Pemetrexed [137281-23-3]

Katalog-Nummer HY-10820-1mL

Size : 10mM/1mL

Marke : MedChemExpress


Beschreibung

Pemetrexed (LY231514) is an antifolate, the Ki values of the pentaglutamate of Pemetrexed (LY231514) are 1.3, 7.2, and 65 nM for inhibits thymidylate synthase (TS), dihydrofolate reductase (DHFR), and glycinamide ribonucleotide formyltransferase (GARFT), respectively[1].

IC50 & Target

Ki: 1.3 nM (TS), 7.2 nM (DHFR), 65 nM (GARFT)[1]

Cellular Effect
Cell Line Type Value Description References
A2780 IC50
39.4 nM
Compound: PMX
Antiproliferative activity against human A2780 cells after 96 hrs by Cell-Titer Blue assay
Antiproliferative activity against human A2780 cells after 96 hrs by Cell-Titer Blue assay
[PMID: 29701475]
A549 IC50
0.08 μM
Compound: PMX
Cytotoxicity against human A549 cells assessed as growth inhibition after 72 hrs by MTT assay
Cytotoxicity against human A549 cells assessed as growth inhibition after 72 hrs by MTT assay
[PMID: 25668494]
A549 IC50
1.26 μM
Compound: PMX
Antiproliferative activity against human A549 cells after 72 hrs by MTT assay in presence of leucovorin
Antiproliferative activity against human A549 cells after 72 hrs by MTT assay in presence of leucovorin
[PMID: 27017552]
A549 IC50
1260 nM
Compound: PMX
Antiproliferative activity against human A549 cells assessed as reduction in cell viability after 72 hrs by MTT assay
Antiproliferative activity against human A549 cells assessed as reduction in cell viability after 72 hrs by MTT assay
[PMID: 31200235]
A549 IC50
2.07 μM
Compound: PTX
Antiproliferative activity against human A549 cells assessed as inhibition of cell growth incubated for 24 hrs by MTT assay
Antiproliferative activity against human A549 cells assessed as inhibition of cell growth incubated for 24 hrs by MTT assay
[PMID: 37437348]
A549 IC50
3.31 μM
Compound: PTX
Antiproliferative activity against human A549 cells after 24 hrs by MTT assay
Antiproliferative activity against human A549 cells after 24 hrs by MTT assay
[PMID: 29807332]
BEAS-2B CC50
151.16 μM
Compound: PTX
Cytotoxicity against human BEAS-2B cells assessed as reduction in cell viability incubated for 24 hrs by MTT assay
Cytotoxicity against human BEAS-2B cells assessed as reduction in cell viability incubated for 24 hrs by MTT assay
[PMID: 37437348]
CCRF-CEM IC50
1.6 x 10-8 M
Compound: 15
Compound was evaluated for the half-maximal inhibition against human CCRF-CEM lymphoblastic leukemic cell growth
Compound was evaluated for the half-maximal inhibition against human CCRF-CEM lymphoblastic leukemic cell growth
[PMID: 1447744]
CHO IC50
13.2 nM
Compound: PMX
Antitumor activity against CHO cells expressing PCFT (R2/PCFT4) transporter assessed as inhibition of cell growth measured upto 96 hrs by Cell titer blue assay
Antitumor activity against CHO cells expressing PCFT (R2/PCFT4) transporter assessed as inhibition of cell growth measured upto 96 hrs by Cell titer blue assay
[PMID: 37582241]
CHO IC50
138 nM
Compound: PMX
Antitumor activity against CHO cells expressing human RFC (PC43-10) transporter assessed as inhibition of cell growth measured upto 96 hrs by Cell titer blue assay
Antitumor activity against CHO cells expressing human RFC (PC43-10) transporter assessed as inhibition of cell growth measured upto 96 hrs by Cell titer blue assay
[PMID: 37582241]
CHO IC50
42 nM
Compound: PMX
Antitumor activity against CHO cells expressing human FR-alpha (RT16) transporter assessed as inhibition of cell growth measured upto 96 hrs by Cell titer blue assay
Antitumor activity against CHO cells expressing human FR-alpha (RT16) transporter assessed as inhibition of cell growth measured upto 96 hrs by Cell titer blue assay
