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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
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.
M57037	MK-6240	MK-6240 is a tau positron emission tomography (PET) tracer for neurofibrillary tangles (NFTs), exhibiting high specificity and selectivity for binding to NFTs.
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.
M57032	GLPG0259	GLPG0259 is a ATP-competitive inhibitor of MAPK-activated protein kinase 5 (MK5) with oral activity.
M57031	3BrB-PP1	3BrB-PP1 is an ATP-competitive analog.
M57030	Kebuzone	Kebuzone is a non-steroidal anti-inflammatory substance that may be studied in inflammatory diseases such as thrombophlebitis and rheumatoid arthritis.
M57029	Pamabrom	Pamabron is a common over-the-counter diuretic used for relief of menstrual-associated symptoms.
M57028	SBP-3264	SBP-3264 is a valuable chemical probe for understanding the roles of STK3 and STK4 in acute myeloid leukemia (AML).
M57027	CGS35066	CGS35066 is a potent and selective aminophosphonate inhibitor of endothelin-converting enzyme-1 (ECE-1).
M57026	BTB09089	BTB09089 is a T cell death-associated gene 8 (TDAG8/GPR65) specific agonist.

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