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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
M42967	EBOV/MARV-IN-2	EBOV/MARV-IN-2 is an Ebolavirus (EBOV, IC50=0.9 μM) and Marburg virus (MARV, IC50=2.7 μM) inhibitor.
M42966	L-AP6	L-AP6 is a selective agonist for a quisqualate-sensitized site in hippocampal CA1 pyramidal neurons.
M42965	PAP-IN-1	PAP-IN-1 is an inhibitor of purple acid phosphatases (PAPs), a ubiquitous binuclear metallohydrolase.
M42964	MGAT2-IN-4	MGAT2-IN-4 is an inhibitor of monoacylglycerol transferase 2 (MGAT2), with liver metabolic stability.
M42963	A1AT modulator 1	A1AT modulator 1 is a potent inhibitor of Z ai-antitrypsin polymerisation with a pIC50 value of 8.3 .
M42962	Bipolal	Bipolal (KM 01) is a natural product isolated from the culture fluid of bipolar algae (Bipolaris sp.).
M42961	2-Quinizarincarboxylic acid	2-Quinizarincarboxylic acid is a glucose uptake inhibitor, with the inhibitory rate of 24.9% at 50 μM.
M42960	S07-1066	S07-1066 is an aldo-keto reductase 1C3 (AKR1C3) inhibitor, synergizing doxorubicin (DOX) cytotoxicity.
M42959	M351-110	M351-110 is a T-cell activating V-domain immunoglobulin inhibitory factor agonist for cancer research.
M42958	BMS-195270	BMS-195270 is a small molecule that inhibits Carbachol-evoked tonicity of isolated rat bladder strips.
M42957	Isoindigo	Isoindigo is the acceptor of donor-acceptor (D-A) conjugated polymer, as well as an Indigo series dye.
M42956	3-Fluoro-L-tyrosine	3-Fluoro-L-tyrosine is a tyrosine analogue, inhibits transamination by tyrosine aminotransferase (TAT).
M42955	L-Arginine butanoate	L-Arginine butanoate ((S)-(+)-Arginine butanoate) is a compound consisting of L-Arginine and butanoate.
M42954	Fosigotifator	Fosigotifator is modulates the integrated stress response (ISR) for inhibition of ISR-related diseases.
M42952	Squalene synthase-IN-1	Squalene synthase-IN-1 is a potent antihyperlipidemic agent acting through Squalene Synthase inhibition.
M42951	Dilaurylglycerosulfate sodium	Dilaurylglycerosulfate sodium is a co-emulsifier in the diagnostic test for the determination of lipase.
M42949	Methyl 2-acetoxybenzoate	Methyl 2-acetoxybenzoate (Methyl acetylsalicylate) is a safe and simple anti-inflammatory aspirin precursor.
M42948	α-Amylase-IN-4	α-Amylase-IN-4 show maximum inhibition of amylase activity with IC50 value 17.83 ± 0.14 μg/mL.
M42947	Fecosterol	Fecosterol is a metabolite of Saccharomyces cerevisiae and can be used in the research of phytosterolemia.
M42946	Viloxazine hydrochloride	Viloxazine hydrochloride is the inactive isomer of Viloxazine, and can be used as an experimental control.

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