[PMID: 37582241]
CHO IC50
60 nM
Compound: PMX
Antitumor activity against CHO cells expressing human FR-beta (D4) transporter assessed as inhibition of cell growth measured upto 96 hrs by Cell titer blue assay
Antitumor activity against CHO cells expressing human FR-beta (D4) transporter assessed as inhibition of cell growth measured upto 96 hrs by Cell titer blue assay
[PMID: 37582241]
CHO IC50
894 nM
Compound: PMX
Cytotoxicity against transporter-null (R2) CHO cells assessed as inhibition of cell growth measured upto 96 hrs by Cell titer blue assay
Cytotoxicity against transporter-null (R2) CHO cells assessed as inhibition of cell growth measured upto 96 hrs by Cell titer blue assay
[PMID: 37582241]
Calu-1 IC50
5.12 μM
Compound: PTX
Antiproliferative activity against human Calu-1 cells assessed as inhibition of cell growth incubated for 24 hrs by MTT assay
Antiproliferative activity against human Calu-1 cells assessed as inhibition of cell growth incubated for 24 hrs by MTT assay
[PMID: 37437348]
HUVEC IC50
1.73 μM
Compound: PMX
Cytotoxicity against HUVEC assessed as reduction in cell viability after 72 hrs by MTT assay
Cytotoxicity against HUVEC assessed as reduction in cell viability after 72 hrs by MTT assay
[PMID: 31200235]
HepG2 IC50
1.26 μM
Compound: PMX
Cytotoxicity against human HepG2 cells assessed as growth inhibition after 72 hrs by MTT assay
Cytotoxicity against human HepG2 cells assessed as growth inhibition after 72 hrs by MTT assay
[PMID: 25668494]
IGROV-1 IC50
102 nM
Compound: PMX, LY-231514
Antiproliferative activity against human IGROV1 cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs
Antiproliferative activity against human IGROV1 cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs
[PMID: 21879757]
IGROV-1 IC50
102 nM
Compound: pemetrexed
Antiproliferative activity against human RFC and FRalpha expressing human IGROV1 cells
Antiproliferative activity against human RFC and FRalpha expressing human IGROV1 cells
[PMID: 18680275]
IGROV-1 IC50
104 nM
Compound: PMX
Antiproliferative activity against wild type human IGROV1 cells after 96 hrs by Cell-Titer Blue assay
Antiproliferative activity against wild type human IGROV1 cells after 96 hrs by Cell-Titer Blue assay
[PMID: 29701475]
IGROV-1 IC50
200 nM
Compound: PMX, LY-231514
Antiproliferative activity against human IGROV1 cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs in the presence of 200 nM folic acid
Antiproliferative activity against human IGROV1 cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs in the presence of 200 nM folic acid
[PMID: 21879757]
IGROV-1 IC50
200 nM
Compound: pemetrexed
Antiproliferative activity against human RFC and FRalpha expressing human IGROV1 cells in presence of folic acid
Antiproliferative activity against human RFC and FRalpha expressing human IGROV1 cells in presence of folic acid
[PMID: 18680275]
IGROV-1 IC50
22.2 nM
Compound: PMX
Antiproliferative activity against FRalpha knockout human IGROV1 KD10 cells after 96 hrs by Cell-Titer Blue assay
Antiproliferative activity against FRalpha knockout human IGROV1 KD10 cells after 96 hrs by Cell-Titer Blue assay
[PMID: 29701475]
IGROV-1 IC50
46.6 nM
Compound: PMX
Antiproliferative activity against FRalpha knockout human IGROV1 KD4 cells after 96 hrs by Cell-Titer Blue assay
Antiproliferative activity against FRalpha knockout human IGROV1 KD4 cells after 96 hrs by Cell-Titer Blue assay
[PMID: 29701475]
IGROV-1 IC50
71 nM
Compound: 1; PMX
