About 6 results found for searched term "Cyclophosphamide" (0.294 seconds)
Cat.No. | Name | Target |
---|---|---|
M3671 | Cyclophosphamide monohydrate | Animal Modeling |
Cyclophosphamide hydrate | ||
Cyclophosphamide monohydrate is a nitrogen mustard alkylating agent, it attaches the alkyl group to the guanine base of DNA. *The compound is unstable in solutions, freshly prepared is recommended | ||
M3746 | Cyclophosphamide | DNA/RNA Synthesis |
Cyclophosphamide is a synthetic alkylating agent chemically related to the nitrogen mustards with antineoplastic and immunosuppressive activities. *The compound is unstable in solutions, freshly prepared is recommended | ||
M45348 | 4-Hydroperoxy cyclophosphamide | DNA Alkylator/Crosslinker |
4-Hydroperoxy cyclophosphamide, the active metabolite form of the precursor Cyclophosphamide, cross-links DNA and induces T-cell apoptosis independent of caspase receptor activation, as well as activating the mitochondrial death pathway through the generation of reactive oxygen species (ROS). It can be used in studies related to rheumatoid arthritis and autoimmune diseases. | ||
M11549 | Palifosfamide | DNA Alkylator/Crosslinker |
Isophosphoramide mustard; IPM; ZIO-201 | ||
Palifosfamide(Isophosphoramide mustard; IPM; Zio-201) is a new DNA alkylation agent and active metabolite of isocyclophosphamide, which has anticancer activity. | ||
M27931 | Cetrorelix | LHRH/GnRH |
SB-75 | ||
Cetrorelix is a potent gonadotrophin-releasing hormone (GnRH) antagonist. Cetrorelix inhibits the endogenous luteinizing hormone surge during ovarian stimulation. Cetrorelix reduces cyclophosphamide induced ovarian follicular destruction in mice. | ||
M30115 | ONO-8130 | Prostaglandin Receptor |
ONO-8130 is an orally active and selective prostanoid EP1 receptor antagonist. ONO-8130 blocks phosphorylation of ERK in the L6 spinal cord. ONO-8130 relieves bladder pain in mice with cyclophosphamide-induced cystitis. ONO-8130 can be used for interstitial cystitis research. |
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