94371-89-8
Chemical Structure
1,2-Diphenylethane-d14
- CAS No.: 94371-89-8
- Formula:C14D14
- Molecular Weight:196.35
IUPAC Name: (S)-2-(2-((6-oxo-5-(trifluoromethyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1,6-dihydropyridazin-4-yl)amino)propoxy)isoindoline-1,3-dione
InChIKey: QWUWMCYKGHVNAV-BOAKRTBXSA-N
SMILES: [2H]C1=C([2H])C([2H])=C([2H])C([2H])=C1C([2H])([2H])C([2H])([2H])C2=C([2H])C([2H])=C([2H])C([2H])=C2[2H]
Biological Activity: 1,2-Diphenylethane-d14 is the d14-labeled Bibenzyl (HY-78004). Bibenzyl (s-Diphenylethane; Dibenzyl) is the parent core structure of bibenzyl-type natural products and an intermediate in organic synthesis. Hydroxyl-substituted derivatives of Bibenzyl are mainly isolated from plants such as Dendrobium (Orchidaceae) and Cannabaceae. These derivatives accumulate when plants are exposed to fungal infection and biotic stress, and exhibit antioxidant, anti-inflammatory, and anti-hepatic steatosis activities[1][2][3].
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1,2-Diphenylethane-d14 | 99.5% | 1,2-Diphenylethane-d14 is the d14-labeled Bibenzyl (HY-78004). Bibenzyl (s-Diphenylethane; Dibenzyl) is the parent core structure of bibenzyl-type natural products and an intermediate in organic synthesis. Hydroxyl-substituted derivatives of Bibenzyl are mainly isolated from plants such as Dendrobium (Orchidaceae) and Cannabaceae. These derivatives accumulate when plants are exposed to fungal infection and biotic stress, and exhibit antioxidant, anti-inflammatory, and anti-hepatic steatosis activities. | ||||||||||||||||||||
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1,2-Diphenylethane-d4 | 1,2-Diphenylethane-d4 (Dibenzil-d4; s-Diphenylethane-d4; Bibenzyl-d4) is the d4-labeled Bibenzyl (HY-78004). Bibenzyl (s-Diphenylethane; Dibenzyl) is the parent core structure of bibenzyl-type natural products and an intermediate in organic synthesis. Hydroxyl-substituted derivatives of Bibenzyl are mainly isolated from plants such as Dendrobium (Orchidaceae) and Cannabaceae. These derivatives accumulate when plants are exposed to fungal infection and biotic stress, and exhibit antioxidant, anti-inflammatory, and anti-hepatic steatosis activities. | |||||||||||||||||||||
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Bibenzyl | 99.97% | Bibenzyl (s-Diphenylethane; Dibenzyl) is the parent core structure of bibenzyl-type natural products and an intermediate in organic synthesis. Hydroxyl-substituted derivatives of Bibenzyl are mainly isolated from plants such as Dendrobium (Orchidaceae) and Cannabaceae. These derivatives accumulate when plants are exposed to fungal infection and biotic stress, and exhibit antioxidant, anti-inflammatory, and anti-hepatic steatosis activities. | ||||||||||||||||||||
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- [1]. Kongkatitham V, et al. Anti-oxidant and anti-inflammatory effects of new bibenzyl derivatives from Dendrobium parishii in hydrogen peroxide and lipopolysaccharide treated RAW264. 7 cells[J]. Phytochemistry Letters, 2018, 24: 31-38.
- [2]. Zhang ZM, et al. Bibenzyl and naphthalene derivatives from Dendrobium chrysanthum and their anti-hepatic-steatosis activities. Bioorganic chemistry. 2024 Apr;145:107236.
- [3]. Boddington KF, et al. Bibenzyl synthesis in Cannabis sativa L. Plant J. 2022 Feb;109(3):693-707. [Content Brief]
