Details of the Drug

General Information of Drug (ID: DMINOX3)

Drug Name
Vincristine
Synonyms
LCR; Leurocristine; Marqibo; Oncovine; Tecnocris; VCR; VIN; Vincasar; Vincristina; Vincristinum; Vincrstine; Vincrystine; Vinkristin; Indole alkaloid; Liposomal Vincristine; Onco TCS; Vincristina [DCIT]; Oncovin (TN); Tecnocris (TN); Vincristine (INN); Vincristine [INN:BAN]; Vincristinum [INN-Latin]; Lilly37231 (1:1 sulfate salt); Oncovin (1:1 sulfate salt); Vincasar (1:1 sulfate salt); Vincrex (1:1 sulfate salt); Vincaleukoblastine, 22-oxo-22-Oxovincaleukoblastine; Z-D-Val-Lys(Z)-OH; 22-Oxovincaleukoblastine
Indication
Disease Entry ICD 11 Status REF
Acute lymphoblastic leukaemia 2A85 Approved [1]
Adult kidney Wilms tumor N.A. Approved [2]
Beckwith-Wiedemann syndrome N.A. Approved [2]
Burkitt lymphoma N.A. Approved [2]
Central nervous system neoplasm N.A. Approved [2]
Childhood acute lymphoblastic leukemia N.A. Approved [2]
Childhood kidney Wilms tumor N.A. Approved [2]
Hamartoma N.A. Approved [2]
Kidney neoplasm N.A. Approved [2]
Leukemia N.A. Approved [2]
MALT lymphoma N.A. Approved [2]
Nodal marginal zone lymphoma 2A85.0 Approved [2]
Plasma cell myeloma 2A83.1 Approved [2]
Primitive neuroectodermal tumor N.A. Approved [2]
Splenic marginal zone lymphoma N.A. Approved [2]
Testicular lymphoma N.A. Approved [2]
Wilms tumor N.A. Approved [2]
Classic Hodgkin lymphoma N.A. Investigative [2]
Follicular lymphoma 2A80 Investigative [2]
Neuroblastoma 2D11.2 Investigative [2]
⏷ Show the Full List of Indication(s)
Therapeutic Class
Anticancer Agents
Drug Type
Small molecular drug
Structure
3D MOL 2D MOL
#Ro5 Violations (Lipinski): 2 Molecular Weight (mw) 825
Logarithm of the Partition Coefficient (xlogp) 2.8
Rotatable Bond Count (rotbonds) 10
Hydrogen Bond Donor Count (hbonddonor) 3
Hydrogen Bond Acceptor Count (hbondacc) 12
ADMET Property
BDDCS Class
Biopharmaceutics Drug Disposition Classification System (BDDCS) Class 1: high solubility and high permeability [3]
Clearance
The drug present in the plasma can be removed from the body at the rate of 2 mL/min/kg [4]
Elimination
15% of drug is excreted from urine in the unchanged form [3]
Half-life
The concentration or amount of drug in body reduced by one-half in 5 minutes (alpha), 2.3 hours (beta), and 85 hours (gamma) [4]
Metabolism
The drug is metabolized via the hepatic []
Unbound Fraction
The unbound fraction of drug in plasma is 0.4% [4]
Vd
Fluid volume that would be required to contain the amount of drug present in the body at the same concentration as in the plasma 2.4 L/kg [4]
Water Solubility
The ability of drug to dissolve in water is measured as 10 mg/mL [3]
Chemical Identifiers
Formula
C46H56N4O10
IUPAC Name
methyl (1R,9R,10S,11R,12R,19R)-11-acetyloxy-12-ethyl-4-[(13S,15S,17S)-17-ethyl-17-hydroxy-13-methoxycarbonyl-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-4(12),5,7,9-tetraen-13-yl]-8-formyl-10-hydroxy-5-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-10-carboxylate
Canonical SMILES
CC[C@@]1(C[C@@H]2C[C@@](C3=C(CCN(C2)C1)C4=CC=CC=C4N3)(C5=C(C=C6C(=C5)[C@]78CCN9[C@H]7[C@@](C=CC9)([C@H]([C@@]([C@@H]8N6C=O)(C(=O)OC)O)OC(=O)C)CC)OC)C(=O)OC)O
InChI
InChI=1S/C46H56N4O10/c1-7-42(55)22-28-23-45(40(53)58-5,36-30(14-18-48(24-28)25-42)29-12-9-10-13-33(29)47-36)32-20-31-34(21-35(32)57-4)50(26-51)38-44(31)16-19-49-17-11-15-43(8-2,37(44)49)39(60-27(3)52)46(38,56)41(54)59-6/h9-13,15,20-21,26,28,37-39,47,55-56H,7-8,14,16-19,22-25H2,1-6H3/t28-,37+,38-,39-,42+,43-,44-,45+,46+/m1/s1
