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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
M42988	LK-44	hCES2A-IN-2 is an orally active human carboxylesterase 2 (hCES2A) inhibitor (IC50: 5.02 μM).
M42986	IZS-M	IZS-M is an amino acid-derived corrosion inhibitor, based on the green chemistry principles.
M42985	IZS-P	IZS-P is an amino acid-derived corrosion inhibitor, based on the green chemistry principles.
M42984	SYNTi	SYNTi is a PDZ domain inhibitor targeting the syndecan/syntenin protein-protein Interaction.
M42983	Mofebutazone	Mofebutazone, a monophenyl analogue of Phenylbutazone (DPB), is an anti-inflammatory compound.
M42982	Vamagloxistat	Vamagloxistat is glycolate oxidase inhibitor, used to inhibit hyperoxaluria and kidney stones.
M42981	MSN8C	MSN8C, an analog of mansonone E, is a novel catalytic inhibitor of human DNA topoisomerase II.
M42980	LJP 1586	LJP 1586 is an amine-based inhibitor of semicarbazide-sensitive amine oxidase (SSAO) activity.
M42979	Atilotrelvir	Atilotrelvir is antiviral agent, can inhibit coronavirus, picornavirus and norovirus infection.
M42978	RS5517	RS5517 is a specific PDZ1-domain antagonist of NHERF1 that prevented its ectopic nuclear entry.
M42977	Mip-IN-1	Mip-IN-1（S,S-28i）is a new rapamycin-derived macrophage infectivity potentiator (Mip) inhibitor.
M42976	Azure C	Azure C is the product of sequential enzymatic oxidation of Methylene blue (MB) or Azure B (AB).
M42975	Vacquinol-1 dihydrochloride	Vacquinol-1 (NSC13316) dihydrochloride is a MKK4-specific activator that activates MAPK pathways.
M42974	Benzyl DC-81	Benzyl DC-81 is an anticancer agent with antiproliferative activity against A375 and MCF-7 cells.
M42973	SN-38-CO-DMEDA TFA	SN-38-CO-DMEDA TFA is the intermediate product for synthesizing antibody-conjugated drug LND1035.
M42972	Azimsulfuron	Azimsulfuron (DPX-A8947) is a sulfonylurea herbicide useful in controlling weeds in paddy fields.
M42971	GPAT-IN-1	GPAT-IN-1 is a glycerol-3-phosphate acyltransferase (GPAT) inhibitor with an IC50 value of 8.9 μM.
M42970	AC-099	AC-099 is a selective NPFF2R full agonist (EC50=1189 nM) and NPFF1R partial agonist (EC50=2370 nM).
M42969	3-Acetylphenyl acetate	3-Acetylphenyl acetate (Tetramethyl thiol alcynic acid) can be used as pharmaceutical intermediates.
M42968	rTRD01	rTRD01 is a TDP-43 ligand that binds to TDP-43’s RRM1 and RRM2 domains (Kd=89 uM for TDP-43102–269).

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