [30]
PMID18986805C9b DMFU6AI Discovery agent N.A. Investigative [31]
PYRAZOLOPYRIDAZINE 1 DMKTB5U Discovery agent N.A. Investigative [32]
PYRAZOLOPYRIDAZINE 2 DMI7AUJ Discovery agent N.A. Investigative [32]
Ro-0505124 DMLVERQ Discovery agent N.A. Investigative [33]
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⏷ Show the Full List of 21 Investigative Drug(s)
Molecule Interaction Atlas

References

1 Agreement signed with Prostagenics to develop prostate cancer treatment. Innovate Oncology, Inc. 2005.
2 Interpreting expression profiles of cancers by genome-wide survey of breadth of expression in normal tissues. Genomics 2005 Aug;86(2):127-41.
3 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2017
4 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services.
5 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2021
6 Dual CDK4/CDK6 inhibition induces cell-cycle arrest and senescence in neuroblastoma. Clin Cancer Res. 2013 Nov 15;19(22):6173-82.
7 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
8 Liposarcoma: molecular genetics and therapeutics. Sarcoma. 2011;2011:483154.
9 Cell cycle kinases as therapeutic targets for cancer. Nat Rev Drug Discov. 2009 Jul;8(7):547-66.
10 A comparison of physicochemical property profiles of marketed oral drugs and orally bioavailable anti-cancer protein kinase inhibitors in clinical development. Curr Top Med Chem. 2007;7(14):1408-22.
11 Clinical pipeline report, company report or official report of Fochon Pharmaceuticals.
12 Clinical pipeline report, company report or official report of Gan & Lee Pharmaceuticals.
13 ClinicalTrials.gov (NCT04541225) Phase 1/2 Dose Escalation, Safety, Pharmacokinetics, and Efficacy Study of NUV-422 in Adults With Recurrent or Refractory High-grade Gliomas and Solid Tumors. U.S.National Institutes of Health.
14 Discovery of 4-((7H-Pyrrolo[2,3-d]pyrimidin-4-yl)amino)-N-(4-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-pyrazole-3-carboxamide (FN-1501), an FLT3- and CDK-Kinase Inhibitor with Potentially High Efficiency against Acute Myelocytic Leukemia. J Med Chem. 2018 Feb 22;61(4):1499-1518.
15 ClinicalTrials.gov (NCT04557449) Study to Test the Safety and Tolerability of PF-07220060 in Participants With Advance Solid Tumors (CDK4). U.S. National Institutes of Health.
16 Clinical pipeline report, company report or official report of Regor Therapeutics
17 Cyclin-dependent kinase inhibitors for cancer therapy: a patent review (2009 - 2014).Expert Opin Ther Pat. 2015;25(9):953-70.
18 Hedgehog inhibitors: a patent review (2013 - present).Expert Opin Ther Pat. 2015 May;25(5):549-65.
19 c-Jun N-terminal kinase inhibitors: a patent review (2010 - 2014).Expert Opin Ther Pat. 2015;25(8):849-72.
20 Pharmacological inhibitors of cyclin-dependent kinases. Trends Pharmacol Sci. 2002 Sep;23(9):417-25.
21 Structure-based generation of a new class of potent Cdk4 inhibitors: new de novo design strategy and library design. J Med Chem. 2001 Dec 20;44(26):4615-27.
22 Anthraquinones and betaenone derivatives from the sponge-associated fungus Microsphaeropsis species: novel inhibitors of protein kinases. J Nat Prod. 2000 Jun;63(6):739-45.
23 Design, synthesis, and biological evaluation of 3,4-diarylmaleimides as angiogenesis inhibitors. J Med Chem. 2006 Feb 23;49(4):1271-81.
24 4-arylazo-3,5-diamino-1H-pyrazole CDK inhibitors: SAR study, crystal structure in complex with CDK2, selectivity, and cellular effects. J Med Chem. 2006 Nov 2;49(22):6500-9.
25 5-Arylamino-2-methyl-4,7-dioxobenzothiazoles as inhibitors of cyclin-dependent kinase 4 and cytotoxic agents. Bioorg Med Chem Lett. 2000 Mar 6;10(5):461-4.
26 Synthesis, structure-activity relationship, and biological studies of indolocarbazoles as potent cyclin D1-CDK4 inhibitors. J Med Chem. 2003 May 22;46(11):2027-30.
27 Design, synthesis and biological evaluation of new tryptamine and tetrahydro-beta-carboline-based selective inhibitors of CDK4. Bioorg Med Chem. 2008 Aug 15;16(16):7728-39.
28 The p16 status of tumor cell lines identifies small molecule inhibitors specific for cyclin-dependent kinase 4. Clin Cancer Res. 1999 Dec;5(12):4279-86.
29 Dissecting the determinants of cyclin-dependent kinase 2 and cyclin-dependent kinase 4 inhibitor selectivity. J Med Chem. 2006 Sep 7;49(18):5470-7.
30 Potentiation of paclitaxel-induced apoptosis by the novel cyclin-dependent kinase inhibitor NU6140: a possible role for survivin down-regulation. Mol Cancer Ther. 2005 Sep;4(9):1328-37.
31 Imidazole pyrimidine amides as potent, orally bioavailable cyclin-dependent kinase inhibitors. Bioorg Med Chem Lett. 2008 Dec 15;18(24):6486-9.
32 N-Phenyl-4-pyrazolo[1,5-b]pyridazin-3-ylpyrimidin-2-amines as potent and selective inhibitors of glycogen synthase kinase 3 with good cellular effi... J Med Chem. 2004 Sep 9;47(19):4716-30.
33 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: 1976).