InChIKey
OGWKCGZFUXNPDA-XQKSVPLYSA-N
Cross-matching ID
PubChem CID
5978
ChEBI ID
CHEBI:28445
CAS Number
57-22-7
DrugBank ID
DB00541
TTD ID
D09QVV
VARIDT ID
DR00143
INTEDE ID
DR1692
Combinatorial Drugs (CBD) Click to Jump to the Detailed CBD Information of This Drug
Repurposed Drugs (RPD) Click to Jump to the Detailed RPD Information of This Drug

Molecular Interaction Atlas of This Drug


Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Tubulin beta (TUBB) TTYFKSZ NOUNIPROTAC Modulator [5]

Drug Transporter (DTP)
DTP Name DTP ID UniProt ID MOA REF
Multidrug resistance-associated protein 2 (ABCC2) DTFI42L MRP2_HUMAN Substrate [6]
Multidrug resistance-associated protein 1 (ABCC1) DTSYQGK MRP1_HUMAN Substrate [7]
Breast cancer resistance protein (ABCG2) DTI7UX6 ABCG2_HUMAN Substrate [8]
P-glycoprotein 1 (ABCB1) DTUGYRD MDR1_HUMAN Substrate [9]

Drug-Metabolizing Enzyme (DME)
DME Name DME ID UniProt ID MOA REF
Cytochrome P450 3A4 (CYP3A4) DE4LYSA CP3A4_HUMAN Substrate [10]
Cytochrome P450 3A5 (CYP3A5) DEIBDNY CP3A5_HUMAN Substrate [10]
Cytochrome P450 3A7 (CYP3A7) DERD86B CP3A7_HUMAN Substrate [11]
Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This Drug

Drug-Drug Interaction (DDI) Information of This Drug

Coadministration of a Drug Treating the Same Disease as Vincristine
DDI Drug Name DDI Drug ID Severity Mechanism Disease REF
Clofarabine DMCVJ86 Moderate Increased risk of hepatotoxicity by the combination of Vincristine and Clofarabine. Mature B-cell lymphoma [2A85] [12]
Blinatumomab DMGECIJ Moderate Decreased metabolism of Vincristine caused by Blinatumomab mediated inhibition of CYP450 enzyme. Mature B-cell lymphoma [2A85] [13]
Coadministration of a Drug Treating the Disease Different from Vincristine (Comorbidity)
DDI Drug Name DDI Drug ID Severity Mechanism Comorbidity REF
Remdesivir DMBFZ6L Moderate Increased risk of hepatotoxicity by the combination of Vincristine and Remdesivir. 1D6YCoronavirus Disease 2019 [1D6YCoronavirus Disease 2019] [14]
Ivosidenib DM8S6T7 Moderate Increased metabolism of Vincristine caused by Ivosidenib mediated induction of CYP450 enzyme. Acute myeloid leukaemia [2A60] [15]
Midostaurin DMI6E0R Moderate Decreased clearance of Vincristine due to the transporter inhibition by Midostaurin. Acute myeloid leukaemia [2A60] [16]
Arn-509 DMT81LZ Moderate Accelerated clearance of Vincristine due to the transporter induction by Arn-509. Acute myeloid leukaemia [2A60] [16]
Gilteritinib DMTI0ZO Moderate Decreased clearance of Vincristine due to the transporter inhibition by Gilteritinib. Acute myeloid leukaemia [2A60] [17]
Siltuximab DMGEATB Moderate Additive immunosuppressive effects by the combination of Vincristine and Siltuximab. Anemia [3A00-3A9Z] [16]
Dronedarone DMA8FS5 Moderate Decreased clearance of Vincristine due to the transporter inhibition by Dronedarone. Angina pectoris [BA40] [18]
Bedaquiline DM3906J Moderate Increased risk of hepatotoxicity by the combination of Vincristine and Bedaquiline. Antimicrobial drug resistance [MG50-MG52] [19]
Voriconazole DMAOL2S Major Decreased clearance of Vincristine due to the transporter inhibition by Voriconazole. Aspergillosis [1F20] [20]
Posaconazole DMUL5EW Major Decreased clearance of Vincristine due to the transporter inhibition by Posaconazole. Aspergillosis [1F20] [20]
