39791-20-3

Nilestriol Chemical Structure
39791-20-3

Chemical Structure

Nilestriol

Synonym(s): Nylestriol; EE3CPE

  • CAS No.: 39791-20-3
  • Formula:C25H32O3
  • Molecular Weight:380.52

IUPAC Name: (8R,9S,13S,14S,16R,17R)-3-(cyclopentyloxy)-17-ethynyl-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthrene-16,17-diol

InChIKey: CHZJRGNDJLJLAW-RIQJQHKOSA-N

SMILES: C#C[C@]1(O)[C@H](O)C[C@@]2([H])[C@]3([H])CCC4=C(C=CC(OC5CCCC5)=C4)[C@@]3([H])CC[C@]12C

Biological Activity: Nilestriol is a estriol derivative, which inhibits osteoporosis on ovariectomized rats or postmenopausal women[1].

Cat. No. Product Name Purity Description Pricing
HY-121528
Nilestriol 98.93% Nilestriol is a estriol derivative, which inhibits osteoporosis on ovariectomized rats or postmenopausal women.
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HY-160976
Ethynyl estradiol 3-sulfate Ethynyl estradiol 3-sulfate (17α-Ethynylestradiol-3-sulfate; EE-3-SO4) can prolong the median survival time of rats in an acute severe blood loss model by approximately 6 times, with a 6-hour survival rate of 80%.
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HY-B0216
Ethinylestradiol 99.96% Ethinylestradiol is an orally active steroidal estrogen. Ethinylestradiol is widely used in research on menopausal symptoms, gynecological conditions, and certain hormone-sensitive cancers.
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HY-B0216S2
Ethynyl Estradiol-13C2 98.64% Ethynyl Estradiol-13C2 is the 13C-labeled Ethynyl Estradiol. Ethynyl Estradiol-13C2 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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HY-B0390
Mestranol 99.69% Mestranol is an inactive proagent and becomes biologically active on conversion to ethinyl estradiol (EE). Mestranol acts as an estrogen receptor agonist. Mestranol combines with a progestin in vivo and can be used for the research of menopausal hormone or menstrual disorders. Mestranol is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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HY-B0709
Estradiol acetate Estradiol acetate is a novel orally active Estradiol (HY-B0141) prodrug. Estradiol acetate reduces the frequency and severity of postmenopause symptoms. Estradiol acetate can be used in the research of menopausal symptoms.
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HY-B1012
Quinestrol 99.19% Quinestrol (W-3566) is an orally effective synthetic estrogen compound that acts on CYP3A4, CYP1A2, and GnRH. Quinestrol interferes with GnRH release and disrupts the hypothalamic-pituitary-ovarian axis. Quinestrol downregulates the gene expression of follicle-stimulating hormone β and luteinizing hormone β, induces oxidative stress, damages reproductive organs, reduces sperm density and motility, increases sperm malformation rate, and alters the levels of sex hormones such as testosterone, luteinizing hormone, estradiol, and progesterone. Quinestrol can be used in studies related to reproductive function regulation.
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HY-W008581
Estradiol 3-methyl ether 99.07% Estradiol 3-methyl ether (EDME) is a highly selective TRPML1 ion channel antagonist and microtubule (microtubule) depolymerizing agent, with IC50 values of 0.22 μM and 3.8 μM against TRPML1 and TRPML2, respectively; it shows no activity against TRPML3. Estradiol 3-methyl ether induces the disruption of cytoplasmic microtubule networks in mammalian cells, with an EC50 of 9 μM. Independent of estrogen receptors, Estradiol 3-methyl ether blocks autophagy (autophagy), TFEB nuclear translocation, and inhibits the migration and invasion of triple-negative breast cancer cells by suppressing TRPML1. Estradiol 3-methyl ether is applicable for relevant research on triple-negative breast cancer.
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HY-Z2771
Estradiol Valerate impurity 6 Estradiol Valerate impurity 6 is an impurity of Estradiol Valerate.
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HY-Z7989
Estriol impurity 2 Estriol impurity 2 (3-Methoxyestriol) is an impurity of Estriol.
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HY-Z8973
Ethinylestradiol impurity 3 Ethinylestradiol impurity 3 (17beta-Ethinylestradiol) is an impurity of Ethinylestradiol.
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References