NP-MRD: Showing NP-Card for [(1r,3s,3ar,3bs,5s,5as,7s,9as,9br,11ar)-3a,3b,5,7-tetrahydroxy-1-[(2r,5e)-7-hydroxy-6-methylhept-5-en-2-yl]-9a,11a-dimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxidanesulfonic acid (NP0170210)

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Record Information

Version

2.0

Created at

2022-09-03 06:19:27 UTC

Updated at

2022-09-03 06:19:28 UTC

NP-MRD ID

NP0170210

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1r,3s,3ar,3bs,5s,5as,7s,9as,9br,11ar)-3a,3b,5,7-tetrahydroxy-1-[(2r,5e)-7-hydroxy-6-methylhept-5-en-2-yl]-9a,11a-dimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxidanesulfonic acid

Description

(24E)-15alpha-(Sulfooxy)-5alpha-cholesta-24-ene-3beta,6alpha,8,14,26-pentaol belongs to the class of organic compounds known as tetrahydroxy bile acids, alcohols and derivatives. These are prenol lipids structurally characterized by a bile acid or alcohol which bears four hydroxyl groups. [(1r,3s,3ar,3bs,5s,5as,7s,9as,9br,11ar)-3a,3b,5,7-tetrahydroxy-1-[(2r,5e)-7-hydroxy-6-methylhept-5-en-2-yl]-9a,11a-dimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxidanesulfonic acid is found in Archaster typicus. Based on a literature review very few articles have been published on (24E)-15alpha-(Sulfooxy)-5alpha-cholesta-24-ene-3beta,6alpha,8,14,26-pentaol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032208192D          

 37 40  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309032208192D          

 37 40  0  0  1  0            999 V2000
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    6.6095   -1.3047    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4216   -1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9534   -1.7902    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.7655   -1.6450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6731   -2.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8610   -2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3292   -2.0807    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0489   -2.8566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5171   -2.2259    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2368   -3.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4247   -3.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8928   -2.5163    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5330   -3.2587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5116   -1.2739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0180   -1.9252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  8  6  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  2  0  0  0  0
 12 15  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 23 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 18 31  1  0  0  0  0
 31 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
  8 34  1  0  0  0  0
 16 34  1  0  0  0  0
 34 35  1  1  0  0  0
  2 36  1  0  0  0  0
 36 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0170210

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CC\C=C(/C)CO)[C@H]1C[C@H](OS(O)(=O)=O)[C@]2(O)[C@]1(C)CC[C@@H]1[C@@]3(C)CC[C@H](O)C[C@@H]3[C@@H](O)C[C@@]21O

> <INCHI_IDENTIFIER>
InChI=1S/C27H46O9S/c1-16(15-28)6-5-7-17(2)19-13-23(36-37(33,34)35)27(32)25(19,4)11-9-22-24(3)10-8-18(29)12-20(24)21(30)14-26(22,27)31/h6,17-23,28-32H,5,7-15H2,1-4H3,(H,33,34,35)/b16-6+/t17-,18+,19-,20-,21+,22-,23+,24+,25-,26+,27+/m1/s1

> <INCHI_KEY>
IHMGTTNKQOBQFC-MXVFAFKXSA-N

> <FORMULA>
C27H46O9S

> <MOLECULAR_WEIGHT>
546.72

> <EXACT_MASS>
546.286254235

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
59.76451871072591

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(1R,2S,5S,7S,8S,10S,11R,12S,14R,15R)-5,8,10,11-tetrahydroxy-14-[(2R,5E)-7-hydroxy-6-methylhept-5-en-2-yl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-12-yl]oxidanesulfonic acid