Roflumilast DMPGHY8 Moderate Additive immunosuppressive effects by the combination of Vincristine and Roflumilast. Asthma [CA23] [16]
Ofloxacin DM0VQN3 Minor Decreased absorption of Vincristine due to intestinal mucosa variation caused by Ofloxacin. Bacterial infection [1A00-1C4Z] [21]
Dalfopristin DM4LTKV Moderate Decreased metabolism of Vincristine caused by Dalfopristin mediated inhibition of CYP450 enzyme. Bacterial infection [1A00-1C4Z] [22]
Clarithromycin DM4M1SG Major Decreased clearance of Vincristine due to the transporter inhibition by Clarithromycin. Bacterial infection [1A00-1C4Z] [20]
Trovafloxacin DM6AN32 Minor Decreased absorption of Vincristine due to intestinal mucosa variation caused by Trovafloxacin. Bacterial infection [1A00-1C4Z] [21]
Sparfloxacin DMB4HCT Minor Decreased absorption of Vincristine due to intestinal mucosa variation caused by Sparfloxacin. Bacterial infection [1A00-1C4Z] [21]
Gemifloxacin DMHT34O Minor Decreased absorption of Vincristine due to intestinal mucosa variation caused by Gemifloxacin. Bacterial infection [1A00-1C4Z] [21]
Norfloxacin DMIZ6W2 Minor Decreased absorption of Vincristine due to intestinal mucosa variation caused by Norfloxacin. Bacterial infection [1A00-1C4Z] [21]
ABT-492 DMJFD2I Minor Decreased absorption of Vincristine due to intestinal mucosa variation caused by ABT-492. Bacterial infection [1A00-1C4Z] [21]
Levofloxacin DMS60RB Minor Decreased absorption of Vincristine due to intestinal mucosa variation caused by Levofloxacin. Bacterial infection [1A00-1C4Z] [21]
Troleandomycin DMUZNIG Major Decreased clearance of Vincristine due to the transporter inhibition by Troleandomycin. Bacterial infection [1A00-1C4Z] [20]
Lomefloxacin DMVRH9C Minor Decreased absorption of Vincristine due to intestinal mucosa variation caused by Lomefloxacin. Bacterial infection [1A00-1C4Z] [21]
Telithromycin DMZ4P3A Major Decreased clearance of Vincristine due to the transporter inhibition by Telithromycin. Bacterial infection [1A00-1C4Z] [20]
Erdafitinib DMI782S Moderate Decreased clearance of Vincristine due to the transporter inhibition by Erdafitinib. Bladder cancer [2C94] [23]
Pexidartinib DMS2J0Z Major Increased risk of hepatotoxicity by the combination of Vincristine and Pexidartinib. Bone/articular cartilage neoplasm [2F7B] [24]
Lomustine DMMWSUL Minor Decreased metabolism of Vincristine caused by Lomustine mediated inhibition of CYP450 enzyme. Brain cancer [2A00] [25]
Lapatinib DM3BH1Y Moderate Decreased clearance of Vincristine due to the transporter inhibition by Lapatinib. Breast cancer [2C60-2C6Y] [26]
Tucatinib DMBESUA Major Decreased clearance of Vincristine due to the transporter inhibition by Tucatinib. Breast cancer [2C60-2C6Y] [20]
Palbociclib DMD7L94 Moderate Decreased metabolism of Vincristine caused by Palbociclib mediated inhibition of CYP450 enzyme. Breast cancer [2C60-2C6Y] [27]
Capecitabine DMTS85L Minor Increased plasma concentrations of Vincristine and Capecitabine due to competitive inhibition of the same metabolic pathway. Colorectal cancer [2B91] [25]
Mifepristone DMGZQEF Moderate Decreased metabolism of Vincristine caused by Mifepristone mediated inhibition of CYP450 enzyme. Cushing syndrome [5A70] [16]
Ivacaftor DMZC1HS Moderate Decreased clearance of Vincristine due to the transporter inhibition by Ivacaftor. Cystic fibrosis [CA25] [28]
