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  1. General Info
  2. Effects Info
  3. Reference
Drug Details
01. General Information
Name Ponatinib
PubChem CID 24826799
Molecular Weight 532.6g/mol
Synonyms

PONATINIB, 943319-70-8, AP24534, Ponatinib (AP24534), AP 24534, 3-(imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide, ponatinibum, AP-24534, UNII-4340891KFS, CHEBI:78543, HSDB 8184, 3-(2-Imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-N-[4-[(4-methyl-1-piperazinyl)methyl]-3-(trifluoromethyl)phenyl]benzamide, 4340891KFS, CHEMBL1171837, DTXSID50241426, 943319-70-8 (free base), 3-(2-imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-N-[4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl]benzamide, 3-(Imidazo[1,2-B]pyridazin-3-Ylethynyl)-4-Methyl-N-{4-[(4-Methylpiperazin-1-Yl)methyl]-3-(Trifluoromethyl)phenyl}benzamide, Benzamide, 3-(2-imidazo(1,2-b)pyridazin-3-ylethynyl)-4-methyl-N-(4-((4-methyl-1- piperazinyl)methyl)-3-(trifluoromethyl)phenyl)-, AP24534(Ponatinib), 3-(2-(Imidazo(1,2-b)pyridazin-3-yl)ethynyl)-4-methyl-N-(4-((4-methylpiperazin-1- yl)methyl)-3-(trifluoromethyl)phenyl)benzamide, 3-(imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide., Ponatinib [USAN], Ponatinib [USAN:INN], 0LI, 3-(2-(IMIDAZO(1,2-B)PYRIDAZIN-3-YL)ETHYNYL)-4-METHYL-N-(4-((4-METHYLPIPERAZIN-1-YL)METHYL)-3-(TRIFLUOROMETHYL)PHENYL)BENZAMIDE, 3-(2-(Imidazo[1,2-b]pyridazin-3-yl)ethynyl)-4-methyl-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide, 3-(2-{imidazo[1,2-b]pyridazin-3-yl}ethynyl)-4-methyl-N-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}benzamide, 3-(imidazo(1,2-b)pyridazin-3-ylethynyl)-4-methyl-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide, 3-(imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-N-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}benzam ide, 3-[2-(imidazo[1,2-b]pyridazin-3-yl)ethynyl]-4-methyl-n-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}benzamide, BENZAMIDE, 3-(2-IMIDAZO(1,2-B)PYRIDAZIN-3-YLETHYNYL)-4-METHYL-N-(4-((4-METHYL-1-PIPERAZINYL)METHYL)-3-(TRIFLUOROMETHYL)PHENYL)-, BENZAMIDE, 3-(2-IMIDAZO[1,2-B]PYRIDAZIN-3-YLETHYNYL)-4-METHYL-N-[4-[(4-METHYL-1-PIPERAZINYL)METHYL]-3-(TRIFLUOROMETHYL)PHENYL]-, Benzamide, 3-(2-imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-N-[4-[(4-methyl-1-piperazinyl)methyl]-3-(trifluoromethyl)phenyl]-; 3-(2-Imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-N-[4-[(4-methyl-1-piperazinyl)methyl]-3-(trifluoromethyl)phenyl]benzamide; AP 24534; Iclusig; Ponatinib, Ponatinib, Free Base, AP24534,Ponatinib, PONATINIB [INN], PONATINIB [MI], Ponatinib (USAN/INN), PONATINIB [VANDF], AP24534 (Ponatinib), PONATINIB [WHO-DD], MLS006010166, SCHEMBL589260, GTPL5890, DTXCID50163917, EX-A067, L01XE24, BCPP000397, HMS3295I23, HMS3654H16, BCP02037, BDBM50322535, MFCD17215203, NSC758487, NSC800855, AKOS015995214, AM81261, BCP9000307, CCG-264900, CS-0204, DB08901, NSC-758487, NSC-800855, PB34916, NCGC00263152-01, NCGC00263152-02, NCGC00263152-12, NCGC00263152-14, 3-(2-(imidazo(1,2-b)pyridazin-3-yl)ethynyl)-4-methyl-N-(4-((4-methylpiperazin-y-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide, AC-26973, AS-19133, HY-12047, SMR004701274, FT-0660376, NS00072196, S1490, SW218091-2, A24930, D09950, AB01565847_03, EN300-6733072, Q198728, BRD-K44227013-001-02-3, Z1828098700, 3-(imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-N-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}benzam, Benzamide, 3-(2-Imidazo(1,2-B)Pyridazin-3-Ylethynyl)-4-Methyl-N-(4-((4-Methyl-1-Piperazinyl)Methyl)-3-(Trifluoromethyl)Phenyl), Ponatinib;3-(2-(imidazo[1,2-b]pyridazin-3-yl)ethynyl)-4-methyl-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)benzamide