Antiproliferative activity against human IGROV-1 cells assessed as inhibition of cell growth incubated for 96 hrs by CellTiter-Blue cell viability assay
Antiproliferative activity against human IGROV-1 cells assessed as inhibition of cell growth incubated for 96 hrs by CellTiter-Blue cell viability assay
[PMID: 38116433]
IGROV-1 IC50
71 nM
Compound: PMX
Antiproliferative activity against human IGROV1 cells harboring non targeted control shRNA sequence after 96 hrs by Cell-Titer Blue assay
Antiproliferative activity against human IGROV1 cells harboring non targeted control shRNA sequence after 96 hrs by Cell-Titer Blue assay
[PMID: 29701475]
IGROV-1 IC50
> 20 μM
Compound: PMX
Anticlonogenic activity against human IGROV1 cells incubated for 24 hrs followed by compound wash out and measured after 10 days by methylene blue staining-based assay
Anticlonogenic activity against human IGROV1 cells incubated for 24 hrs followed by compound wash out and measured after 10 days by methylene blue staining-based assay
[PMID: 29701475]
KB IC50
0.07 μM
Compound: PMX
Cytotoxicity against human KB cells assessed as growth inhibition after 72 hrs by MTT assay
Cytotoxicity against human KB cells assessed as growth inhibition after 72 hrs by MTT assay
[PMID: 25668494]
KB IC50
0.07 μM
Compound: PMX
Antiproliferative activity against human KB cells after 72 hrs by MTT assay in presence of leucovorin
Antiproliferative activity against human KB cells after 72 hrs by MTT assay in presence of leucovorin
[PMID: 27017552]
KB IC50
11.74 nM
Compound: 6, Pemetrexed, PMX, Alimta
Inhibition of GARFTase in human KB cells assessed as incorporation of [14C]-glycine into [14C]-formyl GAR incubated 30 mins prior to [14C]-glycine addition measured after 16 hrs by radiometric assay in presence of azaserin
Inhibition of GARFTase in human KB cells assessed as incorporation of [14C]-glycine into [14C]-formyl GAR incubated 30 mins prior to [14C]-glycine addition measured after 16 hrs by radiometric assay in presence of azaserin
[PMID: 24256410]
KB IC50
11.74 nM
Compound: PMX, LY231514
Inhibition of GARFTase in human KB cells expressing RFC/FRalpha/PCFT assessed as incorporation of [U-14C]-glycine into [14C]-formyl glycinamide ribonucleotide incubated for 1 hr followed by [U-14C]-glycine addition measured after 16 hrs
Inhibition of GARFTase in human KB cells expressing RFC/FRalpha/PCFT assessed as incorporation of [U-14C]-glycine into [14C]-formyl glycinamide ribonucleotide incubated for 1 hr followed by [U-14C]-glycine addition measured after 16 hrs
[PMID: 25602637]
KB IC50
30 nM
Compound: PMX
Inhibition of GARFTase in human KB cells assessed as inhibition of incorporation of [14C]glycine into [14C]formyl GAR after 30 mins in presence of azaserine
Inhibition of GARFTase in human KB cells assessed as inhibition of incorporation of [14C]glycine into [14C]formyl GAR after 30 mins in presence of azaserine
[PMID: 19371039]
KB IC50
30 nM
Compound: pemetrexed
Inhibition of GARFTase in human KB cells assessed as inhibition of [14C]glycine incorporation into [14C]formylGAR in presence of azaserine
Inhibition of GARFTase in human KB cells assessed as inhibition of [14C]glycine incorporation into [14C]formylGAR in presence of azaserine
[PMID: 18680275]
KB IC50
30 μM
Compound: PMX
Inhibition of GARFtase in human KB cells assessed as [14C]glycine incorporation in to [14C]FGAR in folate free RPMI medium with 2 nM LCV by in-situassay
Inhibition of GARFtase in human KB cells assessed as [14C]glycine incorporation in to [14C]FGAR in folate free RPMI medium with 2 nM LCV by in-situassay
[PMID: 20085328]
KB IC50
327 nM
Compound: PMX
