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| Product | Description | |
|---|---|---|
| Chavicol | Chavicol (p-Hydroxyallylbenzene, compound 6) can inhibit acetylcholinesterase ( Cholinesterase (ChE) ), with an IC 50 of 7.42 μM. Chavicol has anti-cancer activity and can suppress the growth, survival, migration, and invasion of cancer cells. Chavicol cytotoxic effect is significant, approximately 31 μg/mL in A-549 cells [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: p-Hydroxyallylbenzene. CAS No. 501-92-8. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-W159754. |  |
| Methyl Chavicol FCC | Methyl Chavicol FCC (Estragole). CAS No. 140-67-0. FEMA No. 2411. Kosher: Y. VIGON Item # 500885. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Aromatherapy, Essetial Oils. |  America & Internationally |
| 4-Allylphenol | 4-Allylphenol is a useful building block naturally occurring in Syzygium aromaticum leaves. 4-Allylphenol has been used in the synthetic, regioselective preparation of gamma-lactones. Group: Biochemicals. Alternative Names: Chavicol (6CI); Phenol, 4-(2-propenyl)- (9CI); Phenol, p-allyl- (7CI,8CI); 4-(2-Propen-1-yl)phenol; (4-Hydroxyphenyl)-2-propene; 3-(p-Hydroxyphenyl)-1-propene; 4-(2-Propenyl)phenol; NSC 290195; p-Allylphenol; p-Hydroxyallylbenzene; γ-(p-Hydroxyphenyl)-α-propylene. Grades: Highly Purified. CAS No. 501-92-8. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C?H??O, Molecular Weight: 134.18. US Biological Life Sciences. |  Worldwide |
| Estragole FCC | Estragole FCC (Methyl Chavicol). CAS No. 140-67-0. FEMA No. 2411. Kosher: Y. VIGON Item # 500885. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Aromatherapy, Essetial Oils. | America & Internationally |
| eugenol synthase | The enzyme acts in the opposite direction. The enzymes from the plants Ocimum basilicum (sweet basil), Clarkia breweri and Petunia hybrida only accept coniferyl acetate and form eugenol. The enzyme from Pimpinella anisum (anise) forms anol (from 4-coumaryl acetate) in vivo, although the recombinant enzyme can form eugenol from coniferyl acetate. The enzyme from Larrea tridentata (creosote bush) also forms chavicol from a coumaryl ester and can use NADH. Group: Enzymes. Synonyms: LtCES1; EGS1; EGS2. Enzyme Commission Number: EC 1.1.1.318. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0230; eugenol synthase; EC 1.1.1.318; LtCES1; EGS1; EGS2. Cat No: EXWM-0230. |  |
| (iso)eugenol O-methyltransferase | Acts on eugenol and chavicol as well as isoeugenol. Group: Enzymes. Enzyme Commission Number: EC 2.1.1.146. CAS No. 191744-33-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1742; (iso)eugenol O-methyltransferase; EC 2.1.1.146; 191744-33-9. Cat No: EXWM-1742. | |
| p-Allylphenol | A useful research chemical. Synonyms: 4-(2-propenyl)-pheno; 4-(Prop-2-enyl)-phenol; Chavicol; gamma-(p-Hydroxyphenyl)-alpha-propylene; p-Allylphenol; p-Chavicol; Phenol, 4-(2-propenyl)-; Phenol, p-allyl-. Grades: 95%. CAS No. 501-92-8. Molecular formula: C9H10O. Mole weight: 134.18. |  |
| trans-anol O-methyltransferase | The enzyme from anise (Pimpinella anisum) is highly specific for substrates in which the double bond in the propenyl side chain is located between C7 and C8, and, in contrast to EC 2.1.1.146, (iso)eugenol O-methyltransferase, does not have activity with eugenol or chavicol. Group: Enzymes. Synonyms: AIMT1; S-adenosyl-L-methionine:t-anol/isoeugenol O-methyltransferase; t-anol O-methyltransferase. Enzyme Commission Number: EC 2.1.1.279. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1885; trans-anol O-methyltransferase; EC 2.1.1.279; AIMT1; S-adenosyl-L-methionine:t-anol/isoeugenol O-methyltransferase; t-anol O-methyltransferase. Cat No: EXWM-1885. | |
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