JTC-801 is a selective opioid receptor-like1 (ORL1) receptor antagonist with IC50 of 94 nM, and weakly inhibits receptors δ, κ, and μ.

Juglone significantly inhibits the proliferation and induce the apoptosis of SiHa cells and Caski cells, stimulates suicidal erythrocyte death or eryptosis at least in part by upregulation of ceramide abundance, energy depletion and activation of PKC, and prevents high-fat diet-induced liver injury and nerve inflammation in mice through inhibition of inflammatory cytokine secretion, NF-kappa B […]

Juglone significantly inhibits the proliferation and induce the apoptosis of SiHa cells and Caski cells, stimulates suicidal erythrocyte death or eryptosis at least in part by upregulation of ceramide abundance, energy depletion and activation of PKC, and prevents high-fat diet-induced liver injury and nerve inflammation in mice through inhibition of inflammatory cytokine secretion, NF-kappa B […]

Junipediol A is a natural product isolated and purified from the leaves of Peucedanum japonicum Thunb..

Junipediol A is a natural product isolated and purified from the leaves of Peucedanum japonicum Thunb..

JX06 is a selective covalent PDK1 inhibitor with IC50 values of 49, 101 and 313nM for PDK-1, PDK-2 and PDK-3, respectively.

JX06 is a selective covalent PDK1 inhibitor with IC50 values of 49, 101 and 313nM for PDK-1, PDK-2 and PDK-3, respectively.

JX06 is a selective covalent PDK1 inhibitor with IC50 values of 49, 101 and 313nM for PDK-1, PDK-2 and PDK-3, respectively.

JX06 is a selective covalent PDK1 inhibitor with IC50 values of 49, 101 and 313nM for PDK-1, PDK-2 and PDK-3, respectively.

JX06 is a selective covalent PDK1 inhibitor with IC50 values of 49, 101 and 313nM for PDK-1, PDK-2 and PDK-3, respectively.

K-604 dihydrochloride is a potent and selective acyl-CoA:cholesterol acyltransferase 1 (ACAT-1) inhibitor with an IC50 of 0.45±0.06 μM.

K-604 dihydrochloride is a potent and selective acyl-CoA:cholesterol acyltransferase 1 (ACAT-1) inhibitor with an IC50 of 0.45±0.06 μM.

K-Ras(G12C) inhibitor 6 is an allosteric, and selective inhibitor of oncogenic K-Ras (G12C).

K-Ras(G12C) inhibitor 6 is an allosteric, and selective inhibitor of oncogenic K-Ras (G12C).

K-Ras(G12C) inhibitor 6 is an allosteric, and selective inhibitor of oncogenic K-Ras (G12C).

K-Ras(G12C) inhibitor 6 is an allosteric, and selective inhibitor of oncogenic K-Ras (G12C).

K-Ras(G12C) inhibitor 6 is an allosteric, and selective inhibitor of oncogenic K-Ras (G12C).

K-Ras(G12C) inhibitor 6 is an allosteric, and selective inhibitor of oncogenic K-Ras (G12C).

Kaempferol 3-O-arabinoside is a natural product isolated and purified from the roots of Ligusticum jeholense Nakai et Kitag displaying cytotoxic and high antioxidant activity.

Kaempferol 3,7,4′-trimethylether is a natural product isolated and purified from the rhizomes of Curcuma aromatica, shows selective cyctoxic activities against the nine tested cancer cell lines.

Kaempferol 3,7,4′-trimethylether is a natural product isolated and purified from the rhizomes of Curcuma aromatica, shows selective cyctoxic activities against the nine tested cancer cell lines.

Kaempferol 7-O-rhamnoside is a natural product isolated and purified from the herbs of Maytenus hookeri.

Kaempferol 7-O-rhamnoside is a natural product isolated and purified from the herbs of Maytenus hookeri.

Kaempferol tetraacetate, a natural product isolated and purified from the herbs of Cudrania tricuspidata, exhibits significant cytotoxicity in vitro against three human cell lines HL-60, U937 and SK-MEL-1, and is a potent antiplatelet agent.

Kaempferol-3-O-β-d-galactoside is a natural product isolated and purified from the aerial part of Calluna vulgaris L with antioxidant, anti-inflammatory and antinociceptive activities.

Kaempferol-7-O-D-glucopyranoside is a natural product isolated and purified from the herbs of Hosta plantaginea with antiinflammatory activity.

Kaempferol-7-O-D-glucopyranoside is a natural product isolated and purified from the herbs of Hosta plantaginea with antiinflammatory activity.

Kaerophyllin, a natural product isolated and purified from the roots of Bupleurum chinense DC., protects the rat liver from TAA-caused injury and fibrogenesis by suppressing hepatic inflammation and inhibiting HSC activation, possibly through upregulation of PPAR-γ expression, and inhibits AB-induced LX-2 activation and migration with downregulation of Akt/ERK phosphorylations and NF-κB activity.

Kaerophyllin, a natural product isolated and purified from the roots of Bupleurum chinense DC., protects the rat liver from TAA-caused injury and fibrogenesis by suppressing hepatic inflammation and inhibiting HSC activation, possibly through upregulation of PPAR-γ expression, and inhibits AB-induced LX-2 activation and migration with downregulation of Akt/ERK phosphorylations and NF-κB activity.

Kalii dehydrographolidi succinas is an immune system drug that can be used in viral upper respiratory infection.