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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
M7829	6β-Hydroxytestosterone	6β-Hydroxytestosterone is a CYP3A4 metabolite; androgenic.
M7820	GW8510	GW8510 is an inhibitor of cyclin kinase 2 (CDK2).
M7804	5-Fluoro-2′-deoxycytidine	5-Fluoro-2′-deoxycytidine is a mechanism based DNMT (DNA cytosine-5 methyltransferase) inhibitor, that forms a covalent link with the cysteine residue in the active site of DNMT.
M7802	Fadrozole hydrochloride	Fadrozole is a nonsteroidal aromatase inhibitor.
M7773	dPPA	Selective activator of PKC beta.
M7761	Diacylglycerol Kinase Inhibitor II	Diacylglycerol kinase inhibitor.
M7746	Dexrazoxane	Dexrazoxane (ICRF-187, ADR-529, DXZ) is an iron chelator that can be used to prevent DOX-induced cardiotoxicity.
M7741	DNQX	DNQX is a competitive kainate, quisqualate (non-NMDA) glutamate receptor antagonist.
M7720	Caerulomycin A	Caerulomycins produced by Streptomyces caeruleus are bipyridinic molecules endowed with antibiotic properties.
M7696	Choline bitartrate	Acyl group acceptor.
M7643	Bongkrekic acid solution	An antiapoptotic agent, it protects against NMDA receptor induced neuronal apoptosis, extends cell survival in cells undergoing apoptosis following infection with viral vectors and abrogates apoptosis induced by hydrogen peroxide in T-cells.
M7639	BF-170 hydrochloride	BF-170 is a new probe for neurofibrillary tangles (tau fibrils).
M7610	Ancitabine hydrochloride	Antineoplastic.
M7598	Amifostine trihydrate	Amifostine trihydrate is a broad-spectrum cytoprotection agent against the DNA damaging effects of ionizing radiation.
M7596	4′-Aminomethyltrioxsalen hydrochloride	4′-Aminomethyltrioxsalen hydrochloride is used to inactivate DNA and RNA viruses, including HIV-1, by nucleic acid cross-linking followed by UV irradiation.
M7580	GJ103 sodium salt	GJ103 sodium salt is an active analog of the read-through compound GJ072.
M7577	ML-7 hydrochloride	ML-7 hydrochloride is a naphthalene sulphonamide derivative, potently inhibits MLCK (IC50=300 nM) and TRPC6 channel (IC50>10 μM).
M7571	PCI-27483	PCI-27483 is a FVIIa/tissue factor inhibitor, with antitumour effects.
M7564	PF-06282999	PF-06282999 is a potent and selective myeloperoxidase inhibitor which is potential useful for the treatment of cardiovascular diseases.
M7556	G007-LK	G007-LK is a potent and selective inhibitor of TNKS1 and TNKS2, with IC50s of 46 nM and 25 nM, respectively.

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