Others Others

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
M9614	SB-204990	SB-204990 is a potent and specific ATP citrate-lyase inhibitor.
M9599	NB-598	NB-598 is a potent competitive inhibitor of squalene epoxidase (SE).
M9594	EDC.HCl Crosslinker	EDC.HCl Crosslinker is a zero-length crosslinker that can be used to conjugate carboxyl functional groups to primary amines.
M9593	Iminodiacetic acid	Iminodiacetic acid is a bovine liver glutamate dehydrogenase inhibitor.
M9591	D-(+)-Trehalose Anhydrous	D-(+)-Trehalose is used as a food ingredient and pharmaceutical excipient.
M9583	Dansylsarcosine piperidinium salt	Dansylsarcosine piperidinium salt
M9582	Tris Dodecyl Sulfate	Tris Dodecyl Sulfate
M9579	XMD-17-51	XMD-17-51 is a potent and selective NUAK1 inhibitor.
M9574	Ginkgetin	Ginkgetin is a natural biflavonoid isolated from leaves of Ginkgo biloba L. with effects of anti-inflammation and anticancer activity. Ginkgetin is also a potent inhibitor of Wnt signaling, with an IC50 of 5.92 μΜ.
M9571	API-1	API-1 is a Pin1 inhibitor with an IC50 of 72.3 nM. API-1 directly and specifically binds to the Pin1 peptidyl-prolyl isomerase (PPIase) domain and potently inhibits Pin1 cis-trans isomerizing activity.
M9568	SC-26196	SC-26196 is a potent, orally active D6D inhibitor (IC50 = 0.2 µM in a rat liver microsomal assay) that completely blocks the conversion of linoleic acid to arachidonic acid (AA).
M9567	Leptin (116-130) mouse	Leptin (116-130) mouse is a synthetic leptin peptide fragment.
M9563	2,1,3-Benzothiadiazole-5-carbaldehyde	2,1,3-Benzothiadiazole-5-carbaldehyde
M9560	Paquinimod	Paquinimod is a S100A9 inhibitor preventing S100A9 binding to TLR-4.
M9557	BAY-1816032	BAY-1816032 is a potent and oral available BUB1 (budding uninhibited by benzimidazoles 1) kinase inhibitor with an IC50 of 7 nM.
M9543	Dextran (Mw 40000)	Dextran (Dextran 40000) has an inhibitory effect on thrombocyte aggregation.
M9531	NADP disodium salt	NADP disodium salt is a participant coenzyme in aerobic and anaerobic oxidations.
M9523	PEG6000	PEG6000 is a neutral and biocompatible hydrophilic polymer.
M9517	Sodium hippurate	Hippuric acid is a low molecular weight phenolic carboxylic acid urinary metabolite that may be a useful urinary biomarker for certain cancers such as gastric cancer and oxidative stress.
M9511	DO264	DO264 is a potent selective, and in vivo active ABHD12 inhibitor, with an IC50 of 11 nM.

By Signaling Pathways

By Product Type

Signaling Pathways

Others Others

Get to Know Us

Customer Support

Resources

Contact Us