Structure Database (LMSD)

Common Name
Beta-estradiol
Systematic Name
estra-1,3,5(10)-triene-3,17β-diol
Synonyms
  • Beta-estradiol
  • 17beta-Estradiol
  • 17b-Oestradiol
  • 3,17b-Dihydroxyestra-1,3,5(10)-triene
LM ID
LMST02010001
Formula
Exact Mass
Calculate m/z
272.17763
Sum Composition
Status
Curated




Classification

Biological Context

17β-Estradiol is the major pre-menopausal bioactive estrogen and an active metabolite of testosterone.1,2,3 It is produced primarily by the ovary, and to a lesser extent, by the adrenals, testes, and adipose tissue, as well as by the placenta during pregnancy.1 17β-Estradiol binds to estrogen receptors localized to the nucleus, cytoplasm, and plasma membrane and induces gene transcription or non-genomic intracellular signaling in a location-dependent manner.2 It regulates reproductive development in females and spermatogenesis in males, as well as various non-reproductive processes including lipid and glucose homeostasis, bone mass maintenance, cognition, energy balance, and dilation of blood vessels.2,3 17β-Estradiol deficiency due to hypogonadism or 17α-hydroxylase/17,20-lyase deficiency is associated with fatigue, incontinence, osteoporosis, depression, emotional instability, and hot flashes. Formulations containing 17β-estradiol have been used in the treatment of menopause symptoms and the prevention of osteoporosis.

This information has been provided by Cayman Chemical

References

Reactions

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Reactions graph legend

String Representations

InChiKey (Click to copy)
VOXZDWNPVJITMN-ZBRFXRBCSA-N
InChi (Click to copy)
InChI=1S/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-17,19-20H,2,4,6-9H2,1H3/t14-,15-,16+,17+,18+/m1/s1
SMILES (Click to copy)
C1=CC2[C@@]3([H])CC[C@]4(C)[C@@H](O)CC[C@@]4([H])[C@]3([H])CCC=2C=C1O

Other Databases

Wikipedia
KEGG ID
HMDB ID
CHEBI ID
LIPIDBANK ID
SST0064
PubChem CID
SwissLipids ID
Cayman ID
PDB ID
GuidePharm ID

Calculated Physicochemical Properties

Heavy Atoms 20
Rings 4
Aromatic Rings 1
Rotatable Bonds 0
Van der Waals Molecular Volume 269.28
Topological Polar Surface Area 40.46
Hydrogen Bond Donors 2
Hydrogen Bond Acceptors 2
logP 3.90
Molar Refractivity 79.24

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Updated at
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