Details
Stereochemistry | EPIMERIC |
Molecular Formula | C32H47F5O3S |
Molecular Weight | 606.771 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 6 / 7 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@]3([H])C4=C(C[C@H](CCCCCCCCC[S+]([O-])CCCC(F)(F)C(F)(F)F)[C@@]23[H])C=C(O)C=C4
InChI
InChIKey=VWUXBMIQPBEWFH-MSCODYEVSA-N
InChI=1S/C32H47F5O3S/c1-30-17-15-26-25-12-11-24(38)21-23(25)20-22(29(26)27(30)13-14-28(30)39)10-7-5-3-2-4-6-8-18-41(40)19-9-16-31(33,34)32(35,36)37/h11-12,21-22,26-29,38-39H,2-10,13-20H2,1H3/t22-,26+,27-,28-,29+,30-,41?/m0/s1
Fulvestrant Beta-Isomer, also known as Fulvestrant EP Impurity A. Fulvestrant, sold under the trade name Faslodex among others, is an estrogen receptor antagonist indicated for the treatment of hormone receptor (HR)-positive metastatic breast cancer in postmenopausal women with disease progression as well as HR-positive, HER2-negative advanced breast cancer in combination with palbociclib in women with disease progression after endocrine therapy.
Approval Year
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
DTXSID40193748
Created by
admin on Sat Dec 16 05:14:52 GMT 2023 , Edited by admin on Sat Dec 16 05:14:52 GMT 2023
|
PRIMARY | |||
|
71317003
Created by
admin on Sat Dec 16 05:14:52 GMT 2023 , Edited by admin on Sat Dec 16 05:14:52 GMT 2023
|
PRIMARY | |||
|
407577-53-1
Created by
admin on Sat Dec 16 05:14:52 GMT 2023 , Edited by admin on Sat Dec 16 05:14:52 GMT 2023
|
PRIMARY | |||
|
L8HA5DT6RS
Created by
admin on Sat Dec 16 05:14:52 GMT 2023 , Edited by admin on Sat Dec 16 05:14:52 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD