Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C20H21N7O7.2Na |
Molecular Weight | 517.403 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].[Na+].NC1=NC(=O)C2=C(NC[C@H](CNC3=CC=C(C=C3)C(=O)N[C@@H](CCC([O-])=O)C([O-])=O)N2C=O)N1
InChI
InChIKey=FSDMNNPYPVJNAT-NJHZPMQHSA-L
InChI=1S/C20H23N7O7.2Na/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);;/q;2*+1/p-2/t12-,13-;;/m0../s1
Molecular Formula | Na |
Molecular Weight | 22.9898 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C20H21N7O7 |
Molecular Weight | 471.4234 |
Charge | -2 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Levoleucovorin is the pharmacologically active isomer of leucovorin or 5-formyl tetrahydrofolic acid, a folate analog . Levoleucovorin does not require reduction by the enzyme dihydrofolate reductase in order to participate in reactions utilizing folates as a source of “onecarbon” moieties. Administration of levoleucovorin can counteract the therapeutic and toxic effects of folic acid antagonists such as methotrexate, which act by inhibiting dihydrofolate reductase. Levoleucovorin can enhance the therapeutic and toxic effects of fluoropyrimidines used in cancer therapy such as 5-fluorouracil. 5-fluorouracil is metabolized to 5-fluoro-2'-deoxyuridine-5'-monophosphate (FdUMP), which binds to and inhibits thymidylate synthase (an enzyme important in DNA repair and replication). Levoleucovorin is readily converted to another reduced folate, 5,10-methylenetetrahydrofolate, which acts to stabilize the binding of FdUMP to thymidylate synthase and thereby enhances the inhibition of this enzyme. Fusilev® (levoleucovorin) is approved by FDA for i) rescue after high-dose methotrexate therapy in osteosarcoma, ii) diminishing the toxicity and counteracting the effects of impaired methotrexate elimination and of inadvertent overdosage of folic acid antagonists and iii) in combination chemotherapy with 5-fluorouracil in the palliative treatment of patients with advanced metastatic colorectal cancer.
Approval Year
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Secondary | FUSILEV Approved UseFusilev is a folate analog indicated for: Rescue after high-dose methotrexate therapy in osteosarcoma. Diminishing the toxicity and counteracting the effects of impaired methotrexate elimination and of inadvertent overdosage of folic acid antagonists. Use in combination chemotherapy with 5-fluorouracil in the palliative treatment of patients with advanced metastatic colorectal cancer. Launch Date1.20484803E12 |
|||
Palliative | FUSILEV Approved UseFusilev is a folate analog indicated for: Rescue after high-dose methotrexate therapy in osteosarcoma. Diminishing the toxicity and counteracting the effects of impaired methotrexate elimination and of inadvertent overdosage of folic acid antagonists. Use in combination chemotherapy with 5-fluorouracil in the palliative treatment of patients with advanced metastatic colorectal cancer. Launch Date1.20484803E12 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
10895 ng/mL |
200 mg/m² single, intravenous dose: 200 mg/m² route of administration: Intravenous experiment type: SINGLE co-administered: |
LEVOLEUCOVORIN unknown | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
340 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/8405015/ |
12.5 mg single, oral dose: 12.5 mg route of administration: Oral experiment type: SINGLE co-administered: |
LEVOMEFOLIC ACID serum | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
275 ng/mL |
15 mg single, intravenous dose: 15 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
LEVOMEFOLIC ACID serum | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
4930 ng/mL |
200 mg/m² single, intravenous dose: 200 mg/m² route of administration: Intravenous experiment type: SINGLE co-administered: |
LEVOMEFOLIC ACID unknown | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
30719 ng × h/mL |
200 mg/m² single, intravenous dose: 200 mg/m² route of administration: Intravenous experiment type: SINGLE co-administered: |
LEVOLEUCOVORIN unknown | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
1563 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/8405015/ |
12.5 mg single, oral dose: 12.5 mg route of administration: Oral experiment type: SINGLE co-administered: |
LEVOMEFOLIC ACID serum | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
52105 ng × h/mL |
200 mg/m² single, intravenous dose: 200 mg/m² route of administration: Intravenous experiment type: SINGLE co-administered: |