MK-8228 DMOB58Q Moderate Decreased metabolism of Vincristine caused by MK-8228 mediated inhibition of CYP450 enzyme. Cytomegaloviral disease [1D82] [29]
Aprepitant DM053KT Moderate Decreased metabolism of Vincristine caused by Aprepitant mediated inhibition of CYP450 enzyme. Depression [6A70-6A7Z] [30]
Nefazodone DM4ZS8M Major Decreased metabolism of Vincristine caused by Nefazodone mediated inhibition of CYP450 enzyme. Depression [6A70-6A7Z] [20]
Primidone DM0WX6I Moderate Increased metabolism of Vincristine caused by Primidone mediated induction of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [31]
Oxcarbazepine DM5PU6O Moderate Increased metabolism of Vincristine caused by Oxcarbazepine mediated induction of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [32]
Cenobamate DM8KLU9 Moderate Increased metabolism of Vincristine caused by Cenobamate mediated induction of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [33]
Fosphenytoin DMOX3LB Moderate Accelerated clearance of Vincristine due to the transporter induction by Fosphenytoin. Epilepsy/seizure [8A61-8A6Z] [34]
Rufinamide DMWE60C Moderate Increased metabolism of Vincristine caused by Rufinamide mediated induction of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [16]
Phenobarbital DMXZOCG Moderate Increased metabolism of Vincristine caused by Phenobarbital mediated induction of CYP450 enzyme. Epilepsy/seizure [8A61-8A6Z] [31]
Carbamazepine DMZOLBI Moderate Accelerated clearance of Vincristine due to the transporter induction by Carbamazepine. Epilepsy/seizure [8A61-8A6Z] [31]
Cannabidiol DM0659E Moderate Increased risk of hepatotoxicity by the combination of Vincristine and Cannabidiol. Epileptic encephalopathy [8A62] [16]
Tazemetostat DMWP1BH Moderate Increased metabolism of Vincristine caused by Tazemetostat mediated induction of CYP450 enzyme. Follicular lymphoma [2A80] [35]
Itraconazole DMCR1MV Major Decreased metabolism of Vincristine caused by Itraconazole mediated inhibition of CYP450 enzyme. Fungal infection [1F29-1F2F] [20]
Miconazole DMPMYE8 Moderate Decreased metabolism of Vincristine caused by Miconazole mediated inhibition of CYP450 enzyme. Fungal infection [1F29-1F2F] [36]
Ketoconazole DMPZI3Q Major Decreased metabolism of Vincristine caused by Ketoconazole mediated inhibition of CYP450 enzyme. Fungal infection [1F29-1F2F] [20]
Boceprevir DMBSHMF Major Decreased metabolism of Vincristine caused by Boceprevir mediated inhibition of CYP450 enzyme. Hepatitis virus infection [1E50-1E51] [20]
Telaprevir DMMRV29 Major Decreased clearance of Vincristine due to the transporter inhibition by Telaprevir. Hepatitis virus infection [1E50-1E51] [20]
Rifampin DMA8J1G Moderate Accelerated clearance of Vincristine due to the transporter induction by Rifampin. HIV-infected patients with tuberculosis [1B10-1B14] [31]
Rifapentine DMCHV4I Moderate Accelerated clearance of Vincristine due to the transporter induction by Rifapentine. HIV-infected patients with tuberculosis [1B10-1B14] [31]
Brentuximab vedotin DMWLC57 Moderate Increased risk of hepatotoxicity by the combination of Vincristine and Brentuximab vedotin. Hodgkin lymphoma [2B30] [37]
Delavirdine DM3NF5G Major Decreased metabolism of Vincristine caused by Delavirdine mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [20]
