Details
| Stereochemistry | EPIMERIC |
| Molecular Formula | C20H21N7O7.Ca.5H2O |
| Molecular Weight | 601.578 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O.O.O.O.O.[Ca++].NC1=NC(=O)C2=C(NCC(CNC3=CC=C(C=C3)C(=O)N[C@@H](CCC([O-])=O)C([O-])=O)N2C=O)N1
InChI
InChIKey=NPPBLUASYYNAIG-ZIGBGYJWSA-L
InChI=1S/C20H23N7O7.Ca.5H2O/c21-20-25-16-15(18(32)26-20)27(9-28)12(8-23-16)7-22-11-3-1-10(2-4-11)17(31)24-13(19(33)34)5-6-14(29)30;;;;;;/h1-4,9,12-13,22H,5-8H2,(H,24,31)(H,29,30)(H,33,34)(H4,21,23,25,26,32);;5*1H2/q;+2;;;;;/p-2/t12?,13-;;;;;;/m0....../s1
| Molecular Formula | Ca |
| Molecular Weight | 40.078 |
| Charge | 2 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | H2O |
| Molecular Weight | 18.0153 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C20H23N7O7 |
| Molecular Weight | 473.4393 |
| Charge | 0 |
| Count |
|
| Stereochemistry | EPIMERIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Leucovorin is a compound similar to folic acid, which is a necessary vitamin. It has been around and in use for many decades. Leucovorin is a medication frequently used in combination with the chemotherapy drugs fluoruracil and methotrexate. Leucovorin is not a chemotherapy drug itself, however it is used in addition to these chemotherapy drugs to enhance anticancer effects (with fluorouracil) or to help prevent or lessen side effects (with methotrexate). Leucovorin is also used by itself to treat certain anemia problems when folic acid deficiency is present.
CNS Activity
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: P04818 Gene ID: 7298.0 Gene Symbol: TYMS Target Organism: Homo sapiens (Human) |
|||
Target ID: P00374 Gene ID: 1719.0 Gene Symbol: DHFR Target Organism: Homo sapiens (Human) Sources: http://www.ncbi.nlm.nih.gov/pubmed/2260989 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Secondary | LEUCOVORIN CALCIUM Approved UseLeucovorin rescue is indicated after high dose methotrexate therapy in osteosarcoma. Leucovorin is also indicated to diminish the toxicity and counteract the effects of impaired methotrexate elimination and of inadvertent overdosages of folic acid antagonists. Leucovorin is indicated in the treatment of megaloblastic anemias due to folic acid deficiency when oral therapy is not feasible. Leucovorin is also indicated for use in combination with 5-fluorouracil to prolong survival in the palliative treatment of patients with advanced colorectal cancer. Launch Date1953 |
|||
| Palliative | LEUCOVORIN CALCIUM Approved UseLeucovorin rescue is indicated after high dose methotrexate therapy in osteosarcoma. Leucovorin is also indicated to diminish the toxicity and counteract the effects of impaired methotrexate elimination and of inadvertent overdosages of folic acid antagonists. Leucovorin is indicated in the treatment of megaloblastic anemias due to folic acid deficiency when oral therapy is not feasible. Leucovorin is also indicated for use in combination with 5-fluorouracil to prolong survival in the palliative treatment of patients with advanced colorectal cancer. Launch Date1953 |
|||
| Palliative | LEUCOVORIN CALCIUM Approved UseLeucovorin rescue is indicated after high dose methotrexate therapy in osteosarcoma. Leucovorin is also indicated to diminish the toxicity and counteract the effects of impaired methotrexate elimination and of inadvertent overdosages of folic acid antagonists. Leucovorin is indicated in the treatment of megaloblastic anemias due to folic acid deficiency when oral therapy is not feasible. Leucovorin is also indicated for use in combination with 5-fluorouracil to prolong survival in the palliative treatment of patients with advanced colorectal cancer. Launch Date1953 |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
391 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/8405015/ |
25 mg single, oral dose: 25 mg route of administration: Oral experiment type: SINGLE co-administered: |
5-METHYLTETRAHYDROFOLIC ACID plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
21.3 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/8405015/ |
25 mg single, oral dose: 25 mg route of administration: Oral experiment type: SINGLE co-administered: |
LEUCOVORIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
258 ng/mL |
25 mg single, intravenous dose: 25 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
5-METHYLTETRAHYDROFOLIC ACID serum | Homo sapiens population: UNKNOWN age: ADULT sex: MALE food status: UNKNOWN |
|
226 ng/mL |
25 mg single, intramuscular dose: 25 mg route of administration: Intramuscular experiment type: SINGLE co-administered: |
5-METHYLTETRAHYDROFOLIC ACID serum | Homo sapiens population: UNKNOWN age: ADULT sex: MALE food status: UNKNOWN |
|
360 ng/mL |
25 mg single, intramuscular dose: 25 mg route of administration: Intramuscular experiment type: SINGLE co-administered: |
LEUCOVORIN serum | Homo sapiens population: UNKNOWN age: ADULT sex: MALE food status: UNKNOWN |
|
96 μM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3260621 |
500 mg/m² 1 times / week other, intravenous dose: 500 mg/m² route of administration: Intravenous experiment type: OTHER co-administered: FLUOROURACIL |
LEUCOVORIN CALCIUM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
51 μM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3260621 |
500 mg/m² 1 times / 5 weeks other, intravenous dose: 500 mg/m² route of administration: Intravenous experiment type: OTHER co-administered: FLUOROURACIL |
LEUCOVORIN CALCIUM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
1810 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/8405015/ |
25 mg single, oral dose: 25 mg route of administration: Oral experiment type: SINGLE co-administered: |
5-METHYLTETRAHYDROFOLIC ACID plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
65.5 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/8405015/ |
25 mg single, oral dose: 25 mg route of administration: Oral experiment type: SINGLE co-administered: |
LEUCOVORIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
28.4 mg × min/L |
25 mg single, intravenous dose: 25 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
5-METHYLTETRAHYDROFOLIC ACID serum | Homo sapiens population: UNKNOWN age: ADULT sex: MALE food status: UNKNOWN |
|
71 mM × min EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3260621 |
500 mg/m² 1 times / week other, intravenous dose: 500 mg/m² route of administration: Intravenous experiment type: OTHER co-administered: FLUOROURACIL |
LEUCOVORIN CALCIUM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
364 mM × min EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3260621 |
500 mg/m² 1 times / 5 weeks other, intravenous dose: 500 mg/m² route of administration: Intravenous experiment type: OTHER co-administered: FLUOROURACIL |
LEUCOVORIN CALCIUM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
6.2 h |
25 mg single, intravenous dose: 25 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
5-METHYLTETRAHYDROFOLIC ACID serum | Homo sapiens population: UNKNOWN age: ADULT sex: MALE food status: UNKNOWN |
|
6.2 h |
25 mg single, intramuscular dose: 25 mg route of administration: Intramuscular experiment type: SINGLE co-administered: |
5-METHYLTETRAHYDROFOLIC ACID serum | Homo sapiens population: UNKNOWN age: ADULT sex: MALE food status: UNKNOWN |
|
6.2 h |
25 mg single, intramuscular dose: 25 mg route of administration: Intramuscular experiment type: SINGLE co-administered: |
LEUCOVORIN serum | Homo sapiens population: UNKNOWN age: ADULT sex: MALE food status: UNKNOWN |
|
8 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/3260621 |
500 mg/m² 1 times / week other, intravenous dose: 500 mg/m² route of administration: Intravenous experiment type: OTHER co-administered: FLUOROURACIL |
LEUCOVORIN CALCIUM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
Doses
| Dose | Population | Adverse events |
|---|---|---|
20 mg/m2 1 times / week multiple, intravenous MTD Dose: 20 mg/m2, 1 times / week Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / week Sources: |
unhealthy, Median age 52 years Health Status: unhealthy Age Group: Median age 52 years Sex: M+F Sources: |
Other AEs: Neurotoxicity, Diarrhea... Other AEs: Neurotoxicity (grade 1, 83.3%) Sources: Diarrhea (grade 1, 66.7%) Diarrhea (grade 3, 16.7%) Nausea (grade 1, 16.7%) Nausea (grade 2, 33.3%) Vomiting (grade 1, 33.3%) Vomiting (grade 2, 16.7%) |
