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Natural Products

Cat.No.  Name Information
M17797 Quillaic acid Quillaic acid is an anti-gastric cancer and anti-proliferation agent that can promote apoptosis of cancer cells. Quillaic acid also has analgesic and local anti-inflammatory activity.
M17793 16-Oxoalisol A 16-Oxoalisol A
M17784 Oleanonic acid Oleanonic acid (3-Oxooleanolic acid) is an orally available triterpene that has anti-inflammatory and insecticidal properties. In vitro, oleanonic acid can improve oxidative stress, autophagy defects, ferroptosis, mitochondrial damage, and endoplasmic reticulum stress induced by Amyloid-β, and in vivo, it can alleviate myocardial hypertrophy in rats.
M17770 Pyracrenic acid Pyracrenic acid
M17765 Ginsenoside Rk3 Ginsenoside Rk3 significantly inhibits TNF-α-induced NF-κB transcriptional activity, with an IC50 of 14.24±1.30 μM in HepG2 cells.
M17749 Ganodermanontriol Ganodermanontriol is a sterol isolated from Ganoderma lucidum, induces anti-inflammatory activity in tert-butyl hydroperoxide (t-BHP)-damaged hepatic cells through the expression of HO-1.
M17652 Zeaxanthin dipalmitate Zeaxanthin dipalmitate
M17651 Tigogenin Tigogenin
M17619 7-Oxo-β-sitosterol 7-Oxo-β-sitosterol
M17603 Cedrol Cedrol is a potent competitive inhibitor of cytochrome P-450 (CYP) enzymes. Cedrol inhibits CYP2B6-mediated bupropion hydroxylase and CYP3A4-mediated midazolam hydroxylation with Ki of 0.9 μM and 3.4 μM, respectively. Cedrol also has weak inhibitory effect on CYP2C8, CYP2C9, and CYP2C19 enzymes.
M17591 Heliangin Heliangin
M17579 Brevilin A Brevilin A is an orally active STAT3/JAK inhibitor, with IC50 of 10.6 μM against STAT3.
M17577 Axinysone B Axinysone B
M17572 Tagitinin A Tagitinin A is a sesquiterpene with anti-hyperglycemic activity. Tagitinin A significantly inhibits glucose uptake in differentiated 3T3-L1 adipocytes.
M17553 Bullatantriol Bullatantriol
M17477 Aromadendrane-4β,10α-diol Aromadendrane-4β,10α-diol
M17451 3,6'-Disinapoylsucrose 3,6'-Disinapoylsucrose
M17443 Lapachol Lapachol is a naturally occurring naphthoquinone and orally active, potent inhibitor of dihydroorotic acid dehydrogenase (DHODH).Lapachol has immunosuppressive activity against lymphocytes by inhibiting pyrimidine synthesis through direct blockade of DHODH activity. In addition, Lapachol is a vitamin K antagonist with antitumor and antileishmanial activity that inhibits DNA and RNA synthesis in tumor cells.
M17442 Miltirone Miltirone is an orally active natural compound found in the root of Salvia miltiorrhiza. Miltirone is a central benzodiazepine receptor partial agonist, with an IC50 of 0.3 μM. Miltirone induces ROS - and-p53 dependent apoptosis. Miltirone inhibits carboxylesterase 2 (CES2; Ki = 0.04 μM) and SARS-CoV main protease (Mpro).
M17425 2,6-Dimethoxy-1,4-benzoquinone 2,6-Dimethoxy-1,4-benzoquinone

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