T0477 |
Zileuton |
Zileuton is a synthetic derivative of hydroxyurea with antiasthmatic properties. The leukotriene inhibitor zileuton blocks 5-lipoxygenase, which catalyzes the formation of leukotri |
T0646 |
Mesalamine |
Mesalamine is an anti-inflammatory agent, structurally related to the SALICYLATES, which is active in INFLAMMATORY BOWEL DISEASE. It is considered to be the active moiety of SULPHA |
T1296 |
Aminopar |
Aminosalicylic Acid is an analog of para-aminobenzoic acid (PABA) with antitubercular activity. |
T1401 |
Meclofenoxate hydrochloride |
Meclofenoxate hydrochloride is an ester of DIMETHYLAMINOETHANOL and para-chlorophenoxyacetic acid. It has been shown to improve memory and general cognition, and mentally stimulati |
T1420 |
Diethylcarbamazine citrate |
Diethylcarbamazine citrate is an anthelmintic used primarily as the citrate in the treatment of filariasis, particular infestations with Wucheria bancrofti or Loa loa. It is an inh |
T1558 |
Resveratrol |
Resveratrol is a polyphenolic phytoalexin with antioxidant and chemopreventive activities. It has a wide spectrum of targets including COX, SIRT, LOC, etc. |
T1677 |
Montelukast |
Montelukast is an orally available leukotriene receptor antagonist which is widely used for the prophylaxis and chronic treatment of asthma and has been linked to rare cases of cli |
T6485 |
Embelin |
Embelin, isolated from the Japanese Ardisia herb, is an inhibitor of the X-linked inhibitor of apoptosis (IC50: 4.1 uM). |
T4347 |
ML355 |
ML355, a specific, effective 12-Lipoxygenase(12-LOX) inhibitors(IC50=0.34 μM), possess favorable ADME properties. |
T6S1699 |
6-Shogaol |
1. 6-Shogaol has antipyretic and analgesic effects in addition to inhibitory effect on lipoxygenase activity. 2. 6-shogaol has anti-inflammatory property, reduces the inflammatory |
TJS0315 |
7,8-Dihydroxy-4-methylcoumarin |
1. 4-Methyldaphnetin is a potent inhibitor (low micromolar) of lipid peroxidation and scavengers of superoxide anion radicals and of aqueous alkylperoxyl radicals, but may be pro-o |
T3879 |
Silychristin |
Silychristin is a plant growth regulator. Silychristin is an anti-hepatotoxic agent. Silychristin is the inhibitor of horseradish peroxidases and lipoxygenase. |
T4571 |
Balsalazide |
Balsalazide is an anti-inflammatory compound used in the treatment of Inflammatory Bowel Disease. |
T5759 |
marmesin |
Marmesin is a coumarin originally isolated from the mature bark of A. marmelos,exhibiting COX-2/5-LOX dual inhibitory activity. |
T5714 |
5-DEMETHYLNOBILETIN |
5-DEMETHYLNOBILETIN is a natual product, has anti-inflammatory activity, it may act through a direct inhibition of 5-LOX, without affecting the expression of COX-2. |
TQ0180 |
Chebulagic acid |
Chebulagic acid, isolated from the Terminalia chebula Retz, is a COX-LOX dual inhibitor. |
T3090 |
Abietic Acid |
Abietic Acid is the primary component of resin acid isolated from rosin. |
T8002 |
3-Hydroxycoumarin |
3-Hydroxycoumarin is a natural compound, and is human 15-LOX-1 inhibitors |
T8260 |
4',5-Dihydroxyflavone |
4',5-Dihydroxyflavone is a soybean LOX-1(Ki: 102.6 μM) and yeast α-Glucosidase inhibitor (IC50: 66 μM). |
T8356 |
FPL 62064 |
FPL 62064 is a potent dual inhibitor of 5-lipoxygenase (5-LOX) and COX (IC50 of 3.5 μM and 3.1 μM for RBL-1 cytosolic 5-lipoxygenase and prostaglandin synthetase, respectively) |
TN1255 |
3-O-Acetyl-11-hydroxy-beta-boswellic acid |
3-O-Acetyl-11-hydroxy-beta-boswellic acid is the precursor of 3-O-acetyl-9, 11-dehydro-beta-boswellic acid(a 5-lipoxygenase inhibitor ). |
TN1291 |
5-Hydroxy-3',4',7-trimethoxyflavone |
5-Hydroxy-3',4',7-trimethoxyflavone has anti-inflammatory, antibacterial and antifungal activities, it also shows moderate antitrypanosomal activity with MIC value of 19.0 ug/ml |
TN1244 |
3'-Demethylnobiletin |
3'-Demethylnobiletin has chemopreventive effects on colon carcinogenesis, it can significantly inhibit the growth of human colon cancer cells, cause cell-cycle arrest, induce apopt |
