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| Stem definition | Drug id | CAS RN |
|---|---|---|
| tyrosine kinase inhibitors | 5507 | 937272-79-2 |
None
None
| Property | Description | Value | Unit | Confidence | Similarity |
|---|---|---|---|---|---|
| kinase-safety-class | ACVR2B,ACVRL1,AKT2,AKT3,ALK,AURKA,AXL,BRAF,BTK,CAMK2B,CAMK2D,CDK5,CDK9,DDR1,DYRK1B,EGFR,EIF2AK3,EPHB4,ERBB2,FLT3,GAK,GRK2,GSK3B,INSR,ITK,JAK2,JAK3,KDR,KIT,MAP3K1,MAP3K21,MAP3K7,MAP4K1,MAP4K3,MAPK10,MAPK7,MAPKAPK2,MARK4,MELK,MET,NTRK2,PDK1,PDK2,PDK4,PDPK1,PIK3CA,PIK3CB,PIK3CD,PIK3CG,PIM2,PRKCD,PRKDC,SIK2,SIK3,STK33,SYK,TEK,TGFBR1,TTK | 59 | |||
| kinase-selectivity-class | AXL,CDK4,SIK2 | 3 | |||
| pfas-class | PFAS structural alert (1 = True, 0 = False) | 0 |
| Date | Agency | Company | Orphan |
|---|---|---|---|
| March 18, 2022 | FDA | MARINUS PHARMA INC |
None
None
| MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
|---|---|---|---|---|---|---|
| Off label use | 98.94 | 56.12 | 61 | 321 | 1500124 | 109088793 |
| Platelet count abnormal | 90.01 | 56.12 | 16 | 366 | 6266 | 110582651 |
| Haemoglobin abnormal | 71.77 | 56.12 | 14 | 368 | 9024 | 110579893 |
| Death | 56.98 | 56.12 | 33 | 349 | 698836 | 109890081 |
None
| Source | Code | Description |
|---|---|---|
| ATC | L01EJ03 | ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS ANTINEOPLASTIC AGENTS PROTEIN KINASE INHIBITORS Janus-associated kinase (JAK) inhibitors |
| FDA MoA | N0000020001 | Tyrosine Kinase Inhibitors |
| MeSH PA | D000075242 | Janus Kinase Inhibitors |
| MeSH PA | D000092004 | Tyrosine Kinase Inhibitors |
| MeSH PA | D000970 | Antineoplastic Agents |
| MeSH PA | D004791 | Enzyme Inhibitors |
| MeSH PA | D047428 | Protein Kinase Inhibitors |
| FDA EPC | N0000175605 | Kinase Inhibitor |
| FDA MoA | N0000182138 | Cytochrome P450 1A2 Inhibitors |
| FDA MoA | N0000182141 | Cytochrome P450 3A4 Inhibitors |
| FDA MoA | N0000185503 | P-Glycoprotein Inhibitors |
| FDA MoA | N0000190113 | Breast Cancer Resistance Protein Inhibitors |
| FDA MoA | N0000190857 | Janus Kinase Inhibitors |
| FDA MoA | N0000191265 | Organic Cation Transporter 1 Inhibitors |
| CHEBI has role | CHEBI:35610 | antineoplastic agent |
| CHEBI has role | CHEBI:67079 | anti-inflammatory agent |
| CHEBI has role | CHEBI:68495 | apoptosis inducer |
| CHEBI has role | CHEBI:76617 | EC 2.7.10.2 (non-specific protein-tyrosine kinase) inhibitor |
| CHEBI has role | CHEBI:233423 | antifibrotic agent |
| Disease | Relation | SNOMED_ID | DOID |
|---|---|---|---|
| Myelofibrosis | indication | 52967002 | DOID:4971 |
| Drug inhibition of cytochrome p450 CYP3A enzyme | contraindication | 423819001 |
None
None
None
| Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Patent number | Patent expiration date | Patent use |
|---|---|---|---|---|---|---|---|---|---|---|
| EQ 100MG BASE | VONJO | SOBI | N208712 | Feb. 28, 2022 | RX | CAPSULE | ORAL | 9573964 | May 5, 2028 | TREATMENT OF MYELOFIBROSIS WITH PACRITINIB |