20 mg/m2 1 times / week multiple, intravenous Studied dose Dose: 20 mg/m2, 1 times / week Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / week Sources: |
unhealthy, Median age 52 years Health Status: unhealthy Age Group: Median age 52 years Sex: M+F Sources: |
DLT: Neutropenia... Dose limiting toxicities: Neutropenia (20%) Sources: |
20 mg/m2 1 times / week multiple, intravenous Studied dose Dose: 20 mg/m2, 1 times / week Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / week Sources: |
unhealthy, Median age 52 years Health Status: unhealthy Age Group: Median age 52 years Sex: M+F Sources: |
DLT: Diarrhea... Dose limiting toxicities: Diarrhea (grade 3, 40%) Sources: |
20 mg/m2 1 times / week multiple, intravenous Studied dose Dose: 20 mg/m2, 1 times / week Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / week Sources: |
unhealthy, Median age 52 years Health Status: unhealthy Age Group: Median age 52 years Sex: M+F Sources: |
DLT: Diarrhea... Dose limiting toxicities: Diarrhea (grade 3, 33.3%) Sources: |
20 mg/m2 1 times / day multiple, intravenous Studied dose Dose: 20 mg/m2, 1 times / day Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / day Sources: |
unhealthy, Median age 60.5 years Health Status: unhealthy Age Group: Median age 60.5 years Sex: M+F Sources: |
DLT: Nausea, Vomiting... Dose limiting toxicities: Nausea (grade 3, 33.3%) Sources: Vomiting (grade 3, 33.3%) Diarrhea (grade 3, 33.3%) Paresthesia (grade 3, 33.3%) Febrile neutropenia (grade 4, 33.3%) |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Nausea | grade 1, 16.7% | 20 mg/m2 1 times / week multiple, intravenous MTD Dose: 20 mg/m2, 1 times / week Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / week Sources: |
unhealthy, Median age 52 years Health Status: unhealthy Age Group: Median age 52 years Sex: M+F Sources: |
| Vomiting | grade 1, 33.3% | 20 mg/m2 1 times / week multiple, intravenous MTD Dose: 20 mg/m2, 1 times / week Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / week Sources: |
unhealthy, Median age 52 years Health Status: unhealthy Age Group: Median age 52 years Sex: M+F Sources: |
| Diarrhea | grade 1, 66.7% | 20 mg/m2 1 times / week multiple, intravenous MTD Dose: 20 mg/m2, 1 times / week Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / week Sources: |
unhealthy, Median age 52 years Health Status: unhealthy Age Group: Median age 52 years Sex: M+F Sources: |
| Neurotoxicity | grade 1, 83.3% | 20 mg/m2 1 times / week multiple, intravenous MTD Dose: 20 mg/m2, 1 times / week Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / week Sources: |
unhealthy, Median age 52 years Health Status: unhealthy Age Group: Median age 52 years Sex: M+F Sources: |
| Vomiting | grade 2, 16.7% | 20 mg/m2 1 times / week multiple, intravenous MTD Dose: 20 mg/m2, 1 times / week Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / week Sources: |
unhealthy, Median age 52 years Health Status: unhealthy Age Group: Median age 52 years Sex: M+F Sources: |
| Nausea | grade 2, 33.3% | 20 mg/m2 1 times / week multiple, intravenous MTD Dose: 20 mg/m2, 1 times / week Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / week Sources: |
unhealthy, Median age 52 years Health Status: unhealthy Age Group: Median age 52 years Sex: M+F Sources: |
| Diarrhea | grade 3, 16.7% | 20 mg/m2 1 times / week multiple, intravenous MTD Dose: 20 mg/m2, 1 times / week Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / week Sources: |
unhealthy, Median age 52 years Health Status: unhealthy Age Group: Median age 52 years Sex: M+F Sources: |
| Neutropenia | 20% DLT |
20 mg/m2 1 times / week multiple, intravenous Studied dose Dose: 20 mg/m2, 1 times / week Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / week Sources: |
unhealthy, Median age 52 years Health Status: unhealthy Age Group: Median age 52 years Sex: M+F Sources: |
| Diarrhea | grade 3, 40% DLT |
20 mg/m2 1 times / week multiple, intravenous Studied dose Dose: 20 mg/m2, 1 times / week Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / week Sources: |
unhealthy, Median age 52 years Health Status: unhealthy Age Group: Median age 52 years Sex: M+F Sources: |
| Diarrhea | grade 3, 33.3% DLT |