Fosamprenavir DM4W9B3 Major Decreased metabolism of Vincristine caused by Fosamprenavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [20]
Cobicistat DM6L4H2 Major Decreased clearance of Vincristine due to the transporter inhibition by Cobicistat. Human immunodeficiency virus disease [1C60-1C62] [20]
Efavirenz DMC0GSJ Moderate Increased metabolism of Vincristine caused by Efavirenz mediated induction of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [38]
Saquinavir DMG814N Major Decreased metabolism of Vincristine caused by Saquinavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [20]
Etravirine DMGV8QU Moderate Increased metabolism of Vincristine caused by Etravirine mediated induction of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [39]
Zalcitabine DMH7MUV Moderate Increased risk of peripheral neuropathy by the combination of Vincristine and Zalcitabine. Human immunodeficiency virus disease [1C60-1C62] [40]
Amprenavir DMLMXE0 Major Decreased metabolism of Vincristine caused by Amprenavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [20]
Darunavir DMN3GCH Moderate Decreased metabolism of Vincristine caused by Darunavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [41]
Atazanavir DMSYRBX Major Decreased metabolism of Vincristine caused by Atazanavir mediated inhibition of CYP450 enzyme. Human immunodeficiency virus disease [1C60-1C62] [20]
Mipomersen DMGSRN1 Major Increased risk of hepatotoxicity by the combination of Vincristine and Mipomersen. Hyper-lipoproteinaemia [5C80] [42]
Teriflunomide DMQ2FKJ Major Increased risk of hepatotoxicity by the combination of Vincristine and Teriflunomide. Hyper-lipoproteinaemia [5C80] [43]
BMS-201038 DMQTAGO Major Increased risk of hepatotoxicity by the combination of Vincristine and BMS-201038. Hyper-lipoproteinaemia [5C80] [44]
Verapamil DMA7PEW Minor Increased plasma concentration of Vincristine and Verapamil due to competitive binding of plasma proteins. Hypertension [BA00-BA04] [45]
Conivaptan DM1V329 Major Decreased metabolism of Vincristine caused by Conivaptan mediated inhibition of CYP450 enzyme. Hypo-osmolality/hyponatraemia [5C72] [20]
Tolvaptan DMIWFRL Moderate Decreased clearance of Vincristine due to the transporter inhibition by Tolvaptan. Hypo-osmolality/hyponatraemia [5C72] [17]
Berotralstat DMWA2DZ Moderate Decreased metabolism of Vincristine caused by Berotralstat mediated inhibition of CYP450 enzyme. Innate/adaptive immunodeficiency [4A00] [46]
Amobarbital DM0GQ8N Moderate Increased metabolism of Vincristine caused by Amobarbital mediated induction of CYP450 enzyme. Insomnia [7A00-7A0Z] [31]
Methotrexate DM2TEOL Moderate Increased risk of hepatotoxicity by the combination of Vincristine and Methotrexate. Leukaemia [2A60-2B33] [16]
Glycerol phenylbutyrate DMDGRQO Moderate Increased metabolism of Vincristine caused by Glycerol phenylbutyrate mediated induction of CYP450 enzyme. Liver disease [DB90-DB9Z] [16]
Denosumab DMNI0KO Moderate Additive myelosuppressive effects by the combination of Vincristine and Denosumab. Low bone mass disorder [FB83] [47]
Crizotinib DM4F29C Moderate Decreased metabolism of Vincristine caused by Crizotinib mediated inhibition of CYP450 enzyme. Lung cancer [2C25] [48]
Brigatinib DM7W94S Moderate Increased metabolism of Vincristine caused by Brigatinib mediated induction of CYP450 enzyme. Lung cancer [2C25] [49]
