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Evodia

3,5,6-trihydroxysitostane
T84308133697-68-4In house
3,5,6-trihydroxysitostane is a steroid natural product derived from the fruits of Evodia rutaecarpa.
  • $195
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Stigmastane-3,5,6-triol
TN506720835-91-0
Stigmastane-3,5,6-triol and derivatives could be used for preparing antiviral medicine.
  • $460
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Evodosin A
TN40441291053-38-7
Evodosin A is a natural product for research related to life sciences. The catalog number is TN4044 and the CAS number is 1291053-38-7.
  • $660
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Evodine
TCS23366989-38-4
1. Evodine has antinociceptive activity.
  • $50
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1-Methyl-2-[(Z)-6-undecenyl]-4(1H)-quinolone
TN6057120693-49-4
(Z)-1-Methyl-2-(undec-6-enyl)quinolin-4(1H)-one shows strong inhibitory activity on leukotriene biosynthesis in human polymorphonuclear granulocytes, and it is very effective against mycobacteria.
  • $660
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Glaucin B
TN4135115458-73-6
Glaucin B is a new bitter limonoid.
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1-Methyl-2-undecyl-4(1H)-quinolone
TN255359443-02-6
1-Methyl-2-undecyl-4(1H)-quinolone, along with dihydroevocarpine and evodiamine, should serve as chemical markers for the quality control of Evodia rutaecarpa (Juss.) Benth. This compound selectively inhibits type B MAO (MAO-B) activity with an IC(50) value of 15.3 microM using the substrate kynuramine, while not inhibiting type A MAO (MAO-A) activity. It can mitigate high phosphate-induced calcification in human aortic valve interstitial cells (HAVICs) by inhibiting phosphate cotransporter (PiT-1) gene expression and exhibits moderate antiangiogenic activity against human tumor cells.
  • $540
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Flavaprin
TN406153846-49-4
Flavaprin is a natural product of Evodia, Rutaceae. The catalog number is TN4061 and the CAS number is 53846-49-4. Flavaprin can be used as a reference standard.
  • $2,250
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7-Isopentenyloxy-gamma-fagarine
TN323723417-92-7
7-Isopentenyloxy-gamma-fagarine has highly cytotoxicity against the MCF-7and Jurkat cell line. It has been used as a precursor for the chemical asymmetric synthesis of the enantiopure alkaloids: evoxine, anhydroevoxine and evodine.
  • $2,298
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Limonexic acid
TN444099026-99-0
Limonexic acid shows antinociceptive actions , it produces dose-related inhibition of glutamate- and capsaicin-induced pain. Limonexic acid can effectively protect hepatocyte against CCl4-induced injury.
  • $2,198
7-10 days
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12alpha-Hydroxyevodol
TN2604120722-04-5
12alpha-Hydroxyevodol is a natural product for research related to life sciences. The catalog number is TN2604 and the CAS number is 120722-04-5.
  • $660
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1-Hydroxyrutaecarpine
TN117353600-24-1
1-Hydroxyrutaecarpine exhibits cytotoxicities (ED50 values < 4 microg mL) against P-388 or HT-29 cell lines in vitro.
  • $620
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Elasticamide
TN2681154801-30-6
(2S,3S,4R,2'R)-2-(2'-hydroxytetracosanoylamino)octadecane-1,3,4-triol shows selectively inhibitory activity against phospholipase A 2 (PLA 2) secreted from Crotalus adamenteus venom at concentration of 100 ug/mL.
  • $5,200
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Hydroxyevodiamine
TN17521238-43-3
Hydroxyevodiamine is a natural product
  • $160
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6-Acetonyl-N-methyl-dihydrodecarine
TN31511253740-09-8
6-Acetonyl- N -methyl-dihydrodecarine has mosquito larvicidal activity against the malaria vector Anopheles gambiae.
  • $660
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1-Methyl-2-nonylquinolin-4(1H)-one
TN255268353-24-2
1-Methyl-2-nonylquinolin-4(1H)-one has anti-inflammatory activity, it exhibits inhibitory activity on leukotriene biosynthesis in a bioassay using human polymorphonuclear granulocytes, with IC50 values of 12.1 microM.
  • $520
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Evodol
TN163822318-10-1
Evodol may as an anti-inflammatory agent or lead compound, it shows inhibitory activity on nitric oxide (NO) production in lipopolysaccharide -activated RAW264.7 macrophages. Evodol and limonin possess larvicidal activity against the Asian tiger mosquitoe
  • $598
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1-Methyl-2-pentyl-4(1H)-quinolinone
TN117522048-98-2
1-Methyl-2-pentyl-4(1H)-quinolinone, a natural product,
  • $236
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5-Methoxy-2',3'-dehydromarmesin
TN267354087-32-0
5-Methoxy-2',3'-dehydromarmesin is a natural product for research related to life sciences. The catalog number is TN2673 and the CAS number is 54087-32-0.
  • $899
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Dihydroevocarpine
TN109915266-35-0
Dihydroevocarpine shows potent anti-Helicobacter pylori activity with the minimum inhibitory concentration (MIC) value of 10-20 microg ml. Dihydroevocarpine is a moderate modulator of p-glycoprotein (p-gp) activity; it shows more potent inhibitory effects against MAO-B compared to MAO-A.
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