| 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. |
| M43061 | HCAR2 agonist 1 | HCAR2 agonist 1 is a Gi protein-biased allosteric modulator of HCAR2. |
| M43060 | CD33 splicing modulator 1 hydrochloride | CD33 splicing modulator 1 hydrochloride is a CD33 splicing modulator. |
| M43059 | ELOVL6-IN-3 | ELOVL6-IN-1 is a potent, orally active and selective ELOVL6 inhibitor. |
| M43058 | Licostinel | Licostinel (ACEA-1021) is a glycine receptor antagonist (IC50: 59 nM). |
| M43057 | hCES2A-IN-1 | hCES2A-IN-1 is a potent hCES2A inhibitor, with an IC50 value of 1.6 nM. |
| M43056 | Kallikrein 5-IN-2 | Kallikrein 5-IN-2 is a selective Kallikrein KLK5 inhibitor (pIC50=7.1). |
| M43055 | Pandamine | Pandamine is a natural alkaloid that can be extracted from Panda oleosa. |
| M43053 | hCES2-IN-1 | hCES2-IN-1 is a reversible and selective hCES2 inhibitor (IC50: 6.72 μM). |
| M43052 | Dimiracetam | Dimiracetam is an orally active compound, with anti-neuropathic activity. |
| M43051 | Abefolastat tesaroxetan | Abefolastat tesaroxetan (SarbisPSMA) is a bivalent sarcophagine conjugate. |
| M43050 | N-Acetylsulfanilamide | N-Acetylsulfanilamide is a compound with potential anti-infective activity. |
| M43049 | BLK degrader 1 | BLK degrader 1 is a selective degrader of B-lymphoid tyrosine kinase (BLK). |
| M43048 | E235 | E235 is an expression regulator of activates transcription factor 4 (ATF4). |
| M43047 | PRDX1-IN-1 | PRDX1-IN-1 is a selective inhibtor of PRDX1 with an IC50 value of 0.164 μM. |
| M43046 | RASP-IN-1 | RASP-IN-1 is a lipophili ccompound used for macular degeneration inhibition. |
| M43045 | Tibric acid | Tibric acid (CP 18524) has similar effects to those of hypolipidemic agents. |
| M43044 | 21-Desacetyldeflazacort | 21-Desacetyldeflazacort (21-desDFZ) is the active metabolite of Deflazacort. |
| M43043 | Clibucaine | Clibucaine is a piperidine derivative possessing local anesthetic properties. |
| M43042 | IA1-8H2 | IA1-8H2 is a non-covalent, non-competitive inhibitor of PHPT1 (IC50: 3.4 μM). |
| M43041 | NCP2 Anchor | NCP2 Anchor can be used in the synthesis of exon jumping oligomer conjugates. |
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