Ceritinib DMB920Z Major Decreased metabolism of Vincristine caused by Ceritinib mediated inhibition of CYP450 enzyme. Lung cancer [2C25] [20]
PF-06463922 DMKM7EW Moderate Increased metabolism of Vincristine caused by PF-06463922 mediated induction of CYP450 enzyme. Lung cancer [2C25] [50]
Osimertinib DMRJLAT Moderate Increased metabolism of Vincristine caused by Osimertinib mediated induction of CYP450 enzyme. Lung cancer [2C25] [16]
Capmatinib DMYCXKL Moderate Decreased clearance of Vincristine due to the transporter inhibition by Capmatinib. Lung cancer [2C25] [51]
Selpercatinib DMZR15V Moderate Decreased metabolism of Vincristine caused by Selpercatinib mediated inhibition of CYP450 enzyme. Lung cancer [2C25] [16]
Calaspargase pegol DMQZBXI Moderate Increased risk of hepatotoxicity by the combination of Vincristine and Calaspargase pegol. Malignant haematopoietic neoplasm [2B33] [52]
Idelalisib DM602WT Major Decreased metabolism of Vincristine caused by Idelalisib mediated inhibition of CYP450 enzyme. Mature B-cell leukaemia [2A82] [20]
IPI-145 DMWA24P Moderate Decreased metabolism of Vincristine caused by IPI-145 mediated inhibition of CYP450 enzyme. Mature B-cell leukaemia [2A82] [53]
LGX818 DMNQXV8 Moderate Increased metabolism of Vincristine caused by LGX818 mediated induction of CYP450 enzyme. Melanoma [2C30] [54]
Dabrafenib DMX6OE3 Moderate Increased metabolism of Vincristine caused by Dabrafenib mediated induction of CYP450 enzyme. Melanoma [2C30] [16]
Lasmiditan DMXLVDT Moderate Decreased clearance of Vincristine due to the transporter inhibition by Lasmiditan. Migraine [8A80] [55]
Exjade DMHPRWG Moderate Decreased metabolism of Vincristine caused by Exjade mediated inhibition of CYP450 enzyme. Mineral absorption/transport disorder [5C64] [56]
Thalidomide DM70BU5 Major Additive thrombogenic effects by the combination of Vincristine and Thalidomide. Multiple myeloma [2A83] [57]
Tecfidera DM2OVDT Moderate Additive immunosuppressive effects by the combination of Vincristine and Tecfidera. Multiple sclerosis [8A40] [58]
Siponimod DM2R86O Major Additive immunosuppressive effects by the combination of Vincristine and Siponimod. Multiple sclerosis [8A40] [17]
Fingolimod DM5JVAN Major Additive immunosuppressive effects by the combination of Vincristine and Fingolimod. Multiple sclerosis [8A40] [59]
Ocrelizumab DMEZ2KH Moderate Additive immunosuppressive effects by the combination of Vincristine and Ocrelizumab. Multiple sclerosis [8A40] [60]
Ozanimod DMT6AM2 Major Additive immunosuppressive effects by the combination of Vincristine and Ozanimod. Multiple sclerosis [8A40] [16]
Rifabutin DM1YBHK Moderate Increased metabolism of Vincristine caused by Rifabutin mediated induction of CYP450 enzyme. Mycobacterium infection [1B10-1B21] [31]
Fedratinib DM4ZBK6 Moderate Decreased metabolism of Vincristine caused by Fedratinib mediated inhibition of CYP450 enzyme. Myeloproliferative neoplasm [2A20] [16]
Nilotinib DM7HXWT Moderate Decreased clearance of Vincristine due to the transporter inhibition by Nilotinib. Myeloproliferative neoplasm [2A20] [61]
Imatinib DM7RJXL Moderate Decreased metabolism of Vincristine caused by Imatinib mediated inhibition of CYP450 enzyme. Myeloproliferative neoplasm [2A20] [62]
Dasatinib DMJV2EK Moderate Decreased metabolism of Vincristine caused by Dasatinib mediated inhibition of CYP450 enzyme. Myeloproliferative neoplasm [2A20] [63]