20 mg/m2 1 times / week multiple, intravenous Studied dose Dose: 20 mg/m2, 1 times / week Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / week Sources: |
unhealthy, Median age 52 years Health Status: unhealthy Age Group: Median age 52 years Sex: M+F Sources: |
| Diarrhea | grade 3, 33.3% DLT |
20 mg/m2 1 times / day multiple, intravenous Studied dose Dose: 20 mg/m2, 1 times / day Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / day Sources: |
unhealthy, Median age 60.5 years Health Status: unhealthy Age Group: Median age 60.5 years Sex: M+F Sources: |
| Nausea | grade 3, 33.3% DLT |
20 mg/m2 1 times / day multiple, intravenous Studied dose Dose: 20 mg/m2, 1 times / day Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / day Sources: |
unhealthy, Median age 60.5 years Health Status: unhealthy Age Group: Median age 60.5 years Sex: M+F Sources: |
| Paresthesia | grade 3, 33.3% DLT |
20 mg/m2 1 times / day multiple, intravenous Studied dose Dose: 20 mg/m2, 1 times / day Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / day Sources: |
unhealthy, Median age 60.5 years Health Status: unhealthy Age Group: Median age 60.5 years Sex: M+F Sources: |
| Vomiting | grade 3, 33.3% DLT |
20 mg/m2 1 times / day multiple, intravenous Studied dose Dose: 20 mg/m2, 1 times / day Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / day Sources: |
unhealthy, Median age 60.5 years Health Status: unhealthy Age Group: Median age 60.5 years Sex: M+F Sources: |
| Febrile neutropenia | grade 4, 33.3% DLT |
20 mg/m2 1 times / day multiple, intravenous Studied dose Dose: 20 mg/m2, 1 times / day Route: intravenous Route: multiple Dose: 20 mg/m2, 1 times / day Sources: |
unhealthy, Median age 60.5 years Health Status: unhealthy Age Group: Median age 60.5 years Sex: M+F Sources: |
Overview
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
OverviewOther
| Other Inhibitor | Other Substrate | Other Inducer |
|---|---|---|
Drug as perpetrator
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
| no [IC50 133 uM] | ||||
| no [IC50 133 uM] | ||||
| no [IC50 133 uM] | ||||
| no [IC50 133 uM] | ||||
Page: - |
no | |||
Sources: https://molpharm.aspetjournals.org/content/83/6/1257 Page: - |
yes [Inhibition 10 uM] | |||
Sources: https://molpharm.aspetjournals.org/content/83/6/1257 Page: - |
yes [Inhibition 10 uM] |
Drug as victim
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Page: - |
no [Km 1740 uM] | |||
Page: - |
no [Km 640 uM] |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Methotrexate-induced bone marrow adiposity is mitigated by folinic acid supplementation through the regulation of Wnt/β-catenin signalling. | 2015-03 |
|
| Methotrexate induces production of IL-1 and IL-6 in the monocytic cell line U937. | 2014-01-20 |
|
| Prognostic and predictive role of JWA and XRCC1 expressions in gastric cancer. | 2012-05-15 |
|
| Low-dose methotrexate inhibits methionine S-adenosyltransferase in vitro and in vivo. | 2012-05-09 |
|
| Synthesis, biological, and antitumor activity of a highly potent 6-substituted pyrrolo[2,3-d]pyrimidine thienoyl antifolate inhibitor with proton-coupled folate transporter and folate receptor selectivity over the reduced folate carrier that inhibits β-glycinamide ribonucleotide formyltransferase. | 2011-10-27 |
|
| Dihydrofolate reductase deficiency due to a homozygous DHFR mutation causes megaloblastic anemia and cerebral folate deficiency leading to severe neurologic disease. | 2011-02-11 |
|
| Identification and characterization of an inborn error of metabolism caused by dihydrofolate reductase deficiency. | 2011-02-11 |
|
| Effect of methotrexate and leucovorin on female reproductive tract of albino rats. | 2011-01-08 |
|
| Exploratory study of hepatic arterial infusion oxaliplatin with systemic 5-fluorouracil/bevacizumab in patients with refractory solid tumor and extensive liver metastases. | 2010-12 |
|
| Interleukin-10 and -12 predict chemotherapy-associated toxicity in esophageal adenocarcinoma. | 2010-11 |
|
| Hepatotoxicity of intra-arterial combination chemotherapy in patients with liver cirrhosis and advanced hepatocellular carcinoma. | 2010-11 |
|
