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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
Structure of ELACESTRANT HYDROCHLORIDE

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

HIDE SMILES / InChI

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.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P03372
Gene ID: 2099.0
Gene Symbol: ESR1
Target Organism: Homo sapiens (Human)
PubMed

PubMed

TitleDatePubMed
Elacestrant (RAD1901), a Selective Estrogen Receptor Degrader (SERD), Has Antitumor Activity in Multiple ER(+) Breast Cancer Patient-derived Xenograft Models.
2017 Aug 15

Sample Use Guides

400 mg/day once daily
Route of Administration: Oral
Elacestrant treatment also inhibited E2-mediated proliferation in MCF7 and T47D cells in a dose-dependent manner
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:42:51 GMT 2023
Edited
by admin
on Sat Dec 16 09:42:51 GMT 2023
Record UNII
8NZT0PR8AL
Record Status Validated (UNII)
Record Version
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Name Type Language
ELACESTRANT HYDROCHLORIDE
USAN  
Official Name English
ELACESTRANT DIHYDROCHLORIDE
Preferred Name English
RAD1901 DIHYDROCHLORIDE
Code English
ORSERDU
Brand Name English
2-Naphthalenol, 6-[2-[ethyl[[4-[2-(ethylamino)ethyl]phenyl]methyl]amino]-4-methoxyphenyl]-5,6,7,8-tetrahydro-, hydrochloride (1:2), (6R)-
Systematic Name English
(6R)-6-{2-[ethyl({4-[2-(ethylamino)ethyl]phenyl}methyl)amino]-4-methoxyphenyl}-5,6,7,8-tetrahydronaphthalen-2-ol hydrochloride (1:2)
Systematic Name English
ELACESTRANT HYDROCHLORIDE [USAN]
Common Name English
RAD-1901 DIHYDROCHLORIDE
Code English
Code System Code Type Description
NCI_THESAURUS
C171898
Created by admin on Sat Dec 16 09:42:51 GMT 2023 , Edited by admin on Sat Dec 16 09:42:51 GMT 2023
PRIMARY
USAN
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
PRIMARY
MANUFACTURER PRODUCT INFORMATION
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
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.
CAS
1349723-93-8
Created by admin on Sat Dec 16 09:42:51 GMT 2023 , Edited by admin on Sat Dec 16 09:42:51 GMT 2023
PRIMARY
EVMPD
SUB184532
Created by admin on Sat Dec 16 09:42:51 GMT 2023 , Edited by admin on Sat Dec 16 09:42:51 GMT 2023
PRIMARY
FDA UNII
8NZT0PR8AL
Created by admin on Sat Dec 16 09:42:51 GMT 2023 , Edited by admin on Sat Dec 16 09:42:51 GMT 2023
PRIMARY
PUBCHEM
67479909
Created by admin on Sat Dec 16 09:42:51 GMT 2023 , Edited by admin on Sat Dec 16 09:42:51 GMT 2023
PRIMARY
SMS_ID
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
PRIMARY
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