General Information of Drug (ID: DMZM6FW)

Drug Name
Oxazolyl methylthiothiazole derivative 1 Drug Info
Synonyms PMID26161698-Compound-52
Cross-matching ID
PubChem CID
25195503
TTD Drug ID
DMZM6FW

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Clinical Trial Drug(s)
Patented Agent(s)
Approved Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
RGB-286638 DMEGOQP Haematological malignancy 2B33.Y Phase 1 [2]
Nitrogen mustard derivative 1 DMXDSYU N. A. N. A. Patented [1]
PMID26161698-Compound-17 DMB92RA N. A. N. A. Patented [1]
Drug Name Drug ID Indication ICD 11 Highest Status REF
Flavopiridol DMKSUOI Acute myeloid leukaemia 2A60 Phase 2 [3]
P276-00 DM9DJL2 Mantle cell lymphoma 2A85.5 Phase 2 [4]
RGB-286638 DMEGOQP Haematological malignancy 2B33.Y Phase 1 [2]
SNS-032 DMEITAS Solid tumour/cancer 2A00-2F9Z Phase 1 [5]
BTX-A51 DMC8XHQ Advanced solid tumour 2A00-2F9Z Phase 1 [6]
CYC065 DM9ODT6 Lymphoma 2A80-2A86 Phase 1 [3]
AZD4573 DMOYPTK Haematological malignancy 2B33.Y Phase 1 [3]
TP-1287 DM3Z07E Solid tumour/cancer 2A00-2F9Z Phase 1 [7]
VIP-152 DMBQ5OL Chronic lymphocytic leukaemia 2A82.0 Phase 1 [8]
AZD7503 DM8XJD2 Non-alcoholic steatohepatitis DB92.1 Phase 1 [9]
⏷ 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 [4]
Ro 31-7453 DM83QCL Solid tumour/cancer 2A00-2F9Z Phase 2 [10]
P276-00 DM9DJL2 Mantle cell lymphoma 2A85.5 Phase 2 [4]
P-276 DMMJUHD Breast cancer 2C60-2C65 Phase 2 [11]
RGB-286638 DMEGOQP Haematological malignancy 2B33.Y Phase 1 [2]
AG-024322 DMY4WVK Solid tumour/cancer 2A00-2F9Z Phase 1 [4]
PHA-793887 DM2Y4FG Solid tumour/cancer 2A00-2F9Z Phase 1 [12]
PMID25991433-Compound-A1 DM89LF0 N. A. N. A. Patented [13]
KENPAULLONE DMAGVXW Discovery agent N.A. Patented [14]
Roscovitine derivative 1 DMD1G3Z N. A. N. A. Patented [1]
⏷ 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 [4]
Samuraciclib DM54FQA Breast cancer 2C60-2C65 Phase 1/2 [15]
SNS-032 DMEITAS Solid tumour/cancer 2A00-2F9Z Phase 1 [5]
BTX-A51 DMC8XHQ Advanced solid tumour 2A00-2F9Z Phase 1 [6]
SY-1365 DMK48PM Solid tumour/cancer 2A00-2F9Z Phase 1 [3]
LY3405105 DMB51K2 Solid tumour/cancer 2A00-2F9Z Phase 1 [16]
SY-5609 DMNW3LH Solid tumour/cancer 2A00-2F9Z Phase 1 [17]
Roscovitine derivative 1 DMD1G3Z N. A. N. A. Patented [1]
Tricyclic benzimidazole derivative 1 DM5SD9E N. A. N. A. Patented [1]
Pyrazolo-triazine derivative 2 DML6V78 N. A. N. A. Patented [1]
⏷ Show the Full List of 10 Drug(s)
Drug(s) Targeting Histone deacetylase (HDAC)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Valproate DMCFE9I Epilepsy 8A60-8A68 Approved [18]
Sodium phenylbutyrate DMXLBCQ Spinal muscular atrophy 8B61 Approved [19]
HBI-8000 DMDWYUN Non-small-cell lung cancer 2C25.Y Registered [3]
ITF2357 DMFZBNE Duchenne dystrophy 8C70 Phase 3 [20]
Pracinostat DMTD7AB Acute myeloid leukaemia 2A60 Phase 3 [21]
NVP-LAQ824 DM8JWNA Mood disorder 6A60-6E23 Phase 3 [22]
SNDX-275 DMH7W9X Breast cancer 2C60-2C65 Phase 3 [3]
CMS-024-02 DMC4X7L Solid tumour/cancer 2A00-2F9Z Phase 3 [23]
Abexinostat DM91LGU Follicular lymphoma 2A80 Phase 3 [24]
PDX-101 DM6OC53 Plasma cell myeloma 2A83.1 Phase 2 [25]
⏷ 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 [4]
Ro 31-7453 DM83QCL Solid tumour/cancer 2A00-2F9Z Phase 2 [10]
PHA848125 DMS2Q9G Thymic cancer 2C27 Phase 2 [26]
TG02 DMZFIGQ Anaplastic astrocytoma 2A00.0 Phase 1/2 [27]
NUV-422 DMQJQNT Malignant glioma 2A00.0 Phase 1/2 [28]
RGB-286638 DMEGOQP Haematological malignancy 2B33.Y Phase 1 [2]
FN-1501 DM7BMD6 Solid tumour/cancer 2A00-2F9Z Phase 1 [29]
AG-024322 DMY4WVK Solid tumour/cancer 2A00-2F9Z Phase 1 [4]
PHA-793887 DM2Y4FG Solid tumour/cancer 2A00-2F9Z Phase 1 [12]
SNS-032 DMEITAS Solid tumour/cancer 2A00-2F9Z Phase 1 [5]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Apremilast DMTWS9E Psoriasis vulgaris EA90 Approved [30]
LY2835219 DM93VBZ Breast cancer 2C60-2C65 Approved [25]
Palbociclib DMD7L94 Breast cancer 2C60-2C65 Approved [31]
Ribociclib Succinate DM9CIUW Breast cancer 2C60-2C65 Approved [32]
Trilaciclib DMP5A4T Small-cell lung cancer 2C25.Y Approved [33]
LEE011 DMMX75K Breast cancer 2C60-2C65 Phase 3 [34]
Ro 31-7453 DM83QCL Solid tumour/cancer 2A00-2F9Z Phase 2 [10]
P276-00 DM9DJL2 Mantle cell lymphoma 2A85.5 Phase 2 [4]
P-276 DMMJUHD Breast cancer 2C60-2C65 Phase 2 [35]
G1T38 DMQO2IT Breast cancer 2C60-2C65 Phase 2 [3]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Apremilast DMTWS9E Psoriasis vulgaris EA90 Approved [30]
LY2835219 DM93VBZ Breast cancer 2C60-2C65 Approved [25]
Palbociclib DMD7L94 Breast cancer 2C60-2C65 Approved [31]
Ribociclib Succinate DM9CIUW Breast cancer 2C60-2C65 Approved [32]
Trilaciclib DMP5A4T Small-cell lung cancer 2C25.Y Approved [33]
LEE011 DMMX75K Breast cancer 2C60-2C65 Phase 3 [34]
G1T38 DMQO2IT Breast cancer 2C60-2C65 Phase 2 [3]
GLR2007 DM7DWLY Glioblastoma of brain 2A00.00 Phase 1/2 [36]
FCN-437 DMQ8VUW Breast cancer 2C60-2C65 Phase 1/2 [37]
NUV-422 DMQJQNT Malignant glioma 2A00.0 Phase 1/2 [28]
⏷ 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 3 (CDK3) TTMYWL7 CDK3_HUMAN Inhibitor [1]
Cyclin-dependent kinase 4 (CDK4) TT0PG8F CDK4_HUMAN Inhibitor [1]
Cyclin-dependent kinase 6 (CDK6) TTO0FDJ CDK6_HUMAN Inhibitor [1]
Cyclin-dependent kinase 7 (CDK7) TTQYF7G CDK7_HUMAN Inhibitor [1]
Cyclin-dependent kinase 9 (CDK9) TT1LVF2 CDK9_HUMAN Inhibitor [1]
Histone deacetylase (HDAC) TTBH0VX NOUNIPROTAC Inhibitor [1]