Cytotoxicity against human KB cells assessed as cell growth inhibition incubated up to 96 hrs in presence of 200 nM folic acid by Celltiter-blue cell viability assay
Cytotoxicity against human KB cells assessed as cell growth inhibition incubated up to 96 hrs in presence of 200 nM folic acid by Celltiter-blue cell viability assay
[PMID: 25234128]
KB IC50
327 nM
Compound: PMX
Antiproliferative activity against human KB cells expressing human RFC/FR-alpha/PCFT assessed as reduction in cell viability measured after 96 hrs in presence of folic acid by Cell-Titer Blue assay
Antiproliferative activity against human KB cells expressing human RFC/FR-alpha/PCFT assessed as reduction in cell viability measured after 96 hrs in presence of folic acid by Cell-Titer Blue assay
[PMID: 29425443]
KB IC50
327 nM
Compound: PMX
Inhibition of DHFR in human KB cells expressing RFC/FRalpha/PCFT assessed as reduction in cell growth after 96 hrs in presence of folic acid by Cell-Titer Blue assay
Inhibition of DHFR in human KB cells expressing RFC/FRalpha/PCFT assessed as reduction in cell growth after 96 hrs in presence of folic acid by Cell-Titer Blue assay
[PMID: 32503687]
KB IC50
327 nM
Compound: PMX, LY-231514
Antiproliferative activity against human KB cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs in the presence of 200 nM folic acid
Antiproliferative activity against human KB cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs in the presence of 200 nM folic acid
[PMID: 21879757]
KB IC50
327 nM
Compound: PMX, pemetrexed
Growth inhibition of human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTiter-blue assay in presence of folic acid
Growth inhibition of human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTiter-blue assay in presence of folic acid
[PMID: 24111942]
KB IC50
327 nM
Compound: pemetrexed
Antiproliferative activity against human RFC and FRalpha expressing human KB cells in presence of folic acid
Antiproliferative activity against human RFC and FRalpha expressing human KB cells in presence of folic acid
[PMID: 18680275]
KB IC50
68 nM
Compound: PMX
Cytotoxicity against human KB cells assessed as cell growth inhibition incubated up to 96 hrs by Celltiter-blue cell viability assay
Cytotoxicity against human KB cells assessed as cell growth inhibition incubated up to 96 hrs by Celltiter-blue cell viability assay
[PMID: 25234128]
KB IC50
68 nM
Compound: PMX
Antiproliferative activity against human KB cells expressing human RFC/FR-alpha/PCFT assessed as reduction in cell viability measured after 96 hrs by Cell-Titer Blue assay
Antiproliferative activity against human KB cells expressing human RFC/FR-alpha/PCFT assessed as reduction in cell viability measured after 96 hrs by Cell-Titer Blue assay
[PMID: 29425443]
KB IC50
68 nM
Compound: PMX
Inhibition of DHFR in human KB cells expressing RFC/FRalpha/PCFT assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
Inhibition of DHFR in human KB cells expressing RFC/FRalpha/PCFT assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
[PMID: 32503687]
KB IC50
68 nM
Compound: PMX
Antitumor activity against human KB cells expressing RFC transporter coexpressing FR-alpha and PCFT transporter assessed as inhibition of cell growth measured upto 96 hrs by Cell titer blue assay
Antitumor activity against human KB cells expressing RFC transporter coexpressing FR-alpha and PCFT transporter assessed as inhibition of cell growth measured upto 96 hrs by Cell titer blue assay
[PMID: 37582241]
KB IC50
68 nM
Compound: PMX, LY-231514
Antiproliferative activity against human KB cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs
