Search Result
Results for "
Monoterpenoids
" in MedChemExpress (MCE) Product Catalog:
Cat. No. |
Product Name |
Target |
Research Areas |
Chemical Structure |
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- HY-N2700
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Others
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Cancer
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6a-Hydroxymedicarpin is a monoterpenoid indole alkaloid that can be isolated from Ochrosia elliptica. 6a-Hydroxymedicarpin has anticancer activity .
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- HY-N4156
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Others
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Others
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Pteropodine (compound 3) is a monoterpenoid oxindole alkaloid that can be isolated from Hamelia patens. Pteropodine modulates the functions of M1 muscarinic and 5-HT2 receptors. Pteropodine has antioxidant and antimutagenic properties .
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- HY-W013571
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Cuminic acid; p-Isopropyl benzoic acid
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Fungal
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Infection
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4-Isopropylbenzoic acid (Cuminic acid; p-Isopropyl benzoic acid) an aromatic monoterpenoid, is isolated from the stem bark of Bridelia retusa. 4-Isopropylbenzoic acid exhibits antifungal activities. 4-Isopropylbenzoic acid is also a reversible and uncompetitive inhibitor of mushroom tyrosinase .
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- HY-N9572
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Others
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Others
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Cadambine is a monoterpenoid gluco-indole alkaloid that can be isolated from Nauclea cadamba .
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- HY-N3116
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Others
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Others
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Paeonilactone C is a monoterpenoid, that can be isolated from paeony root .
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- HY-N0675
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Others
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Cancer
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Anhydrovinblastine is a monoterpenoid indole alkaloid that can be isolated from Catharanthus roseus leaves .
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- HY-N0675A
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Microtubule/Tubulin
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Cancer
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Anhydrovinblastine sulfate is a monoterpenoid indole alkaloid that can be isolated from Catharanthus roseus leaves .
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- HY-N9161
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Others
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Cancer
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Echitoveniline, a monoterpenoid indole alkaloid, can be isolated from Alstonia mairei. Echitoveniline has no significant cytotoxicity against cancer cells (IC50: > 40 μM) .
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- HY-N9735
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Bacterial
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Infection
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8-Hydroxy-9,10-diisobutyryloxythymol is a natural monoterpenoid with antibacterial properties. 8-Hydroxy-9,10-diisobutyryloxythymol against S. aureus, S. flexneri, and S. paratyphi-B with MIC values of 6.25 μg/mL .
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- HY-N1680
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Others
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Metabolic Disease
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3,7-Dimethyloct-1-ene-3,6,7-triol is a class of monoterpenoid polyols. 3, 7-dimethyloct-1-ene-3,6,7-triol has anti-HIV activity. 3, 7-dimethyloct-1-ene-3,6,7-triol can be used to study the isolation method of this drug from natural fruit ofCnidium monnieri .
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- HY-W979008
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- HY-N3664
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Others
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Others
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Cyclocerberidol is a Monoterpenoids product that can be isolated from the herbs of Cerbera manghas .
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- HY-N3143
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Others
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Others
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Oleuropeic acid is a Monoterpenoids product that can be isolated from the leaves of Eucalyptus maideni .
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- HY-N3568
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Others
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Others
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Cerberidol is a Monoterpenoids product that can be isolated from the barks of Cerbera manghas .
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- HY-N3450
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Others
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Others
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Isotschimgin is a Monoterpenoids product that can be isolated from the herbs of Piper puberulilimbum .
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- HY-N3118
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Others
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Others
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Paeonilactone A is a Monoterpenoids product that can be isolated from the roots of Paeonia albiflora .
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- HY-N8871
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Others
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Others
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Rauvovertine B is a hexacyclic monoterpenoid indole alkaloid that can be found in Rauvolfia verticillata .
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- HY-N2937
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Others
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Others
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Biondinin C is a Monoterpenoids product that can be isolated from the fruits of Illicium simonsii .
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- HY-N4324
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4-p-Menthan-1,8-diol
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Others
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Infection
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cis-p-Menthan-1,8-diol is a natural menthane monoterpenoid .