References

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2 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.
3 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
4 Cell cycle kinases as therapeutic targets for cancer. Nat Rev Drug Discov. 2009 Jul;8(7):547-66.
5 Mechanism of action of SNS-032, a novel cyclin-dependent kinase inhibitor, in chronic lymphocytic leukemia. Blood. 2009 May 7;113(19):4637-45.
6 Clinical pipeline report, company report or official report of BioTheryX.
7 Clinical pipeline report, company report or official report of Sumitomo Dainippon Pharma.
8 VIP152 is a selective CDK9 inhibitor with pre-clinical in vitro and in vivo efficacy in chronic lymphocytic leukemia. Leukemia. 2023 Feb;37(2):326-338.
9 ClinicalTrials.gov (NCT05560607) An Open-label, Non-randomized, Multiple-dose Study to Assess the Knockdown of Hepatic HSD17B13 mRNA Expression, Pharmacokinetics, Safety, and Tolerability Following Administration of AZD7503 in Participants With Non-alcoholic Fatty Liver Disease. U.S.National Institutes of Health.
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 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.
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 CDK7 inhibitors as anticancer drugs. Cancer Metastasis Rev. 2020 Sep;39(3):805-823.
17 Clinical pipeline report, company report or official report of Syros Pharmaceuticals.
18 Transcription-independent heritability of induced histone modifications in the mouse preimplantation embryo. PLoS One. 2009 Jun 30;4(6):e6086.
19 Histone Deacetylase inhibitors: new promise in the treatment of immune and inflammatory diseases. Curr Drug Targets. 2010 Nov;11(11):1430-8.
20 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
21 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: 8365).
22 Emerging therapies for multiple myeloma. Expert Opin Emerg Drugs. 2009 Mar;14(1):99-127.
23 US patent application no. 2012,0302,505, Cyclodextrin-based polymers for therapeutic delivery.
24 Phase 1 study of the oral histone deacetylase inhibitor abexinostat in patients with Hodgkin lymphoma, non-Hodgkin lymphoma, or chronic lymphocytic leukaemia. Invest New Drugs. 2015 Apr;33(2):423-31.
25 Interpreting expression profiles of cancers by genome-wide survey of breadth of expression in normal tissues. Genomics 2005 Aug;86(2):127-41.
26 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.
27 Preclinical metabolism and pharmacokinetics of SB1317 (TG02), a potent CDK/JAK2/FLT3 inhibitor. Drug Metab Lett. 2012 Mar;6(1):33-42.
28 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.
29 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.
30 Agreement signed with Prostagenics to develop prostate cancer treatment. Innovate Oncology, Inc. 2005.
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33 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2021
34 Dual CDK4/CDK6 inhibition induces cell-cycle arrest and senescence in neuroblastoma. Clin Cancer Res. 2013 Nov 15;19(22):6173-82.
35 Liposarcoma: molecular genetics and therapeutics. Sarcoma. 2011;2011:483154.
36 Clinical pipeline report, company report or official report of Gan & Lee Pharmaceuticals.
37 Clinical pipeline report, company report or official report of Fochon Pharmaceuticals.