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
M6890	Lalistat 2	Lalistat 2 is a selective LAL inhibitor. Lalistat 2 is an inhibitor of many lipases especially Lysosomal acid lipase (LAL, IC50 = 152 nM), which is a key enzyme that degrades neutral lipids at an acidic pH in lysosomes.
M6866	KL 001	KL 001 is a first-in-class cryptochrome protein (CRY) stabilizer that interacts specifically with CRY1 and CRY2 to prevent ubiquitin-dependent CRY degradation, thereby prolonging the circadian cycle. In addition, KL001 has the potential to control fasting hormone-induced gluconeogenesis.
M6857	JX 06	JX 06 is a potent and selective pyruvate dehydrogenase kinase (PDK) 1/2/3 inhibitor.
M6841	J-147	J 147 is a neuroprotective and neurotrophic compound; reduces Aβ40 and Aβ42 levels.
M6834	IPTG	IPTG is a used in cloning procedures with X-GAL.
M6830	INH1	INH1 is a hec1 inhibitor; causes arrest of mitosis.
M6814	IDE 1	IDE 1 is a induces definitive endoderm formation in mouse and human ESCs.
M6756	GN 44028	GN 44028 is a potent HIF-1α inhibitor.
M6747	GGsTop	GGsTop is a highly selective and irreversible inhibitor of γ-glutamyl transpeptidase (GGT), with a Ki of 170 μM for Human GGT.
M6740	G-36	G-36 is a selective GPER antagonist.
M6700	Eeyarestatin I	Eeyarestatin I is a potent endoplasmic reticulum-associated protein degradation (ERAD) and translocation inhibitor. Eeyarestatin I inhibits Sec61 translocon. Eeyarestatin I targets the p97-associated deubiquitinating process (PAD) and inhibits atx3-dependent deubiquitination.
M6692	DSP-4 hydrochloride	DSP-4 hydrochloride is a highly and selective adrenergic neurotoxin. DSP-4 hydrochloride can cross the blood brain barrier.
M6672	DIM-C-pPhOCH3	DIM-C-pPhOCH3 is an agonist of the orphan receptor nuclear receptor related protein 77 (Nur77).
M6656	DCA	DCA (Sodium dichloroacetate) is a mitochondrial pyruvate dehydrogenase kinase (PDK) inhibitor.
M6648	Cytosporone B	Cytosporone B is a high affinity nuclear receptor Nur77 agonist (IC50 = 0.278 nM).
M6628	CP 809101 hydrochloride	CP 809101 hydrochloride is a potent and selective 5-HT _2C agonist.
M6623	CORM 2	CORM 2 is a carbon monoxide-releasing molecule.
M6609	CITCO	CITCO is a selective Constitutive androstane receptor (CAR) agonist. CITCO inhibits growth and expansion of brain tumour stem cells (BTSCs) and has an EC50 of 49 nM over pregnane X receptor (PXR).
M6601	CID 5951923	CID 5951923 is a krüppel-like factor 5 (KLF5) inhibitor.
M6593	CHES	CHES is a buffering agent.

By Signaling Pathways

By Product Type

Signaling Pathways

Others Others

Get to Know Us

Customer Support

Resources

Contact Us