(+)-Viroallosecurinine is a natural alkaloid with antibacterial activity. It exhibits a MIC of 0.48 μg/mL for Ps. Aeruginosa and Staph. aureus.

(+)-Viroallosecurinine is a natural alkaloid with antibacterial activity. It exhibits a MIC of 0.48 μg/mL for Ps. Aeruginosa and Staph. aureus.

(+)-Viroallosecurinine is a natural alkaloid with antibacterial activity. It exhibits a MIC of 0.48 μg/mL for Ps. Aeruginosa and Staph. aureus.

(+)-Viroallosecurinine is a natural alkaloid with antibacterial activity. It exhibits a MIC of 0.48 μg/mL for Ps. Aeruginosa and Staph. aureus.

(+)-Viroallosecurinine is a natural alkaloid with antibacterial activity. It exhibits a MIC of 0.48 μg/mL for Ps. Aeruginosa and Staph. aureus.

(+)-Wikstromol is a useful organic compound for research related to life sciences and the catalog number is T130443.

(+)-Xylariamide A is a probe used for mycobacterial and fungal carbonic anhydrase.

(+)-δ-Cadinene is a sesquiterpene from G. hirsutum with antibacterial, insecticidal, anticancer and antiproliferative activities. It showed a MIC value of 31.25 μg/ml against S. pneumoniae and LC50s values of 8.23, 9. 2 and 3 against third instar larvae of A. stephensi, A. aegypti and C. quinquefasciatust, respectively.(+)-δ-Cadinene (10, 50 and 100 μM) induced apoptosis and […]

(+)-δ-Cadinene is a sesquiterpene from G. hirsutum with antibacterial, insecticidal, anticancer and antiproliferative activities. It showed a MIC value of 31.25 μg/ml against S. pneumoniae and LC50s values of 8.23, 9. 2 and 3 against third instar larvae of A. stephensi, A. aegypti and C. quinquefasciatust, respectively.(+)-δ-Cadinene (10, 50 and 100 μM) induced apoptosis and […]

(+)-δ-Cadinene is a sesquiterpene from G. hirsutum with antibacterial, insecticidal, anticancer and antiproliferative activities. It showed a MIC value of 31.25 μg/ml against S. pneumoniae and LC50s values of 8.23, 9. 2 and 3 against third instar larvae of A. stephensi, A. aegypti and C. quinquefasciatust, respectively.(+)-δ-Cadinene (10, 50 and 100 μM) induced apoptosis and […]

(+/-)- Adomeglivant, also known as LY2409021, is a potent and selective glucagon receptor antagonist. LY2409021 lowers blood glucose in healthy people and in those with type 2 diabetes. Blockade of glucagon signalling in patients with type 2 diabetes is well tolerated and results in substantial reduction of fasting and postprandial glucose with minimal hypoglycaemia, but […]

(+/-)- Adomeglivant, also known as LY2409021, is a potent and selective glucagon receptor antagonist. LY2409021 lowers blood glucose in healthy people and in those with type 2 diabetes. Blockade of glucagon signalling in patients with type 2 diabetes is well tolerated and results in substantial reduction of fasting and postprandial glucose with minimal hypoglycaemia, but […]

(+/-)- Adomeglivant, also known as LY2409021, is a potent and selective glucagon receptor antagonist. LY2409021 lowers blood glucose in healthy people and in those with type 2 diabetes. Blockade of glucagon signalling in patients with type 2 diabetes is well tolerated and results in substantial reduction of fasting and postprandial glucose with minimal hypoglycaemia, but […]

(+/-)-Homoproline is a GABA-uptake inhibitor derived from proline.

(+/-)-Homoproline is a GABA-uptake inhibitor derived from proline.

(+/-)-Homoproline is a GABA-uptake inhibitor derived from proline.

(+/-)-Homoproline hydrochloride is a GABA-uptake inhibitor derived from proline.

(+/-)-Homoproline hydrochloride is a GABA-uptake inhibitor derived from proline.

(+/-)-Homoproline hydrochloride is a GABA-uptake inhibitor derived from proline.

(+/-)-Longamide is a marine derived natural products found in Sponge Homaxinella sp.

(+/-)-Longamide is a marine derived natural products found in Sponge Homaxinella sp.

(+/-)-Longamide is a marine derived natural products found in Sponge Homaxinella sp.

(+/-)-Longamide is a marine derived natural products found in Sponge Homaxinella sp.

(+/-)-Longamide is a marine derived natural products found in Sponge Homaxinella sp.

(+/-)-Longamide is a marine derived natural products found in Sponge Homaxinella sp.

(+/-)-Longamide is a marine derived natural products found in Sponge Homaxinella sp.

(+/-)-Lunacridine is a bioactive chemical.

(+/-)-Lunacridine is a bioactive chemical.

Marmesin is a novel angiogenesis inhibitor.

Marmesin is a novel angiogenesis inhibitor.

Marmesin is a novel angiogenesis inhibitor.

(+/-)-Pinocembrin, a natural product from axillary pines, is a GPR120 ligand that promotes wound healing in the HaCaT cell line.

(+/-)-Pinocembrin, a natural product from axillary pines, is a GPR120 ligand that promotes wound healing in the HaCaT cell line.

(+/-)-Pinocembrin, a natural product from axillary pines, is a GPR120 ligand that promotes wound healing in the HaCaT cell line.

(+/-)-Pinocembrin, a natural product from axillary pines, is a GPR120 ligand that promotes wound healing in the HaCaT cell line.

(+/-)-Pinocembrin, a natural product from axillary pines, is a GPR120 ligand that promotes wound healing in the HaCaT cell line.

(+/-)-Pinocembrin, a natural product from axillary pines, is a GPR120 ligand that promotes wound healing in the HaCaT cell line.

(+/-)-Pinocembrin, a natural product from axillary pines, is a GPR120 ligand that promotes wound healing in the HaCaT cell line.

Selective sigma (σ) receptor ligand. Displays high affinity for σ1; also binds at σ2 sites (Ki = 1.5 nM and 50.8 nM respectively). Selective over a range of receptor types including dopaminergic and muscarinic receptors, DAT and SERT.

Selective sigma (σ) receptor ligand. Displays high affinity for σ1; also binds at σ2 sites (Ki = 1.5 nM and 50.8 nM respectively). Selective over a range of receptor types including dopaminergic and muscarinic receptors, DAT and SERT.

Selective sigma (σ) receptor ligand. Displays high affinity for σ1; also binds at σ2 sites (Ki = 1.5 nM and 50.8 nM respectively). Selective over a range of receptor types including dopaminergic and muscarinic receptors, DAT and SERT.

(+/-)-Salsolinol hydrochloride is a full Gi protein agonist of the μ-opioid receptor (μOR).