Estrogens, Conjugated
sodium [(13S)-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl] sulfate
Molecular Identity
Estrogens, Conjugated
sodium [(13S)-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl] sulfate
PubChem CID: 45357473
Conjugated Estrogens can cause cancer according to California Labor Code. It can cause developmental toxicity according to state or federal government labeling requirements.
2D Structure
Properties
C18H21NaO5S
Molecular Formula
372.40
Molecular Weight
g/mol
372.1007
Exact Mass
Da
91.9
TPSA
Good oral absorption (< 140 A²)
0
H-Bond Donors
5
H-Bond Acceptors
630
Complexity
SMILES
Canonical SMILES
SMILES: CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)OS(=O)(=O)[O-].[Na+]Isomeric SMILES
SMILES: C[C@]12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)OS(=O)(=O)[O-].[Na+]Synonyms(20)
ClimopaxOestro FeminalEstro FeminalEstro-FeminalConjugated EstrogenEstrogen, ConjugatedEquine Estrogen, ConjugatedEstrogen, Conjugated EquineEquine Estrogens, ConjugatedEstrogens, conjugated (USP)SodestrinPremarin CreamConjugated Estrogenic SubstancesPremarin VaginalEstrogens,conjugated
Data from PubChem (NCBI)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Drug Network
Trials and conditions connected to Estrogens, Conjugated
Loading drug network...