84-17-3
84-17-3
Chemical Structure
Dienestrol
- CAS No.: 84-17-3
- Formula:C18H18O2
- Molecular Weight:266.33
IUPAC Name: 4,4'-((2E,4E)-hexa-2,4-diene-3,4-diyl)diphenol
InChIKey: NFDFQCUYFHCNBW-SCGPFSFSSA-N
SMILES: C/C=C(C1=CC=C(O)C=C1)/C(C2=CC=C(O)C=C2)=C/C
Biological Activity: Dienestrol is an orally active nonsteroidal estrogen. Dienestrol prevents the formation of implantation swellings in the uterus by inhibiting ovum discharge[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Dienestrol | 98.04% | Dienestrol is an orally active nonsteroidal estrogen. Dienestrol prevents the formation of implantation swellings in the uterus by inhibiting ovum discharge. | ||||||||||||||||||||
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Dienestrol (Standard) | ≥98% | Dienestrol (Standard) is the analytical standard of Dienestrol (HY-B1403). This product is intended for research and analytical applications. Dienestrol is an orally active nonsteroidal estrogen. Dienestrol prevents the formation of implantation swellings in the uterus by inhibiting ovum discharge. | ||||||||||||||||||||
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Dienestrol-d8 | Dienestrol-d8 is the deuterated-labeled Dienestrol (HY-B1403). Dienestrol is an orally active nonsteroidal estrogen. Dienestrol prevents the formation of implantation swellings in the uterus by inhibiting ovum discharge. | |||||||||||||||||||||
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Dienestrol-d2 | Dienestrol-d2 is a deuterium labeled Dienestrol (HY-B1403). Dienestrol is an orally active nonsteroidal estrogen. Dienestrol prevents the formation of implantation swellings in the uterus by inhibiting ovum discharge. | |||||||||||||||||||||
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Nyasol | Nyasol ((-)-Nyasol) is an active compound that has antifungal, antibacterial, antileishmanial, hyaluronidase inhibition activities. Nyasol inhibits LTB4 binding to human neutrophils. Nyasol suppresses neuroinflammatory response through the inhibition of I-κB degradation in LPS (HY-D1056)-stimulated BV-2 microglial cells. | |||||||||||||||||||||
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Diethylstilbestrol | 99.62% | Diethylstilbestrol is a non-steroidal female hormone that has oral activity and can act on menopausal and postmenopausal disorders. Diethylstilbestrol can induce DNA oxidation and Apoptosis of spermatogonial stem cells. Diethylstilbestrol can induce thymocyte Autophagy Diethylstilbestrol is a 11β-hydroxysteroid dehydrogenase 2 (HSD11B2) inhibitor.. | ||||||||||||||||||||
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Diethylstilbestrol-d3 | Diethylstilbestrol-d3 is deuterium labeled Diethylstilbestrol. | |||||||||||||||||||||
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(-)-Hinokiresinol | 98.0% | (-)-Hinokiresinol (Hinokiresinol; trans-Hinokiresinol) can be isolated from Chamaecyparis obtusa. (-)-Hinokiresinol has weak termiticidal activity but strong antifeedant and repellent activity. | ||||||||||||||||||||
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cis-Hinkiresinol | cis-Hinkiresinol is a bioactive constituent of Rhizoma anemarrhenae. Rhizoma anemarrhenae is reprted to have anti-pathogenic microorganism, hypoglycemic effects, anti-inflammatory, antipyretic effects and anti-platelet aggregation. | |||||||||||||||||||||
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(+)-Nyasol | (+)-Nyasol is a stilbene-type organic compound that can be naturally extracted from the dried roots of Asparagus filicinus Ham. ex D. Don (an Asparagus species) from Fenna, Tibet, China. This plant is traditionally used in the study of bronchitis, cough, and pneumonia, and can be used in research related to respiratory diseases. | |||||||||||||||||||||
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Bisphenol E | 99.90% | Bisphenol E (4,4'-Ethylidenediphenol) is a biochemical reagent. | ||||||||||||||||||||
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Isodienestrol | Isodienestrol, a Diethylstilbestrol (HY-14598) derivative, is a Microtubule inhibitor. Isodienestrol can be used for cancers research | |||||||||||||||||||||
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Bisphenol A-13C2 | Bisphenol A-13C2 is 13C labeled Bisphenol A. Bisphenol A is a phenolic, organic synthetic compound widely used in the production of polycarbonate plastics and epoxy resins. Bisphenol A is a reproductive, developmental, and systemic toxicant, often classified as an endocrine-disrupting compound (EDC). Bisphenol A is associated with many diseases, including cardiovascular diseases, respiratory diseases, diabetes, kidney diseases, obesity, and reproductivedisorders. | |||||||||||||||||||||
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References
- [1]. Yearley E J, et al. Experimental electron density studies of non-steroidal synthetic estrogens: Diethylstilbestrol and dienestrol[J]. Journal of Molecular Structure, 2008, 890(1-3): 240-248.
- [2]. Harper MJ. Interference with early pregnancy in rats by estrogen: mechanism of action of dienestrol. Anat Rec. 1968 Dec;162(4):433-52. [Content Brief]