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- HY-N12187
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Others
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Others
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5,22-Dioxokopsane is a monoterpenoid indole alkaloid derived from Kopsia officinalis .
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- HY-N3899
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8-Carboxygeraniol
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Others
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Others
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Foliamenthic acid is a monoterpenoid compound that can be isolated from methanol extracts of the roots and leaves of the foliate .
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- HY-N3236
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Others
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Others
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Mullilam diol is a Monoterpenoids product that can be isolated from the herbs of Zanthoxylum budrunga Wall. .
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- HY-N8575A
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Others
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Others
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(1R)-Chrysanthemolactone is a Monoterpenoids product that can be isolated from the flowers of Dendranthema indicum .
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- HY-N8575
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Others
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Others
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(1S)-Chrysanthemolactone is a Monoterpenoids product that can be isolated from the flowers of Dendranthema indicum .
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- HY-111664A
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(-)-Citronellal
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Endogenous Metabolite
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Metabolic Disease
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(S)-(-)-Citronellal ((-)-Citronellal) is a monoterpenoid compound found in Corymbia citriodora and Cymbopogon nardus essential oils .
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- HY-W393870
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Others
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Others
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(-)-Dihydrocarvyl acetate is a Monoterpenoids product that can be isolated from the essential oil of Mentha spicata L. var. crispa Benth. .
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- HY-W012440
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Others
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Others
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(1S)-(+)-Menthyl chloroformate is a Monoterpenoids product that can be isolated from the herbs of Mentha canadensis L. .
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- HY-N8530
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Others
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Inflammation/Immunology
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Conodurine is a monoterpenoid indole alkaloid.
Conodurine can inhibit lysosomal acidification. Conodurineis isolated from the natural
Tabernaemontana corymbosa .
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- HY-N3039
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Others
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Others
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p-Menthane-1,3,8-triol is a Monoterpenoids product that can be isolated from the herbs of Mentha canadensis L. .
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- HY-W923189
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- HY-N1648
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Others
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Others
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2,2,5,5-Tetramethylcyclohexane-1,4-dione is a Monoterpenoids product that can be isolated from the herbs of Liriodendron tulipifera .
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- HY-N8751
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Others
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Others
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4-Hydroxy-2,6,6-trimethyl-1-cyclohexenecarboxylic acid is a Monoterpenoids product that can be isolated from the herbs of Salvia dugesii .
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- HY-N1679
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Others
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Others
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2,6-Dimethyl-3,7-octadiene-2,6-diol is a Monoterpenoids product that can be isolated from the fruits of Gardenia jasminoides Ellis .
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- HY-111664
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(+)-Citronellal
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Endogenous Metabolite
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Metabolic Disease
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(R)-(+)-Citronellal, isolated from citrus, lavender and eucalyptus oils, is a monoterpenoid and main component of citronellal oil with a distinct lemon scent. A flavouring agent. Used for insect repellent and antifungal properties .
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- HY-N7601
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Paeonivayin
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Others
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Inflammation/Immunology
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Benzoylalbiflorin, a monoterpenoid, is isolated from paeonia lactiflora. paeonia lactiflora is a traditional Chinese medicine that has been used for the research of rheumatoid arthritis, to alleviate inflammation, amenorrhea, epistaxis, abdominal pain, and other symptoms .
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- HY-119963A
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Bacterial
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Infection
Inflammation/Immunology
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trans-β-terpineol, a monoterpenoid compound, can be isolated from the leaves of Schinus terebinthifolius. Terpineol has antioxidant and antibacterial activity. trans-β-terpineol is a bioactive compound that plays an antibacterial role in Schinus terebinthifolius .
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- HY-N2004
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(±)-Isoborneol
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HSV
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Infection
Neurological Disease
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Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1) .
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- HY-N7851
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Others
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Infection
Others
Inflammation/Immunology
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Terpineol is a monoterpenoid alcohol compound that is widely found in plants, especially in the peels of citrus fruits. Terpineol has antioxidant, anti-inflammatory and antibacterial activities and is commonly used in the fragrance industry as an additive in food, beverages, cosmetics and perfumes .