LEVOMEFOLIC ACID unknown | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
6.8 h |
15 mg single, intravenous dose: 15 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
LEVOMEFOLIC ACID serum | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
Doses
Dose | Population | Adverse events |
---|---|---|
250 mg/m2 1 times / 2 weeks multiple, intravenous Higher than recommended Dose: 250 mg/m2, 1 times / 2 weeks Route: intravenous Route: multiple Dose: 250 mg/m2, 1 times / 2 weeks Co-administed with:: irinotecan, i.v(200 mg/m2) Sources: Page: p.2075-fluorouracil, i.v(850 mg/m2) |
unhealthy, 39 n = 254 Health Status: unhealthy Condition: Colorectal cancer Age Group: 39 Sex: M+F Population Size: 254 Sources: Page: p.207 |
Other AEs: Neutropenia... |
300 mg/m2 1 times / day multiple, intravenous Highest studied dose Dose: 300 mg/m2, 1 times / day Route: intravenous Route: multiple Dose: 300 mg/m2, 1 times / day Co-administed with:: etoposide, i.v(100 mg/m2/day; days 2-4) Sources: Page: p.3205-fluorouracil, i.v(500 mg/m2/day; days 1-5) |
unhealthy, 66 n = 36 Health Status: unhealthy Condition: Gastric cancer Age Group: 66 Sex: M+F Population Size: 36 Sources: Page: p.320 |
Other AEs: Leucopenia... |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Neutropenia | grade 4, 15% | 250 mg/m2 1 times / 2 weeks multiple, intravenous Higher than recommended Dose: 250 mg/m2, 1 times / 2 weeks Route: intravenous Route: multiple Dose: 250 mg/m2, 1 times / 2 weeks Co-administed with:: irinotecan, i.v(200 mg/m2) Sources: Page: p.2075-fluorouracil, i.v(850 mg/m2) |
unhealthy, 39 n = 254 Health Status: unhealthy Condition: Colorectal cancer Age Group: 39 Sex: M+F Population Size: 254 Sources: Page: p.207 |
Leucopenia | grade 4 | 300 mg/m2 1 times / day multiple, intravenous Highest studied dose Dose: 300 mg/m2, 1 times / day Route: intravenous Route: multiple Dose: 300 mg/m2, 1 times / day Co-administed with:: etoposide, i.v(100 mg/m2/day; days 2-4) Sources: Page: p.3205-fluorouracil, i.v(500 mg/m2/day; days 1-5) |
unhealthy, 66 n = 36 Health Status: unhealthy Condition: Gastric cancer Age Group: 66 Sex: M+F Population Size: 36 Sources: Page: p.320 |
PubMed
Title | Date | PubMed |
---|---|---|
Intrathecal leucovorin after intrathecal methotrexate overdose. | 1996 Aug |
|
Marked suppression of the activity of some, but not all, antifolate compounds by augmentation of folate cofactor pools within tumor cells. | 2001 Apr 1 |
|
Lack of catalytic activity of a murine mRNA cytoplasmic serine hydroxymethyltransferase splice variant: evidence against alternative splicing as a regulatory mechanism. | 2001 Apr 24 |
|
Ontogeny of hepatic enzymes involved in serine- and folate-dependent one-carbon metabolism in rabbits. | 2001 May |
|
Mitochondria from cultured cells derived from normal and thiamine-responsive megaloblastic anemia individuals efficiently import thiamine diphosphate. | 2002 Apr 25 |
|
Role of the E45K-reduced folate carrier gene mutation in methotrexate resistance in human leukemia cells. | 2002 Dec |
|
Cloning and characterization of methenyltetrahydrofolate synthetase from Saccharomyces cerevisiae. | 2002 Jun 7 |
|
Transport of 5-formyltetrahydrofolate into primary cultured rat astrocytes. | 2003 Feb 1 |
|
Residues 45 and 404 in the murine reduced folate carrier may interact to alter carrier binding and mobility. | 2003 Jun 27 |
|
A prominent low-pH methotrexate transport activity in human solid tumors: contribution to the preservation of methotrexate pharmacologic activity in HeLa cells lacking the reduced folate carrier. | 2004 Jan 15 |
|
Cloning, expression, and purification of 5,10-methenyltetrahydrofolate synthetase from Mus musculus. | 2004 Jun |
|
Serine hydroxymethyltransferase: role of glu75 and evidence that serine is cleaved by a retroaldol mechanism. | 2004 Jun 8 |
|
Characterization of a folate transporter in HeLa cells with a low pH optimum and high affinity for pemetrexed distinct from the reduced folate carrier. | 2004 Sep 15 |
|
Development of a simplified method for the determination of folates in baker's yeast by HPLC with ultraviolet and fluorescence detection. | 2005 Apr 6 |
|
Loss of reduced folate carrier function and folate depletion result in enhanced pemetrexed inhibition of purine synthesis. | 2005 Feb 1 |
|
5-Formyltetrahydrofolate is an inhibitory but well tolerated metabolite in Arabidopsis leaves. | 2005 Jul 15 |
|
Investigation of the extraction behavior of the main monoglutamate folates from spinach by liquid chromatography-electrospray ionization tandem mass spectrometry. | 2005 Jun 17 |