Antiproliferative activity against human KB cells expressing human RFC, FRalpha and PCFT assessed as reduction of viable cells after 96 hrs
[PMID: 21879757]
KB IC50
68 nM
Compound: PMX, LY231514
Antiproliferative activity against human KB cells expressing RFC/FRalpha/PCFT after 96 hrs by CellTiter-Blue assay
Antiproliferative activity against human KB cells expressing RFC/FRalpha/PCFT after 96 hrs by CellTiter-Blue assay
[PMID: 25602637]
KB IC50
68 nM
Compound: PMX, pemetrexed
Growth inhibition of human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTiter-blue assay
Growth inhibition of human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTiter-blue assay
[PMID: 24111942]
KB IC50
68 nM
Compound: pemetrexed
Antiproliferative activity against human RFC and FRalpha expressing human KB cells
Antiproliferative activity against human RFC and FRalpha expressing human KB cells
[PMID: 18680275]
KB IC50
690 nM
Compound: 6, Pemetrexed, PMX, Alimta
Cytotoxicity against human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTitre-Blue fluorescence assay in presence of folic acid
Cytotoxicity against human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTitre-Blue fluorescence assay in presence of folic acid
[PMID: 24256410]
KB IC50
70.2 nM
Compound: PMX
Antiproliferative activity against human KB cells assessed as reduction in cell viability after 72 hrs by MTT assay
Antiproliferative activity against human KB cells assessed as reduction in cell viability after 72 hrs by MTT assay
[PMID: 31200235]
KB IC50
9.94 nM
Compound: 6, Pemetrexed, PMX, Alimta
Cytotoxicity against human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTitre-Blue fluorescence assay
Cytotoxicity against human KB cells expressing human RFC/FRalpha/PCFT after 96 hrs by CellTitre-Blue fluorescence assay
[PMID: 24256410]
KB IC50
9.95 nM
Compound: 1; PMX
Antiproliferative activity against human KB cells assessed as cell growth inhibition incubated for 96 hrs by CellTiter-Blue cell viability assay
Antiproliferative activity against human KB cells assessed as cell growth inhibition incubated for 96 hrs by CellTiter-Blue cell viability assay
[PMID: 38116433]
L1210 IC50
2.2 x 10-8 M
Compound: 15
Compound was evaluated for the half-maximal inhibition against mouse L1210 leukemic cell growth
Compound was evaluated for the half-maximal inhibition against mouse L1210 leukemic cell growth
[PMID: 1447744]
MCF7 IC50
0.65 μM
Compound: PMX
Antiproliferative activity against human MCF7 cells in folate free medium after 72 hrs in presence of leucovorin by MTT assay
Antiproliferative activity against human MCF7 cells in folate free medium after 72 hrs in presence of leucovorin by MTT assay
[PMID: 28830032]
MDA-MB-231 IC50
3.85 μM
Compound: PTX
Antiproliferative activity against human MDA-MB-231 cells after 24 hrs by MTT assay
Antiproliferative activity against human MDA-MB-231 cells after 24 hrs by MTT assay
[PMID: 29807332]
NCI-H1975 IC50
2.13 μM
Compound: PTX
Antiproliferative activity against human NCI-H1975 cells assessed as inhibition of cell growth incubated for 24 hrs by MTT assay
Antiproliferative activity against human NCI-H1975 cells assessed as inhibition of cell growth incubated for 24 hrs by MTT assay
[PMID: 37437348]
OVCAR-3 IC50
6.9 μM
Compound: PTX
Antiproliferative activity against human OVCAR3 cells after 24 hrs by MTT assay
Antiproliferative activity against human OVCAR3 cells after 24 hrs by MTT assay
[PMID: 29807332]
R2 IC50
13.2 nM
Compound: PMX
Inhibition of DHFR in Chinese Hamster MTXRII-OuaR2-4 R2 cells expressing human PCFT assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
