| 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. |
| M13495 | Aviptadil | Aviptadil is an analog vasoactive intestinal polypeptide (VIP) with potent vasodilatory effects. |
| M13492 | Kukoamine A | Kukoamine A is a natural occurring spermine derivative, acts as a potent inhibitor of trypanothione reductase (Ki, 1.8 μM), with antihypertensive activity. |
| M13483 | Vebicorvir | Vebicorvir (ABI-H0731) is a first-generation hepatitis B virus (HBV) core protein inhibitor. |
| M13481 | Carbendazim | Carbendazim is a potent and orally active broad-spectrum benzimidazole fungicide and can be acts as a pesticide for fungal diseases research, such as Seproria, Fusarium and Sclerotina. |
| M13452 | MMAF-OMe | MMAF-Ome, an antitubulin agent, is also an ADC cytotoxin. MMAF-Ome inhibits several tumor cell lines with IC50s of 0.056 nM, 0.166 nM, 0.183 nM, and 0.449 nM for MDAMB435/5T4, MDAMB361DYT2, MDAMB468, and Raji (5T4-) cell lines, respectively. |
| M13450 | 3',4',5',5,7-Pentamethoxyflavone | 3',4',5',5, 7-pentamethoxyflavone is a natural brass compound extracted from Rutaceae. |
| M13446 | Protein hydrolyzates, silk | Protein hydrolyzates, silk (96690-41-4) is obtained by hydrolysis of mulberry silk protein under appropriate conditions. |
| M13433 | NVP-DKY709 | NVP-DKY709 is a potent and effective (IKAROS Family Zinc Finger 2, IKZF2) inhibitor that contributes to cancer research.DKY709 acts as a CRBN binder to induce the formation of the CRBN-DKY709-IKZF2 ternary complex. This ternary complex promotes the ubiquitination and degradation of IKZF2. |
| M13432 | RBN013209 | RBN013209 is a potent CD38 inhibitor that can be used in cancer research. |
| M13427 | Tanshindiol A | Tanshindiol A is derived from the root of salvia miltiorrhiza. |
| M13410 | R-1479 | R-1479, a nucleoside analogue, is a HCV replication inhibitor (IC50: 1.28 μM) in the HCV subgenomic replication subsystem. |
| M13377 | NE-CARBOXYMETHYL-L-LYSINE | NE-CARBOXYMETHYL-L-LYSINE is a unique post-translational modification (PTM) of proteins that is generated by the non-enzymatic glycation of lysine residues. Nε-(Carboxymethyl)-L-lysine is a major component of the advanced glycation endproducts (AGEs). |
| M13364 | Tricyclazole | Tricyclazole is a biosynthetic inhibitor of pentaketone melanin and a unique fungicide for rice blast control. |
| M13348 | LyP-1 TFA | Lyp-1 TFA is a circular 9-amino acid tumor-targeting peptide that selectively binds its P32 receptor protein in a variety of tumor-associated cells. |
| M13347 | FR901464 | FR901464 is an effective spliceosome inhibitor with significant antitumor and anticancer effects. |
| M13344 | Tidiacic | Tidiacic acid, a carboxylic acid derivative, can be used as pharmaceutical intermediates. |
| M11546 | CD38 inhibitor 1 | CD38 inhibitor 1 (COMPOUND 78c, CD38-in-78C) was an effective INHIBITOR of CD38, with IC50 of 7.3 nM and 1.9 nM for human AND mouse CD38 respectively. |
| M11525 | 2'-Deoxy-5-formylcytidine | 2' -deoxy-5-formylcytidine is an effective internal triplet photosensitizer in DNA. 2' -deoxy-5-formylcytidine can be used as a new hot spot for DNA photodamage. |
| M11513 | Ammonium formate | Ammonium Ammonium Formate is the Ammonium form of formic acid, which is widely used in a variety of organic reactions. Formic acid is an intermediate product of normal metabolism. |
| M11510 | DL-Propargylglycine | Dl-proparyngine (PAG) is an irreversible inhibitor of cysteine γ -lyase (GCL), a key enzyme involved in glutathione synthesis, regulation of homocysteine concentration and metabolism to sulfur pathway that mediates cysteine synthesis. |
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