Omacetaxine mepesuccinate DMPU2WX Moderate Additive immunosuppressive effects by the combination of Vincristine and Omacetaxine mepesuccinate. Myeloproliferative neoplasm [2A20] [64]
Modafinil DMYILBE Minor Increased metabolism of Vincristine caused by Modafinil mediated induction of CYP450 enzyme. Narcolepsy [7A20] [65]
Rolapitant DM8XP26 Moderate Decreased clearance of Vincristine due to the transporter inhibition by Rolapitant. Nausea/vomiting [MD90] [66]
Entrectinib DMMPTLH Moderate Decreased metabolism of Vincristine caused by Entrectinib mediated inhibition of CYP450 enzyme. Non-small cell lung cancer [2C25] [67]
Rucaparib DM9PVX8 Moderate Decreased metabolism of Vincristine caused by Rucaparib mediated inhibition of CYP450 enzyme. Ovarian cancer [2C73] [68]
Abametapir DM2RX0I Moderate Decreased metabolism of Vincristine caused by Abametapir mediated inhibition of CYP450 enzyme. Pediculosis [1G00] [69]
Lefamulin DME6G97 Moderate Decreased metabolism of Vincristine caused by Lefamulin mediated inhibition of CYP450 enzyme. Pneumonia [CA40] [70]
Lonafarnib DMGM2Z6 Major Decreased metabolism of Vincristine caused by Lonafarnib mediated inhibition of CYP450 enzyme. Premature ageing appearance [LD2B] [20]
Enzalutamide DMGL19D Moderate Accelerated clearance of Vincristine due to the transporter induction by Enzalutamide. Prostate cancer [2C82] [71]
Ustekinumab DMHTYK3 Moderate Additive myelosuppressive effects by the combination of Vincristine and Ustekinumab. Psoriasis [EA90] [16]
Tildrakizumab DMLW9HG Moderate Additive myelosuppressive effects by the combination of Vincristine and Tildrakizumab. Psoriasis [EA90] [16]
Risankizumab DMM32GT Moderate Additive immunosuppressive effects by the combination of Vincristine and Risankizumab. Psoriasis [EA90] [16]
Ixekizumab DMXW92T Moderate Additive myelosuppressive effects by the combination of Vincristine and Ixekizumab. Psoriasis [EA90] [16]
Bosentan DMIOGBU Moderate Increased metabolism of Vincristine caused by Bosentan mediated induction of CYP450 enzyme. Pulmonary hypertension [BB01] [72]
Temsirolimus DMS104F Moderate Increased plasma concentrations of Vincristine and Temsirolimus due to competitive inhibition of the same metabolic pathway. Renal cell carcinoma [2C90] [73]
Gatifloxacin DMSL679 Minor Decreased absorption of Vincristine due to intestinal mucosa variation caused by Gatifloxacin. Respiratory infection [CA07-CA4Z] [21]
Tocilizumab DM7J6OR Moderate Additive immunosuppressive effects by the combination of Vincristine and Tocilizumab. Rheumatoid arthritis [FA20] [16]
Canakinumab DM8HLO5 Moderate Additive myelosuppressive effects by the combination of Vincristine and Canakinumab. Rheumatoid arthritis [FA20] [16]
Rilonacept DMGLUQS Moderate Additive immunosuppressive effects by the combination of Vincristine and Rilonacept. Rheumatoid arthritis [FA20] [16]
Golimumab DMHZV7X Major Additive immunosuppressive effects by the combination of Vincristine and Golimumab. Rheumatoid arthritis [FA20] [74]
Dexamethasone DMMWZET Moderate Increased metabolism of Vincristine caused by Dexamethasone mediated induction of CYP450 enzyme. Rheumatoid arthritis [FA20] [31]
Sarilumab DMOGNXY Moderate Additive myelosuppressive effects by the combination of Vincristine and Sarilumab. Rheumatoid arthritis [FA20] [16]
