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Biological and Environmental Research Ontology
| Id | http://purl.obolibrary.org/obo/NCIT_C104055
http://purl.obolibrary.org/obo/NCIT_C104055
|
|---|---|
| Preferred Name | Telapristone Acetate |
| Definitions |
The acetate form of the 21-substituted-19-nor-progestin telapristone, an orally available selective progesterone receptor modulator (SPRM), with potential anti-progesterone and antineoplastic activities. Upon oral administration, CDB-4124 competitively binds to the progesterone receptor (PR) in progesterone-responsive tissue and inhibits PR-mediated gene expression. This interferes with progesterone activity in the reproductive system. As a result, this agent may suppress ovulation and inhibit proliferation of endometrial tissue. Also, this agent may prevent cell growth and induce apoptosis in estrogen receptor (ER) and PR-positive breast cancer cells through a reduction in progesterone levels, ER downregulation and a suppression of the expression of cyclin-dependent kinases (CDK) 2 and 4, ultimately leading to G1/S cell cycle arrest. Unlike some other SPRMs, this agent does not exert any estrogenic, androgenic, anti-estrogenic, and anti-androgenic activities.
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | The acetate form of the 21-substituted-19-nor-progestin telapristone, an orally available selective progesterone receptor modulator (SPRM), with potential anti-progesterone and antineoplastic activities. Upon oral administration, CDB-4124 competitively binds to the progesterone receptor (PR) in progesterone-responsive tissue and inhibits PR-mediated gene expression. This interferes with progesterone activity in the reproductive system. As a result, this agent may suppress ovulation and inhibit proliferation of endometrial tissue. Also, this agent may prevent cell growth and induce apoptosis in estrogen receptor (ER) and PR-positive breast cancer cells through a reduction in progesterone levels, ER downregulation and a suppression of the expression of cyclin-dependent kinases (CDK) 2 and 4, ultimately leading to G1/S cell cycle arrest. Unlike some other SPRMs, this agent does not exert any estrogenic, androgenic, anti-estrogenic, and anti-androgenic activities. |
|---|---|
| prefLabel | Telapristone Acetate
|
| label | Telapristone Acetate
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| PDQ_Closed_Trial_Search_ID | 598776
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| code | C104055
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| Has_Target | |
| prefixIRI | NCIT:C104055
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| in_subset |
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| Display_Name | Telapristone Acetate
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| Preferred_Name | Telapristone Acetate
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| FDA_UNII_Code | 1K9EYK92PQ
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| Contributing_Source |
CTRP
FDA
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| Maps_To | Telapristone Acetate
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| CAS_Registry | 198414-31-2
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| NCI_Drug_Dictionary_ID | 598776
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| type | |
| Is_Value_For_GDC_Property | |
| subClassOf | |
| PDQ_Open_Trial_Search_ID | 598776
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| Semantic_Type |
Organic Chemical
Pharmacologic Substance
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| UMLS_CUI | C3501648
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