TN1016 |
Kukoamine A |
Kukoamine A possesses anticancer, cytoprotective, antioxidant, and anti-inflammatory activities, it also has neuroprotective effects through inhibiting oxidative stress and apoptos |
TN1871 |
Ligustroside |
Ligustroside shows little antioxidant, and anti-inflammatory properties, it shows a significant inhibition effect on prostaglandin E2 (PGE2)-release. Ligustroside shows moderate an |
T10151 |
5-Lipoxygenase-In-1 |
5-Lipoxygenase-In-1 (compound example 4.10) is a 5-Lipoxygenase inhibitor extracted from patent EP 331232 A2. |
T10438 |
AZD 4407 |
AZD 4407 is a potent inhibitor of 5-lipoxygenase. |
TN1182 |
11-Keto-beta-boswellic acid |
11-Keto-beta-boswellic acid, a novel Nrf2 activator, and a selective 5-lipoxygenase (5-LOX) inhibitor; it exerts dose dependent cardioprotective effect manifested by dose-dependent |
T12784 |
RWJ 63556 |
RWJ 63556 is an orally active inhibitor of COX-2 selective/5-lipoxygenase, shows anti-inflammatory activities. |
T11196 |
Enazadrem |
Enazadrem is a 5-lipoxygenase inhibitor with antiinflammatory activities. |
T10719 |
CCT365623 hydrochloride |
CCT365623 hydrochloride is an orally active inhibitor of lysyl oxidase (LOX) (IC50: 0.89 μM). It suppresses EGFR (pY1068) and AKT phosphorylation driven by EGF. |
T10821 |
Cirsiliol |
Cirsiliol is a selective inhibitor of 5-lipoxygenase and a competitive low-affinity ligand of benzodiazepine receptors. |
T10098 |
PGS-IN-1 |
PGS-IN-1 is a potent inhibitor of prostaglandin synthetase (PGS; IC50: 0.28 μM) and also inhibits 5-lipoxygenase (IC50: 1.05 μM). |
T16503 |
PF-4191834 |
PF-4191834 is an orally active, noniron chelating, and non-redox inhibitor of the 5-Lipoxygenase (5-LOX) (IC50=229 nM). PF-4191834 shows ~300-fold selectivity for 5-LOX over 12-LOX |
T13764 |
Lycopodine |
Lycopodine inhibits proliferation of HeLa cells through induction of apoptosis via caspase-3 activation. Lycopodine, a pharmacologically important bioactive component derived from |
T22398 |
Phenidone |
Phenidone, a dual inhibitor of cyclooxygenase (COX) and lipoxygenase (LOX), is an organic compound primarily used as a photographic developer. |
TL0014 |
Pinusolide |
Pinusolide is a platelet activating factor ( PAF) antagonist, it may prove of therapeutic value in the treatment of hypotension, it has antileukemic potential, and could be used to |
TN4331 |
Isotachioside |
Isotachioside has15-lipoxygenase (15-LO) inhibitory activities. |
TN4783 |
Picralinal |
Picralinal has anti-inflammatory and analgesic effects. |
TN5020 |
(+/-)-Sigmoidin A |
Sigmoidin A has moderate antioxidant, antimicrobial and anti-inflammatory activity. |
TN5174 |
Trichosanatine |
Trichosanatine and squamosamide, as potential candidates as lead compounds for further study in drug development process with the PP2A- α protein. Trichosanatine can alleviate oxi |
T2807 |
Caffeic Acid |
Caffeic Acid is an orally bioavailable, hydroxycinnamic acid derivative and polyphenol, with potential anti-oxidant, anti-inflammatory, and antineoplastic activities. |
T2798 |
Esculetin |
Esculetin is a coumarin derivative from various natural plant products with various biological and pharmaceutical properties including anti-edema, anti-inflammatory and anti-tumour |
T21902 |
ML351 |
ML351 is a potent and selective inhibitor of human 15-lipoxygenase-1 (15 LOX)(IC50: 200 nM). |
TN1097 |
Beta-boswellic acid |
Beta-boswellic acid and its derivatives (the major constituents of Boswellin) have anti-carcinogenic, anti-tumor, and anti-hyperlipidemic activities. |
T6576 |
Malotilate |
Malotilate is a medicine used for the therapy of liver cirrhosis. |
TN2330 |
Caffeic Acid 3-Methyl Phenethyl Ester |
Caffeic Acid 3-Methyl Phenethyl Ester has chemopreventive properties against chemically induced colon carcinogenesis. It enhances apoptosis in azoxymethane induced colon tumors. |