General Information of Drug (ID: DMCUSG3)

Drug Name
NU6140 Drug Info
Synonyms
Cdk2 Inhibitor IV, NU6140; 444723-13-1; NU 6140; CHEMBL1802728; 4-(6-Cyclohexylmethoxy-9H-purin-2-ylamino)-N,N-diethylbenzamide; 4-{[6-(cyclohexylmethoxy)-7H-purin-2-yl]amino}-N,N-diethylbenzamide; Cdk2 inhibitor IV; SCHEMBL2169233; GTPL5949; CTK8E7940; DTXSID30436732; MolPort-023-276-742; MolPort-044-561-419; HMS3229E18; IN1369; ZINC22309248; BDBM50347924; AKOS024457537; CCG-206836; NCGC00370819-01; NU6140, > RT-011957; 4-(6-cyclohexylmethoxy-9hpurin-2-ylamino)-N,N-diethyl-benzamide
Indication
Disease Entry ICD 11 Status REF
Discovery agent N.A. Investigative [1]
Cross-matching ID
PubChem CID
10202471
CAS Number
CAS 444723-13-1
TTD Drug ID
DMCUSG3

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
DOT
Drug Status:
Patented Agent(s)
Investigative Drug(s)
Preclinical Drug(s)
Discontinued Drug(s)
Clinical Trial Drug(s)
Approved Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
US9650366, 12 DMR3Z49 N. A. N. A. Patented [3]
US9650366, 2 DM9HZ03 N. A. N. A. Patented [3]
US9650366, 9 DMUCIPE N. A. N. A. Patented [3]
ASN-11124542 DMFNZOI Discovery agent N.A. Investigative [4]
indirubin derivative E804 DMFP1C5 Discovery agent N.A. Investigative [2]
Drug Name Drug ID Indication ICD 11 Highest Status REF
KENPAULLONE DMAGVXW Discovery agent N.A. Patented [5]
Roscovitine derivative 1 DMD1G3Z N. A. N. A. Patented [6]
Tricyclic benzimidazole derivative 1 DM5SD9E N. A. N. A. Patented [6]
4-(thiazol-5-yl)-pyrimidine derivative 2 DMMQFCN N. A. N. A. Patented [6]
Pyrazolo[1,5-a]-1,3,5-triazine derivative 1 DMOK7CW N. A. N. A. Patented [6]
Naphthyridine and isoquinoline derivative 1 DMTGIP7 N. A. N. A. Patented [6]
PMID26161698-Compound-18 DM6JVR5 N. A. N. A. Patented [6]
Flavonoid derivative 7 DM6A9UR N. A. N. A. Patented [6]
L-751250 DMOERXK Obesity 5B81 Preclinical [7]
Olomoucine DMNAFG1 N. A. N. A. Terminated [7]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
R-roscovitine DMSH108 Non-small-cell lung cancer 2C25.Y Phase 2 [8]
Ro 31-7453 DM83QCL Solid tumour/cancer 2A00-2F9Z Phase 2 [9]
P276-00 DM9DJL2 Mantle cell lymphoma 2A85.5 Phase 2 [8]
P-276 DMMJUHD Breast cancer 2C60-2C65 Phase 2 [10]
RGB-286638 DMEGOQP Haematological malignancy 2B33.Y Phase 1 [11]
AG-024322 DMY4WVK Solid tumour/cancer 2A00-2F9Z Phase 1 [8]
PHA-793887 DM2Y4FG Solid tumour/cancer 2A00-2F9Z Phase 1 [12]
Oxazolyl methylthiothiazole derivative 1 DMZM6FW N. A. N. A. Patented [6]
PMID25991433-Compound-A1 DM89LF0 N. A. N. A. Patented [13]
KENPAULLONE DMAGVXW Discovery agent N.A. Patented [14]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
R-roscovitine DMSH108 Non-small-cell lung cancer 2C25.Y Phase 2 [8]
Samuraciclib DM54FQA Breast cancer 2C60-2C65 Phase 1/2 [15]
SNS-032 DMEITAS Solid tumour/cancer 2A00-2F9Z Phase 1 [16]