| EQ 100MG BASE | VONJO | SOBI | N208712 | Feb. 28, 2022 | RX | CAPSULE | ORAL | 9573964 | May 5, 2028 | USE OF PACRITINIB FOR INHIBITING JANUS ASSOCIATED KINASE 2(JAK2) |
| EQ 100MG BASE | VONJO | SOBI | N208712 | Feb. 28, 2022 | RX | CAPSULE | ORAL | 8153632 | Jan. 17, 2029 | TREATMENT OF MYELOFIBROSIS WITH PACRITINIB |
| EQ 100MG BASE | VONJO | SOBI | N208712 | Feb. 28, 2022 | RX | CAPSULE | ORAL | 8153632 | Jan. 17, 2029 | USE OF PACRITINIB FOR INHIBITING JANUS ASSOCIATED KINASE 2(JAK2) |
| EQ 100MG BASE | VONJO | SOBI | N208712 | Feb. 28, 2022 | RX | CAPSULE | ORAL | 8980873 | March 25, 2030 | TREATMENT OF MYELOFIBROSIS WITH PACRITINIB |
| EQ 100MG BASE | VONJO | SOBI | N208712 | Feb. 28, 2022 | RX | CAPSULE | ORAL | 8980873 | March 25, 2030 | USE OF PACRITINIB FOR INHIBITING JANUS ASSOCIATED KINASE 2(JAK2) |
| Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Exclusivity date | Description |
|---|---|---|---|---|---|---|---|---|---|
| EQ 100MG BASE | VONJO | SOBI | N208712 | Feb. 28, 2022 | RX | CAPSULE | ORAL | Feb. 28, 2027 | NEW CHEMICAL ENTITY |
| EQ 100MG BASE | VONJO | SOBI | N208712 | Feb. 28, 2022 | RX | CAPSULE | ORAL | Feb. 28, 2029 | TREATMENT OF ADULTS WITH INTERMEDIATE OR HIGH-RISK PRIMARY OR SECONDARY (POST-POLYCYTHEMIA VERA OR POST-ESSENTIAL THROMBOCYTHEMIA) MYELOFIBROSIS (MF) WITH A PLATELET COUNT BELOW 50 X 10^9/L |
| Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
|---|---|---|---|---|---|---|---|---|---|
| Receptor-type tyrosine-protein kinase FLT3 | Kinase | INHIBITOR | IC50 | 8.52 | DRUG LABEL | DRUG LABEL | |||
| Tyrosine-protein kinase JAK2 | Kinase | INHIBITOR | IC50 | 9 | DRUG LABEL | DRUG LABEL | |||
| Ribosyldihydronicotinamide dehydrogenase [quinone] | Enzyme | Kd | 8.40 | CHEMBL | |||||
| Platelet-derived growth factor receptor beta | Kinase | Kd | 5.57 | CHEMBL | |||||
| Tyrosine-protein kinase Lck | Kinase | Kd | 5.18 | CHEMBL | |||||
| Mitogen-activated protein kinase 8 | Kinase | Kd | 5.71 | CHEMBL | |||||
| Tyrosine-protein kinase JAK1 | Kinase | INHIBITOR | IC50 | 5.89 | IUPHAR | ||||
| Protein kinase C beta type | Kinase | Kd | 5.14 | CHEMBL | |||||
| Protein kinase C alpha type | Kinase | Kd | 6.03 | CHEMBL | |||||
| AP2-associated protein kinase 1 | Kinase | Kd | 7.38 | CHEMBL | |||||
| Serine/threonine-protein kinase 10 | Kinase | Kd | 5.54 | CHEMBL | |||||
| Tyrosine-protein kinase Fer | Kinase | Kd | 5.44 | CHEMBL | |||||
| Serine/threonine-protein kinase 16 | Kinase | Kd | 5.73 | CHEMBL | |||||
| TRAF2 and NCK-interacting protein kinase | Kinase | Kd | 7.05 | CHEMBL | |||||
| BMP-2-inducible protein kinase | Kinase | Kd | 7.41 | CHEMBL | |||||
| Dual specificity protein kinase CLK1 | Kinase | Kd | 6.86 | CHEMBL | |||||
| Cyclin-G-associated kinase | Kinase | Kd | 6.17 | CHEMBL | |||||
| Cyclin-dependent kinase 16 | Kinase | Kd | 5.51 | CHEMBL | |||||
| Activated CDC42 kinase 1 | Kinase | Kd | 5.03 | CHEMBL | |||||
| Calcium/calmodulin-dependent protein kinase kinase 2 | Kinase | Kd | 5.11 | CHEMBL | |||||
| Epithelial discoidin domain-containing receptor 1 | Kinase | Kd | 4.15 | CHEMBL | |||||
