Cat. No. | Product Name | Field of Application | Chemical Structure |
---|---|---|---|
DC7762 | RX-3117 Featured |
RX-3117 is an orally available and potent DNA synthesis inhibitor with potential antineoplastic activity.
More description
|
![]() |
DC8111 | Idarubicin Hydrochloride Featured |
Idarubicin Hcl is an anthracycline antibiotic and a DNA topoisomerase II (topo II) inhibitor.
More description
|
![]() |
DC4184 | Vinorelbine Ditartrate Featured |
Vinorelbine (Navelbine) is an anti-mitotic agent which inhibits the proliferation of Hela cells with IC50 of 1.25 nM.
More description
|
![]() |
DCAPI1525 | 5-Azacytidine Featured |
5-Azacytidine is a potent growth inhibitor and a cytotoxic agent. 5-Azacytidine acts as a demethylating agent by inhibiting DNA methyltransferase (Dnmt), forming covalent adducts with cellular DNMT1 depleting enzyme activity. 5-Azacytidine also improves t
More description
|
![]() |
DC2099 | cis-Diaminedichloroplatinum Featured |
Cisplatin is an inorganic platinum agent (cis-diamminedichloroplatinum) with antineoplastic activity.
More description
|
![]() |
DC7530 | Voreloxin Featured |
Voreloxin(SNS-595; AG 7352) is a small molecule and a naphthyridine analogue with antineoplastic activity; inhibitor of Topo II.
More description
|
![]() |
DC6906 | Aprepitant (MK-0869, L-754030) Featured |
Substance P antagonists (SPA).
More description
|
![]() |
DC8940 | Raltitrexed Featured |
Raltitrexed(ZD1694), an inhibitor of thymidylate synthase, is an antimetabolite drug used in cancer chemotherapy.
More description
|
![]() |
DC8149 | Pemetrexed disodium Featured |
Pemetrexed disodium is a novel antifolate and antimetabolite for TS, DHFR and GARFT with Ki of 1.3 nM, 7.2 nM and 65 nM, respectively.
More description
|
![]() |
DC5885 | Oxaliplatin Featured |
Oxaliplatin is a second generation potent platinum-based anti-neoplastic agent that is believed to form inter- and intrastrand DNA adducts which activate signaling pathways culminating in apoptosis. The development of Oxaliplatin was inspired from the eff
More description
|
![]() |
DC9298 | thiotepa Featured |
N,N’N’-triethylenethiophosphoramide (ThioTEPA) is a cancer chemotherapeutic member of the alkylating agent group.
More description
|
![]() |
DC4182 | Temozolomide Featured |
Methazolastone (Temozolomide, Temodar, Temodal) is a DNA damage inducer.
More description
|
![]() |
DC10406 | Imisopasem manganese |
Imisopasem manganese (M40403) is a stable non-peptidyl mimetic of manganese superoxide MnSOD.
More description
|
![]() |
DC5882 | Fosbretabulin disodium Featured |
Fosbretabulin disodium(CA 4DP; CA 4P) is a microtubule destabilizing drug, a type of vascular-targeting agent, a drug designed to damage the vasculature (blood vessels) of cancer tumors causing central necrosis.
More description
|
![]() |
DC7069 | Daunorubicin HCL Featured |
Daunorubicin HCl inhibits both DNA and RNA synthesis and inhibits DNA synthesis with Ki of 0.02 μM.
More description
|
![]() |
DC9013 | Cyclophosphamide Featured |
Cyclophosphamide is a synthetic alkylating agent chemically related to the nitrogen mustards with antineoplastic and immunosuppressive activities.
More description
|
![]() |
DC9095 | Carboplatin Featured |
Carboplatin is a chemotherapy drug by binding to DNA and interfering with the cell's repair mechanism.
More description
|
![]() |
DC7023 | Ombrabulin Featured |
Ombrabulin (AVE8062) hydrochloride is a synthetic derivative of CA-4-P, which inhibits growth in a large number of drug-resistant animal tumors and carcinogen-induced tumors.
More description
|
![]() |
DC9359 | Pralatrexate Featured |
Pralatrexate(Folotyn) is an antifolate, and structurally a folate analog.
More description
|
![]() |
DC9050 | Melphalan Featured |
Melphalan(Sarcolysin; L-PAM) is a chemotherapy drug belonging to the class of nitrogen mustard alkylating agents; attaches the alkyl group to the guanine base of DNA.
More description
|
![]() |
DC9832 | Betulinic acid Featured |
Betulinic acid, a pentacyclic triterpene, selectively induces apoptosis in tumor cells, also is a inhibitor of HIV-1 with EC50 of 1.4 μ M.
More description
|
![]() |
DC8962 | Tegafur Featured |
Tegafur (also known as Ftorafur) is a chemotherapeutic 5-FU prodrug used in the treatment of cancers; is a component of tegafur-uracil.
More description
|
![]() |
DC10444 | Sapacitabine (CYC682) Featured |
Sapacitabine is an orally bioavailable pyrimidine analogue prodrug with potential antineoplastic activity.
More description
|
![]() |
DC9014 | Ifosfamide |
Ifosfamide is a nitrogen mustard alkylating agent used in the treatment of cancer.
More description
|
![]() |
DC8946 | Gimeracil |
Gimeracil(Gimestat) is an inhibitor of dihydropyrimidine dehydrogenase (DPYD), which degrades pyrimidine including 5-fluorouracil in the blood; inhibits homologous recombination.
More description
|
![]() |
DC2108 | Gemcitabine free base |
Gemcitabine(Gemzar) belongs to the group of medicines called antimetabolites.
More description
|
![]() |
DC11192 | Elacytarabine |
Elacytarabine (CP-4055, CP4055) is a fatty acid derivative of cytarabine with potential antineoplastic activity.
More description
|
![]() |
DCAPI1475 | Dexrazoxane Hydrochloride |
Dexrazoxane Hydrochloride
More description
|
![]() |
DC4186 | Cabazitaxel |
Cabazitaxel (Jevtana, XRP6258) is a semi-synthetic derivative of a natural taxoid.
More description
|
![]() |
DC8923 | AS-1413(Amonafide) |
Amonafide(AS1413) produces protein-associated DNA-strand breaks through a topoisomerase II-mediated reaction, but does not produce topoisomerase I-mediated DNA cleavage.
More description
|
![]() |