| Cat.No. | Name | Information |
|---|---|---|
| M6098 | Baicalein | Baicalein is a CYP2C9 and prolyl endopeptidase inhibitor, IC50 value of 3.12 mM. |
| M9325 | EGTA | EGTA is a specific calcium chelator with a Kd of 60.5 nM at physiological pH (7.4) and a high specificity for Ca2+ than for Mg2+.EGTA significantly inhibits the substrate adhesion capacity of inflammatory macrophages. |
| M9330 | Brij-35 | Brij-35 (Polidocanol) is a high HLB, ethoxylated, nonionic ether of lauryl alcohol with broad pH stability. |
| M6154 | 2-PMPA tetrasodium | 2-PMPA (PMPA tetrasodium salt) is a potent and selective inhibitor of glutamate carboxypeptidase II (GCPII) with an IC50 of 300 pM. |
| M2250 | Pamidronate disodium | Pamidronate disodium is a nitrogen containing bisphosphonate, used to the research of preventing osteoporosis. |
| M9916 | DPPH | DPPH (2,2-Diphenyl-1-picrylhydrazyl) is a stable free radical that measures the free radical scavenging activity of antioxidants. |
| M9194 | Insulin (human) | Insulin (human) is a polypeptide hormone that regulates the level of sugar (glucose) in the blood and is produced by beta cells of islets. |
| M3409 | Formestane | Formestane is a second generation selective aromatase inhibitor with an IC50 of 80 nM. |
| M9665 | N-(2-amino-2-oxoethyl)acrylamide | N-(2-Amino-2-oxoethyl)acrylamide |
| M7791 | Exo-1 | Exo1 is a reversible inhibitor of exocytosis, also a Golgi ARF 1 (ADP-Ribosylation Factor) GTPase activator. |
| M42975 | Vacquinol-1 dihydrochloride | Vacquinol-1 (NSC13316) dihydrochloride is a MKK4-specific activator that activates MAPK pathways. |
| M42974 | Benzyl DC-81 | Benzyl DC-81 is an anticancer agent with antiproliferative activity against A375 and MCF-7 cells. |
| M42973 | SN-38-CO-DMEDA TFA | SN-38-CO-DMEDA TFA is the intermediate product for synthesizing antibody-conjugated drug LND1035. |
| M42971 | GPAT-IN-1 | GPAT-IN-1 is a glycerol-3-phosphate acyltransferase (GPAT) inhibitor with an IC50 value of 8.9 μM. |
| M42970 | AC-099 | AC-099 is a selective NPFF2R full agonist (EC50=1189 nM) and NPFF1R partial agonist (EC50=2370 nM). |
| M42969 | 3-Acetylphenyl acetate | 3-Acetylphenyl acetate (Tetramethyl thiol alcynic acid) can be used as pharmaceutical intermediates. |
| M42968 | rTRD01 | rTRD01 is a TDP-43 ligand that binds to TDP-43’s RRM1 and RRM2 domains (Kd=89 uM for TDP-43102–269). |
| M42967 | EBOV/MARV-IN-2 | EBOV/MARV-IN-2 is an Ebolavirus (EBOV, IC50=0.9 μM) and Marburg virus (MARV, IC50=2.7 μM) inhibitor. |
| M42966 | L-AP6 | L-AP6 is a selective agonist for a quisqualate-sensitized site in hippocampal CA1 pyramidal neurons. |
| M42965 | PAP-IN-1 | PAP-IN-1 is an inhibitor of purple acid phosphatases (PAPs), a ubiquitous binuclear metallohydrolase. |
| M42964 | MGAT2-IN-4 | MGAT2-IN-4 is an inhibitor of monoacylglycerol transferase 2 (MGAT2), with liver metabolic stability. |
| M42963 | A1AT modulator 1 | A1AT modulator 1 is a potent inhibitor of Z ai-antitrypsin polymerisation with a pIC50 value of 8.3 . |
| M42962 | Bipolal | Bipolal (KM 01) is a natural product isolated from the culture fluid of bipolar algae (Bipolaris sp.). |
| M42961 | 2-Quinizarincarboxylic acid | 2-Quinizarincarboxylic acid is a glucose uptake inhibitor, with the inhibitory rate of 24.9% at 50 μM. |
| M42960 | S07-1066 | S07-1066 is an aldo-keto reductase 1C3 (AKR1C3) inhibitor, synergizing doxorubicin (DOX) cytotoxicity. |
| M42959 | M351-110 | M351-110 is a T-cell activating V-domain immunoglobulin inhibitory factor agonist for cancer research. |
| M42958 | BMS-195270 | BMS-195270 is a small molecule that inhibits Carbachol-evoked tonicity of isolated rat bladder strips. |
| M42957 | Isoindigo | Isoindigo is the acceptor of donor-acceptor (D-A) conjugated polymer, as well as an Indigo series dye. |
| M42956 | 3-Fluoro-L-tyrosine | 3-Fluoro-L-tyrosine is a tyrosine analogue, inhibits transamination by tyrosine aminotransferase (TAT). |
| M42955 | L-Arginine butanoate | L-Arginine butanoate ((S)-(+)-Arginine butanoate) is a compound consisting of L-Arginine and butanoate. |
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