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Cat.No.	Name	Information
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
M7791	Exo-1	Exo1 is a reversible inhibitor of exocytosis, also a Golgi ARF 1 (ADP-Ribosylation Factor) GTPase activator.
M57054	ML179	ML179 (SR-1309) is a inverse LRH1 (Liver receptor homologue-1) agonist with IC50 of 320 nM.
M57053	HOPan	HoPan inhibits phosphopantotenoylcysteine synthetase activity.
M57052	IND24	IND24 is a potent antiprion agent with an EC50 value of 1.27 µM.
M57051	MKI-1	MKI-1, an inhibitor of MASTL (microtubule-associated serine/threonine kinase-like) with an IC50 of 9.9 μM, exerts antitumor and radiosensitizer activities through PP2A activation in breast cancer.
M57050	CIL62	CIL62 is a caspase-3/7-independent cell death inducer.
M57049	ML095	ML095 is a biochemical inhibitor of PLAP.
M57048	Valnivudine hydrochloride	FV-100 is a potent, selective and orally active anti-varicella zoster virus agent.
M57047	GPi688	GPi688 is a potent and orally active glycogen phosphorylase (GPa) inhibitor with IC50s of 19 nM, 61 nM and 12 nM for human liver GPa, rat liver GPa and human skeletal muscle GPa, respectively.
M57046	DL-AP4	DL-AP4 (2-Amino-4-phosphonobutyric acid) is a glutamate antagonist.
M57045	HPA-12	HPA-12 is an intracellular ceramide transport protein inhibitor.
M57044	ZY-444	ZY-444 is a small molecule that suppresses breast cancer progression by targeting pyruvate carboxylase.
M57043	SBI-477	SBI-477 is a chemical probe stimulated insulin signaling by deactivating the transcription factor MondoA, leading to reduced expression of the insulin pathway suppressors thioredoxin-interacting protein (TXNIP) and arrestin domain–containing 4 (ARRDC4).
M57041	AA41612	AA41612 is a potent antagonist of melanopsin-mediated phototransduction.
M57040	UNC7467	UNC7467 is a potent IP6K inhibitor with values of 4.9, 8.9 and 1320 nM for IP6K2, IP6K1 and IP6K6, respectively.
M57039	BLU2864	BLU2864 is an orally active, highly selective, ATP-competitive PRKACA inhibitor (IC50=0.3 nM).
M57038	BAY-069	BAY-069 is a potent branched-chain amino acid transaminases 1 (BCAT1) and BCAT2 inhibitor with IC50 values of 31 nM and 153 nM, respectively.
M57036	LY88074	LY88074 is a Raloxifene analog lacking the basic side chain.
M57035	GSK-114	GSK-114 is a highly selective, orally active TNNI3K inhibitor (IC50= 25 nM).
M57034	RuBiNic	RuBiNic is a cage compound based on the photochemistry of Ru-bpy complexes and releases nicotine by irradiation with visible light up to 532 nm.
M57033	HSR6071	HSR6071, a pyrazinecarboxamide derivative, is an orally active and potent antiallergic agent.

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