NP-MRD: Showing NP-Card for 17-beta-Estradiol 3-sulfate-17-(beta-D-glucuronide) (NP0090911)

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Record Information

Version

2.0

Created at

2022-05-11 18:25:47 UTC

Updated at

2022-05-11 18:25:47 UTC

NP-MRD ID

NP0090911

Secondary Accession Numbers

None

Natural Product Identification

Common Name

17-beta-Estradiol 3-sulfate-17-(beta-D-glucuronide)

Description

17-Beta-estradiol 3-sulfate-17-(beta-D-glucuronide), also known as estradiol 17b-glucuronide 3-sulfuric acid, belongs to the class of organic compounds known as steroidal glycosides. These are sterol lipids containing a carbohydrate moiety glycosidically linked to the steroid skeleton. 17-Beta-estradiol 3-sulfate-17-(beta-D-glucuronide) is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 02241200522D          

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M  END

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  Mrv0541 02241200522D          

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 11 27  1  6  0  0  0
 12 14  1  0  0  0  0
 13 15  1  0  0  0  0
 16 19  1  0  0  0  0
 18 20  2  0  0  0  0
 18 21  1  0  0  0  0
 19 20  1  0  0  0  0
 20 22  1  0  0  0  0
 21 23  2  0  0  0  0
 22 24  2  0  0  0  0
 23 24  1  0  0  0  0
 31 28  1  6  0  0  0
 29 31  1  0  0  0  0
 29 34  1  0  0  0  0
 32  2  1  1  0  0  0
 35 30  1  1  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 35  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  6  0  0  0
 29 37  1  1  0  0  0
 38 30  1  0  0  0  0
 39 30  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0090911

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12CC[C@H](O[C@@H]3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)C(O)=O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(OS(O)(=O)=O)C=C3

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O11S/c1-24-9-8-14-13-5-3-12(35-36(30,31)32)10-11(13)2-4-15(14)16(24)6-7-17(24)33-23-20(27)18(25)19(26)21(34-23)22(28)29/h3,5,10,14-21,23,25-27H,2,4,6-9H2,1H3,(H,28,29)(H,30,31,32)/t14-,15-,16+,17+,18+,19+,20-,21+,23-,24+/m1/s1

> <INCHI_KEY>
VRMSCBRLZUCJBX-QXYWQCSFSA-N

> <FORMULA>
C24H32O11S

> <MOLECULAR_WEIGHT>
528.569

> <EXACT_MASS>
528.166532556

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
53.252132805695204

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S,4S,5R,6R)-3,4,5-trihydroxy-6-{[(1S,10R,11S,14S,15S)-15-methyl-5-(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-2(7),3,5-trien-14-yl]oxy}oxane-2-carboxylic acid

> <ALOGPS_LOGP>
0.25

> <JCHEM_LOGP>
0.1555711541923268

> <ALOGPS_LOGS>
-2.63

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.627462206078711

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.746081858354322

> <JCHEM_PKA_STRONGEST_BASIC>
-3.686499496639547

> <JCHEM_POLAR_SURFACE_AREA>
180.04999999999998

> <JCHEM_REFRACTIVITY>
122.1772

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.25e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,4S,5R,6R)-3,4,5-trihydroxy-6-{[(1S,10R,11S,14S,15S)-15-methyl-5-(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-2(7),3,5-trien-14-yl]oxy}oxane-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  S   UNK     0      16.764 -14.281   0.000  0.00  0.00           S+0
HETATM    2  O   UNK     0      28.336  -8.423   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0      18.094 -15.056   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      15.433 -13.506   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      15.989 -15.612   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      17.539 -12.950   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      26.400 -10.356   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      26.400 -11.896   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      25.066 -12.666   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      27.857  -9.886   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      23.732 -11.896   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      27.857 -12.365   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      25.066  -9.586   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      28.756 -11.126   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      23.732 -10.356   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      25.091 -14.269   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      26.400  -8.816   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      22.331 -12.676   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      23.708 -15.082   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      22.319 -14.280   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      20.904 -11.807   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      20.878 -15.127   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      19.444 -12.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      19.431 -14.291   0.000  0.00  0.00           C+0
HETATM   25  H   UNK     0      26.538 -13.197   0.000  0.00  0.00           H+0
HETATM   26  H   UNK     0      25.076 -11.001   0.000  0.00  0.00           H+0
HETATM   27  H   UNK     0      23.840 -13.166   0.000  0.00  0.00           H+0
HETATM   28  O   UNK     0      29.876  -5.755   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      32.186  -7.089   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      32.956 -11.090   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      30.646  -7.089   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      29.876  -8.423   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      30.646  -9.756   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      32.956  -8.423   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      32.186  -9.756   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      34.496  -8.423   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      32.956  -5.755   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      32.186 -12.424   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      34.496 -11.090   0.000  0.00  0.00           O+0
CONECT    1    3    4    5    6                                             
CONECT    2   10   32                                                       
CONECT    3    1   24                                                       
CONECT    4    1                                                            
CONECT    5    1                                                            
CONECT    6    1                                                            
CONECT    7    8   10   13   17                                             
CONECT    8    7    9   12   25                                             
CONECT    9    8   11   16   26                                             
CONECT   10    2    7   14                                                  
CONECT   11    9   15   18   27                                             
CONECT   12    8   14                                                       
CONECT   13    7   15                                                       
CONECT   14   10   12                                                       
CONECT   15   11   13                                                       
CONECT   16    9   19                                                       
CONECT   17    7                                                            
CONECT   18   11   20   21                                                  
CONECT   19   16   20                                                       
CONECT   20   18   19   22                                                  
CONECT   21   18   23                                                       
CONECT   22   20   24                                                       
CONECT   23   21   24                                                       
CONECT   24    3   22   23                                                  
CONECT   25    8                                                            
CONECT   26    9                                                            
CONECT   27   11                                                            
CONECT   28   31                                                            
CONECT   29   31   34   37                                                  
CONECT   30   35   38   39                                                  
CONECT   31   28   29   32                                                  
CONECT   32    2   31   33                                                  
CONECT   33   32   35                                                       
CONECT   34   29   35   36                                                  
CONECT   35   30   33   34                                                  
CONECT   36   34                                                            
CONECT   37   29                                                            
CONECT   38   30                                                            
CONECT   39   30                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

