123-35-3
123-35-3
Chemical Structure
Myrcene,75% (stabilized with BHT)
Synonym(s): β-Myrcene
- CAS No.: 123-35-3
- Formula:C10H16
- Molecular Weight:136.23
IUPAC Name: 7-methyl-3-methyleneocta-1,6-diene
InChIKey: UAHWPYUMFXYFJY-UHFFFAOYSA-N
SMILES: C=CC(CC/C=C(C)/C)=C
Biological Activity: Myrcene (β-Myrcene) is a type of aromatic compound that inhibits TNFα and NF-κB activity. Myrcene has anti-invasive action, inhibits cell cycle, and leads to cancer cell apoptosis. Myrcene has strong blood protection effect, anti-inflammation, and anti-inflammatory activity[1][2][3][4][5].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Myrcene,75% (stabilized with BHT) | 75.0% | Myrcene (β-Myrcene) is a type of aromatic compound that inhibits TNFα and NF-κB activity. Myrcene has anti-invasive action, inhibits cell cycle, and leads to cancer cell apoptosis. Myrcene has strong blood protection effect, anti-inflammation, and anti-inflammatory activity. | ||||||||||||||||||||
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Myrcene-13C3 | Myrcene-13C3 is 13C labeled Myrcene (HY-N0803). Myrcene (β-Myrcene) is a type of aromatic compound that inhibits TNFα and NF-κB activity. Myrcene has anti-invasive action, inhibits cell cycle, and leads to cancer cell apoptosis. Myrcene has strong blood protection effect, anti-inflammation, and anti-inflammatory activity. | |||||||||||||||||||||
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Myrcene-d6 | Myrcene-d6 is the deuterium labeled Myrcene. Myrcene (β-Myrcene) is a type of aromatic compound that inhibits TNFα and NF-κB activity. Myrcene has anti-invasive action, inhibits cell cycle, and leads to cancer cell apoptosis. Myrcene has strong blood protection effect, anti-inflammation, and anti-inflammatory activity. | |||||||||||||||||||||
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β-Ocimene | 90.0% | Beta-Ocimene is a naturally occurring organic compound that belongs to the terpene family. β-Ocimene exists as a mixture of two isomers: cis-β-ocimene and trans-β-ocimene. Possessing a pleasant, sweet, and herbaceous aroma, β-ocimene is found in many plants, including mint, basil, parsley, and kumquat. Due to its distinctive scent and flavor, β-ocimene is widely used in the fragrance and flavor industries. It also holds potential applications in agriculture as a natural insect repellent and as a pheromone that attracts beneficial insects. Additionally, β-ocimene exhibits potential anti-inflammatory and anti-cancer activities. | ||||||||||||||||||||
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Farnesene (mixture of isomers) | 98.01% | Farnesene (mixture of isomers) is a farnesene with mixture of isomers. Farnesene is a herbivore-induced plant volatile (HIPV). Farnesene has an important effect on insect resistance in many plant species. | ||||||||||||||||||||
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Geraniol | 98.62% | Geraniol is an olefin terpene with oral activity. Geraniol inhibits cell proliferation and promotes apoptosis. Geraniol has antibacterial, antifungal, antioxidant, anti-inflammatory and antitumor activities. Geraniol can be used to study diabetes. | ||||||||||||||||||||
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(E)-β-Farnesene | 99.92% | (E)-β-Farnesene (trans-β-Farnesene) is an aphid alarm pheromone, which can be found in Phlomis aurea Decne essential oil. (E)-β-Farnesene shows good binding score with a value of -30.64 kcal/mol to the CDK2 receptor. (E)-β-Farnesene also exhibits good affinity to odorant-binding protein 3 (OBP3). (E)-β-Farnesene can be used as a feeding stimulant for the sand fly Lutzomyia longipalpis. | ||||||||||||||||||||
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Sulcatone (Standard) | 99.59% | Sulcatone (Standard) (6-Methyl-5-hepten-2-one (Standard)) is the analytical standard of Sulcatone (HY-W010435). This product is intended for research and analytical applications. Sulcatone (6-Methyl-5-hepten-2-one) is a plant-derived volatile organic compound with activities such as insecticidal, antifungal, and blood pressure-lowering effects. Sulcatone also serves as an insect pheromone and an endogenous metabolite, which can be found in feces. Changes in Sulcatone levels can be used for the auxiliary diagnosis of ulcerative colitis. | ||||||||||||||||||||
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(3E)-4,8-Dimethylnona-1,3,7-triene | (3E)-4,8-Dimethylnona-1,3,7-triene, a sesquiterpene, is the major herbivore-induced plant volatile that help in defense directly by acting as repellants and indirectly by recruiting insects' natural enemies. (3E)-4,8-Dimethylnona-1,3,7-triene attractes Asian corn borer (ACB, Ostrinia furnacalis) larvae. External supplementation with (3E)-4,8-Dimethylnona-1,3,7-triene hampered the larvae's ability to locate pre-infested maize. | |||||||||||||||||||||
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(±)-Ipsdienol | 92.85% | (±)-Ipsdienol is a sex pheromone with an inducing effect on male spruce beetles (Dendroctonus rufipennis Kirby), which can be isolated from the subspecies of spruce beetles (Ips tridens Mannerheim). | ||||||||||||||||||||
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Dihydromyrcene | 90.04% | Dihydromyrcene is a volatile terpenoid compound found in essential oil from Rosa indica L. petals. Dihydromyrcene has potential vasorelaxant and antispasmodic effects. | ||||||||||||||||||||
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Deoxygeraniol | 96.67% | Deoxygeraniol, a monoterpenoid, has been reported in Camellia sinensis, Magnolia sieboldii, and Zingiber officinale. It is commonly used as an intermediate in the synthesis of fragrances or flavorings. | ||||||||||||||||||||
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References
- [1]. Eunson Hwang, et al. Myrcene, an Aromatic Volatile Compound, Ameliorates Human Skin Extrinsic Aging via Regulation of MMPs Production. Am J Chin Med. 2017;45(5):1113-1124. [Content Brief]
- [2]. Jeong-Ho Lee, et al. Anti-invasive effect of β-myrcene, a component of the essential oil from Pinus koraiensis cones, in metastatic MDA-MB-231 human breast cancer cells. Journal of the Korean Society for Applied Biological Chemistry volume 58, pages563–569.
- [3]. Bai X, et al. Myrcene exhibits antitumor activity against lung cancer cells by inducing oxidative stress and apoptosis mechanisms[J]. Natural Product Communications, 2020, 15(9): 1934578X20961189.
- [4]. Islam AUS, et al. Myrcene Attenuates Renal Inflammation and Oxidative Stress in the Adrenalectomized Rat Model. Molecules. 2020 Sep 30;25(19):4492. [Content Brief]
- [5]. Kumar R, et al. Ameliorative effect of myrcene in mouse model of Alzheimer's disease. Eur J Pharmacol. 2021 Nov 15;911:174529. [Content Brief]