BTX-A51 DMC8XHQ Advanced solid tumour 2A00-2F9Z Phase 1 [17]
SY-1365 DMK48PM Solid tumour/cancer 2A00-2F9Z Phase 1 [18]
LY3405105 DMB51K2 Solid tumour/cancer 2A00-2F9Z Phase 1 [19]
SY-5609 DMNW3LH Solid tumour/cancer 2A00-2F9Z Phase 1 [20]
Oxazolyl methylthiothiazole derivative 1 DMZM6FW N. A. N. A. Patented [6]
Roscovitine derivative 1 DMD1G3Z N. A. N. A. Patented [6]
Tricyclic benzimidazole derivative 1 DM5SD9E N. A. N. A. Patented [6]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
R-roscovitine DMSH108 Non-small-cell lung cancer 2C25.Y Phase 2 [8]
Ro 31-7453 DM83QCL Solid tumour/cancer 2A00-2F9Z Phase 2 [9]
PHA848125 DMS2Q9G Thymic cancer 2C27 Phase 2 [21]
TG02 DMZFIGQ Anaplastic astrocytoma 2A00.0 Phase 1/2 [22]
NUV-422 DMQJQNT Malignant glioma 2A00.0 Phase 1/2 [23]
RGB-286638 DMEGOQP Haematological malignancy 2B33.Y Phase 1 [11]
FN-1501 DM7BMD6 Solid tumour/cancer 2A00-2F9Z Phase 1 [24]
AG-024322 DMY4WVK Solid tumour/cancer 2A00-2F9Z Phase 1 [8]
PHA-793887 DM2Y4FG Solid tumour/cancer 2A00-2F9Z Phase 1 [12]
SNS-032 DMEITAS Solid tumour/cancer 2A00-2F9Z Phase 1 [16]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Apremilast DMTWS9E Psoriasis vulgaris EA90 Approved [25]
LY2835219 DM93VBZ Breast cancer 2C60-2C65 Approved [26]
Palbociclib DMD7L94 Breast cancer 2C60-2C65 Approved [27]
Ribociclib Succinate DM9CIUW Breast cancer 2C60-2C65 Approved [28]
Trilaciclib DMP5A4T Small-cell lung cancer 2C25.Y Approved [29]
LEE011 DMMX75K Breast cancer 2C60-2C65 Phase 3 [30]
Ro 31-7453 DM83QCL Solid tumour/cancer 2A00-2F9Z Phase 2 [9]
P276-00 DM9DJL2 Mantle cell lymphoma 2A85.5 Phase 2 [8]
P-276 DMMJUHD Breast cancer 2C60-2C65 Phase 2 [31]
G1T38 DMQO2IT Breast cancer 2C60-2C65 Phase 2 [18]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Fulvestrant DM0YZC6 Breast cancer 2C60-2C65 Approved [32]
Gefitinib DM15F0X Colon adenocarcinoma Approved [33]
Hydrogen peroxide DM1NG5W Infectious disease 1A00-CA43.1 Approved [34]
Nitric Oxide DM1RBYG Hypertension BA00-BA04 Approved [35]
Etretinate DM2CZFA Keratosis ED56 Approved [36]
Sulindac DM2QHZU Acute myelogenous leukaemia 2A41 Approved [37]
Simvastatin DM30SGU Arteriosclerosis BD40 Approved [38]
Lapatinib DM3BH1Y Breast cancer 2C60-2C65 Approved [39]
Quercetin DM3NC4M Obesity 5B81 Approved [40]
Troglitazone DM3VFPD Diabetic complication 5A2Y Approved [41]
⏷ 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
Cyclin-dependent kinase 1 (CDK1) TTH6V3D CDK1_HUMAN Inhibitor [1]
Cyclin-dependent kinase 2 (CDK2) TT7HF4W CDK2_HUMAN Inhibitor [1]
Cyclin-dependent kinase 4 (CDK4) TT0PG8F CDK4_HUMAN Inhibitor [1]
Cyclin-dependent kinase 5 (CDK5) TTL4Q97 CDK5_HUMAN Inhibitor [1]
Cyclin-dependent kinase 7 (CDK7) TTQYF7G CDK7_HUMAN Inhibitor [1]
Tyrosine-protein kinase EIF2AK2 (p68) TTXEZJ4 E2AK2_HUMAN Inhibitor [2]

