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  3. Lauraceae

Lauraceae

Lauraceae (29):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-N2037A
    Higenamine hydrochloride 11041-94-4 99.06%
    Higenamine hydrochloride (Norcoclaurine hydrochloride), a β2-AR agonist, is a key component of the Chinese herb aconite root that prescribes for treating symptoms of heart failure in the oriental Asian countries. Higenamine hydrochloride (Norcoclaurine hydrochloride) has anti-apoptotic effects.
    Higenamine hydrochloride
  • HY-N0222
    Avicularin 572-30-5 99.25%
    Avicularin is a bio-active flavonoid from plants, anti-inflammatory, anti-allergic, anti-oxidant, hepatoprotective, and anti-tumor activities. Avicularin exhibits anti-inflammatory activity through the suppression of ERK signaling pathway in LPS-stimulated RAW 264.7 macrophage cells. Avicularin ameliorates human hepatocellular carcinoma via the regulation of NF κB (p65), COX 2 and PPAR γ activities.
    Avicularin
  • HY-W019711
    trans-Cinnamaldehyde 14371-10-9 99.41%
    trans-Cinnamaldehyde can be used to prepare highly polyfunctionalized furan ring by reaction of alkyl isocyanides with dialkyl acetylenedicarboxylate. trans-Cinnamaldehyde can be used to synthesize trans-cinnamaldehyde -β-cyclodextrin complex, an antimicrobial edible coating that increases the shelf life of fresh-cut fruits.
    trans-Cinnamaldehyde
  • HY-N7083
    Citral 5392-40-5
    Citral is a monoterpene found in Cymbopogon citratus essential oil, with antihyperalgesic, anti-nociceptive and anti-inflammatory effects.
    Citral
  • HY-N0808
    Camphor 76-22-2 ≥98.0%
    Camphor ((±)-Camphor) is a topical anti-infective and anti-pruritic and internally as a stimulant and carminative. However, Camphor is poisonous when ingested. Antiviral, antitussive, and anticancer activities. Camphor is a TRPV3 agonist.
    Camphor
  • HY-N3379
    Linderone 1782-79-2
    Linderone is an antioxidant agent.
    Linderone
  • HY-N6973
    Boldine 476-70-0 99.68%
    Boldine is an aporphine isoquinoline alkaloid extracted from the root of Litsea cubeba and also possesses these properties, including antioxidant, anti-inflammatory and cytoprotective effects. Boldine suppresses osteoclastogenesis, improves bone destruction by down-regulating the OPG/RANKL/RANK signal pathway and may be a potential therapeutic agent for rheumatoid arthritis.
    Boldine
  • HY-N0610
    trans-Cinnamic acid 140-10-3 99.98%
    trans-Cinnamic acid is a natural antimicrobial, with minimal inhibitory concentration (MIC) of 250 μg/mL against fish pathogen A. sobria, SY-AS1.
    trans-Cinnamic acid
  • HY-N0688
    Linderane 13476-25-0 98.86%
    Linderane, isolated from the root of Lindera strychnifolia, is an irreversible inhibitor cytochrome P450 2C9 (CYP2C9). Linderane has the potential to relieve pain and cramp.
    Linderane
  • HY-W046353
    2-Methoxycinnamaldehyde 1504-74-1 ≥98.0%
    2-Methoxycinnamaldehyde (o-Methoxycinnamaldehyde) is a natural compound of Cinnamomum cassia, with antitumor activity. 2-Methoxycinnamaldehyde inhibits proliferation and induces apoptosis by mitochondrial membrane potential (ΔΨm) loss, activation of both caspase-3 and caspase-9. 2-Methoxycinnamaldehyde effectively inhibits platelet-derived growth factor (PDGF)-induced HASMC migration.
    2-Methoxycinnamaldehyde
  • HY-N1356
    Reticuline 485-19-8 98.11%
    Reticuline shows anti-inflammatory effects through JAK2/STAT3 and NF-κB signaling pathways. Reticuline inhibits mRNA expressions of TNF-α, and IL-6 and reduces the phosphorylation levels of JAK2 and STAT3. Reticuline exhibits cardiovascular effects.
    Reticuline
  • HY-N0781
    Linderalactone 728-61-0 ≥98.0%
    Linderalactone is an important sesquiterpene lactone isolated from Radix linderae. Linderalactone inhibits cancer growth by modulating the expression of apoptosis-related proteins and inhibition of JAK/STAT signalling pathway. Linderalactone also inhibits the proliferation of the lung cancer A-549 cells with an IC50 of 15 µM.
    Linderalactone
  • HY-122808
    (-)-Camphoric acid 560-09-8 ≥98.0%
    (-)-Camphoric acid is the less active enantiomer of Camphoric acid. Camphoric acid stimulates osteoblast differentiation and induces glutamate receptor expression. Camphoric acid also significantly induced the activation of NF-κB and AP-1.
    (-)-Camphoric acid
  • HY-U00462
    D-Mannoheptulose 3615-44-9 ≥98.0%
    D-Mannoheptulose is a major non-structural carbohydrate in avocado. D-mannoheptulose is a specific inhibitor of D-glucose phosphorylation. D-Mannoheptulose can block insulin release and utilization of carbohydrate in rat.
    D-Mannoheptulose
  • HY-W012531
    2-Hydroxycinnamic acid 614-60-8
    2-Hydroxycinnamic acid is isolated from the methanol extract of Cinnamomum cassia. 2-Hydroxycinnamic acid shows inhibitory effects on infection of HIV/SARS-CoV S pseudovirus with an IC50 of 0.3 mM
    2-Hydroxycinnamic acid
  • HY-N7136
    α-​Terpinyl acetate 80-26-2
    α-Terpinyl acetate is a monoterpene ester isolated from Laurus nobilis L. essential oil. α-Terpinyl acetate is a competitive P450 2B6 substrate which binding to the active site of P450 2B6 with a Kd value of 5.4 μM.
    α-​Terpinyl acetate
  • HY-N2352
    Laurolitsine 5890-18-6 98.73%
    Laurolitsine ((+)-Norboldine) is an alkaloid isolated from the leaves of Peumus boldus Molina.
    Laurolitsine
  • HY-N0586
    Norisoboldine 23599-69-1 99.44%
    Norisoboldine is an orally active natural aryl hydrocarbon receptor (AhR) agonist. Norisoboldine, as a major isoquinoline alkaloid present in Radix Linderae, can be used for the research of Rheumatoid arthritis and Ulcerative colitis.
    Norisoboldine
  • HY-B1173
    (+)-Camphor 464-49-3 ≥98.0%
    (+)-Camphor is an ingredient in cooking, and as an embalming fluid for medicinal purposes,
    (+)-Camphor
  • HY-77995
    2-Methoxybenzaldehyde 135-02-4 98.71%
    2-Methoxybenzaldehyde (o-Anisaldehyde), isolated from cinnamon essential oil (CEO), exists antibacterial and antifungal activity.
    2-Methoxybenzaldehyde