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Antineoplastic Agents

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CAS:320-67-2
Molecular Formula:C8H12N4O5
Vidaza; Ladakamycin; 5-Azacitidine; Azacitidine; 5-Ac; 5-Azac; Azgr; 5 Azc; [14C]-Azacitidine; 5-Azcr; 5-Ac-15N4; 5'-Azacytidine; Mylosar; 1,3,5-Triazine-2(1H)-One, 4-Amino-1-α-D-Ribofuranosyl-
Brief Introduction
Antimetabolic drugs. The main indication is acute myeloid leukemia which is ineffective to conventional treatment. It is also used for breast cancer, melanoma, intestinal cancer and so on. The main manifestations of toxicity were leucopenia, thrombocytopenia and anemia. Nausea and vomiting are common adverse reactions. Symptoms can be improved by continuous infusion for a long time, or antiemetic agents can be used 24 to 48 hours before treatment. Other toxic effects were diarrhea, neuromuscular disorders, fever, hypotension and rash. The preparation is freshly prepared 3-4h before use.
CAS:3543-75-7
Molecular Formula:C16H22Cl3N3O2
Treanda; Cytostasan; Cytostasanhcl; Bendamustinum; Bendamustin Hydrochloride; Bendamustin Hcl; Bendamustinhydrochlorid; Zimet-33/93; Ribomustin; Bendamustine Hydrochloride Hydrate; 4-(5-(Bis(2-Chloroethyl)Amino)-1-Methyl-1H-Benzo[D]Imidazol-2-Yl)Butanoic Acid Hydrochloride
Brief Introduction
Bendamostine hydrochloride was first developed by ozegowski and his colleagues in the microbial experimental Association in Jena, Germany in the early 1860s. The initial purpose was to connect an alkylated nitrogen mustard (a non effective alkylating agent) with a purine and an amino acid. Compared with nitrogen mustard phenylbutyrate, the main advantage of the newly synthesized compound is its water solubility. It was widely used, but until the end of the cold war, the drug has been carried out in Europe for many single drugs or other drugs for the treatment of various hematological malignancies or non Hodgkin's lymphoma, multiple myeloma, CLL and breast cancer. The clinical effect is very significant, significantly reducing the rate of recurrence and mortality, and has little side effects. Good security. So far, bendamostine hydrochloride single drug or combined treatment has been designated as the first-line or second-line treatment option for a variety of hematological malignancies by European and American clinical guidelines.
CAS:54965-24-1
Molecular Formula:C32H37NO8
Istubal; Tamoxifen (Citrate); Tamoxifen Citrate Salt; Unii-7Frv7310N6; Ici 46474; 2-[4-[(Z)-1,2-Diphenylbut-1-Enyl]Phenoxy]-N,N-Dimethylethanamine;2-Hydroxypropane-1,2,3-Tricarboxylic Acid; Zitazonium; Caditam; Farmifeno; Ginarsan; Jenoxifen
Brief Introduction
Tamoxifen citrate is a kind of estrogen competitive antagonist, which is a non steroidal anti estrogen drug. It can compete with estrogen in vivo and combine with estrogen receptor of breast cancer cells, so as to inhibit the effect of estrogen on cancer cells, hinder the growth and development of tumor cells, and play an anti-cancer effect. It is commonly used in the treatment of various types of breast cancer. It is especially suitable for women with postmenopausal breast cancer who have estrogen receptor and progesterone receptor positive and low level of prostate specific antigen.
CAS:90357-06-5
Molecular Formula:C18H14F4N2O4S
4-Cyano-3-Trifluoromethyl-N-(3-P-Fluorophenylsulfonyl-2-Hydroxy-2-Methylpropionyl)Aniline; N-[4-Cyano-3-(Trifluoromethyl)Phenyl]-3-(4-Fluorophenyl)Sulfonyl-2-Hydroxy-2-Methyl-Propanamid
Brief Introduction
This product can be used as medicine raw material and anti-tumor drug.
CAS:61825-94-3
Molecular Formula:C8H14N2O4Pt
Oxalato(Trans-l-1,2-Cyclohexanediamine)Platinum(II); cis-Oxalato-Trans-l-1,2-Diaminocyclohexaneplatinum(II); [(1S,2S)-2-Azanidylcyclohexyl]Azanide; Oxalate; Platinum(4+)
Brief Introduction
Oxaliplatin, which belongs to platinum derivatives and is clinically used to treat patients with colorectal cancer metastases after failure of fluorouracil treatment, either alone or in combination with fluorouracil, is the third-generation novel platinum based antitumor compound after cisplatin, carboplatin and the only complex platinum based drug with significant activity against colorectal cancer to date. The principle of action is to act on DNA by producing alkylated conjugates, forming intra - and interstrand crosslinks that inhibit DNA synthesis and replication. It also inhibited proliferation in ovarian cancer and melanoma cell lines.
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