|
Structural and functional characterization of a 5,10-methenyltetrahydrofolate synthetase from Mycoplasma pneumoniae (GI: 13508087). | 2005 Nov 1 |
|
Spontaneous neural tube defects in splotch mice supplemented with selected micronutrients. | 2006 May 15 |
|
Methenyltetrahydrofolate synthetase is a high-affinity catecholamine-binding protein. | 2006 Nov 15 |
|
Commentary: a case for minimizing folate supplementation in clinical regimens with pemetrexed based on the marked sensitivity of the drug to folate availability. | 2007 Jul |
|
Application of liquid chromatography-electrospray ionisation mass spectrometry for determination of dietary folates: effects of buffer nature and mobile phase composition on sensitivity and selectivity. | 2007 Mar 2 |
|
pH stability of individual folates during critical sample preparation steps in prevision of the analysis of plant folates. | 2007 Nov-Dec |
|
Investigations of the roles of arginine 115 and lysine 120 in the active site of 5,10-methenyltetrahydrofolate synthetase from Mycoplasma pneumoniae. | 2008 Aug |
|
Effect of folate derivatives on the activity of antifolate drugs used against malaria and cancer. | 2008 May |
|
Folate in wheat genotypes in the HEALTHGRAIN Diversity Screen. | 2008 Nov 12 |
|
The clinical course and genetic defect in the PCFT gene in a 27-year-old woman with hereditary folate malabsorption. | 2008 Sep |
|
The proton-coupled folate transporter: impact on pemetrexed transport and on antifolates activities compared with the reduced folate carrier. | 2008 Sep |
|
High-dose folate and dietary purines promote scavenging of peroxynitrite-derived radicals--clinical potential in inflammatory disorders. | 2009 Nov |
|
Cerebral folate deficiency presenting as adolescent catatonic schizophrenia: a case report. | 2010 Jul |
|
The effect of folinic acid supplementation on homocysteine concentrations in newborns. | 2010 Nov |
|
Mutation of the proton-coupled folate transporter gene (PCFT-SLC46A1) in Turkish siblings with hereditary folate malabsorption. | 2010 Nov |
|
Development and analysis of an in vivo-compatible metabolic network of Mycobacterium tuberculosis. | 2010 Nov 23 |
|
Production of folate by bacteria isolated from oat bran. | 2010 Sep 30 |
Sample Use Guides
Fusilev Rescue After High-Dose Methotrexate Therapy:
Fusilev rescue recommendations are based on a methotrexate dose of 12 grams/m2 administered by intravenous infusion over 4 hours. Fusilev rescue at a dose of 7.5 mg (approximately 5 mg/m2) every 6 hours for 10 doses starts 24 hours after the beginning of the methotrexate infusion.
Fusilev Administration in Combination with 5-Fluorouracil (5-FU):
The following regimens have been used historically for the treatment of colorectal cancer:
1. Fusilev is administered at 100 mg/m2 by slow intravenous injection over a minimum of 3 minutes, followed by 5-FU at 370 mg/m2 by intravenous
injection.
2. Fusilev is administered at 10 mg/m by 2 intravenous injection followed by 5-FU at 425 mg/m2 by intravenous injection.
Route of Administration:
Intravenous
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:49:16 UTC 2023
by
admin
on
Sat Dec 16 08:49:16 UTC 2023
|
Record UNII |
5TXQ76K65T
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
135565660
Created by
admin on Sat Dec 16 08:49:16 UTC 2023 , Edited by admin on Sat Dec 16 08:49:16 UTC 2023
|
PRIMARY | |||
|
DBSALT001890
Created by
admin on Sat Dec 16 08:49:16 UTC 2023 , Edited by admin on Sat Dec 16 08:49:16 UTC 2023
|
PRIMARY | |||
|
SUB63746
Created by
admin on Sat Dec 16 08:49:16 UTC 2023 , Edited by admin on Sat Dec 16 08:49:16 UTC 2023
|
PRIMARY | |||
|
5TXQ76K65T
Created by
admin on Sat Dec 16 08:49:16 UTC 2023 , Edited by admin on Sat Dec 16 08:49:16 UTC 2023
|
PRIMARY | |||
|
D11394
Created by
admin on Sat Dec 16 08:49:16 UTC 2023 , Edited by admin on Sat Dec 16 08:49:16 UTC 2023
|
PRIMARY | |||
|
5TXQ76K65T
Created by
admin on Sat Dec 16 08:49:16 UTC 2023 , Edited by admin on Sat Dec 16 08:49:16 UTC 2023
|
PRIMARY | |||
|
100000134700
Created by
admin on Sat Dec 16 08:49:16 UTC 2023 , Edited by admin on Sat Dec 16 08:49:16 UTC 2023
|
PRIMARY | |||
|
1141892-29-6
Created by
admin on Sat Dec 16 08:49:16 UTC 2023 , Edited by admin on Sat Dec 16 08:49:16 UTC 2023
|
PRIMARY | |||
|
2107308
Created by
admin on Sat Dec 16 08:49:16 UTC 2023 , Edited by admin on Sat Dec 16 08:49:16 UTC 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
PARENT -> SALT/SOLVATE |
|
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |
|