NP-MRD: Showing NP-Card for (1's,2r,2's,4s,4's,7'r,8'r,9's,11's,12's,13's,15'r,16's,18's)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-yl acetate (NP0250436)

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Record Information

Version

2.0

Created at

2022-09-07 13:15:18 UTC

Updated at

2022-09-07 13:15:18 UTC

NP-MRD ID

NP0250436

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,2r,2's,4s,4's,7'r,8'r,9's,11's,12's,13's,15'r,16's,18's)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-yl acetate

Description

CHEMBL507260 belongs to the class of organic compounds known as furospirostanes and derivatives. These are heterocyclic steroids containing a furospirostane moiety, which a skeleton characterized by the presence of a 1,6-dioxaspiro[4.4]Nonane ring system and an androstane moiety. (1's,2r,2's,4s,4's,7'r,8'r,9's,11's,12's,13's,15'r,16's,18's)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-yl acetate is found in Isis hippuris. Based on a literature review very few articles have been published on CHEMBL507260.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072215152D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309072215152D          

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    2.8172   -1.5578    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6332   -1.6795    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0011   -0.9411    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3690   -0.2026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1849   -0.3243    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7630    0.2643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3214   -1.1379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1163   -0.9172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6240   -1.9054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5897   -1.5191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4125   -0.3630    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0489    0.1620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9569    0.3248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6808   -0.7442    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6055   -0.7744    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2376   -0.0359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0611   -0.0866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8845   -0.1372    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3401    0.5506    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
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  6  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 21 20  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 21 28  1  0  0  0  0
 21 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  1  0  0  0
 32 29  1  1  0  0  0
 19 32  1  0  0  0  0
 15 32  1  0  0  0  0
 11 33  1  0  0  0  0
  7 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
  5 36  1  0  0  0  0
 36 37  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0250436

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C[C@@]2(O[C@H]3C[C@H]4[C@@H]5CC[C@H]6C[C@H](OC(C)=O)[C@H](O)C[C@]6(C)[C@H]5[C@@H](O)C[C@]4(C)[C@H]3[C@@]2(C)O)OC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C30H48O7/c1-15-12-30(37-26(15,3)4)29(7,34)25-23(36-30)11-19-18-9-8-17-10-22(35-16(2)31)20(32)13-27(17,5)24(18)21(33)14-28(19,25)6/h15,17-25,32-34H,8-14H2,1-7H3/t15-,17-,18-,19-,20+,21-,22-,23-,24+,25-,27-,28-,29+,30+/m0/s1

> <INCHI_KEY>
CLRGSPLGNCTOOL-YKVVPRMGSA-N

> <FORMULA>
C30H48O7

> <MOLECULAR_WEIGHT>
520.707

> <EXACT_MASS>
520.340003886

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
59.24559958242553

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'S,2R,2'S,4S,4'S,7'R,8'R,9'S,11'S,12'S,13'S,15'R,16'S,18'S)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosane]-16'-yl acetate

> <JCHEM_LOGP>
2.639532664666665

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.178919672795054

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.83398052043087

> <JCHEM_PKA_STRONGEST_BASIC>
-0.31019389813840614

> <JCHEM_POLAR_SURFACE_AREA>
105.45000000000002

> <JCHEM_REFRACTIVITY>
137.35150000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2R,2'S,4S,4'S,7'R,8'R,9'S,11'S,12'S,13'S,15'R,16'S,18'S)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosane]-16'-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.129  -0.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.592  -0.445   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -5.905   0.933   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -5.742  -1.729   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -4.204  -1.635   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.354  -2.918   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.817  -2.824   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.967  -4.108   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.571  -4.013   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.257  -2.635   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.407  -1.351   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.094   0.027   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.243   1.311   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.631   0.122   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.481  -1.162   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.308   0.137   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.794  -2.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.893  -3.619   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.259  -2.908   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.782  -3.135   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.469  -1.757   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.155  -0.378   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.679  -0.605   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.758   0.493   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.933  -2.124   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.417  -1.712   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.498  -3.557   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       8.567  -2.836   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.370  -0.678   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.558   0.302   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       5.520   0.606   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       5.004  -1.389   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.130  -1.445   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.444  -0.067   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.981  -0.162   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -3.518  -0.256   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -4.368   1.028   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   36                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   33                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12   33                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17   32                                             
CONECT   16   15                                                            
CONECT   17   15   10   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   32                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   28   29                                             
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25   21                                                       
CONECT   29   21   30   31   32                                             
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   29   19   15                                                  
CONECT   33   11    7   34   35                                             
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35    5   37                                                  
CONECT   37   36                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₈O₇

