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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 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
M7254 SB 215505 SB 215505 is a 5-HT 2B/2C antagonist.
M7253 SB 206553 hydrochloride SB 206553 hydrochloride is a potent, selective 5-HT 2C/5-HT 2B antagonist. Orally active.
M7251 SB 204741 SB 204741 is a potent, selective 5-HT 2B antagonist.
M7250 SB 204070 SB 204070 is a potent and selective 5-HT 4 antagonist.
M7247 SAR7334 dihydrochloride SAR7334 dihydrochloride is a novel, highly potent and bioavailable inhibitor of TRPC6 channels, inhibiting TRPC6 currents with IC50 of 7.9 nM.
M7245 Salsolinol-1-carboxylic acid Salsolinol-1-carboxylic acid is a endogenous amino acid.
M7243 SAG 21k SAG 21k is a hedgehog signaling activator; brain penetrant and orally bioavailable.
M7241 SA 57 SA 57 is a potent FAAH inhibitor.
M7240 SA 47 SA 47 is a selective FAAH inhibitor.
M7239 S4 S4 is a high affinity and selective CA IX and CA XII inhibitor.
M7238 S 32826 S 32826 is a potent autotaxin inhibitor.
M7236 S 18986 S 18986 is a positive allosteric modulator of AMPA.
M7235 Ryuvidine Ryuvidine is a sETD8 inhibitor; also CDK4 inhibitor.
M7233 RWJ 52353 RWJ 52353 is a α 2D agonist.
M7232 RWJ 50271 RWJ 50271 is a inhibitor of LFA-1/ICAM mediated cell adhesion.
M7231 RWJ 21757 RWJ 21757 is a toll-like receptor 7 (TLR7) agonist.
M7230 RuBi-4AP RuBi-4AP is a caged 4-aminopyridine; a non-selective K V channel blocker.
M7229 RU 58668 RU 58668 is a pure antiestrogen.
M7228 RU 28318, potassium salt RU 28318, potassium salt is a potent, selective mineralocorticoid receptor antagonist.
M7225 RS 56812 hydrochloride RS 56812 hydrochloride is a 5-HT 3 partial agonist.




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