| Activin receptor type-1 | Kinase | Kd | 7.66 | CHEMBL | |||||
| Cyclin-dependent kinase 9 | Kinase | Kd | 6 | CHEMBL | |||||
| Glycogen synthase kinase-3 alpha | Kinase | Kd | 5.29 | CHEMBL | |||||
| Non-receptor tyrosine-protein kinase TNK1 | Kinase | Kd | 6.05 | CHEMBL | |||||
| Non-receptor tyrosine-protein kinase TYK2 | Kinase | Kd | 7.42 | CHEMBL | |||||
| Mitogen-activated protein kinase kinase kinase MLT | Kinase | Kd | 5.53 | CHEMBL | |||||
| Casein kinase II subunit alpha' | Kinase | Kd | 6.41 | CHEMBL | |||||
| Inhibitor of nuclear factor kappa-B kinase subunit epsilon | Kinase | Kd | 6.15 | CHEMBL | |||||
| LIM domain kinase 2 | Kinase | Kd | 4.28 | CHEMBL | |||||
| Serine/threonine-protein kinase STK11 | Kinase | Kd | 8.52 | CHEMBL | |||||
| Interleukin-1 receptor-associated kinase 3 | Kinase | Kd | 7.46 | CHEMBL | |||||
| Mitogen-activated protein kinase kinase kinase kinase 1 | Kinase | Kd | 6.80 | CHEMBL | |||||
| Aurora kinase B | Kinase | Kd | 6.19 | CHEMBL | |||||
| Mitogen-activated protein kinase kinase kinase kinase 4 | Kinase | Kd | 6.53 | CHEMBL | |||||
| Serine/threonine-protein kinase Nek9 | Kinase | Kd | 5.75 | CHEMBL | |||||
| Mitogen-activated protein kinase kinase kinase kinase 2 | Kinase | Kd | 5.43 | CHEMBL | |||||
| Serine/threonine-protein kinase TBK1 | Kinase | Kd | 4.30 | CHEMBL | |||||
| Serine/threonine-protein kinase ICK | Kinase | Kd | 6.57 | CHEMBL | |||||
| Interleukin-1 receptor-associated kinase 1 | Kinase | Kd | 6.59 | CHEMBL | |||||
| Serine/threonine-protein kinase TAO1 | Kinase | Kd | 5.66 | CHEMBL | |||||
| Serine/threonine-protein kinase TAO2 | Kinase | Kd | 5.47 | CHEMBL | |||||
| Macrophage colony-stimulating factor 1 receptor | Kinase | IC50 | 7.40 | CHEMBL | |||||
| cGMP-dependent protein kinase 1 | Kinase | Kd | 5.82 | CHEMBL | |||||
| Ferrochelatase, mitochondrial | Enzyme | Kd | 4.17 | CHEMBL | |||||
| Uncharacterized protein FLJ45252 | Unclassified | Kd | 7.28 | CHEMBL | |||||
| Uncharacterized aarF domain-containing protein kinase 1 | Kinase | Kd | 7.48 | CHEMBL | |||||
| Tyrosine-protein kinase JAK3 | Kinase | INHIBITOR | IC50 | 6.28 | IUPHAR | ||||
| Tyrosine-protein kinase JAK2 | Kinase | IC50 | 5.97 | CHEMBL |
| ID | Source |
|---|---|
| CHEBI:231350 | CHEBI |
| 6T3 | PDB_CHEM_ID |
| CHEMBL2035187 | ChEMBL_ID |
| C561234 | MESH_SUPPLEMENTAL_RECORD_UI |
| 7793 | IUPHAR_LIGAND_ID |
| DB11697 | DRUGBANK_ID |
| 4041252 | VANDF |
| C3467842 | UMLSCUI |
| CHEMBL5095049 | ChEMBL_ID |
| D04300 | KEGG_DRUG |
| 9385 | INN_ID |
| 1228923-42-9 | SECONDARY_CAS_RN |
| 46216796 | PUBCHEM_CID |
| 357763 | MMSL |
| 40530 | MMSL |
| 40560 | MMSL |
| d09865 | MMSL |
| 018971 | NDDF |
| 018972 | NDDF |
| G22N65IL3O | UNII |
| 2595242 | RXNORM |
| G22N65IL3O | INXIGHT DRUGS |
| Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
|---|---|---|---|---|---|---|---|---|
| Vonjo | HUMAN PRESCRIPTION DRUG LABEL | 1 | 72482-100 | CAPSULE | 100 mg | ORAL | NDA | 32 sections |
| Vonjo | HUMAN PRESCRIPTION DRUG LABEL | 1 | 72482-100 | CAPSULE | 100 mg | ORAL | NDA | 32 sections |