Average Mass

520.7070 Da

Monoisotopic Mass

520.34000 Da

IUPAC Name

(1'S,2R,2'S,4S,4'S,7'R,8'R,9'S,11'S,12'S,13'S,15'R,16'S,18'S)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosane]-16'-yl acetate

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@H]1C[C@@]2(O[C@H]3C[C@H]4[C@@H]5CC[C@H]6C[C@H](OC(C)=O)[C@H](O)C[C@]6(C)[C@H]5[C@@H](O)C[C@]4(C)[C@H]3[C@@]2(C)O)OC1(C)C

InChI Identifier

InChI=1S/C30H48O7/c1-15-12-30(37-26(15,3)4)29(7,34)25-23(36-30)11-19-18-9-8-17-10-22(35-16(2)31)20(32)13-27(17,5)24(18)21(33)14-28(19,25)6/h15,17-25,32-34H,8-14H2,1-7H3/t15-,17-,18-,19-,20+,21-,22-,23-,24+,25-,27-,28-,29+,30+/m0/s1

InChI Key

CLRGSPLGNCTOOL-YKVVPRMGSA-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
Isis hippuris	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as furospirostanes and derivatives. These are heterocyclic steroids containing a furospirostane moiety, which a skeleton characterized by the presence of a 1,6-dioxaspiro[4.4]Nonane ring system and an androstane moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Furospirostanes and derivatives

Direct Parent

Furospirostanes and derivatives

Alternative Parents

Substituents

Furospirostane-skeleton
Triterpenoid
Spirostane skeleton
20-hydroxysteroid
Steroid ester
2-hydroxysteroid
Hydroxysteroid
11-beta-hydroxysteroid
11-hydroxysteroid
Ketal
Monosaccharide
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Carboxylic acid ester
Secondary alcohol
Monocarboxylic acid or derivatives
Acetal
Organoheterocyclic compound
Carboxylic acid derivative
Oxacycle
Polyol
Carbonyl group
Alcohol
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	2.64	ChemAxon
pKa (Strongest Acidic)	12.83	ChemAxon
pKa (Strongest Basic)	-0.31	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	105.45 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	137.35 m³·mol⁻¹	ChemAxon
Polarizability	59.25 Å³	ChemAxon
Number of Rings	6	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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9618667

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11443805

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,2r,2's,4s,4's,7'r,8'r,9's,11's,12's,13's,15'r,16's,18's)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-yl acetate (NP0250436)

MOL for NP0250436 ((1's,2r,2's,4s,4's,7'r,8'r,9's,11's,12's,13's,15'r,16's,18's)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-yl acetate)

3D MOL for NP0250436 ((1's,2r,2's,4s,4's,7'r,8'r,9's,11's,12's,13's,15'r,16's,18's)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-yl acetate)

3D SDF for NP0250436 ((1's,2r,2's,4s,4's,7'r,8'r,9's,11's,12's,13's,15'r,16's,18's)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-yl acetate)

3D-SDF for NP0250436 ((1's,2r,2's,4s,4's,7'r,8'r,9's,11's,12's,13's,15'r,16's,18's)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-yl acetate)

PDB for NP0250436 ((1's,2r,2's,4s,4's,7'r,8'r,9's,11's,12's,13's,15'r,16's,18's)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-yl acetate)

3D PDB for NP0250436 ((1's,2r,2's,4s,4's,7'r,8'r,9's,11's,12's,13's,15'r,16's,18's)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-yl acetate)

SMILES for NP0250436 ((1's,2r,2's,4s,4's,7'r,8'r,9's,11's,12's,13's,15'r,16's,18's)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-yl acetate)

INCHI for NP0250436 ((1's,2r,2's,4s,4's,7'r,8'r,9's,11's,12's,13's,15'r,16's,18's)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-yl acetate)

Structure for NP0250436 ((1's,2r,2's,4s,4's,7'r,8'r,9's,11's,12's,13's,15'r,16's,18's)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-yl acetate)

3D Structure for NP0250436 ((1's,2r,2's,4s,4's,7'r,8'r,9's,11's,12's,13's,15'r,16's,18's)-7',11',15'-trihydroxy-4,5,5,7',9',13'-hexamethyl-5'-oxaspiro[oxolane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-16'-yl acetate)