3572-64-3
3572-64-3
Chemical Structure
Dihydrojasmonic acid
- CAS No.: 3572-64-3
- Formula:C12H20O3
- Molecular Weight:212.29
IUPAC Name: 2-(3-oxo-2-pentylcyclopentyl)acetic acid
InChIKey: PQEYTAGBXNEUQL-UHFFFAOYSA-N
SMILES: O=C(O)CC1C(CCCCC)C(CC1)=O
Biological Activity: Dihydrojasmonic acid is a pentacyclic oxygen-containing lipid plant growth regulator related to Jasmonic acid (HY-122464), with activities including growth inhibition, promotion of leaf senescence, and induction of the accumulation of some plant secondary metabolites. Dihydrojasmonic acid serves as a substrate for metabolic modification and undergoes biotransformation via side-chain hydroxylation, glycosylation, and amino acid conjugation in the aerial parts and seedlings of barley (Hordeum vulgare). Dihydrojasmonic acid inhibits the growth of dwarf rice seedlings and can induce the synthesis of secondary metabolites in some plant cell culture species, with its activity being species-dependent. Dihydrojasmonic acid is involved in studies related to the regulation of plant growth and development[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Dihydrojasmonic acid | 99.92% | Dihydrojasmonic acid is a pentacyclic oxygen-containing lipid plant growth regulator related to Jasmonic acid (HY-122464), with activities including growth inhibition, promotion of leaf senescence, and induction of the accumulation of some plant secondary metabolites. Dihydrojasmonic acid serves as a substrate for metabolic modification and undergoes biotransformation via side-chain hydroxylation, glycosylation, and amino acid conjugation in the aerial parts and seedlings of barley (Hordeum vulgare). Dihydrojasmonic acid inhibits the growth of dwarf rice seedlings and can induce the synthesis of secondary metabolites in some plant cell culture species, with its activity being species-dependent. Dihydrojasmonic acid is involved in studies related to the regulation of plant growth and development. | ||||||||||||||||||||
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Dihydrojasmonic acid (Standard) | ≥98% | Dihydrojasmonic acid (Standard) is the analytical standard of Dihydrojasmonic acid (HY-131116). This product is intended for research and analytical applications. Dihydrojasmonic acid is a pentacyclic oxygen-containing lipid plant growth regulator related to Jasmonic acid (HY-122464), with activities including growth inhibition, promotion of leaf senescence, and induction of the accumulation of some plant secondary metabolites. Dihydrojasmonic acid serves as a substrate for metabolic modification and undergoes biotransformation via side-chain hydroxylation, glycosylation, and amino acid conjugation in the aerial parts and seedlings of barley (Hordeum vulgare). Dihydrojasmonic acid inhibits the growth of dwarf rice seedlings and can induce the synthesis of secondary metabolites in some plant cell culture species, with its activity being species-dependent. Dihydrojasmonic acid is involved in studies related to the regulation of plant growth and development. | ||||||||||||||||||||
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(±)-Jasmonic acid | 99.88% | (±)-Jasmonic acid is an endogenous growth regulator closely related to plant resistance to abiotic stresses, used to activate defense responses to wounding, herbivory, and pathogen attacks. (±)-Jasmonic acid does not play an independent regulatory role, but works in a complex signaling network with other plant hormone signaling pathways. In addition, (±)-Jasmonic acid can also reduce chlorophyll levels in green and etiolated barley leaf segments and inhibit the elongation of rice seedlings. | ||||||||||||||||||||
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Jasmonic acid | Jasmonic acid ((-)-Jasmonic acid) is a plant growth regulator and a derivative of Linolenic acid (HY-N0728). Jasmonic acid enhances plant resistance and is widely used as a stress protectant. Jasmonic acid is an endogenous plant hormone and a plant growth inhibitor. | |||||||||||||||||||||
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7-epi Jasmonic acid | 7-epi Jasmonic acid is the isomer of (±)-Jasmonic acid (HY-122464). (±)-Jasmonic acid is a plant growth regulator and a derivative of α-linolenic acid. (±)-Jasmonic acid decreases chlorophyll levels in green and etiolated barley leaf segments and inhibits elongation of rice seedlings. | |||||||||||||||||||||
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GIV3727 | GIV3727 is an orally active bitter taste receptor antagonist targeting TAS2R4, TAS2R7, TAS2R20, TAS2R31, TAS2R40, and TAS2R43, with orthosteric, insurmountable antagonism at hTAS2R31. GIV3727 blocks TAS2R4 and prevents Gallic acid-induced upregulation of GDF15 mRNA expression. GIV3727 inhibits agonist-evoked receptor activation. GIV3727 reduces the perceived bitterness of acesulfame K and saccharin without affecting sweet taste perception. GIV3727 can be used for obesity research. | |||||||||||||||||||||
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(-)-Dihydrojasmonic acid | (-)-Dihydrojasmonic acid ((-)-9,10-Dihydrojasmonic acid) is a compound that can be isolated from the immature fruits of Vicia faba L. and belongs to plant endogenous cyclopentanoid metabolites. | |||||||||||||||||||||
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(+)-Dihydrojasmonic acid | (+)-Dihydrojasmonic acid is a fatty acid. | |||||||||||||||||||||
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Octanoate, 99% sodium | 99.92% | Octanoate, 99% sodium is an oily liquid with a slightly unpleasant rancid taste and used commercially in the production of esters used in perfumery and also in the manufacture of dyes. Octanoate, 99% sodium is also an orally active tremor-suppressing agent. | ||||||||||||||||||||
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(Rac)-Jasmonic acid | (Rac)-Jasmonic acid is the racemate of Jasmonic acid (HY-122464A). Jasmonic acid ((-)-Jasmonic acid) is a plant growth regulator and a derivative of Linolenic acid (HY-N0728). | |||||||||||||||||||||
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2-Pentylcyclohexanone | 2-Pentylcyclohexanone is a compound that can be isolated from Chenopodium ambrosioides essential oil. | |||||||||||||||||||||
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References
- [1]. Meyer A, et al. Metabolism of the plant growth regulator dihydrojasmonic acid in barley shoots. Phytochemistry, 1989, 28(4):1007‑1011.
- [2]. Koda Y. The Role of Jasmonic Acid and Related Compounds in the Regulation of Plant Development. International Review of Cytology, 1992, 135:155‑199.
- [3]. Gundlach H. Biological activity and biosynthesis of pentacyclic oxylipins: The linoleic acid pathway. Phytochemistry, 1998, 47(4):527‑537.