Drug Type Small molecule
Formula C₂₉H₂₇F₃N₆O
SMILES CC1=C(C=C(C=C1)C(=O)NC2=CC(=C(C=C2)CN3CCN(CC3)C)C(F)(F)F)C#CC4=CN=C5N4N=CC=C5
InChI 1S/C29H27F3N6O/c1-20-5-6-22(16-21(20)8-10-25-18-33-27-4-3-11-34-38(25)27)28(39)35-24-9-7-23(26(17-24)29(30,31)32)19-37-14-12-36(2)13-15-37/h3-7,9,11,16-18H,12-15,19H2,1-2H3,(H,35,39)
InChIKey PHXJVRSECIGDHY-UHFFFAOYSA-N
CAS Number 943319-70-8
ChEMBL ID CHEMBL1171837
ChEBI ID CHEBI:78543
TTD ID D0H0EQ
Drug Bank ID DB08901
KEGG ID D09950
Toxicity Organism Test Type Route(Dose)
rat LD50 intraperitoneal(165 mg/kg)
mouse LD50 intraperitoneal(254 mg/kg)
rat LD50 oral(322 mg/kg)
Structure 2D-img
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2D MOL 3D MOL
02. Combinatorial Therapeutic Effect(s)
Synergistic Effect
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Enhancing Drug Efficacy
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Combination Pair ID: 465
Pair Name Gossypol, Ponatinib
Partner Name Gossypol
Disease Info [ICD-11: 2A00-2F9Z] Solid tumour or cancer Investigative
Biological Phenomena Inhibition-->Angiogenesis
Gene Regulation Up-regulation Expression BAX hsa581
Down-regulation Expression BCL2 hsa596
Up-regulation Expression CASP9 hsa842
Down-regulation Expression FGFR4 hsa2264
Up-regulation Expression TP53 hsa7157
Down-regulation Expression VEGFA hsa7422
In Vivo Model EAC cells were maintained through serial intraperitoneal inoculation of saline solution containing 106 cells/mouse into female Swiss albino mice (El-Wahab and Fouda, 2009). After 10 days, the host mice were euthanized by cervical dislocation, and the cells were recovered by collecting them using a syringe, washing them in normal saline, and counting them.
Result Gossypol could be used as an adjuvant medication for ponatinib in cancer treatment, possibly leading to successful dose reductions and fewer side effects; however, further research is needed before a clinical application could be feasible.
Combination Pair ID: 965
Pair Name Forskolin, Ponatinib
Partner Name Forskolin
Disease Info [ICD-11: 2A20.1] Chronic myelogenous leukemia Investigative
Gene Regulation Down-regulation Phosphorylation CRKL hsa1399
In Vitro Model KCL-22 Chronic myelogenous leukemia, BCR-ABL1 positive Homo sapiens (Human) CVCL_2091
K-562 Blast phase chronic myelogenous leukemia Homo sapiens (Human) CVCL_0004
HH [Human lymphoma] Primary cutaneous T-cell non-Hodgkin lymphoma Homo sapiens (Human) CVCL_1280
HEK293 Healthy Homo sapiens (Human) CVCL_0045
Hep-G2 Hepatoblastoma Homo sapiens (Human) CVCL_0027
Result This study provides new insight into the biological underpinnings of BCR-ABL-driven CML and potential rationale for investigating novel treatment strategies for patients with T315I CML.
03. Reference
No. Title Href
1 The ponatinib/gossypol novel combination provides enhanced anticancer activity against murine solid Ehrlich carcinoma via triggering apoptosis and inhibiting proliferation/angiogenesis. Toxicol Appl Pharmacol. 2021 Dec 1;432:115767. doi: 10.1016/j.taap.2021.115767. Click
2 Sensitivity of imatinib-resistant T315I BCR-ABL CML to a synergistic combination of ponatinib and forskolin treatment. Tumour Biol. 2016 Sep;37(9):12643-12654. doi: 10.1007/s13277-016-5179-7. Click
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