Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C30H38N2O2.2ClH |
Molecular Weight | 531.557 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.Cl.[H][C@]1(CCC2=CC(O)=CC=C2C1)C3=C(C=C(OC)C=C3)N(CC)CC4=CC=C(CCNCC)C=C4
InChI
InChIKey=XGFHYCAZOCBCRQ-FBHGDYMESA-N
InChI=1S/C30H38N2O2.2ClH/c1-4-31-17-16-22-6-8-23(9-7-22)21-32(5-2)30-20-28(34-3)14-15-29(30)26-11-10-25-19-27(33)13-12-24(25)18-26;;/h6-9,12-15,19-20,26,31,33H,4-5,10-11,16-18,21H2,1-3H3;2*1H/t26-;;/m1../s1
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C30H38N2O2 |
Molecular Weight | 458.6349 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Elacestrant (ER-306323 or RAD 1901 [6R)-6-(2-(N-(4-(2-(ethylamino)ethyl)benzyl)-N-ethylamino)-4-methoxyphenyl)-5,6,7,8-tetrahydronaphthalen-2-ol dihydrochloride]) is a selective estrogen receptor (ER) degrader. Elacestrant induces the degradation of ER, inhibits ER-mediated signaling and growth of ER+ breast cancer cell lines in vitro and in vivo, and significantly inhibits tumor growth in breast cancer xenograft models. Elacestrant has the potential for use as a single agent or in combination with other therapies for the treatment of breast cancer. Elacestrant is being developed by Radius Health, for the treatment of estrogen receptor positive breast cancer.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT03778931
400 mg/day once daily
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/28473534
Elacestrant treatment also inhibited E2-mediated proliferation in MCF7 and T47D cells in a dose-dependent manner
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:42:51 GMT 2023
by
admin
on
Sat Dec 16 09:42:51 GMT 2023
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Record UNII |
8NZT0PR8AL
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Record Status |
Validated (UNII)
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Record Version |
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Official Name | English | ||
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Preferred Name | English | ||
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Code | English | ||
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Brand Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Code | English |
Code System | Code | Type | Description | ||
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C171898
Created by
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GH-121
Created by
admin on Sat Dec 16 09:42:51 GMT 2023 , Edited by admin on Sat Dec 16 09:42:51 GMT 2023
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RAD-1901 DIHYDROCHLORIDE
Created by
admin on Sat Dec 16 09:42:51 GMT 2023 , Edited by admin on Sat Dec 16 09:42:51 GMT 2023
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PRIMARY | Description: RAD1901 is an orally available, selective estrogen receptor degrader (SERD) and selective estrogen receptor modulator (SERM), with potential antineoplastic and estrogen-like activities. Upon oral administration of higher doses of RAD1901, this agent acts as a SERD, which binds to the estrogen receptor (ER) and induces a conformational change that results in the degradation of the receptor. This may inhibit the growth and survival of ER-expressing cancer cells. At lower doses of this agent, RAD1901 acts as a SERM and has estrogen-like effects in certain tissues, which can both reduce hot flashes and protect against bone loss. In addition, RAD1901 is able to cross the blood-brain barrier (BBB). (last updated: 5/19/2016).Synonym: RAD1901, RAD-1901, RAD 1901, RAD1901 HCl salt. | ||
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1349723-93-8
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SUB184532
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8NZT0PR8AL
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67479909
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100000170508
Created by
admin on Sat Dec 16 09:42:51 GMT 2023 , Edited by admin on Sat Dec 16 09:42:51 GMT 2023
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