Inhibition of DHFR in Chinese Hamster MTXRII-OuaR2-4 R2 cells expressing human PCFT assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
[PMID: 32503687]
R2 IC50
13.2 nM
Compound: PMX, LY-231514
Antiproliferative activity against chinese hamster R2 cells expressing human PCFT assessed as reduction of viable cells after 96 hrs
Antiproliferative activity against chinese hamster R2 cells expressing human PCFT assessed as reduction of viable cells after 96 hrs
[PMID: 21879757]
R2 IC50
13.2 nM
Compound: PMX, pemetrexed
Growth inhibition of Chinese hamster R2 cells expressing human PCFT4 after 96 hrs by CellTiter-blue assay
Growth inhibition of Chinese hamster R2 cells expressing human PCFT4 after 96 hrs by CellTiter-blue assay
[PMID: 24111942]
R2 IC50
138 nM
Compound: PMX
Antiproliferative activity in Chinese hamster R2 cells deficient in RFC, PCFT, and FRalpha assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
Antiproliferative activity in Chinese hamster R2 cells deficient in RFC, PCFT, and FRalpha assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
[PMID: 29701475]
R2 IC50
22.3 nM
Compound: 6, Pemetrexed, PMX, Alimta
Cytotoxicity against chinese hamster R2 cells expressing human PCFT4 after 96 hrs by CellTitre-Blue fluorescence assay
Cytotoxicity against chinese hamster R2 cells expressing human PCFT4 after 96 hrs by CellTitre-Blue fluorescence assay
[PMID: 24256410]
R2 IC50
4.94 nM
Compound: PMX, LY-231514
Antiproliferative activity against chinese hamster R2 cells expressing human PCFT assessed as inhibition of colony formation after 10 to 14 days
Antiproliferative activity against chinese hamster R2 cells expressing human PCFT assessed as inhibition of colony formation after 10 to 14 days
[PMID: 21879757]
R2 IC50
42 nM
Compound: PMX
Cytotoxicity in RFC-null Chinese hamster R2 cells assessed as reduction in cell viability measured after 96 hrs by Cell-Titer Blue fluorescence analysis
Cytotoxicity in RFC-null Chinese hamster R2 cells assessed as reduction in cell viability measured after 96 hrs by Cell-Titer Blue fluorescence analysis
[PMID: 27458733]
R2 IC50
42 nM
Compound: PMX, LY231514
Cytotoxicity against RFC-deficient Chinese hamster R2 cells assessed as growth inhibition after 96 hrs by CellTiter-Blue assay
Cytotoxicity against RFC-deficient Chinese hamster R2 cells assessed as growth inhibition after 96 hrs by CellTiter-Blue assay
[PMID: 25602637]
R2 IC50
849 nM
Compound: PMX
Cytotoxicity in RFC-null Chinese hamster R2 cells assessed as reduction in cell viability measured after 96 hrs by Cell-Titer Blue assay
Cytotoxicity in RFC-null Chinese hamster R2 cells assessed as reduction in cell viability measured after 96 hrs by Cell-Titer Blue assay
[PMID: 29425443]
R2 IC50
894 nM
Compound: PMX
Cytotoxicity against Chinese hamster R2 cells assessed as cell growth inhibition incubated up to 96 hrs by Celltiter-blue cell viability assay
Cytotoxicity against Chinese hamster R2 cells assessed as cell growth inhibition incubated up to 96 hrs by Celltiter-blue cell viability assay
[PMID: 25234128]
R2 IC50
894 nM
Compound: PMX
Inhibition of DHFR in Chinese Hamster MTXRII-OuaR2-4/FRalpha-null R2 cells assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
Inhibition of DHFR in Chinese Hamster MTXRII-OuaR2-4/FRalpha-null R2 cells assessed as reduction in cell growth after 96 hrs by Cell-Titer Blue assay
[PMID: 32503687]
R2 IC50
894 nM
Compound: PMX, LY-231514
Antiproliferative activity against chinese hamster R2 cells assessed as reduction of viable cells after 96 hrs
Antiproliferative activity against chinese hamster R2 cells assessed as reduction of viable cells after 96 hrs