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- HY-125598
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Cytochrome P450
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Others
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Secologanin, a secoiridoid glucoside, is a pivotal terpenoid intermediate in the biosynthesis of biologically active monoterpenoid indole alkaloids such as reserpine, ajmaline, and vinblastine. Secologanin synthase (cytochrome P450 isoform CYP72A1) catalyzes the oxidative cleavage of loganin into Secologanin .
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- HY-N1004
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Others
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Others
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10-Hydroxy-16-epiaffinine is a natural product that can be isolated from the leaves and twigs of Rauvolfia verticillata .
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-
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- HY-N4035
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(3β)-A'-Neogammacer-17(21)-en-3-ol
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Others
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Others
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Hop-17(21)-en-3-ol ((3β)-A'-Neogammacer-17(21)-en-3-ol) is a Monoterpenoids product that can be isolated from the herbs of Xanthium sibiricum .
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- HY-N2004R
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HSV
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Infection
Neurological Disease
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Isoborneol (Standard) is the analytical standard of Isoborneol. This product is intended for research and analytical applications. Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1) .
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- HY-N3797A
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Ditaine chloride
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Apoptosis
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Cancer
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Echitamine (Ditaine) chloride is the major monoterpene indole alkaloid present in Alstonia scholaris with potent anti-tumour activity. Echitamine chloride induces DNA fragmentation and cells apoptosis. Echitamine chloride inhibits pancreatic lipase with an IC50 of 10.92 μM .
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- HY-43520
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Fluorescent Dye
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Others
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BODIPY-FL is a green fluorescent dye that can be used to label probes or primers. BODIPY-FL fluorescence can be quenched after interacting with uniquely positioned guanine, making it useful for quantifying specific DNA or RNA molecules. BODIPY-FL-labeled sphingolipid analogs can be used to investigate sphingolipid internalization, transport, and endocytosis in mouse embryonic stem cells. BODIPY-FL-labeled monoterpenes can quickly penetrate bacteria, mammalian, and fungal cells, allowing for the detection of characteristics of a broad spectrum of Gram-positive and Gram-negative bacteria, as well as pathogenic fungi. The maximum absorption wavelength of BODIPY-FL is 505 nm, and the maximum emission wavelength is 513 nm .
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- HY-B1021
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Free Fatty Acid Receptor
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Cardiovascular Disease
Metabolic Disease
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Vincamine is a monoterpenoid indole alkaloid extracted from the Madagascar periwinkle. Vincamine is a peripheral vasodilator and exerts a selective vasoregulator action on the brain microcapilar circulation . Vincamine is a GPR40 agonist and acts as a β-cell protector by ameliorating β-cell dysfunction and promoting glucose-stimulated insulin secretion (GSIS). Vincamine improves glucose homeostasis in vivo, and has the potential for the type 2 diabetes mellitus (T2DM) research .
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- HY-B1021R
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Free Fatty Acid Receptor
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Cardiovascular Disease
Metabolic Disease
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Vincamine (Standard) is the analytical standard of Vincamine. This product is intended for research and analytical applications. Vincamine is a monoterpenoid indole alkaloid extracted from the Madagascar periwinkle. Vincamine is a peripheral vasodilator and exerts a selective vasoregulator action on the brain microcapilar circulation . Vincamine is a GPR40 agonist and acts as a β-cell protector by ameliorating β-cell dysfunction and promoting glucose-stimulated insulin secretion (GSIS). Vincamine improves glucose homeostasis in vivo, and has the potential for the type 2 diabetes mellitus (T2DM) research .
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- HY-121615
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alpha-Phellandrene
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Insecticide
Apoptosis
Autophagy
NO Synthase
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Infection
Neurological Disease
Inflammation/Immunology
Cancer
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α-Phellandrene (alpha-Phellandrene) is an orally active monoterpenoid and insecticide. α-Phellandrene can be isolated from plant essential oils. α-Phellandrene induces Apoptosis and Autophagy. α-Phellandrene promotes cAMP signaling pathway and increases NO production. α-Phellandrene has anti-inflammatory and anticancer (sarcoma) activities. α-Phellandrene shows insecticidal activity against Lucilia cuprina L3. α-Phellandrene reduces mechanical hyperalgesia .
