About 8 results found for searched term "U-104" (0.052 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M3099 | U-104 | Carbonic Anhydrase |
| MST-104; SLC-0111 | ||
| U-104 is a potent carbonic anhydrase (CA) inhibitor for CA IX and CA XII with Ki of 45.1 nM and 4.5 nM, respectively, very low inhibition for CA I and CA II. | ||
| M3380 | Pitavastatin Calcium | Autophagy |
| Pitavastatin hemicalcium; NK-104 | ||
| Pitavastatin Calcium is a new type of statin. | ||
| M22202 | Deuterated AZ5104 | Others |
| Deuterated AZ5104 | ||
| M25049 | Tecaginlimab | TNF Receptor |
| BNT-312 DuoBody-CD40x-4-1BB GEN1042 | ||
| Tecaginlimab (BNT-312) is a Fc-inert bispecific antibody for dual targeting and conditional stimulation of CD40 and 4-1BB. Tecaginlimab can enhance priming and reactivation of tumor-specific immunity. | ||
| M25065 | Barecetamab | EGFR/HER2 |
| ISU-104 | ||
| Barecetamab (ISU-104) is a fully human anti-ErbB3 monoclonal antibody. Barecetamab can be used for the research of recurrent/metastatic (R/M) head and neck squamous cell carcinoma (HNSCC). | ||
| M28203 | VU0410425 | GluR |
| VU0410425 is an mGlu1 negative allosteric modulator. VU0410425 exhibits potent inhibitory activity for rat mGlu1 with an IC50 value of 140 nM. VU0410425 can be used for the research of central nervous system disorders. | ||
| M58185 | VU0810464 | Potassium Channel |
| VU0810464 is a potent and selective non-ureaG protein-gated inwardly-rectifying potassium channels (GIRK, Kir3) activator. VU0810464 displays nanomolar potency for neuronal (EC50=165 nM) and GIRK1/4 (EC50=720 nM) channels with improved brain penetration. | ||
| M56443 | (R)-STU104 | p38 MAPK |
| (R)-STU104 is a potent and orally active TAK1-MKK3 interaction inhibitor with IC50s of 0.58 μM and 4.0 μM for TNF-α and MKK3 phosphorylation. | ||
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