Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C20H23N7O7 |
Molecular Weight | 473.4393 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
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=VVIAGPKUTFNRDU-STQMWFEESA-N
InChI=1S/C20H23N7O7/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)/t12-,13-/m0/s1
Molecular Formula | C20H23N7O7 |
Molecular Weight | 473.4393 |
Charge | 0 |
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 Date2008 |
|||
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 Date2008 |
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 |
---|---|---|
Cloning and characterization of methenyltetrahydrofolate synthetase from Saccharomyces cerevisiae. | 2002 Jun 7 |
|
10-formyltetrahydrofolate dehydrogenase, one of the major folate enzymes, is down-regulated in tumor tissues and possesses suppressor effects on cancer cells. | 2002 May |
|
Uptake of 5-methyltetrahydrofolate into PC-3 human prostate cancer cells is carrier-mediated. | 2003 Aug |
|
Methenyltetrahydrofolate synthetase regulates folate turnover and accumulation. | 2003 Aug 8 |
|
Specific and sensitive quantification of folate vitamers in foods by stable isotope dilution assays using high-performance liquid chromatography-tandem mass spectrometry. | 2003 May |
|
Cerebral folate deficiency. | 2004 Dec |
|
Lack of impact of the loss of constitutive folate receptor alpha expression, achieved by RNA Interference, on the activity of the new generation antifolate pemetrexed in HeLa cells. | 2004 Dec 1 |
|
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 |
|
Thymidylate synthase and methylenetetrahydrofolate reductase gene polymorphisms: relationships with 5-fluorouracil sensitivity. | 2004 Jan 26 |
|
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 |
|
Selective preservation of pemetrexed pharmacological activity in HeLa cells lacking the reduced folate carrier: association with the presence of a secondary transport pathway. | 2004 May 1 |
|
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 |
|
The relationship between folate transport activity at low pH and reduced folate carrier function in human Huh7 hepatoma cells. | 2005 Aug 30 |
|
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 |
|
Higher plant plastids and cyanobacteria have folate carriers related to those of trypanosomatids. | 2005 Nov 18 |
|
The inverse relationship between reduced folate carrier function and pemetrexed activity in a human colon cancer cell line. | 2006 Feb |
|
Mining literature for a comprehensive pathway analysis: a case study for retrieval of homocysteine related genes for genetic and epigenetic studies. | 2006 Jan 23 |
|
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 |
|
Inhibition of 5,10-methenyltetrahydrofolate synthetase. | 2007 Feb 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 |
|
High-dose folate and dietary purines promote scavenging of peroxynitrite-derived radicals--clinical potential in inflammatory disorders. | 2009 Nov |
|
Quantification of folate in fruits and vegetables: A fluorescence-based homogeneous assay. | 2010 Jul 15 |
|
Properties of the Arg376 residue of the proton-coupled folate transporter (PCFT-SLC46A1) and a glutamine mutant causing hereditary folate malabsorption. | 2010 Nov |
|
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
Fri Dec 15 16:15:47 GMT 2023
by
admin
on
Fri Dec 15 16:15:47 GMT 2023
|
Record UNII |
990S25980Y
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
LIVERTOX |
554
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
||
|
WHO-ATC |
V03AF10
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
||
|
WHO-ATC |
V03AF04
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
||
|
NCI_THESAURUS |
C2078
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
||
|
FDA ORPHAN DRUG |
48590
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
||
|
FDA ORPHAN DRUG |
48490
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
DTXSID4023204
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
PRIMARY | |||
|
SUB34736
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
PRIMARY | |||
|
C1559
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
PRIMARY | |||
|
68538-85-2
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
PRIMARY | |||
|
877015
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
PRIMARY | RxNorm | ||
|
DB11596
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
PRIMARY | |||
|
4384
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
PRIMARY | |||
|
63606
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
PRIMARY | |||
|
990S25980Y
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
PRIMARY | |||
|
990S25980Y
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
PRIMARY | |||
|
100000128077
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
PRIMARY | |||
|
135398559
Created by
admin on Fri Dec 15 16:15:47 GMT 2023 , Edited by admin on Fri Dec 15 16:15:47 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
SALT/SOLVATE -> PARENT | |||
|
SALT/SOLVATE -> PARENT | |||
|
SALT/SOLVATE -> PARENT | |||
|
SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |