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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 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
M9662 2-(4-Methylpiperazin-1-yl)pyrimidine 2-(4-Methylpiperazin-1-yl)pyrimidine
M9661 MF-438 MF-438 is a potent and orally bioavailable stearoyl-CoA desaturase 1 (SCD1) inhibitor with an EC50 of 2.3 nM for rSCD1.
M9599 NB-598 NB-598 is a potent competitive inhibitor of squalene epoxidase (SE).
M9594 EDC.HCl Crosslinker EDC.HCl Crosslinker is a zero-length crosslinker that can be used to conjugate carboxyl functional groups to primary amines.
M9593 Iminodiacetic acid Iminodiacetic acid is a bovine liver glutamate dehydrogenase inhibitor.
M9591 D-(+)-Trehalose Anhydrous D-(+)-Trehalose is used as a food ingredient and pharmaceutical excipient.
M9583 Dansylsarcosine piperidinium salt Dansylsarcosine piperidinium salt is a chemical compound utilized in biochemical research, holds a pivotal position in the study of NMDA receptors. Owing to its proficiency in fluorescence detection of glutamate or glycine binding sites on these receptors, it may have the potential to augment the therapeutic treatment of prevalent neurological disorders such as Alzheimer's and Parkinson's.
M9582 Tris Dodecyl Sulfate Tris Dodecyl Sulfate
M9579 XMD-17-51 XMD-17-51 is a potent and selective NUAK1 inhibitor.
M9574 Ginkgetin Ginkgetin is a natural biflavonoid isolated from leaves of Ginkgo biloba L. with effects of anti-inflammation and anticancer activity. Ginkgetin is also a potent inhibitor of Wnt signaling, with an IC50 of 5.92 μΜ.
M9571 API-1 API-1 is a Pin1 inhibitor with an IC50 of 72.3 nM. API-1 directly and specifically binds to the Pin1 peptidyl-prolyl isomerase (PPIase) domain and potently inhibits Pin1 cis-trans isomerizing activity.
M9568 SC-26196 SC-26196 is a potent, orally active D6D inhibitor (IC50 = 0.2 µM in a rat liver microsomal assay) that completely blocks the conversion of linoleic acid to arachidonic acid (AA).
M9567 Leptin (116-130) mouse Leptin (116-130) mouse is a synthetic leptin peptide fragment.
M9563 2,1,3-Benzothiadiazole-5-carbaldehyde 2,1,3-Benzothiadiazole-5-carbaldehyde
M9560 Paquinimod Paquinimod is a S100A9 inhibitor preventing S100A9 binding to TLR-4.
M9557 BAY-1816032 BAY-1816032 is a potent and oral available BUB1 (budding uninhibited by benzimidazoles 1) kinase inhibitor with an IC50 of 7 nM.
M9543 Dextran (Mw 40000) Dextran (Dextran 40000) has an inhibitory effect on thrombocyte aggregation.
M9531 NADP disodium salt NADP disodium salt is a participant coenzyme in aerobic and anaerobic oxidations.
M9517 Sodium hippurate Hippuric acid is a low molecular weight phenolic carboxylic acid urinary metabolite that may be a useful urinary biomarker for certain cancers such as gastric cancer and oxidative stress.
M9511 DO264 DO264 is a potent selective, and in vivo active ABHD12 inhibitor, with an IC50 of 11 nM.




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