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- HY-B1173
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D-(+)-Camphor; (1R)-(+)-Camphor
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Bacterial
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Neurological Disease
Inflammation/Immunology
Cancer
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(+)-Camphor (D-(+)-Camphor; (1R)-(+)-Camphor) is an isomer of Camphor. Camphor is an agonist of monoterpenoid transient receptor potential (TRP) channels (such as TRPV1, TRPV3, TRPM8) and an inhibitor of TRPA1 channels. Camphor's derivatives have multiple biological activities, including antibacterial, antiviral, antioxidant, analgesic and anticancer. Camphor can selectively activate cold-sensitive TRP channels and inhibit TRPA1-mediated nociceptive signals. Camphor stimulates the cold-sensing nerve endings in the skin and regulates the activity of ion channels to exert analgesic, anti-inflammatory and anti-itching effects. It also has anti-proliferative and anti-mutagenic activities on tumor cells, which may be related to inhibiting ribosome function or inducing cell apoptosis. Camphor can be absorbed through the skin and (+)-Camphor can be used in the study of muscle and joint pain and inflammation .
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- HY-B1173R
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D-(+)-Camphor (Standard); (1R)-(+)-Camphor (Standard)
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Bacterial
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Neurological Disease
Inflammation/Immunology
Cancer
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(+)-Camphor (Standard) is the analytical standard of (+)-Camphor. This product is intended for research and analytical applications. (+)-Camphor (D-(+)-Camphor; (1R)-(+)-Camphor) is an isomer of Camphor. Camphor is an agonist of monoterpenoid transient receptor potential (TRP) channels (such as TRPV1, TRPV3, TRPM8) and an inhibitor of TRPA1 channels. Camphor's derivatives have multiple biological activities, including antibacterial, antiviral, antioxidant, analgesic and anticancer. Camphor can selectively activate cold-sensitive TRP channels and inhibit TRPA1-mediated nociceptive signals. Camphor stimulates the cold-sensing nerve endings in the skin and regulates the activity of ion channels to exert analgesic, anti-inflammatory and anti-itching effects. It also has anti-proliferative and anti-mutagenic activities on tumor cells, which may be related to inhibiting ribosome function or inducing cell apoptosis. Camphor can be absorbed through the skin and (+)-Camphor can be used in the study of muscle and joint pain and inflammation .
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Cat. No. |
Product Name |
Type |
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- HY-43520
-
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Fluorescent Dyes/Probes
|
BODIPY-FL is a green fluorescent dye that can be used to label probes or primers. BODIPY-FL fluorescence can be quenched after interacting with uniquely positioned guanine, making it useful for quantifying specific DNA or RNA molecules. BODIPY-FL-labeled sphingolipid analogs can be used to investigate sphingolipid internalization, transport, and endocytosis in mouse embryonic stem cells. BODIPY-FL-labeled monoterpenes can quickly penetrate bacteria, mammalian, and fungal cells, allowing for the detection of characteristics of a broad spectrum of Gram-positive and Gram-negative bacteria, as well as pathogenic fungi. The maximum absorption wavelength of BODIPY-FL is 505 nm, and the maximum emission wavelength is 513 nm .