View in JSmol

Synonyms

Value	Source
Estradiol 17beta-glucuronide 3-sulfate	Kegg
Estradiol 17b-glucuronide 3-sulfate	Generator
Estradiol 17b-glucuronide 3-sulfuric acid	Generator
Estradiol 17b-glucuronide 3-sulphate	Generator
Estradiol 17b-glucuronide 3-sulphuric acid	Generator
Estradiol 17beta-glucuronide 3-sulfuric acid	Generator
Estradiol 17beta-glucuronide 3-sulphate	Generator
Estradiol 17beta-glucuronide 3-sulphuric acid	Generator
Estradiol 17β-glucuronide 3-sulfate	Generator
Estradiol 17β-glucuronide 3-sulfuric acid	Generator
Estradiol 17β-glucuronide 3-sulphate	Generator
Estradiol 17β-glucuronide 3-sulphuric acid	Generator
17-b-Estradiol 3-sulfate-17-(b-D-glucuronide)	Generator
17-b-Estradiol 3-sulfuric acid-17-(b-D-glucuronide)	Generator
17-b-Estradiol 3-sulphate-17-(b-D-glucuronide)	Generator
17-b-Estradiol 3-sulphuric acid-17-(b-D-glucuronide)	Generator
17-beta-Estradiol 3-sulfuric acid-17-(beta-D-glucuronide)	Generator
17-beta-Estradiol 3-sulphate-17-(beta-D-glucuronide)	Generator
17-beta-Estradiol 3-sulphuric acid-17-(beta-D-glucuronide)	Generator
17-Β-estradiol 3-sulfate-17-(β-D-glucuronide)	Generator
17-Β-estradiol 3-sulfuric acid-17-(β-D-glucuronide)	Generator
17-Β-estradiol 3-sulphate-17-(β-D-glucuronide)	Generator
17-Β-estradiol 3-sulphuric acid-17-(β-D-glucuronide)	Generator
17beta-Estradiol 3-sulfate-17-(beta-D-glucuronoside)	HMDB
17beta-Estradiol 3-sulfate-17-(beta-delta-glucuronoside)	HMDB
17beta-Estradiol 3-sulphate-17-(beta-D-glucuronoside)	HMDB
17beta-Estradiol 3-sulphate-17-(beta-delta-glucuronoside)	HMDB
Estra-1,3,5(10)-triene-3,17beta-diol 3-sulfate-17-D-glucuronide	HMDB
Estra-1,3,5(10)-triene-3,17beta-diol 3-sulfate-17-D-glucuronoside	HMDB
Estra-1,3,5(10)-triene-3,17beta-diol 3-sulfate-17-delta-glucuronide	HMDB
Estra-1,3,5(10)-triene-3,17beta-diol 3-sulfate-17-delta-glucuronoside	HMDB
Estra-1,3,5(10)-triene-3,17beta-diol 3-sulphate-17-D-glucuronide	HMDB
Estra-1,3,5(10)-triene-3,17beta-diol 3-sulphate-17-D-glucuronoside	HMDB
Estra-1,3,5(10)-triene-3,17beta-diol 3-sulphate-17-delta-glucuronide	HMDB
Estra-1,3,5(10)-triene-3,17beta-diol 3-sulphate-17-delta-glucuronoside	HMDB

Chemical Formula

C₂₄H₃₂O₁₁S

Average Mass

528.5690 Da

Monoisotopic Mass

528.16653 Da

IUPAC Name

(2S,3S,4S,5R,6R)-3,4,5-trihydroxy-6-{[(1S,10R,11S,14S,15S)-15-methyl-5-(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-2(7),3,5-trien-14-yl]oxy}oxane-2-carboxylic acid

