Cat.No. | Name | Information |
---|---|---|
M2206 | TH-302 (Evofosfamide) | TH-302 is a highly potent and selective hypoxia-activated procompound targeting hypoxic regions of solid tumors with IC50 of 19 nM. |
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 prevent 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. |
M9331 | 10-Hydroxy-trans-2-decenoic acid | 10-hydroxy-2-decenoic acid (10-H2DA) is the principal lipid component in royal jelly which is the food for queen and larvae honeybees. |
M11288 | NCGC00229600 | NCGC00229600 is an allosteric reverse agonist of TSHR. NCGC00229600 inhibits TSH and stimulates antibody activation of internally expressed TSHRs in Graves' disease. |
M11285 | HWL-088 | Hwl-088 is a highly effective, orally active free fatty acid receptor 1 (FFA1/GPR40) agonist (EC50 18.9 nM) with moderate PPARδ activity (EC50 570.9 nM). Hwl-088 improves glucose and lipid metabolism. |
M11284 | Cetaben | Cetaben is a PPARα -independent peroxisome proliferator that can effectively reduce cholesterol and triglyceride concentrations. |
M11279 | GNE-6468 | Gne-6468 is a potent and selective RORγ (RORc) reverse agonist with an EC50 value of 2 nM. Gne-6468 inhibited IL-17 in PBMC with EC50 value of 30 nM. |
M11276 | SCO-267 | SCO-267 is a full agonist of the GPCR GPR40, whose activation stimulates secretions of insulin and incretin. |
M11275 | PSB-12379 | Psb-12379 is a nucleotide analogue and a potent ECTO-5 '-nucleotidase (CD73) inhibitor with Kis values of 9.03 nM (rat) and 2.21 nM (human). |
M11274 | Lufenuron | Lufenuron is a bioactive chemical. |
M11273 | UNC5293 | UNC5293 is a potent and selective inhibitor of MERTK (Ki=190 pM). UNC5293 inhibits MERTK (IC50=0.9 nM) and is more selective for Axl, Tyro3 and Flt3. UNC5293 showed excellent pharmacokinetic properties in mice. |
M11185 | 3-Deazaadenosine hydrochloride | 3-deazaadenosine HCl (3-DZA, c3Ado) is an effective s-adenosylhomocysteine hydrolase inhibitor with Ki value of 3.9 μM. 3-deazaadenosine HCl inhibits the transcription of TNF-α and IL-1β induced by bacterial liposolysaccharide. 3-deazaadenosine HCl inhibits NF-κB transcriptional activity, prevents CARBOxyl methylation of Ras induced by FCS, and reduces ERK1/2 and Akt phosphorylation induced by FCS. |
M11174 | Mefentrifluconazole | Mefentrifluconazole, a new azole derivative, is a broad-spectrum antifungal agent. Mefentrifluconazole is a highly selective and orally active fungal CYP51 inhibitor (Kd= 0.5 nM). |
M11173 | PC945 | PC945 is a potent antifungal triazole drug that is resistant to a variety of sensitive and resistant strains of Aspergillus fumigatus. PC945 is a potent, tightly bound inhibitor of aspergilloxine 14α-demethylase (CYP51A/CYP51B) activity.IC50s are 0.23 μM and 0.22 μM, respectively. |
M11138 | 7beta-Hydroxybufalin | 7beta-Hydroxybufalin is a natural product. |
M11135 | DELPHINIDIN-3-O-GALACTOSIDE | Delphinidin-3-O-galactoside chloride has anti-obesity and hypolipidemic effects. Delphinidin-3-O-galactoside (D3G) is a water-soluble anthocyanin with antioxidant activity. D3G is capable of masking the EGCG-induced cytotoxicity and ER stress, presumably through up-regulation of antioxidant enzymes and heat shock proteins. |
M11132 | Cyclanoline | Cyclanoline has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor and a plant metabolite. |
M11123 | Brevicornin | Brevicornin is a flavonol compound isolated from Epimedium. |
M11121 | Dehydrobufotenine | |
M11112 | Tarasaponin IV | Tarasaponin IV is a zymbrane-type triterpene saponin isolated from the bark of the tree. Tarasaponin IV can be used in cancer research. |
M11054 | Norgestrel | Norgestrel, a synthetic analogue of progesterone, is a powerful neuroprotective antioxidant that prevents photoinduced ROS production and cell death in photosensitive cells. |
M11049 | Neriifolin | Neriifolin, a cardiac glycoside that penetrates the central nervous system, is a typeNa, K-ATPase++ of inhibitors. Neriifolin targets beclin 1, inhibits the formation of LC3-associated phagosomes, and improves the development of experimental autoimmune encephalomyelitis (EAE). |
M11046 | Bixin | Bixin (BX) annatoxin isolated from the seeds of Bixa Orellana, a carotenoid with anti-inflammatory, anti-tumor and antioxidant activities. |
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