(+)-Dihydrexidine hydrochloride is an agonist of dopamine D1 receptor(EC50 of 72± 21 nM).

(+)-Dihydrocalanolide A (DHCal A ; NSC 678323) is an orally active nonnucleoside inhibitor of Reverse Transcriptase . (+)-Dihydrocalanolide A can be used to HIV infection research .

(+)-Dihydrocalanolide A (DHCal A ; NSC 678323) is an orally active nonnucleoside inhibitor of Reverse Transcriptase . (+)-Dihydrocalanolide A can be used to HIV infection research .

(+)-Dihydrocalanolide A (DHCal A ; NSC 678323) is an orally active nonnucleoside inhibitor of Reverse Transcriptase . (+)-Dihydrocalanolide A can be used to HIV infection research .

(+)-Donepezil is an isomer of Donepezil — a nootropic acting as an inhibitor of acetylcholinesterase.

(+)-Donepezil is an isomer of Donepezil — a nootropic acting as an inhibitor of acetylcholinesterase.

(+)-Donepezil is an isomer of Donepezil — a nootropic acting as an inhibitor of acetylcholinesterase.

(+)-Dropropizine can inhibit histamine receptor, anti-allergic, and reduce a cough by modulation of neuropeptides involved in the cough reflex and by interfering with stimulus activation of peripheral endings of sensory nerves.

(+)-Epicatechin is a natural product and an antioxidant agent.

(+)-Epicatechin is a natural product and an antioxidant agent.

(+)-Epicatechin is a natural product and an antioxidant agent.

(+)-Epicatechin is a natural product and an antioxidant agent.

(+)-Epicatechin is a natural product and an antioxidant agent.

(+)-Epicatechin is a natural product and an antioxidant agent.

(+)-Epicatechin is a natural product and an antioxidant agent.

(+)-Epicatechin is a natural product and an antioxidant agent.

(+)-Epipinoresinol is a natural product

(+)-Epipinoresinol is a natural product

(+)-Fenchone has anti-inflammatory and antimicrobial activities

(+)-Fluprostenol, an analogue of prostaglandin F2 alpha, is a prostaglandin F2α receptor PTGFR agonist and decreases the expression of Oviductal glycoprotein 1 (OVGP1).

(+)-Fluprostenol, an analogue of prostaglandin F2 alpha, is a prostaglandin F2α receptor PTGFR agonist and decreases the expression of Oviductal glycoprotein 1 (OVGP1).

(+)-Fluprostenol, an analogue of prostaglandin F2 alpha, is a prostaglandin F2α receptor PTGFR agonist and decreases the expression of Oviductal glycoprotein 1 (OVGP1).

(+)-Fluprostenol, an analogue of prostaglandin F2 alpha, is a prostaglandin F2α receptor PTGFR agonist and decreases the expression of Oviductal glycoprotein 1 (OVGP1).

(+)-Fluprostenol, an analogue of prostaglandin F2 alpha, is a prostaglandin F2α receptor PTGFR agonist and decreases the expression of Oviductal glycoprotein 1 (OVGP1).

(+)-Fluprostenol, an analogue of prostaglandin F2 alpha, is a prostaglandin F2α receptor PTGFR agonist and decreases the expression of Oviductal glycoprotein 1 (OVGP1).

(+)-Fluprostenol, an analogue of prostaglandin F2 alpha, is a prostaglandin F2α receptor PTGFR agonist and decreases the expression of Oviductal glycoprotein 1 (OVGP1).

Gallocatechin possesses free radical scavenging ability. Gallocatechin has moderate affinity to the human cannabinoid receptor.

Gallocatechin possesses free radical scavenging ability. Gallocatechin has moderate affinity to the human cannabinoid receptor.

Gallocatechin possesses free radical scavenging ability. Gallocatechin has moderate affinity to the human cannabinoid receptor.

Gallocatechin possesses free radical scavenging ability. Gallocatechin has moderate affinity to the human cannabinoid receptor.

(+)-Geodin is a fungal metabolite. It increases the fibrinolytic activity of bovine aortic endothelial cells (BAECs) when used at concentrations ranging from 50 to 150 μM. (+)-Geodin (1-100 μg/ml) also increases 2-deoxyglucose uptake by rat adipocytes.

(+)-Goniothalesdiol, isolated from the bark of the Malaysian tree G. borneensis, is a tetrahydrofuran compound known to have significant cytotoxic effects against P388 mouse leukemia cells and pesticidal activities. It has been shown to have promising cytotoxic activity against p388 mouse leukemia cells (ED50 ≥30 μg/ml).

(+)-Guaiacin is a compound isolated from the bark of Machilus wangchiana Chun. It shows potent in vitro activities against the release of β-glucuronidase in rat polymorphonuclear leukocytes (PMNs) induced by platelet-activating factor (PAF).

(+)-Intermedine, a pyrrolizidine alkaloid (PA), shows remarkable cytotoxic activity against neural progenitor cells (NPCs).

(+)-Isoampelopsin F is a natural product for research related to life sciences. The catalog number is TN6249 and the CAS number is 354553-38-1.

(+)-Isocorydine is a eukaryote protein kinases Inhibitor.

(+)-Isocorydine is a eukaryote protein kinases Inhibitor.

(+)-Isocorydine is a eukaryote protein kinases Inhibitor.