> <ALOGPS_LOGP>
0.53

> <JCHEM_LOGP>
0.1286250233017121

> <ALOGPS_LOGS>
-2.76

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.411026326079966

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.2213134714880551

> <JCHEM_PKA_STRONGEST_BASIC>
-2.079704094235371

> <JCHEM_POLAR_SURFACE_AREA>
164.75

> <JCHEM_REFRACTIVITY>
138.11860000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.46e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1R,2S,5S,7S,8S,10S,11R,12S,14R,15R)-5,8,10,11-tetrahydroxy-14-[(2R,5E)-7-hydroxy-6-methylhept-5-en-2-yl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-12-yl]oxidanesulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       1.516  -1.373   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.571  -2.589   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.151  -4.015   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.676  -4.226   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.257  -5.652   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.782  -5.863   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.363  -7.289   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.727  -4.647   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.299  -3.168   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.574  -2.304   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.624  -0.764   0.000  0.00  0.00           O+0
HETATM   12  S   UNK     0       5.316   0.049   0.000  0.00  0.00           S+0
HETATM   13  O   UNK     0       6.129   1.357   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       4.503  -1.259   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       4.008   0.862   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.790  -3.249   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       8.159  -1.754   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.306  -2.978   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.725  -1.551   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.829  -1.529   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.345  -1.258   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      11.868   0.190   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      12.338  -2.436   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      13.854  -2.164   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      14.846  -3.342   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      16.362  -3.071   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      14.323  -4.790   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      12.807  -5.061   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.814  -3.884   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.291  -5.332   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.299  -4.155   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.775  -5.603   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.259  -5.874   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.267  -4.697   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.595  -6.083   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -0.955  -2.378   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -1.900  -3.594   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   36                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   34                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12                                                            
CONECT   16   10   17   18   34                                             
CONECT   17   16                                                            
CONECT   18   16   19   20   31                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   29                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   23   30   31                                             
CONECT   30   29                                                            
CONECT   31   29   18   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33    8   16   35                                             
CONECT   35   34                                                            
CONECT   36    2   37                                                       
CONECT   37   36                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   80    0
END

View in JSmol

Synonyms

Value	Source
(24E)-15a-(Sulfooxy)-5a-cholesta-24-ene-3b,6a,8,14,26-pentaol	Generator
(24E)-15a-(Sulphooxy)-5a-cholesta-24-ene-3b,6a,8,14,26-pentaol	Generator
(24E)-15alpha-(Sulphooxy)-5alpha-cholesta-24-ene-3beta,6alpha,8,14,26-pentaol	Generator
(24E)-15Α-(sulfooxy)-5α-cholesta-24-ene-3β,6α,8,14,26-pentaol	Generator
(24E)-15Α-(sulphooxy)-5α-cholesta-24-ene-3β,6α,8,14,26-pentaol	Generator

Chemical Formula

C₂₇H₄₆O₉S

Average Mass

546.7200 Da

Monoisotopic Mass

546.28625 Da

IUPAC Name

[(1R,2S,5S,7S,8S,10S,11R,12S,14R,15R)-5,8,10,11-tetrahydroxy-14-[(2R,5E)-7-hydroxy-6-methylhept-5-en-2-yl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-12-yl]oxidanesulfonic acid

Traditional Name

[(1R,2S,5S,7S,8S,10S,11R,12S,14R,15R)-5,8,10,11-tetrahydroxy-14-[(2R,5E)-7-hydroxy-6-methylhept-5-en-2-yl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-12-yl]oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

C[C@H](CC\C=C(/C)CO)[C@H]1C[C@H](OS(O)(=O)=O)[C@]2(O)[C@]1(C)CC[C@@H]1[C@@]3(C)CC[C@H](O)C[C@@H]3[C@@H](O)C[C@@]21O

InChI Identifier

InChI=1S/C27H46O9S/c1-16(15-28)6-5-7-17(2)19-13-23(36-37(33,34)35)27(32)25(19,4)11-9-22-24(3)10-8-18(29)12-20(24)21(30)14-26(22,27)31/h6,17-23,28-32H,5,7-15H2,1-4H3,(H,33,34,35)/b16-6+/t17-,18+,19-,20-,21+,22-,23+,24+,25-,26+,27+/m1/s1

InChI Key

IHMGTTNKQOBQFC-MXVFAFKXSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Archaster typicus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetrahydroxy bile acids, alcohols and derivatives. These are prenol lipids structurally characterized by a bile acid or alcohol which bears four hydroxyl groups.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Bile acids, alcohols and derivatives

