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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Vincristine
rdfs:subClassOf
Has_Salt_Form
Concept_In_Subset
Semantic_Type
  • Organic Chemical
  • Pharmacologic Substance
Preferred_Name
  • Vincristine
UMLS_CUI
  • C0042679
CAS_Registry
  • 57-22-7
Accepted_Therapeutic_Use_For
  • Acute leukemia; Brain tumors; Chronic lymphocytic leukemia; Gestational trophoblastic neoplasms; Head and Neck squamous cell carcinoma; Kaposis sarcoma; Liver cancer;
  • Lymphoma, Hodgkins, Non-Hodgkins; Malignant thymoma; Multiple myeloma; Osteogenic sarcoma; Ovarian cancer; Pheochromocytoma; Retinoblastoma; Rhabdomyosarcoma; Soft tissue sarcoma; Testicular cancer; Wilms tumor
In_Clinical_Trial_For
  • Myelodysplastic and Myeloproliferative diseases; Neuroblastoma; Osteosarcoma; Rhabdomyosarcoma; Soft Tissue sarcoma; Wilms' Tumor
  • Adrenal Cortex Neoplasms; Brain tumors; Childhood Medulloblastoma; Ependymoma; Ewing's sarcoma; Leukemia; Lymphoma; Glioma(s); Medulloblastoma; Multiple Myeloma;
FDA_UNII_Code
  • 5J49Q6B70F
Contributing_Source
  • FDA
ALT_DEFINITION
  • The active ingredient in a drug used to treat acute leukemia. It is used in combination with other drugs to treat Hodgkin disease, non-Hodgkin lymphoma, rhabdomyosarcoma, neuroblastoma, and Wilms tumor. Vincristine is also being studied in the treatment of other types of cancer. It blocks cell growth by stopping cell division. It is a type of vinca alkaloid and a type of antimitotic agent.NCI-GLOSS
Chemical_Formula
  • C46H56N4O10
Legacy_Concept_Name
  • Vincristine
CHEBI_ID
  • CHEBI:28445
FULL_SYN
  • VincristinePTNCI
  • VincrystineSYNCI
  • LEUROCRISTINESYDTPNSC0067574
  • VincristineSYNCITCGA
  • 22-OxovincaleukoblastineSNNCI
  • vincristinePTNCI-GLOSSCDR0000045435
  • LeurocristineSYNCI
  • VincristinePTDCP02166
  • VCRABNCI
  • VINCRISTINEPTFDA5J49Q6B70F
  • VINCRISTINESYDTPNSC0067574
DEFINITION
  • A natural alkaloid isolated from the plant Vinca rosea Linn. Vincristine binds irreversibly to microtubules and spindle proteins in S phase of the cell cycle and interferes with the formation of the mitotic spindle, thereby arresting tumor cells in metaphase. This agent also depolymerizes microtubules and may also interfere with amino acid, cyclic AMP, and glutathione metabolism; calmodulin-dependent Ca++ -transport ATPase activity; cellular respiration; and nucleic acid and lipid biosynthesis. (NCI04)NCI
code
  • C933
sameAs
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