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Cancer

Cat. No. Product Name CAS No. Information
CSN16255 Doxorubicin HCl 25316-40-9 Doxorubicin hydrochloride is an antibiotic agent that inhibits DNA topoisomerase II and induces DNA damage and apoptosis in tumor cells.
CSN19462 Irinotecan 97682-44-5 Irinotecan is a camptothecin analog prevents DNA from unwinding by inhibition of topoisomerase 1.
CSN15710 Cabozantinib 849217-68-1 Cabozantinib is a potent VEGFR2 inhibitor with IC50 of 0.035 nM and also inhibits c-Met, Ret, Kit, Flt-134, Tie2, and AXL with IC50 of 1.3 nM, 4 nM, 4.6 nM, 12 nM11.3 nM6 nM, 14.3 nM and 7 nM, respectively.
CSN10824 Dimesna 16208-51-8 Dimesna is a kidney selective prodrug to Mesna.
CSN12283 β-Lapachone 4707-32-8 -Lapachone is a naturally occurring quinone obtained from the bark of the lapacho tree (Tabebuia avellanedae) with cancer chemopreventive properties and a potent inhibitor of IDO1 (IC500.44 M).
CSN18312 Amsacrine 51264-14-3 Amsacrine can intercalate into the DNA of tumor cells with antineoplastic activity.
CSN12667 Tivozanib 475108-18-0 Tivozanib is an inhibitor of VEGFR1, VEGFR2 and VEGFR3 with IC50s of 30 nM, 6.5 nM, 15 nM, respectively. It can also inhibit PDGFR and c-Kit.
CSN16298 Etoposide 33419-42-0 Etoposide inhibits DNA synthesis by inhibiting topoisomerase II (IC50 60.3 M).
CSN19463 Irinotecan HCl 100286-90-6 Irinotecan hydrochloride is an inhibitor of topoisomerase 1 that prevents DNA from unwinding.
CSN12454 Vatalanib 2HCl 212141-51-0 Vatalanib dihydrochloride is inhibitor of VEGFR2 or KDR with IC50 of 37 nM.
CSN16117 Salirasib 162520-00-5 Salirasib is an inhibitor of prenylated protein methyltransferase (PPMTase) with Ki of 2.6 M and can inhibit the methylation of Ras.
CSN12234 Zebularine 3690-10-6 Zebularine is a DNA methylation inhibitor which forms a covalent complex with DNA methyltransferases, it also inhibits cytidinedeaminase with Ki of 2 M.
CSN16731 Daunorubicin HCl 23541-50-6 Daunorubicin hydrochloride can inhibit both DNA synthesis (Ki 0.02 M) and RNA synthesis.
CSN12341 BIBF 1120 656247-17-5 Nintedanib is a potent triple angiokinase inhibitor for VEGFR123, FGFR123 and PDGFR with IC50 of 34 nM13 nM13 nM, 69 nM37 nM108 nM and 59 nM65 nM.
CSN10852 DMXAA 117570-53-3 DMXAA is an apoptosis inducer with anti-vascular activity. It can inhibit STING and enzyme DT-diaphorase (Ki 20 M).
CSN15871 Ondansetron HCl 2H2O 103639-04-9 Ondansetron HCl 2H2O is a competitive 5-HT3 receptor antagonist.
CSN11403 Aloin A 1415-73-2 Aloin A, an anthracycline from aloe plants, can be used as a chemopreventive factor with antineoplastic activity. It exhibits inhibition of phosphodiesterase and tyrosinase.
CSN11119 (+)-Griseofulvin 126-07-8 ()-Griseofulvin is a naturally occuring centrosomal clustering inhibitor and induces keratin cytoskeleton alterations. It is also an antifungal drug.
CSN12963 Tipifarnib 192185-72-1 Tipifarnib is an inhibitor of farnesyltransferase with IC50 of 0.6 nM.
CSN13137 Ondansetron 99614-02-5 Ondansetron is a serotonin 5-HT3 receptor antagonist used mainly as anantiemetic (to treat nausea and vomiting), often following chemotherapy.
CSN16581 Campathecin 7689-03-4 Camptothecin is a potent DNA enzyme topoisomerase I (topo I) inhibitor with an IC50 and IC70 of 50 nM and 0.225 M for breast cancer cell line MDA-MB-231.
CSN16877 Cabozantinib Malate 1140909-48-3 Cabozantinib S-malate is a VEGFR2 inhibitor with IC50 of 0.035 nM. It also inhibits c-Met, Ret, Kit, Flt-134, Tie2, and AXL with IC50 of 1.3 nM-11.3 nM.
CSN21898 Cediranib 288383-20-0 Cediranib is a multiple RTKs inhibitor with IC50 values of 0.001M, 0.005M, 0.003M, 0.002M and 0.005M for VEGFR-2, VEGFR-1, VEGFR-3, c-Kit and PDGFR-(measured kinase activity), respectively.