|
Cat. No. |
Product Name |
Category |
Target |
Chemical Structure |
-
- HY-N2700
-
-
-
- HY-N4156
-
-
-
- HY-W013571
-
-
-
- HY-N9572
-
-
-
- HY-N3116
-
-
-
- HY-N0675
-
-
-
- HY-N9161
-
-
-
- HY-N9735
-
-
-
- HY-N1680
-
-
-
- HY-N3664
-
-
-
- HY-N3143
-
-
-
- HY-N3568
-
-
-
- HY-N3450
-
-
-
- HY-N3118
-
-
-
- HY-N8871
-
-
-
- HY-N2937
-
-
-
- HY-N4324
-
-
-
- HY-N12187
-
-
-
- HY-N3899
-
-
-
- HY-N3236
-
-
-
- HY-N8575A
-
-
-
- HY-N8575
-
-
-
- HY-111664A
-
-
-
- HY-W393870
-
-
-
- HY-W012440
-
-
-
- HY-N8530
-
-
-
- HY-N3039
-
-
-
- HY-N1648
-
-
-
- HY-N8751
-
-
-
- HY-N1679
-
-
-
- HY-111664
-
-
-
- HY-N7601
-
-
-
- HY-N2004
-
-
-
- HY-N7851
-
-
-
- HY-125598
-
-
-
- HY-N1004
-
-
-
- HY-N4035
-
-
-
- HY-N2004R
-
-
-
- HY-N3797A
-
-
-
- HY-B1021
-
-
-
- HY-B1021R
-
|
Apocynaceae
Alkaloids
Structural Classification
Source classification
Plants
Indole Alkaloids
Catharanthus roseus (L.) G. Don
|
Free Fatty Acid Receptor
|
Vincamine (Standard) is the analytical standard of Vincamine. This product is intended for research and analytical applications. Vincamine is a monoterpenoid indole alkaloid extracted from the Madagascar periwinkle. Vincamine is a peripheral vasodilator and exerts a selective vasoregulator action on the brain microcapilar circulation . Vincamine is a GPR40 agonist and acts as a β-cell protector by ameliorating β-cell dysfunction and promoting glucose-stimulated insulin secretion (GSIS). Vincamine improves glucose homeostasis in vivo, and has the potential for the type 2 diabetes mellitus (T2DM) research .
|
-
-
- HY-121615
-
-
-
- HY-B1173
-
D-(+)-Camphor; (1R)-(+)-Camphor
|
Structural Classification
Other Monoterpenes
Classification of Application Fields
Terpenoids
Source classification
Other Diseases
Plants
Lauraceae
Cinnamomum camphora
Disease Research Fields
|
Bacterial
|
(+)-Camphor (D-(+)-Camphor; (1R)-(+)-Camphor) is an isomer of Camphor. Camphor is an agonist of monoterpenoid transient receptor potential (TRP) channels (such as TRPV1, TRPV3, TRPM8) and an inhibitor of TRPA1 channels. Camphor's derivatives have multiple biological activities, including antibacterial, antiviral, antioxidant, analgesic and anticancer. Camphor can selectively activate cold-sensitive TRP channels and inhibit TRPA1-mediated nociceptive signals. Camphor stimulates the cold-sensing nerve endings in the skin and regulates the activity of ion channels to exert analgesic, anti-inflammatory and anti-itching effects. It also has anti-proliferative and anti-mutagenic activities on tumor cells, which may be related to inhibiting ribosome function or inducing cell apoptosis. Camphor can be absorbed through the skin and (+)-Camphor can be used in the study of muscle and joint pain and inflammation .
|
-
-
- HY-B1173R
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D-(+)-Camphor (Standard); (1R)-(+)-Camphor (Standard)
|
Structural Classification
Other Monoterpenes
Terpenoids
Source classification
Plants
Lauraceae
Cinnamomum camphora
|
Bacterial
|
(+)-Camphor (Standard) is the analytical standard of (+)-Camphor. This product is intended for research and analytical applications. (+)-Camphor (D-(+)-Camphor; (1R)-(+)-Camphor) is an isomer of Camphor. Camphor is an agonist of monoterpenoid transient receptor potential (TRP) channels (such as TRPV1, TRPV3, TRPM8) and an inhibitor of TRPA1 channels. Camphor's derivatives have multiple biological activities, including antibacterial, antiviral, antioxidant, analgesic and anticancer. Camphor can selectively activate cold-sensitive TRP channels and inhibit TRPA1-mediated nociceptive signals. Camphor stimulates the cold-sensing nerve endings in the skin and regulates the activity of ion channels to exert analgesic, anti-inflammatory and anti-itching effects. It also has anti-proliferative and anti-mutagenic activities on tumor cells, which may be related to inhibiting ribosome function or inducing cell apoptosis. Camphor can be absorbed through the skin and (+)-Camphor can be used in the study of muscle and joint pain and inflammation .
|
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