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Results for "

monoterpenoid

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    20
    TargetMol | Inhibitors_Agonists
  • Natural Products
    15
    TargetMol | Natural_Products
  • Isotope Products
    1
    TargetMol | Isotope_Products
4-Isopropylbenzoic acid
NSC1907, NSC-1907, NSC 1907, Cumic acid
T20488536-66-3
4-Isopropylbenzoic acid (Cumic acid) is an aromatic monoterpenoid isolated from the stem bark of Bridelia retusa. 4-Isopropylbenzoic acid shows antifungal activities. 4-Isopropylbenzoic acid is also a reversible and uncompetitive mushroom tyrosinase inhibitor.
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7-10 days
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(S)​-​(-​)​-​Citronellal
(S)-(-)-3,7-Dimethyl-6-Octenal, (-​)​-​Citronellal
T80135949-05-3
(S)-(-)-Citronellal ((S)-(-)-3,7-Dimethyl-6-Octenal) is a monoterpenoid.
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1,8-Cineole
T1714470-82-6
Eucalyptol, a natural monoterpenoid and cyclic ether found in eucalyptus species, effectively controls excessive airway mucus secretion and asthma by inhibiting pro-inflammatory cytokines. It serves as an efficacious treatment for non-purulent sinusitis, reducing inflammation and pain when applied topically, and demonstrating leukemic cell-killing capabilities in vitro.
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Anhydrovinblastine
3',4'-Anhydrovinblastine
T302238390-45-3
3', 4'-Anhydrovinblastine (3',4'-Anhydrovinblastine) is an antineoplastic agent.
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Paeonilactone B
(+)-Paeonilactone B
TN203698751-78-1
Paeonilactone B ((+)-Paeonilactone B), a monoterpenoid from Paeonilactone, has neuroprotective activity, inhibits oxidative stress, and suppresses H2O2-induced neurotoxicity in rat cortical cells.
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Benzoylalbiflorin
Paeonivayin
TN7027184103-78-4
Benzoylalbiflorin (Paeonivayin) is a monoterpenoid isolated from Radix Paeoniae Alba.
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(+)-Fenchol
1,3,3-Trimethyl-2-norbornanol​,endo-(+)-Fenchyl Alcohol,(+)-α-Fenchol,(1R)-endo-(+)-Fenchyl Alcohol,D-Fenchyl Alcohol
TN75542217-02-9
(+)-Fenchol, a monoterpenoid discovered in various plants including Cannabis, serves both as a precursor in synthesizing other terpenoids and as a chiral building block for the organic synthesis of numerous compounds. Additionally, formulations incorporating (+)-fenchol are employed as fragrance ingredients.
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Vinorine
TN523534020-07-0
Vinorine is a direct biosynthetic precursor along the complex pathway to the monoterpenoid indole alkaloid ajmaline, an antiarrhythmic drug from the Indian medicinal plant Rauvolfia serpentina.
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(-)-Fenchone
TN16417787-20-4
(-)-Fenchone is a bicyclic monoterpenoid widely distributed in plants and can be extracted from Foeniculum vulgare and Peumus boldus. (-)-Fenchone has a wide range of biological activities including antioxidant, wound healing, antidiarrheal, antifungal, anti-injury sensory and bronchodilator activities. (-)-Fenchone is a potential anti-tumor compound.
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(-)-Myrtenol
(1R)-(-)-Myrtenol
TN460819894-97-4
(-)-Myrtenol ((1R)-(-)-Myrtenol) is a naturally occurring plant-derived monoterpenoid with anxiolytic, gastric cytoprotective, and wound-healing activities, and can be used in the study of gastric ulcers.
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(-)-11,12-Methylenedioxykopsinaline
T8361288607-48-1
(-)-11,12-Methylenedioxykopsinaline (Compound 4), a monoterpenoid indole alkaloid, has been isolated from *Kopsia officinalis* [1].
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5,22-Dioxokopsane
T833093703-90-0
5,22-Dioxokopsane, a monoterpenoid indole alkaloid, is derived from the plant Kopsia officinalis [1].
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cis-p-Menthan-1,8-diol
4-p-Menthan-1,8-diol
T13617565-48-0
cis- p- Menthan- 1, 8- diol is a natural menthane monoterpenoid.
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Thymohydroquinone
Thymoquinol
T357492217-60-9
Thymohydroquinone (Thymoquinol) is a monoterpenoid phenolic compound found in thyme, oregano, and other plants in the labiaceae family. Thymohydroquinone inhibits cancer cell growth, reduces oxidative stress and modulates inflammatory responses, scoured 2, 2-diphenyl-1-PicrylHydrazyl radicals in a cell-free assay (IC50 = 2.4 μg ml), In the oxygen radical absorption capacity (ORAC) test at concentrations of 1.6 to 6.4 μg ml, Its Trolox value was 2.6. Thymus hydroquinone inhibited the growth of A2780, OVCAR-8 and CIS-A2780 ovarian cancer cells (IC50 were 3.1, 8.9 and 9.8 μM, respectively) and human ovarian immortalized epithelial cells (IC50 = 14 μM). It also inhibited Plasmodium falciparum in vitro (IC50 = 15.9 μM).
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(+)-Isopulegol
T8275104870-56-6
(+)-Isopulegol is a monoterpenoid from Mentha canadensis L.
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7-10 days
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