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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T14913 | CD38 inhibitor 1 | CD38 | |
CD38 inhibitor 1 is an inhibitor of CD38. For hCD38 and mouse CD38, the IC50s are 7.3 nM and 1.9 nM. | |||
T79732 | CD38 inhibitor 3 | CD38 | |
CD38 Inhibitor 3 (compound 1), with an IC50 of 11 nM, is a potent agent that enhances mitochondrial biogenesis, diminishes lactate levels, and augments both NAD+ content and Nrf2 expression. In a Pus1 -/- mouse model of ... | |||
T61681 | CD38 inhibitor 2 | ||
CD38 inhibitor 2 is a potent CD38 inhibitor ( IC 50 = 0.01 ~ 0.1 μΜ). | |||
T9918 | Daratumumab | Others | |
Daratumumab is a human monoclonal antibody that targets CD38 a cell surface protein that is overexpressed on multiple myeloma MM) cells. | |||
TN1895 | Luteolinidin chloride | CD38 | |
Luteolinidin chloride is a natural product. It is a potent CD38 inhibitor which can protect the heart against I/R injury with preservation of eNOS function and prevention of endothelial dysfunction in vivo. | |||
T24920 | UCD38B HCl | UCD38B hydrochloride,UCD 38 B hydrochloride,UCD-38-B HCl,UCD-38-B Hydrochloride,UCD 38 B HCl | |
UCD38B HCl is a cell-permeable intracellular uPA inhibitor that acts by killing proliferative and non-proliferative high-grade glioma cells by programmed necrosis. | |||
T69940 | NCD38 | ||
NCD38 is a potent, selective LSD1 inhibitor. | |||
T78577 | NCD38 TFA | Histone Demethylase | |
NCD38 TFA serves as a selective inhibitor of LSD1 [1] [2]. | |||
T61933 | MK-0159 | CD38 | |
MK-0159 is an orally available, highly potent CD38 inhibitor with myocardial injury protection for the study of cardiac ischemia and reperfusion injury. | |||
T60099 | RBN013209 | CD38 | |
RBN013209 is a potent CD38 inhibitor. RBN013209 is useful in the treatment of cancer. | |||
T38951 | Isatuximab | SAR-650984,hu38SB19,Isatuximab-irfc | Apoptosis , CD38 |
Isatuximab is a monoclonal antibody targeting the transmembrane receptor and extracellular enzyme CD38 in malignant cells of the hematological system and is a highly expressed protein in multiple myeloma. Isatuximab has ... | |||
T77006 | Felzartamab | TJ-202,MOR-03087,MOR-202 | CD38 |
Felzartamab(MOR-202) is a human-targeted monoclonal antibody to CD38 for the study of multiple myeloma and advanced antibody-mediated rejection of allogeneic kidney transplants. | |||
TN1513 | Clitorin | PKC , Antifection | |
Clitorin has free radical scavenging property. It shows significant interactions with CD38, it may have anti-hyperglycemic potential. | |||
T38730 | Ara-F-NAD+ | ||
Ara-F-NAD+, an arabino analogue of NAD + , is a potent, slow-binding CD38 NADase inhibitor, with a K i of 169 nM. | |||
T77084 | Mezagitamab | ||
Mezagitamab (TAK-079), an IgG1λ anti-CD38 monoclonal antibody, functions by depleting tumor cells that express CD38 through both antibody and complement-dependent cytotoxicity. It shows potential for use in the treatment... | |||
T82440 | Erzotabart | CD38 | |
Erzotabart, an IgG1-kappa monoclonal antibody targeting CD38 (ADP-ribosyl cyclase 1, cyclic ADP-ribose hydrolase 1, cADPr hydrolase 1, cADPR1) in Homo sapiens, exhibits antineoplastic activity [1]. | |||
T37475 | Cyclic ADP-Ribose (ammonium salt) | cADP-Ribose,cADPR,Cyclic ADP-Ribose (ammonium salt) | |
Cyclic ADP-ribose (cADP-ribose) is an endogenous metabolite of NAD+ that mobilizes the release of stored Ca2+ in the endoplasmic reticulum via ryanodine receptors in various cell types.[1],[2],[3],[4],[5] This second mes... | |||
T77091 | Modakafusp alfa | ||
Modakafusp alfa (TAK-573) is a humanized anti-CD38 IgG4 monoclonal antibody, with 2 attenuated IFNα2b molecules fused to it. This compound is researched for potential use in treating multiple myeloma [1]. | |||
T74032 | Ara-F-NAD+ sodium | ||
Ara-F-NAD+ sodium, an arabino analogue of NAD+, serves as a potent, reversible, and slow-binding inhibitor of the CD38 NADase [1] [2]. | |||
T13907 | Sulfo-ara-F-NMN | CZ-48 | Others |
Sulfo-ara-F-NMN is an analogue of nicotinamide mononucleotide (NMN) with cellular permeability. Sulfo-ara-F-NMN was selective to activate SARM1 and inhibited CD38 with an IC50 of about 10 μM. Activation by Sulfo-ara-F-NM... |