Leflunomide DMR8ONJ Major Additive myelosuppressive effects by the combination of Vincristine and Leflunomide. Rheumatoid arthritis [FA20] [43]
Anthrax vaccine DM9GSWY Moderate Antagonize the effect of Vincristine when combined with Anthrax vaccine. Sepsis [1G40-1G41] [75]
Voxelotor DMCS6M5 Moderate Decreased metabolism of Vincristine caused by Voxelotor mediated inhibition of CYP450 enzyme. Sickle-cell disorder [3A51] [76]
Telotristat ethyl DMDIYFZ Moderate Increased metabolism of Vincristine caused by Telotristat ethyl mediated induction of CYP450 enzyme. Small intestine developmental anomaly [DA90] [16]
Larotrectinib DM26CQR Moderate Decreased metabolism of Vincristine caused by Larotrectinib mediated inhibition of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [17]
Armodafinil DMGB035 Minor Increased metabolism of Vincristine caused by Armodafinil mediated induction of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [65]
LEE011 DMMX75K Moderate Decreased metabolism of Vincristine caused by LEE011 mediated inhibition of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [77]
Etoposide DMNH3PG Minor Decreased metabolism of Vincristine caused by Etoposide mediated inhibition of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [25]
Fluorouracil DMUM7HZ Minor Increased plasma concentrations of Vincristine and Fluorouracil due to competitive inhibition of the same metabolic pathway. Solid tumour/cancer [2A00-2F9Z] [25]
Doxorubicin DMVP5YE Minor Decreased metabolism of Vincristine caused by Doxorubicin mediated inhibition of CYP450 enzyme. Solid tumour/cancer [2A00-2F9Z] [25]
Pitolisant DM8RFNJ Moderate Increased metabolism of Vincristine caused by Pitolisant mediated induction of CYP450 enzyme. Somnolence [MG42] [16]
Naltrexone DMUL45H Moderate Increased risk of hepatotoxicity by the combination of Vincristine and Naltrexone. Substance abuse [6C40] [78]
Fostamatinib DM6AUHV Moderate Decreased metabolism of Vincristine caused by Fostamatinib mediated inhibition of CYP450 enzyme. Thrombocytopenia [3B64] [79]
Brilinta DMBR01X Moderate Decreased metabolism of Vincristine caused by Brilinta mediated inhibition of CYP450 enzyme. Thrombosis [DB61-GB90] [16]
Sirolimus DMGW1ID Moderate Increased plasma concentrations of Vincristine and Sirolimus due to competitive inhibition of the same metabolic pathway. Transplant rejection [NE84] [73]
Azathioprine DMMZSXQ Moderate Additive myelosuppressive effects by the combination of Vincristine and Azathioprine. Transplant rejection [NE84] [17]
Tacrolimus DMZ7XNQ Moderate Increased plasma concentrations of Vincristine and Tacrolimus due to competitive inhibition of the same metabolic pathway. Transplant rejection [NE84] [73]
Cinoxacin DM4EWNS Minor Decreased absorption of Vincristine due to intestinal mucosa variation caused by Cinoxacin. Urinary tract infection [GC08] [21]
Nalidixic acid DMRM0JV Minor Decreased absorption of Vincristine due to intestinal mucosa variation caused by Nalidixic acid. Urinary tract infection [GC08] [21]
Ganciclovir DM1MBYQ Moderate Additive myelosuppressive effects by the combination of Vincristine and Ganciclovir. Virus infection [1A24-1D9Z] [17]
Valganciclovir DMS2IUH Moderate Additive myelosuppressive effects by the combination of Vincristine and Valganciclovir. Virus infection [1A24-1D9Z] [17]
⏷ Show the Full List of 141 DDI Information of This Drug

References

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