Pemetrexed disodium
CAS No. 150399-23-8
Pemetrexed disodium( LY231514 disodium | LY 231514 disodium | LY-231514 disodium )
Catalog No. M12095 CAS No. 150399-23-8
A classical multitargeted antifolate that inhibits multiple folate-requiring enzymes TS/DHFR/GARFT with Ki of 1.3/7.2/65 nM respectively.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 37 | In Stock |
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| 25MG | 35 | In Stock |
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| 50MG | 47 | In Stock |
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| 100MG | 61 | In Stock |
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| 200MG | 86 | In Stock |
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| 500MG | 138 | In Stock |
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| 1G | 203 | In Stock |
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Biological Information
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Product NamePemetrexed disodium
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NoteResearch use only, not for human use.
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Brief DescriptionA classical multitargeted antifolate that inhibits multiple folate-requiring enzymes TS/DHFR/GARFT with Ki of 1.3/7.2/65 nM respectively.
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DescriptionA classical multitargeted antifolate that inhibits multiple folate-requiring enzymes TS/DHFR/GARFT with Ki of 1.3/7.2/65 nM respectively; increases the cytotoxicity and antitumor activity of gemcitabine in HT29 colon carcinoma.Chemotherapeutic Agents Approved(In Vitro):Pemetrexed (LY231514) disodium is a novel classical antifolate, the antitumor activity of which may result from simultaneous and multipie inhibition of several key folate-requiring enzymes via its polyglutamated metabolites. Pemetrexed (LY231514) is one of the best substrates that is known for the enzyme FPGS (Km=1.6 μM and Vmax/Km=621). It is likely that polyglutamation and the polyglutamated metabolites of LY231514 play profound roles in determining both the selectivity and the antitumor activity of this novel agent. Whereas LY23l5l4 only moderately inhibits TS (Ki=340 nM, recombinant mouse), the pentaglutamate of LY23l5l4 is 100-fold more potent (Ki=3.4 nM), making LY231514 one of the most potent folate-based TS inhibitors.(In Vivo):The group of mice treated with PC61 plus Pemetrexed demonstrates statistically longer survival than other groups. In a survival analysis, significantly better survival is observed in the group of mice treated with PC61 plus Pemetrexed compare with those treated with PC61 alone, rat IgG plus Pemetrexed, or no treatment.
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In VitroPemetrexed (LY231514) disodium is a novel classical antifolate, the antitumor activity of which may result from simultaneous and multipie inhibition of several key folate-requiring enzymes via its polyglutamated metabolites. Pemetrexed (LY231514) is one of the best substrates that is known for the enzyme FPGS (Km=1.6 μM and Vmax/Km=621). It is likely that polyglutamation and the polyglutamated metabolites of LY231514 play profound roles in determining both the selectivity and the antitumor activity of this novel agent. Whereas LY23l5l4 only moderately inhibits TS (Ki=340 nM, recombinant mouse), the pentaglutamate of LY23l5l4 is 100-fold more potent (Ki=3.4 nM), making LY231514 one of the most potent folate-based TS inhibitors.
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In VivoThe group of mice treated with PC61 plus Pemetrexed demonstrates statistically longer survival than other groups. In a survival analysis, significantly better survival is observed in the group of mice treated with PC61 plus Pemetrexed compare with those treated with PC61 alone, rat IgG plus Pemetrexed, or no treatment.
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SynonymsLY231514 disodium | LY 231514 disodium | LY-231514 disodium
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PathwayCell Cycle/DNA Damage
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TargetAntifolate
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RecptorDHFR|GARFT|Thymidylatesynthase
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Research AreaCancer
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IndicationChemotherapeutic
Chemical Information
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CAS Number150399-23-8
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Formula Weight471.3743
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Molecular FormulaC20H19N5Na2O6
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Purity>98% (HPLC)
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SolubilityH2O: 11.19 mg/mL (Need ultrasonic and warming)
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SMILESC1=CC(=CC=C1CCC2=CNC3=C2C(=O)N=C(N3)N)C(=O)N[C@@H](CCC(=O)[O-])C(=O)[O-].[Na+].[Na+]
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Chemical NameL-Glutamic acid, N-[4-[2-(2-amino-4,7-dihydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-5-yl)ethyl]benzoyl]-, sodium salt (1:2)
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Shih C, et al. Cancer Res. 1997 Mar 15;57(6):1116-23.
2. Tonkinson JL, et al. Cancer Res. 1999 Aug 1;59(15):3671-6.
3. Curtin NJ, et al. Lancet Oncol. 2001 May;2(5):298-306.
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