Dienestrol
Dv, Estraguard (dienestrol) is a small molecule pharmaceutical. Dienestrol was first approved as Dienestrol on 1982-01-01. It is used to treat atrophic vaginitis and vulvar lichen sclerosus in the USA.
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Therapeutic Areas
Therapeutic Area | MeSH |
---|---|
urogenital diseases | D000091642 |
Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Dienestrol
Tradename | Company | Number | Date | Products |
---|---|---|---|---|
DIENESTROL | Johnson & Johnson | N-006110 DISCN | 1982-01-01 | 1 products |
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Labels
FDA
EMA
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Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
---|---|---|---|
atrophic vaginitis | EFO_1001271 | D059268 | — |
vulvar lichen sclerosus | — | D007724 | N90.4 |
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
HCPCS
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Clinical
Clinical Trials
1 clinical trials
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Indications Phases 4
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Indications Phases 3
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Indications Phases 2
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Indications Phases 1
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | DIENESTROL |
INN | dienestrol |
Description | Dienestrol is an olefinic compound that is hexa-2,4-diene substituted by 4-hydroxyphenyl groups at positions 3 and 4 respectively. It has a role as a xenoestrogen. It is a member of phenols and an olefinic compound. |
Classification | Small molecule |
Drug class | estrogens |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | C/C=C(C(=C/C)/c1ccc(O)cc1)\c1ccc(O)cc1 |
Identifiers
PDB | — |
CAS-ID | 13029-44-2 |
RxCUI | — |
ChEMBL ID | CHEMBL1018 |
ChEBI ID | — |
PubChem CID | 667476 |
DrugBank | DB00890 |
UNII ID | RRW32X4U1F (ChemIDplus, GSRS) |
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 167 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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19 adverse events reported
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