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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
M56597	GCPII-IN-1 TFA	GCPII-IN-1 TFA is a glutamate carboxypeptidase II (GCPII, or PSMA) inhibitor scaffold with a Ki of 44.3 nM.
M56596	Carboxylesterase-IN-2	Carboxylesterase-IN-2 is a potent inhibitor of Carboxylesterase Notum with an IC50 less than or equal to 10 nM.
M56590	GlyRS-IN-1	GlyRS-IN-1 is a glycyl-tRNA synthase (GlyRS) inhibitor.
M56583	UT-B-IN-1	UT-B-IN-1 (UTBINH-14) is a reversible, competitive and selective urea transporter-B (UT-B) inhibitor with IC50 values of 10 and 25 nM for human and mouse UT-B, respectively.
M56519	Benzamil	Benzamil (Benzylamiloride), an Amiloride analogue, is a Na+/Ca2+ exchanger (NCX) inhibitor (IC50~100 nM).
M56466	CRAC intermediate 2	CRAC intermediate 2 is a intermediate compound for CRAC inhibitor synthesis.
M56464	RO2959 monohydrochloride	RO2959 monohydrochloride is a potent and selective CRAC channel inhibitor with an IC50 of 402 nM.
M56460	Encecalinol	Encecalinol, extracted from aerial parts of Ageratina grandifolia, is a potent inhibitor of calmodulin inhibitor.
M56459	Beauverolide Ja	Beauverolide Ja, a cyclotetradepsipeptide, is a potent calmodulin (CaM) inhibitor with a Kd of 0.078 μM and a Ki of 0.39 μM for Ca2+-CaM.
M56439	MLKL-IN-2	MLKL-IN-2 is a MLKL inhibitor.
M56391	KF38789	KF38789 is a selective inhibitor of P-selectin-PSGL-1 binding.
M56386	PSB-06126	PSB-06126 is a selective nucleoside triphosphate diphosphohydrolase (NTPDase) inhibitor, with the Ki values of 0.33 μM for rat NTPDase 1, 19.1 μM for NTPDase 2 and 2.22 μM for NTPDase 3, respectively.
M56355	FEN1-IN-4	FEN1-IN-4 is a human flap endonuclease-1 (hFEN1) inhibitor.
M56342	MethADP disodium	MethADP disodium is a specific CD73 inhibitor.
M56341	MethADP sodium	MethADP (sodium salt) (Adenosine 5'-(α,β-methylene)diphosphate (sodium)) is a specific CD73 inhibitor.
M56336	15(S)-HPETE	15(S)-HPETE is a monohydroperoxy polyunsaturated fatty acid (PUFA) produced by the action of 15-lipoxygenase (15-LO) on arachidonic acid.
M56334	SB-706375	SB-706375 is an antagonist of the Urotensin II (UII) receptor.
M56279	EM574	EM574 is a potent motilin receptor agonist in the human gastric antrum and rabbit gastrointestinal tract in vitro.
M56257	GW-803430	GW-803430 (GW-3430) is a potent and selective melanin-concentrating hormone receptor 1 (MCH R1) antagonist with a pIC50 of 9.3.
M56192	BAY-27-9955	BAY-27-9955 is an orally active non-peptide glucagon receptor antagonist.

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