(-)-(1R,3S)-3-Aminocyclopentanecarboxylic acid is used in the synthesis of aminocyclopentanecarboxylic acid-containing cyclic RGD peptides. It is also used to prepare BMS-457, a potent and selective CCR1 antagonist.

(-)-(1S,4R)-4-Aminocyclopent-2-enecarboxylic Acid is a cyclopentane GABA analogue.

(-)-(8,8-Dichlorocamphorylsulfonyl)oxaziridine (CAS# 139628-16-3 ) is a useful research chemical.

(-)-2-(2-Hydroxyethyl)clavam is an oxypenicillane antibiotic produced by Streptomyces antibiotcus var. antibioticus Tu 1718. It has anti-fungal and weak anti-Gram-positive and negative bacteria activity.

(-)-2,3:4,6-Di-O-isopropylidene-2-keto-L-gulonic Acid Monohydrate (CAS# 68539-16-2 ) is a useful research chemical.

(-)-allo-Protolichesterinic acid can inhibit 5-lipoxygenase in vitro.

(-)-Blebbistatin is a cell-permeable inhibitor for non muscle myosin II ATPase with IC50 of ~2 μM, does not inhibit myosin light chain kinase, inhibits contraction of the cleavage furrow without disrupting mitosis or contractile ring assembly.

(-)-Carbovir, is a nucleoside/nucleotide reverse transcriptase inhibitor (NRTI) caused mitochondrial toxicity in human hepatoma carcinoma cell.

(-)-Catechin gallate, a minor polyphenolic constituent in green tea, is used to study its cytotoxicity. It enhances Fe(2+)-induced, lipid peroxidation. It also inhibits aromatase activity, an enzyme that converts androgens to estrogen and is thought to play a role in the etiology of breast cancer.

(-)-Chelidonine is an alkaloid isolated from Glaucium squamigerum.

(-)-Corlumine is a natural alkaloid compound found in some plant.

(-)dihydropertusaric acid is a γ-lactone carboxylic acid derived from the lichen Pertusaria albescens.

(-)-Epiafzelechin exhibits various modes of action in suppressing HSV-2 multiplication.

(−)-Epicatechin gallate (ECG) is a natural catechin with a single galloyl group. Like EGCG, it inhibits the growth of cancer cells and has anti-inflammatory effects. The hydroxyl groups of ECG contribute to its potent antioxidant activity and facilitate the killing of methicillin-resistant strains of S. aureus. (-)-Epicatechin gallate is a natural compound found in the […]

(-)-Epigallocatechin (EGC) is a natural flavonoid isolated from herbs of Berchemia kulingensis Schneid, and it has prominent antiplatelet activity and blood anticoagulation in a dose-dependent manner. (-)-Epigallocatechin is a natural compound, it can also be used in cosmetics material.

EGCG is an antioxidant extracted from green tea, reduces Aβ42-induced cell death in three different cell types and inhibits β-secretase (IC50 = 1.6 μM). (-)-Epigallocatechin gallate is a natural compound found in the woods of Acacia catechu (L.F.) Willd. It can be used in cosmetic material.

EGCG is an antioxidant extracted from green tea, reduces Aβ42-induced cell death in three different cell types and inhibits β-secretase (IC50 = 1.6 μM). (-)-Epigallocatechin gallate is a natural compound found in the woods of Acacia catechu (L.F.) Willd. It can be used in cosmetic material.

(-)-Gallocatechin had been shown to have moderate affinity to the human cannabinoid receptor.

GCG is the ester of gallocatechin and gallic acid and a type of catechin. It is an epimer of epigallocatechin gallate.

It is produced by the strain of Curvularia harveyi. It can inhibit the formation of Sea urchin eggs Spindle.

(-)-Heraclenol is a natural coumarin compound found in several plants.

(-)-Holostyligone is a lignan isolated from the Holostylis reniformis.

(-)-Huperzine A is a potent, highly specific and reversible inhibitor of acetylcholinesterase (AChE) with Ki of 7 nM, exhibiting 200-fold more selectivity for G4 AChE over G1 AChE. Also acts as an NMDA receptor antagonist. Phase 4.

(-)-Lyoniresinol 9′-O-glucoside is purified from the bamboo-sheath of Phyllostachys heterocycla MITF.

(−)-Neplanocin A potently and irreversibly inactivates SAH hydrolase (Ki = 8.39 nM). It has antitumor activity against mouse leukemia L1210 cells and broad-spectrum antiviral activity. Neplanocin A is more potent against vesicular stomatitis than the reversible SAH hydrolase inhibitor 3-deazaneplanocin (ID50 = 0.07 and 0.3 μg/ml, respectively).