| Glucarpidase, leucovorin, and thymidine for high-dose methotrexate-induced renal dysfunction: clinical and pharmacologic factors affecting outcome. | 2010-09-01 |
|
| A phase I study of 5-fluorouracil/leucovorin and arsenic trioxide for patients with refractory/relapsed colorectal carcinoma. | 2010-06-01 |
|
| Methotrexate-induced myelopathy responsive to substitution of multiple folate metabolites. | 2010-05 |
|
| Phase I study of flavopiridol with oxaliplatin and fluorouracil/leucovorin in advanced solid tumors. | 2009-12-01 |
|
| Effect of charcoal hemoperfusion for removal of plasma methotrexate in a patient with acute renal failure. | 2009-10-30 |
|
| Acute methotrexate neurotoxicity with choreiform movements and focal neurological deficits: a case report. | 2009-10 |
|
| Prevention of neurotoxicity by high-dose folinic acid rescue after high-dose methotrexate and intrathecal methotrexate without compromising cure inspite of previous transient leukoencephalopathy after intrathecal methotrexate. | 2009-08 |
|
| Second-line therapy in refractory pancreatic cancer. results of a phase II study. | 2009-03 |
|
| Pharmacogenetic analyses of hematotoxicity in advanced gastric cancer patients receiving biweekly fluorouracil, leucovorin, oxaliplatin and docetaxel (FLOT): a translational study of the Arbeitsgemeinschaft Internistische Onkologie (AIO). | 2009-03 |
|
| [A case of therapy for bevacizumab-induced hypertension]. | 2009-01 |
|
| Damaging effects of chronic low-dose methotrexate usage on primary bone formation in young rats and potential protective effects of folinic acid supplementary treatment. | 2009-01 |
|
| An unusual presentation of hand-foot syndrome at the hidden area: the scrotum and penis. | 2009 |
|
| Protein expression profiling in esophageal adenocarcinoma patients indicates association of heat-shock protein 27 expression and chemotherapy response. | 2008-12-15 |
|
| Early recognition of renal toxicity of high-dose methotrexate therapy: a case report. | 2008-12 |
|
| Fatal thrombocytopenia after oxaliplatin-based chemotherapy. | 2008-11-27 |
|
| Multiple toxic effects of low-dose methotrexate in a patient treated for psoriasis. | 2008-11-15 |
|
| A 50-year-old man with burkitt lymphoma. | 2008-10 |
|
| K-Ras mutations and treatment outcome in colorectal cancer patients receiving exclusive fluoropyrimidine therapy. | 2008-08-01 |
|
| [Genetic polymorphisms related to fluoropyrimidine sensitivity and toxicity]. | 2008-07 |
|
| Methotrexate/naproxen-associated severe hepatitis in a child with juvenile idiopathic arthritis. | 2008-01-05 |
|
| A Phase II study of oxaliplatin with low-dose leucovorin and bolus and continuous infusion 5-fluorouracil (modified FOLFOX-4) for gastric cancer patients with malignant ascites. | 2007-12 |
|
| First clinical experience of orally active epidermal growth factor receptor inhibitor combined with simplified FOLFOX6 as first-line treatment for metastatic colorectal cancer. | 2007-08-15 |
|
| A pilot phase II study of chemotherapy with oxaliplatin, folinic acid, 5-fluorouracil and irinotecan in metastatic gastric cancer. | 2007-08-08 |
|
| Mitochondrial complex I encephalomyopathy and cerebral 5-methyltetrahydrofolate deficiency. | 2007-08 |
|
| Successful carboxypeptidase G2 rescue of a high-risk elderly Hodgkin lymphoma patient with methotrexate intoxication and renal failure. | 2007-08 |
|
| Severe methotrexate toxicity precipitated by intravenous radiographic contrast. | 2007-07 |
|
| Resumption of high-dose methotrexate after methotrexate-induced nephrotoxicity and carboxypeptidase G2 use. | 2007-06-01 |
|
| Carboxypeptidase-G2 rescue in a patient with high dose methotrexate-induced nephrotoxicity. | 2005-04 |
|
| Clinical use of thymidine as a rescue agent from methotrexate toxicity. | 1991-08 |
|
| Diurnal variation of folate concentrations in mouse embryo and plasma: the protective effect of folinic acid on valproic-acid-induced teratogenicity is time dependent. | 1991 |
|
| High dose intravenous methotrexate and reversible focal neurological deficit. | 1990-12 |
|
| Dose response relationship of methotrexate in combination with cisplatin in murine bladder cancer. | 1990-03 |
|
