This HTML5 document contains 65 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

PrefixIRI
n2http://linked.opendata.cz/resource/drugbank/drug/
dctermshttp://purl.org/dc/terms/
n19http://linked.opendata.cz/resource/drugbank/drug/DB00890/identifier/chebi/
n6http://linked.opendata.cz/resource/mesh/concept/
n14http://linked.opendata.cz/resource/drugbank/company/
foafhttp://xmlns.com/foaf/0.1/
n22http://linked.opendata.cz/resource/drugbank/drug/DB00890/identifier/wikipedia/
n21http://linked.opendata.cz/resource/drugbank/drug/DB00890/identifier/pharmgkb/
n20http://bio2rdf.org/drugbank:
n16http://linked.opendata.cz/resource/drugbank/drug/DB00890/identifier/kegg-compound/
admshttp://www.w3.org/ns/adms#
n17http://linked.opendata.cz/resource/drugbank/drug/DB00890/identifier/kegg-drug/
n10http://wifo5-03.informatik.uni-mannheim.de/drugbank/resource/drugs/
n18http://linked.opendata.cz/resource/drugbank/drug/DB00890/identifier/drugbank/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n8http://linked.opendata.cz/resource/drugbank/medicinal-product/
n7http://linked.opendata.cz/ontology/drugbank/
owlhttp://www.w3.org/2002/07/owl#
n5http://linked.opendata.cz/ontology/mesh/
n11http://linked.opendata.cz/resource/drugbank/property/
n4http://www.rxlist.com/cgi/generic2/
xsdhhttp://www.w3.org/2001/XMLSchema#
n13http://linked.opendata.cz/resource/atc/
n12http://linked.opendata.cz/ontology/sukl/drug/

Statements

Subject Item
n2:DB00890
rdf:type
n7:Drug
n7:description
Dienestrol is a synthetic, non-steroidal estrogen. It is an estrogen receptor agonist. Estrogens work partly by increasing a normal clear discharge from the vagina and making the vulva and urethra healthy. Using or applying an estrogen relieves or lessens: dryness and soreness in the vagina, itching, redness, or soreness of the vulva. Conditions that are treated with vaginal estrogens include a genital skin condition (vulvar atrophy), inflammation of the vagina (atrophic vaginitis), and inflammation of the urethra (atrophic urethritis).
n7:group
approved
n7:indication
For use in the treatment of atrophic vaginitis and kraurosis vulvae.
n7:manufacturer
n14:271B5919-363D-11E5-9242-09173F13E4C5 n14:271B591B-363D-11E5-9242-09173F13E4C5 n14:271B591A-363D-11E5-9242-09173F13E4C5
owl:sameAs
n10:DB00890 n20:DB00890
dcterms:title
Dienestrol
adms:identifier
n16:C08090 n17:D00898 n18:DB00890 n19:4518 n21:PA164745534 n22:Dienestrol
n7:mechanismOfAction
Dienestrol is a synthetic, non-steroidal estrogen. Estrogens passively diffuse into target cells of responsive tissues, complex with the estrogen receptors, and enter the cell's nucleus to initiate or enhance gene transcription of protein synthesis after binding to DNA.
n7:packager
n14:271B5918-363D-11E5-9242-09173F13E4C5
n7:synonym
Dienestrolum Dehydrostilbestrol DV Diènestrol Dienestrol
n7:toxicity
Symptoms of overdose include nausea and vomiting, and withdrawal bleeding may occur in females.
n7:proteinBinding
50 to 80%
n7:synthesisReference
Short, W.F. and Hobday, G.1; U.S. Patent 2,464,203; March 15,1949; assigned to Boots Pure Drug Company Limited, England. Adler, E.; U.S. Patent 2,465,505; March 29,1949; assigned to Hoffmann-La Roche Inc.
n5:hasConcept
n6:M0006320
foaf:page
n4:diene.htm
n7:IUPAC-Name
n11:271B5921-363D-11E5-9242-09173F13E4C5
n7:InChI
n11:271B5927-363D-11E5-9242-09173F13E4C5
n7:Molecular-Formula
n11:271B5926-363D-11E5-9242-09173F13E4C5
n7:Molecular-Weight
n11:271B5923-363D-11E5-9242-09173F13E4C5
n7:Monoisotopic-Weight
n11:271B5924-363D-11E5-9242-09173F13E4C5
n7:SMILES
n11:271B5925-363D-11E5-9242-09173F13E4C5
n7:Water-Solubility
n11:271B591F-363D-11E5-9242-09173F13E4C5 n11:271B5937-363D-11E5-9242-09173F13E4C5
n7:logP
n11:271B5920-363D-11E5-9242-09173F13E4C5 n11:271B591D-363D-11E5-9242-09173F13E4C5 n11:271B5939-363D-11E5-9242-09173F13E4C5
n7:logS
n11:271B591E-363D-11E5-9242-09173F13E4C5 n11:271B593A-363D-11E5-9242-09173F13E4C5
n12:hasATCCode
n13:G03CC02 n13:G03CB01
n7:H-Bond-Acceptor-Count
n11:271B592D-363D-11E5-9242-09173F13E4C5
n7:H-Bond-Donor-Count
n11:271B592E-363D-11E5-9242-09173F13E4C5
n7:InChIKey
n11:271B5928-363D-11E5-9242-09173F13E4C5
n7:Polar-Surface-Area--PSA-
n11:271B5929-363D-11E5-9242-09173F13E4C5
n7:Polarizability
n11:271B592B-363D-11E5-9242-09173F13E4C5
n7:Refractivity
n11:271B592A-363D-11E5-9242-09173F13E4C5
n7:Rotatable-Bond-Count
n11:271B592C-363D-11E5-9242-09173F13E4C5
n7:absorption
Systemic absorption and mode of action of dienestrol are undetermined.Estrogens diffuse into their target cells and interact with a protein receptor. Target cells include the female reproductive tract, the mammary gland, the hypothalamus, and the pituitary. Estrogens increase the hepatic synthesis of sex hormone binding globulin (SHBG), thyroid-binding globulin (TBG), and other serum proteins and suppress follicle-stimulating hormone (FSH) from the anterior pituitary. The combination of an estrogen with a progestin suppresses the hypothalamic-pituitary system, decreasing the secretion of gonadotropin-releasing hormone (GnRH).
n7:affectedOrganism
Humans and other mammals
n7:casRegistryNumber
84-17-3
n7:category
n7:containedIn
n8:271B591C-363D-11E5-9242-09173F13E4C5
n7:Bioavailability
n11:271B5933-363D-11E5-9242-09173F13E4C5
n7:Ghose-Filter
n11:271B5935-363D-11E5-9242-09173F13E4C5
n7:MDDR-Like-Rule
n11:271B5936-363D-11E5-9242-09173F13E4C5
n7:Melting-Point
n11:271B5938-363D-11E5-9242-09173F13E4C5
n7:Number-of-Rings
n11:271B5932-363D-11E5-9242-09173F13E4C5
n7:Physiological-Charge
n11:271B5931-363D-11E5-9242-09173F13E4C5
n7:Rule-of-Five
n11:271B5934-363D-11E5-9242-09173F13E4C5
n7:Traditional-IUPAC-Name
n11:271B5922-363D-11E5-9242-09173F13E4C5
n7:pKa--strongest-acidic-
n11:271B592F-363D-11E5-9242-09173F13E4C5
n7:pKa--strongest-basic-
n11:271B5930-363D-11E5-9242-09173F13E4C5