CSN17192 Motesanib Diphosphate 857876-30-3 Motesanib diphosphate is ATP-competitive inhibitor of VEGFR1, VEGFR2 and VEGFR3 with IC50 of 2 nM, 3 nM and 6 nM, respectively. It also shows better inhibitory activity against c-Kit, PDGFR, and RET.
CSN17586 LOXO-101 Sulfate 1223405-08-0 LOXO-101 sulfate blocks the ATP binding site of the TRK family of receptors with IC50 of 2 nM to 20 nM against TRKA, TRKB, and TRKC.
CSN19151 BFH772 890128-81-1 BFH772 selectively targets VEGFR2 kinase with IC50 of 3 nM.
CSN13122 YO-01027 209984-56-5 Dibenzazepine is a dipeptidic -secretase inhibitor with IC50 of 2.6 nM and 2.9 nM in cell-free assays for APPL and Notch cleavage, respectively.
CSN16766 Idarubicin HCl 57852-57-0 Idarubicin hydrochloride is a hydrochloride salt form of idarubicin which is an anthracycline antibiotic and a DNA topoisomerase II (topo II) inhibitor for MCF-7 cells with IC50 of 3.3 ngmL in a cell-free assay.
CSN19726 Fadrozole HCl 102676-31-3 Fadrozole hydrochloride specifically inhibits aromatase, blocking the aromatization of androstenedione and testosterone into estrone and estradiol, respectively.
CSN10166 Trapidil 15421-84-8 Trapidil, a vasodilator and an antiplatelet drug, is also a PDGF antagonist that can inhibit the proliferation of the PDGF-producing glioma cells.
CSN19250 ARQ 092 1313883-00-9 ARQ 092 is a pan-Akt inhibitor with IC50 values of 5nM, 4.5nM and 16nM for Akt1, Akt2 and Akt2, respectively, through blocking membrane translocation of inactive AKT and even dephosphorylating the membrane-associated active form.
CSN16918 Calcipotriol 112965-21-6 Calcipotriol is a synthetic VitD3 analogue with a high affinity for the vitamin D receptor.
CSN18065 Tipifarnib S-Enantiomer 192185-71-0 Tipifarnib S-enantiomer is the enantiomer of tipifarnib, a potent and specific farnesyltransferase inhibitor with an IC50 of 0.6 nM.
CSN17839 1alpha-Hydroxy VD4 143032-85-3 1alpha-Hydroxy VD4 , a 1alpha (OH)D derivative, can effectively induce the differentiation of monoblastic leukaemia U937, P39TSU and P31FUJ cells.
CSN16730 Vatalanib 212141-54-3 Vatalanib is an inhibitor of VEGFR2KDR with IC50 of 37 nM, showing less potent against VEGFR1Flt-1, 18-fold against VEGFR3Flt-4.
CSN17751 INNO-206 1361644-26-9 INNO-206 is the 6-maleimidocaproyl hydrazone derivative prodrug of the anthracycline antibiotic doxorubicin (DOXO-EMCH) with antineoplastic activity.
CSN16968 LOXO-101 1223403-58-4 LOXO-101 is an ATP-competitive inhibitor of TRK with IC50 of nanomolar range for all the family members.
CSN16686 Ondansetron HCl 99614-01-4 Ondansetron is a serotonin 5-HT3 receptor antagonist used mainly as anantiemetic (to treat nausea and vomiting), often following chemotherapy.
CSN18021 Voreloxin 175414-77-4 Voreloxin is a naphthyridine analogue with antineoplastic activity and an inhibitor of Topo II.
CSN12020 Suramin Sodium 129-46-4 Suramin sodium salt is a polysulfonated naphthylurea that inhibits the binding of calmodulin to recognition sites on the ryanodine receptor-1 (IC50 4.9 M), blocks G protein coupling to GPCRs, and non-selectively antagonizes P2 purinergic receptors(10-100 M).
CSN17904 DOXO-EMCH 151038-96-9 DOXO-EMCH is a 6-maleimidocaproyl hydrazone derivative of Doxorubicin, is an albumin binding prodrug.
CSN18023 Voreloxin HCl 175519-16-1 Voreloxin hydrochloride is a naphthyridine analogue with antineoplastic activity and an inhibitor of Topo II.
CSN21384 BNP 1350 203923-89-1 BNP 1350 is a topoisomerase I inhibitor, with potent anti-cancer activity.
CSN18659 AZD3293 1383982-64-6 AZD3293 is an oral beta-secretase 1 cleaving enzyme (BACE) inhibitor.
CSN20465 ATR-101 HCl 133825-81-7
CSN20240 Elocalcitol 199798-84-0 Elocalcitol is a vitamin D3 analog having agonistic activities at vitamin D receptor (VDR).
CSN20400 AEZS-108 139570-93-7
CSN24157 666-15 1433286-70-4 666-15 is a potent and cell-permeable inhibitor of cAMP-response element binding protein (CREB) with efficacious anti-cancer activity both in vitro and in vivo.
CSN24156 E260 1241537-79-0 E260 is an inhibitor of the Fer/FerT kinase with Kd of 0.85 μM, selectively evokes metabolic stress and necrotic death in cancer cells.
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