NP-MRD: Showing NP-Card for (2s,5s,6r,7r,13s,16s,18s)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]icosa-3,8,19-trien-11-one (NP0281848)

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Record Information

Version

2.0

Created at

2022-09-09 08:26:21 UTC

Updated at

2022-09-09 08:26:21 UTC

NP-MRD ID

NP0281848

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,5s,6r,7r,13s,16s,18s)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]icosa-3,8,19-trien-11-one

Description

(2S,5S,6R,7R,13S,16S,18S)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]Icosa-3,8,19-trien-11-one belongs to the class of organic compounds known as isoindoles and derivatives. These are polycyclic compounds containing an isoindole moiety, which is structurally characterized by a cyclohexadiene fused to a pyrrole ring. Based on a literature review very few articles have been published on (2S,5S,6R,7R,13S,16S,18S)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]Icosa-3,8,19-trien-11-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092210262D          

 37 42  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309092210262D          

 37 42  0  0  1  0            999 V2000
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   -1.3843   -2.2690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -1.9385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6753   -0.4116    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0188    0.0344    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8713   -0.0161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0204    0.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7729    1.2540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7537    1.2366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4477    0.7906    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5126    1.6561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2436    1.0079    0.0000 C   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  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
  4 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 22 28  1  0  0  0  0
 29 19  1  6  0  0  0
 15 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 34 35  1  0  0  0  0
 15 35  1  0  0  0  0
 35 36  1  6  0  0  0
 35 37  1  0  0  0  0
  2 37  1  0  0  0  0
 12 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0281848

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC[C@H]2C3C(C(C)=C[C@@]2(C)C1)[C@]1(C)C=C(C)[C@@H](C)[C@H]2[C@](O)(CC4=CC=C(O)C=C4)N=C(O)C12C3=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H41NO4/c1-17-7-12-23-24-25(19(3)14-29(23,5)13-17)30(6)15-18(2)20(4)26-31(37,16-21-8-10-22(34)11-9-21)33-28(36)32(26,30)27(24)35/h8-11,14-15,17,20,23-26,34,37H,7,12-13,16H2,1-6H3,(H,33,36)/t17-,20+,23-,24?,25?,26-,29+,30-,31+,32?/m0/s1

> <INCHI_KEY>
AEKBQYOSHUYACR-NIQPOQINSA-N

> <FORMULA>
C32H41NO4

> <MOLECULAR_WEIGHT>
503.683

> <EXACT_MASS>
503.303558804

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
57.235459197991304

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,5S,6R,7R,13S,16S,18S)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0^{2,10}.0^{6,10}.0^{13,18}]icosa-3,8,19-trien-11-one

> <JCHEM_LOGP>
6.158436074666664

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.502416785988466

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.1386933555810455

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6159591708875545

> <JCHEM_POLAR_SURFACE_AREA>
90.12

> <JCHEM_REFRACTIVITY>
146.28320000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,5S,6R,7R,13S,16S,18S)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0^{2,10}.0^{6,10}.0^{13,18}]icosa-3,8,19-trien-11-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       4.518   4.835   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.881   3.257   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.418   3.345   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.263   2.057   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.053   3.520   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.800   2.146   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.645   0.858   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.250   0.838   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.953  -0.517   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.415  -0.606   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.570   0.682   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.033   0.594   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.070  -0.607   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.398  -2.394   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.629  -0.063   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.723  -1.146   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.256  -1.751   0.000  0.00  0.00           O+0
HETATM   18  N   UNK     0       3.031  -2.522   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       1.509  -2.288   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.106  -2.519   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.456  -3.925   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.067  -4.532   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.104  -6.063   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.515  -6.680   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.755  -5.766   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -4.166  -6.383   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -2.584  -4.236   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.173  -3.619   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.260  -0.768   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.035   0.064   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.626  -0.030   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.038   1.603   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.443   2.341   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.407   2.308   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.702   1.476   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       2.823   3.091   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       4.188   1.881   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   37                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6   11                                             
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    4   12                                                  
CONECT   12   11   13   37                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   29   35                                             
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21   29                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   28                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   22                                                       
CONECT   29   19   15   30                                                  
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   15   36   37                                             
CONECT   36   35                                                            
CONECT   37   35    2   12                                                  
MASTER        0    0    0    0    0    0    0    0   37    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₄₁NO₄

Average Mass

503.6830 Da

Monoisotopic Mass

503.30356 Da

IUPAC Name

(2S,5S,6R,7R,13S,16S,18S)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0^{2,10}.0^{6,10}.0^{13,18}]icosa-3,8,19-trien-11-one

Traditional Name

(2S,5S,6R,7R,13S,16S,18S)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0^{2,10}.0^{6,10}.0^{13,18}]icosa-3,8,19-trien-11-one

CAS Registry Number

Not Available

SMILES

C[C@H]1CC[C@H]2C3C(C(C)=C[C@@]2(C)C1)[C@]1(C)C=C(C)[C@@H](C)[C@H]2[C@](O)(CC4=CC=C(O)C=C4)N=C(O)C12C3=O

InChI Identifier

InChI=1S/C32H41NO4/c1-17-7-12-23-24-25(19(3)14-29(23,5)13-17)30(6)15-18(2)20(4)26-31(37,16-21-8-10-22(34)11-9-21)33-28(36)32(26,30)27(24)35/h8-11,14-15,17,20,23-26,34,37H,7,12-13,16H2,1-6H3,(H,33,36)/t17-,20+,23-,24?,25?,26-,29+,30-,31+,32?/m0/s1

InChI Key

AEKBQYOSHUYACR-NIQPOQINSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoindoles and derivatives. These are polycyclic compounds containing an isoindole moiety, which is structurally characterized by a cyclohexadiene fused to a pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoindoles and derivatives

Sub Class

Not Available

Direct Parent

Isoindoles and derivatives

Alternative Parents

Substituents

Isoindole or derivatives
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Cyclic carboximidic acid
Pyrroline
Ketone
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Alkanolamine
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	6.16	ChemAxon
pKa (Strongest Acidic)	4.14	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	90.12 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	146.28 m³·mol⁻¹	ChemAxon
Polarizability	57.24 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	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

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

163187772

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,5s,6r,7r,13s,16s,18s)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]icosa-3,8,19-trien-11-one (NP0281848)

MOL for NP0281848 ((2s,5s,6r,7r,13s,16s,18s)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]icosa-3,8,19-trien-11-one)

3D MOL for NP0281848 ((2s,5s,6r,7r,13s,16s,18s)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]icosa-3,8,19-trien-11-one)

3D SDF for NP0281848 ((2s,5s,6r,7r,13s,16s,18s)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]icosa-3,8,19-trien-11-one)

3D-SDF for NP0281848 ((2s,5s,6r,7r,13s,16s,18s)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]icosa-3,8,19-trien-11-one)

PDB for NP0281848 ((2s,5s,6r,7r,13s,16s,18s)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]icosa-3,8,19-trien-11-one)

3D PDB for NP0281848 ((2s,5s,6r,7r,13s,16s,18s)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]icosa-3,8,19-trien-11-one)

SMILES for NP0281848 ((2s,5s,6r,7r,13s,16s,18s)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]icosa-3,8,19-trien-11-one)

INCHI for NP0281848 ((2s,5s,6r,7r,13s,16s,18s)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]icosa-3,8,19-trien-11-one)

Structure for NP0281848 ((2s,5s,6r,7r,13s,16s,18s)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]icosa-3,8,19-trien-11-one)

3D Structure for NP0281848 ((2s,5s,6r,7r,13s,16s,18s)-7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]icosa-3,8,19-trien-11-one)