Traditional Name

(2S,3S,4S,5R,6R)-3,4,5-trihydroxy-6-{[(1S,10R,11S,14S,15S)-15-methyl-5-(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-2(7),3,5-trien-14-yl]oxy}oxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

[H][C@@]12CC[C@H](O[C@@H]3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)C(O)=O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(OS(O)(=O)=O)C=C3

InChI Identifier

InChI=1S/C24H32O11S/c1-24-9-8-14-13-5-3-12(35-36(30,31)32)10-11(13)2-4-15(14)16(24)6-7-17(24)33-23-20(27)18(25)19(26)21(34-23)22(28)29/h3,5,10,14-21,23,25-27H,2,4,6-9H2,1H3,(H,28,29)(H,30,31,32)/t14-,15-,16+,17+,18+,19+,20-,21+,23-,24+/m1/s1

InChI Key

VRMSCBRLZUCJBX-QXYWQCSFSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Anas platyrhynchos	FooDB	FooDB
Anatidae	FooDB	FooDB
Anser anser	FooDB	FooDB
Bison bison	FooDB	FooDB
Bos taurus	FooDB	FooDB
Bos taurus X Bison bison	FooDB	FooDB
Bubalus bubalis	FooDB	FooDB
Capra aegagrus hircus	FooDB	FooDB
Cervidae	FooDB	FooDB
Cervus canadensis	FooDB	FooDB
Columba	FooDB	FooDB
Columbidae	FooDB	FooDB
Dromaius novaehollandiae	FooDB	FooDB
Equus caballus	FooDB	FooDB
Gallus gallus	FooDB	FooDB
Lagopus muta	FooDB	FooDB
Leporidae	FooDB	FooDB
Lepus timidus	FooDB	FooDB
Melanitta fusca	FooDB	FooDB
Meleagris gallopavo	FooDB	FooDB
Numida meleagris	FooDB	FooDB
Odocoileus	FooDB	FooDB
Oryctolagus	FooDB	FooDB
Ovis aries	FooDB	FooDB
Phasianidae	FooDB	FooDB
Phasianus colchicus	FooDB	FooDB
Struthio camelus	FooDB	FooDB
Sus scrofa	FooDB	FooDB
Sus scrofa domestica	FooDB	FooDB

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroidal glycosides. These are sterol lipids containing a carbohydrate moiety glycosidically linked to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Steroidal glycosides

Alternative Parents

Substituents

Steroidal glycoside
Sulfated steroid skeleton
Estrane-skeleton
1-o-glucuronide
O-glucuronide
Phenanthrene
Glucuronic acid or derivatives
Glycosyl compound
O-glycosyl compound
Arylsulfate
Tetralin
Beta-hydroxy acid
Sulfate-ester
Sulfuric acid monoester
Hydroxy acid
Monosaccharide
Oxane
Benzenoid
Pyran
Sulfuric acid ester
Organic sulfuric acid or derivatives
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Monocarboxylic acid or derivatives
Acetal
Carboxylic acid derivative
Polyol
Carboxylic acid
Hydrocarbon derivative
Alcohol
Organic oxide
Organooxygen compound
Carbonyl group
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

steroid sulfate (CHEBI:792 )
steroid glucosiduronic acid (CHEBI:792 )
sulfates (C11289 )
C18 steroids (estrogens) and derivatives (C11289 )
Glucuronides (C11289 )
Glucuronides (LMST05010035 )

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	0.25	ALOGPS
logP	0.16	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	-1.7	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	180.05 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	122.18 m³·mol⁻¹	ChemAxon
Polarizability	53.25 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0010358

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB027510

KNApSAcK ID

Not Available

Chemspider ID

4445182

KEGG Compound ID

C11289

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5281895

PDB ID

Not Available

ChEBI ID

792

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 17-beta-Estradiol 3-sulfate-17-(beta-D-glucuronide) (NP0090911)

MOL for NP0090911 (17-beta-Estradiol 3-sulfate-17-(beta-D-glucuronide))

3D MOL for NP0090911 (17-beta-Estradiol 3-sulfate-17-(beta-D-glucuronide))

3D SDF for NP0090911 (17-beta-Estradiol 3-sulfate-17-(beta-D-glucuronide))

3D-SDF for NP0090911 (17-beta-Estradiol 3-sulfate-17-(beta-D-glucuronide))

PDB for NP0090911 (17-beta-Estradiol 3-sulfate-17-(beta-D-glucuronide))

3D PDB for NP0090911 (17-beta-Estradiol 3-sulfate-17-(beta-D-glucuronide))

SMILES for NP0090911 (17-beta-Estradiol 3-sulfate-17-(beta-D-glucuronide))

INCHI for NP0090911 (17-beta-Estradiol 3-sulfate-17-(beta-D-glucuronide))

Structure for NP0090911 (17-beta-Estradiol 3-sulfate-17-(beta-D-glucuronide))

3D Structure for NP0090911 (17-beta-Estradiol 3-sulfate-17-(beta-D-glucuronide))