Enclomiphene citrate
Modify Date: 2025-08-20 08:42:01
Enclomiphene citrate structure
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Common Name | Enclomiphene citrate | ||
|---|---|---|---|---|
| CAS Number | 7599-79-3 | Molecular Weight | 598.08300 | |
| Density | N/A | Boiling Point | 509ºC at 760mmHg | |
| Molecular Formula | C32H36ClNO8 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 261.6ºC | |
Use of Enclomiphene citrateEnclomiphene citrate is a potent and orally active oestrogen receptor antagonist, with antioestrogenic property[1]. |
| Name | 2-{4-[(E)-2-Chloro-1,2-diphenylvinyl]phenoxy}-N,N-diethylethanami ne 2-hydroxy-1,2,3-propanetricarboxylate (1:1) |
|---|---|
| Synonym | More Synonyms |
| Description | Enclomiphene citrate is a potent and orally active oestrogen receptor antagonist, with antioestrogenic property[1]. |
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| Related Catalog | |
| References |
| Boiling Point | 509ºC at 760mmHg |
|---|---|
| Molecular Formula | C32H36ClNO8 |
| Molecular Weight | 598.08300 |
| Flash Point | 261.6ºC |
| Exact Mass | 597.21300 |
| PSA | 144.60000 |
| LogP | 5.31410 |
| InChIKey | PYTMYKVIJXPNBD-BTKVJIOYSA-N |
| SMILES | CCN(CC)CCOc1ccc(C(=C(Cl)c2ccccc2)c2ccccc2)cc1.O=C(O)CC(O)(CC(=O)O)C(=O)O |
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Name: Primary cell-based high-throughput screening assay for identification of compounds th...
Source: Johns Hopkins Ion Channel Center
Target: regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id: JHICC_RGS_Act_HTS
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Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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Name: High throughput fluorescence intensity-based biochemical assay to screen for small mo...
Source: University of Pittsburgh Molecular Library Screening Center
Target: furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id: MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
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Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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Name: Dicer-mediated maturation of pre-microRNA
Source: Center for Chemical Genomics, University of Michigan
Target: N/A
External Id: TargetID_659_CEMA
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify pos...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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Name: Absorbance-based primary biochemical high throughput screening assay to identify acti...
Source: The Scripps Research Institute Molecular Screening Center
Target: caspase-3 preproprotein [Homo sapiens]
External Id: PROCASPASE3_ACT_EPIABS_1536_1X%ACT PRUN
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Name: uHTS identification of small molecule modulators of NR3A
Source: Burnham Center for Chemical Genomics
Target: N/A
External Id: SBCCG-A1015-NR3A-Primary-Assay
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| trans-clomifene citrate |
| Enclomiphene citrate |