| Discoloration of the nails and early anemia after mitoxantrone, folinic acid and 5-fluorouracil. | 1990 |
|
| Folate nephropathy occurring during cytotoxic chemotherapy with high-dose folinic acid and 5-fluorouracil. | 1990 |
|
| Methotrexate-induced leukoencephalopathy is treatable with high-dose folinic acid: a case report and analysis of the literature. | 1990 |
|
| Valproic acid-induced neural tube defects: reduction by folinic acid in the mouse. | 1987-07-06 |
|
| Effects of intraventricular methotrexate on cerebrospinal fluid monoamine metabolites in rhesus monkeys. | 1986-10 |
|
| Leukocytoclastic vasculitis after high-dose methotrexate. | 1986-09 |
|
| Transient cerebral dysfunction following chemotherapy for osteogenic sarcoma. | 1978-05 |
Sample Use Guides
200 mg/m2 or 20 mg/m2 in Advanced Colorectal Cancer, 10 mg/m2 in Leucovorin Rescue After High-Dose Methotrexate Therapy and up to 1 mg daily in Megaloblastic Anemia Due to Folic Acid Deficiency.
Route of Administration:
Intravenous
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3499251
Curator's Comment: The data show that in osteosarcoma cells and in lymphoblasts the cytotoxic effects of 1 uM to 0.1 uM methotrexate can be substantially reversed by 1 uM leucovorin.
RPMI 1788 cells revealed a high intrinsic resistance to methotrexate (MTX). The cytotoxic effect of high concentrations of MTX (10 -5 M) was reversed by relatively low (10 -6 M) concentrations of simultaneously added leucovorin (LV). The enhancement of cell survival was less marked when LV application was delayed for 12 h.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:11:22 GMT 2025
by
admin
on
Mon Mar 31 22:11:22 GMT 2025
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| Record UNII |
R3W57OBQ5W
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| Record Status |
Validated (UNII)
|
| Record Version |
|
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LEUCOVORIN CALCIUM PENTAHYDRATE
Created by
admin on Mon Mar 31 22:11:22 GMT 2025 , Edited by admin on Mon Mar 31 22:11:22 GMT 2025
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PRIMARY | Description: A white or creamy white powder; odourless. Solubility: Very soluble in water; practically insoluble in ethanol (~750 g/l) TS. Category: Cytotoxic drug. Storage: Calcium folinate should be kept in a well-closed container, protected from light. Additional information: CAUTION: Calcium folinate must be handled with care, avoiding contact with the skin and inhalation of airborne particles. Definition: Calcium folinate contains not less than 95.0% and not more than 105.0% of C20H21CaN7O7, calculated with reference to the anhydrous substance. | ||
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6035-45-6
Created by
admin on Mon Mar 31 22:11:22 GMT 2025 , Edited by admin on Mon Mar 31 22:11:22 GMT 2025
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100000137727
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admin on Mon Mar 31 22:11:22 GMT 2025 , Edited by admin on Mon Mar 31 22:11:22 GMT 2025
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DBSALT001441
Created by
admin on Mon Mar 31 22:11:22 GMT 2025 , Edited by admin on Mon Mar 31 22:11:22 GMT 2025
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R3W57OBQ5W
Created by
admin on Mon Mar 31 22:11:22 GMT 2025 , Edited by admin on Mon Mar 31 22:11:22 GMT 2025
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135802074
Created by
admin on Mon Mar 31 22:11:22 GMT 2025 , Edited by admin on Mon Mar 31 22:11:22 GMT 2025
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DTXSID3036999
Created by
admin on Mon Mar 31 22:11:22 GMT 2025 , Edited by admin on Mon Mar 31 22:11:22 GMT 2025
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m5519
Created by
admin on Mon Mar 31 22:11:22 GMT 2025 , Edited by admin on Mon Mar 31 22:11:22 GMT 2025
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SUB76309
Created by
admin on Mon Mar 31 22:11:22 GMT 2025 , Edited by admin on Mon Mar 31 22:11:22 GMT 2025
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| Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |
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ANHYDROUS->SOLVATE |