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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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