Drug Off-Target (DOT)
DOT Name DOT ID UniProt ID Interaction REF
Baculoviral IAP repeat-containing protein 5 (BIRC5) OTILXZYL BIRC5_HUMAN Gene/Protein Processing [1]

References

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2 Identification of new inhibitors of protein kinase R guided by statistical modeling. Bioorg Med Chem Lett. 2011 Jul 1;21(13):4108-14.
3 Heterocycle-substituted pyridyl benzothiophenes as kinase inhibitors. US9650366.
4 Small molecule inhibitors of the RNA-dependent protein kinase. Biochem Biophys Res Commun. 2003 Aug 15;308(1):50-7.
5 1-Azakenpaullone is a selective inhibitor of glycogen synthase kinase-3 beta. Bioorg Med Chem Lett. 2004 Jan 19;14(2):413-6.
6 Cyclin-dependent kinase inhibitors for cancer therapy: a patent review (2009 - 2014).Expert Opin Ther Pat. 2015;25(9):953-70.
7 Pharmacological inhibitors of cyclin-dependent kinases. Trends Pharmacol Sci. 2002 Sep;23(9):417-25.
8 Cell cycle kinases as therapeutic targets for cancer. Nat Rev Drug Discov. 2009 Jul;8(7):547-66.
9 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.
10 P276-00, a novel cyclin-dependent inhibitor induces G1-G2 arrest, shows antitumor activity on cisplatin-resistant cells and significant in vivo efficacy in tumor models. Mol Cancer Ther. 2007 Mar;6(3):926-34.
11 Small-molecule multi-targeted kinase inhibitor RGB-286638 triggers P53-dependent and -independent anti-multiple myeloma activity through inhibition of transcriptional CDKs. Leukemia. 2013 Dec;27(12):2366-75.
12 A first in man, phase I dose-escalation study of PHA-793887, an inhibitor of multiple cyclin-dependent kinases (CDK2, 1 and 4) reveals unexpected h... Cell Cycle. 2011 Mar 15;10(6):963-70.
13 c-Jun N-terminal kinase inhibitors: a patent review (2010 - 2014).Expert Opin Ther Pat. 2015;25(8):849-72.
14 Discovery of novel CDK1 inhibitors by combining pharmacophore modeling, QSAR analysis and in silico screening followed by in vitro bioassay. Eur J Med Chem. 2010 Sep;45(9):4316-30.
15 The CDK7 inhibitor CT7001 (Samuraciclib) targets proliferation pathways to inhibit advanced prostate cancer. Br J Cancer. 2023 Jun;128(12):2326-2337.
16 Mechanism of action of SNS-032, a novel cyclin-dependent kinase inhibitor, in chronic lymphocytic leukemia. Blood. 2009 May 7;113(19):4637-45.
17 Clinical pipeline report, company report or official report of BioTheryX.
18 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
19 CDK7 inhibitors as anticancer drugs. Cancer Metastasis Rev. 2020 Sep;39(3):805-823.
20 Clinical pipeline report, company report or official report of Syros Pharmaceuticals.
21 Identification of N,1,4,4-tetramethyl-8-{[4-(4-methylpiperazin-1-yl)phenyl]amino}-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide (PHA-848125), a potent, orally available cyclin dependent kinase inhibitor. J Med Chem. 2009 Aug 27;52(16):5152-63.
22 Preclinical metabolism and pharmacokinetics of SB1317 (TG02), a potent CDK/JAK2/FLT3 inhibitor. Drug Metab Lett. 2012 Mar;6(1):33-42.
23 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.
24 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.
25 Agreement signed with Prostagenics to develop prostate cancer treatment. Innovate Oncology, Inc. 2005.
26 Interpreting expression profiles of cancers by genome-wide survey of breadth of expression in normal tissues. Genomics 2005 Aug;86(2):127-41.
27 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2017
28 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services.
29 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2021
30 Dual CDK4/CDK6 inhibition induces cell-cycle arrest and senescence in neuroblastoma. Clin Cancer Res. 2013 Nov 15;19(22):6173-82.
31 Liposarcoma: molecular genetics and therapeutics. Sarcoma. 2011;2011:483154.
32 mTOR inhibition reverses acquired endocrine therapy resistance of breast cancer cells at the cell proliferation and gene-expression levels. Cancer Sci. 2008 Oct;99(10):1992-2003. doi: 10.1111/j.1349-7006.2008.00955.x.
33 Leptomycin B reduces primary and acquired resistance of gefitinib in lung cancer cells. Toxicol Appl Pharmacol. 2017 Nov 15;335:16-27. doi: 10.1016/j.taap.2017.09.017. Epub 2017 Sep 21.
34 Assessment of the cytotoxic, genotoxic, and apoptotic potential of flurbiprofen in HeLa and HepG2 cell lines. J Biochem Mol Toxicol. 2021 Jun;35(6):1-11. doi: 10.1002/jbt.22770. Epub 2021 Mar 11.
35 Apoptotic signaling pathways induced by nitric oxide in human lymphoblastoid cells expressing wild-type or mutant p53. Cancer Res. 2004 May 1;64(9):3022-9. doi: 10.1158/0008-5472.can-03-1880.
36 Bexarotene activates the p53/p73 pathway in human cutaneous T-cell lymphoma. Br J Dermatol. 2009 Mar;160(3):519-26. doi: 10.1111/j.1365-2133.2008.08931.x. Epub 2008 Nov 25.
37 Expression profile analysis of colon cancer cells in response to sulindac or aspirin. Biochem Biophys Res Commun. 2002 Mar 29;292(2):498-512.
38 Apoptotic induction by simvastatin in human lung cancer A549 cells via Akt signaling dependent down-regulation of survivin. Invest New Drugs. 2011 Oct;29(5):945-52. doi: 10.1007/s10637-010-9450-2. Epub 2010 May 13.
39 Combining lapatinib (GW572016), a small molecule inhibitor of ErbB1 and ErbB2 tyrosine kinases, with therapeutic anti-ErbB2 antibodies enhances apoptosis of ErbB2-overexpressing breast cancer cells. Oncogene. 2005 Sep 15;24(41):6213-21. doi: 10.1038/sj.onc.1208774.
40 Quercetin inhibit human SW480 colon cancer growth in association with inhibition of cyclin D1 and survivin expression through Wnt/beta-catenin signaling pathway. Cancer Invest. 2009 Jul;27(6):604-12. doi: 10.1080/07357900802337191.
41 Troglitazone sensitizes tumor cells to TRAIL-induced apoptosis via down-regulation of FLIP and Survivin. Apoptosis. 2006 Sep;11(9):1503-12. doi: 10.1007/s10495-006-8896-3.