Direct Parent

Tetrahydroxy bile acids, alcohols and derivatives

Alternative Parents

Substituents

26-hydroxysteroid
Tetrahydroxy bile acid, alcohol, or derivatives
Sulfated steroid skeleton
3-hydroxysteroid
14-hydroxysteroid
6-hydroxysteroid
Hydroxysteroid
3-beta-hydroxysteroid
Sulfate-ester
Sulfuric acid monoester
Alkyl sulfate
Sulfuric acid ester
Organic sulfuric acid or derivatives
Cyclic alcohol
Tertiary alcohol
Secondary alcohol
Polyol
Organic oxide
Primary alcohol
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

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	0.53	ALOGPS
logP	0.13	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	-1.2	ChemAxon
pKa (Strongest Basic)	-2.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	164.75 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	138.12 m³·mol⁻¹	ChemAxon
Polarizability	59.76 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102049448

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(1r,3s,3ar,3bs,5s,5as,7s,9as,9br,11ar)-3a,3b,5,7-tetrahydroxy-1-[(2r,5e)-7-hydroxy-6-methylhept-5-en-2-yl]-9a,11a-dimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxidanesulfonic acid (NP0170210)

MOL for NP0170210 ([(1r,3s,3ar,3bs,5s,5as,7s,9as,9br,11ar)-3a,3b,5,7-tetrahydroxy-1-[(2r,5e)-7-hydroxy-6-methylhept-5-en-2-yl]-9a,11a-dimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxidanesulfonic acid)

3D MOL for NP0170210 ([(1r,3s,3ar,3bs,5s,5as,7s,9as,9br,11ar)-3a,3b,5,7-tetrahydroxy-1-[(2r,5e)-7-hydroxy-6-methylhept-5-en-2-yl]-9a,11a-dimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxidanesulfonic acid)

3D SDF for NP0170210 ([(1r,3s,3ar,3bs,5s,5as,7s,9as,9br,11ar)-3a,3b,5,7-tetrahydroxy-1-[(2r,5e)-7-hydroxy-6-methylhept-5-en-2-yl]-9a,11a-dimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxidanesulfonic acid)

3D-SDF for NP0170210 ([(1r,3s,3ar,3bs,5s,5as,7s,9as,9br,11ar)-3a,3b,5,7-tetrahydroxy-1-[(2r,5e)-7-hydroxy-6-methylhept-5-en-2-yl]-9a,11a-dimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxidanesulfonic acid)

PDB for NP0170210 ([(1r,3s,3ar,3bs,5s,5as,7s,9as,9br,11ar)-3a,3b,5,7-tetrahydroxy-1-[(2r,5e)-7-hydroxy-6-methylhept-5-en-2-yl]-9a,11a-dimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxidanesulfonic acid)

3D PDB for NP0170210 ([(1r,3s,3ar,3bs,5s,5as,7s,9as,9br,11ar)-3a,3b,5,7-tetrahydroxy-1-[(2r,5e)-7-hydroxy-6-methylhept-5-en-2-yl]-9a,11a-dimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxidanesulfonic acid)

SMILES for NP0170210 ([(1r,3s,3ar,3bs,5s,5as,7s,9as,9br,11ar)-3a,3b,5,7-tetrahydroxy-1-[(2r,5e)-7-hydroxy-6-methylhept-5-en-2-yl]-9a,11a-dimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxidanesulfonic acid)

INCHI for NP0170210 ([(1r,3s,3ar,3bs,5s,5as,7s,9as,9br,11ar)-3a,3b,5,7-tetrahydroxy-1-[(2r,5e)-7-hydroxy-6-methylhept-5-en-2-yl]-9a,11a-dimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxidanesulfonic acid)

Structure for NP0170210 ([(1r,3s,3ar,3bs,5s,5as,7s,9as,9br,11ar)-3a,3b,5,7-tetrahydroxy-1-[(2r,5e)-7-hydroxy-6-methylhept-5-en-2-yl]-9a,11a-dimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxidanesulfonic acid)

3D Structure for NP0170210 ([(1r,3s,3ar,3bs,5s,5as,7s,9as,9br,11ar)-3a,3b,5,7-tetrahydroxy-1-[(2r,5e)-7-hydroxy-6-methylhept-5-en-2-yl]-9a,11a-dimethyl-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxidanesulfonic acid)