[PMID: 21879757]
R2 IC50
894 nM
Compound: pemetrexed
Antiproliferative activity against human RFC expressing Chinese hamster R2 cells
Antiproliferative activity against human RFC expressing Chinese hamster R2 cells
[PMID: 18680275]
R2 IC50
974 nM
Compound: PMX
Cytotoxicity against Chinese hamster R2 cells expressing empty vector assessed as cell growth inhibition incubated up to 96 hrs by Celltiter-blue cell viability assay
Cytotoxicity against Chinese hamster R2 cells expressing empty vector assessed as cell growth inhibition incubated up to 96 hrs by Celltiter-blue cell viability assay
[PMID: 25234128]
R2 IC50
> 1000 nM
Compound: 6, Pemetrexed, PMX, Alimta
Cytotoxicity against chinese hamster R2 cells after 96 hrs by CellTitre-Blue fluorescence assay
Cytotoxicity against chinese hamster R2 cells after 96 hrs by CellTitre-Blue fluorescence assay
[PMID: 24256410]
SGC-7901 IC50
9.08 μM
Compound: PTX
Antiproliferative activity against human SGC7901 cells after 24 hrs by MTT assay
Antiproliferative activity against human SGC7901 cells after 24 hrs by MTT assay
[PMID: 29807332]
SW-620 IC50
0.08 μM
Compound: PMX
Antiproliferative activity against human SW620 cells after 72 hrs by MTT assay in presence of leucovorin
Antiproliferative activity against human SW620 cells after 72 hrs by MTT assay in presence of leucovorin
[PMID: 27017552]
SW-620 IC50
0.09 μM
Compound: PMX
Antiproliferative activity against human SW620 cells in folate free medium after 72 hrs in presence of leucovorin by MTT assay
Antiproliferative activity against human SW620 cells in folate free medium after 72 hrs in presence of leucovorin by MTT assay
[PMID: 28830032]
SW-620 IC50
80.2 nM
Compound: PMX
Antiproliferative activity against human SW620 cells assessed as reduction in cell viability after 72 hrs by MTT assay
Antiproliferative activity against human SW620 cells assessed as reduction in cell viability after 72 hrs by MTT assay
[PMID: 31200235]
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[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Lösungsmittel & Löslichkeit
In Vitro: 

DMSO : 250 mg/mL (584.92 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

H2O : < 0.1 mg/mL (insoluble)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.3397 mL 11.6984 mL 23.3967 mL
5 mM 0.4679 mL 2.3397 mL 4.6793 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Select the appropriate dissolution method based on your experimental animal and administration route.

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

  • Protocol 1

    Add each solvent one by one:  10% DMSO    40% PEG300    5% Tween-80    45% Saline

    Solubility: ≥ 2.08 mg/mL (4.87 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

    Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
  • Protocol 2

    Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in Saline)

    Solubility: ≥ 2.08 mg/mL (4.87 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

    Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.

For the following dissolution methods, please prepare the working solution directly. It is recommended to prepare fresh solutions and use them promptly within a short period of time.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

  • Protocol 1

    Add each solvent one by one:  50% PEG300    50% Saline

    Solubility: 20 mg/mL (46.79 mM); Suspended solution; Need ultrasonic

  • Protocol 2

    Add each solvent one by one:  20% SBE-β-CD in Saline

    Solubility: 5 mg/mL (11.70 mM); Clear solution; Need ultrasonic

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