NP-MRD: Showing NP-Card for (1s,4r,8r,9s,11e,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0¹,¹⁸.0⁴,⁸.0¹⁴,¹⁶]henicosa-6,11,20-triene-2,5-dione (NP0252710)

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Record Information

Version

2.0

Created at

2022-09-07 16:18:23 UTC

Updated at

2022-09-07 16:18:23 UTC

NP-MRD ID

NP0252710

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4r,8r,9s,11e,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0¹,¹⁸.0⁴,⁸.0¹⁴,¹⁶]henicosa-6,11,20-triene-2,5-dione

Description

Chaetoglobosin U, also known as penochalasin K, belongs to the class of organic compounds known as chaetoglobosins. These are cytochalasans with a structure in which the hydrogenated isoindole bears an (indol-3-yl)methyl group. Chaetoglobosin U is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. (1s,4r,8r,9s,11e,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0¹,¹⁸.0⁴,⁸.0¹⁴,¹⁶]henicosa-6,11,20-triene-2,5-dione was first documented in 2006 (PMID: 16499339). Based on a literature review very few articles have been published on chaetoglobosin U.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072218182D          

 39 45  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309072218182D          

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   -0.1156    0.6640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3283    2.0223    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4789    1.8521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1582    2.8295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9424    2.5732    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7266    2.3169    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3406    2.8679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1705    3.6751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7846    4.2261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5687    3.9698    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1828    4.5207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7389    3.1625    0.0000 C   0  0  1  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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  7  5  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  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
 17 25  1  0  0  0  0
 20 25  1  0  0  0  0
 26 15  1  6  0  0  0
 11 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 32 31  1  1  0  0  0
 29 32  1  0  0  0  0
 32 33  1  0  0  0  0
 11 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  6  0  0  0
 37 39  1  0  0  0  0
 39  2  1  1  0  0  0
  7 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0252710

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1[C@H]2[C@H](CC3=CNC4=CC=CC=C34)N=C(O)[C@@]22[C@@H](\C=C\C[C@H](C)[C@@H]3[C@@H](CC2=O)C(=O)C(O)=C3C)[C@@H]2O[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C32H36N2O5/c1-15-8-7-10-21-29-31(4,39-29)17(3)26-23(12-18-14-33-22-11-6-5-9-19(18)22)34-30(38)32(21,26)24(35)13-20-25(15)16(2)27(36)28(20)37/h5-7,9-11,14-15,17,20-21,23,25-26,29,33,36H,8,12-13H2,1-4H3,(H,34,38)/b10-7+/t15-,17-,20+,21-,23-,25-,26-,29-,31+,32+/m0/s1

> <INCHI_KEY>
MRENMDHAGXAXRK-QFHPAQOTSA-N

> <FORMULA>
C32H36N2O5

> <MOLECULAR_WEIGHT>
528.649

> <EXACT_MASS>
528.262422267

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
57.3066249660376

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4R,8R,9S,11E,13R,14S,16R,17S,18R,19S)-6,21-dihydroxy-19-[(1H-indol-3-yl)methyl]-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0^{1,18}.0^{4,8}.0^{14,16}]henicosa-6,11,20-triene-2,5-dione

> <JCHEM_LOGP>
3.6949578704460997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.95686775814298

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.746030425234016

> <JCHEM_PKA_STRONGEST_BASIC>
5.401360100472457

> <JCHEM_POLAR_SURFACE_AREA>
115.28000000000002

> <JCHEM_REFRACTIVITY>
149.02130000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4R,8R,9S,11E,13R,14S,16R,17S,18R,19S)-6,21-dihydroxy-19-(1H-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0^{1,18}.0^{4,8}.0^{14,16}]henicosa-6,11,20-triene-2,5-dione

> <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       9.719   5.755   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.312   5.131   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.989   3.625   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       9.017   2.479   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.651   3.565   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.685   2.135   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.833   4.875   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.151   3.368   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.294   2.731   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.322   0.833   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.540   2.818   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.873   2.046   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.281   2.670   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0       4.550   0.540   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       3.018   0.382   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.246  -0.951   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.013  -2.286   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.545  -2.449   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       4.862  -3.956   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       3.527  -4.724   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.204  -6.230   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.739  -6.703   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.596  -5.671   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.919  -4.165   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.385  -3.692   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.394   1.790   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.930   2.268   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.216   1.240   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.613   3.775   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.894   3.457   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       0.295   5.282   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       1.759   4.803   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.223   4.325   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.369   5.353   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.052   6.860   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.198   7.889   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.662   7.410   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.808   8.439   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.979   5.903   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   39                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   39                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   26   33                                             
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   26                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   17   20                                                  
CONECT   26   15   11   27                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31   32                                             
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   29   33                                                  
CONECT   33   32   11   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37    2    7                                                  
MASTER        0    0    0    0    0    0    0    0   39    0   90    0
END

View in JSmol

Synonyms

Value	Source
Chaetoglobosin F	MeSH
Chaetoglobosin K	MeSH
Chaetoglobosin V	MeSH
Chaetoglobosin D	MeSH
Chaetoglobosin T	MeSH
Chaetoglobosin y	MeSH
Chaetoglobosins	MeSH
Chaetoglobosin b	MeSH
Chaetoglobosin e	MeSH
Chaetoglobosin R	MeSH
Chaetoglobosin W	MeSH
Chaetoglobosin a	MeSH
Chaetoglobosin C	MeSH
Chaetoglobosin Q	MeSH
Penochalasin K	MeSH

Chemical Formula

C₃₂H₃₆N₂O₅

Average Mass

528.6490 Da

Monoisotopic Mass

528.26242 Da

IUPAC Name

(1S,4R,8R,9S,11E,13R,14S,16R,17S,18R,19S)-6,21-dihydroxy-19-[(1H-indol-3-yl)methyl]-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0^{1,18}.0^{4,8}.0^{14,16}]henicosa-6,11,20-triene-2,5-dione

Traditional Name

(1S,4R,8R,9S,11E,13R,14S,16R,17S,18R,19S)-6,21-dihydroxy-19-(1H-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0^{1,18}.0^{4,8}.0^{14,16}]henicosa-6,11,20-triene-2,5-dione

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@H]2[C@H](CC3=CNC4=CC=CC=C34)N=C(O)[C@@]22[C@@H](\C=C\C[C@H](C)[C@@H]3[C@@H](CC2=O)C(=O)C(O)=C3C)[C@@H]2O[C@]12C

InChI Identifier

InChI=1S/C32H36N2O5/c1-15-8-7-10-21-29-31(4,39-29)17(3)26-23(12-18-14-33-22-11-6-5-9-19(18)22)34-30(38)32(21,26)24(35)13-20-25(15)16(2)27(36)28(20)37/h5-7,9-11,14-15,17,20-21,23,25-26,29,33,36H,8,12-13H2,1-4H3,(H,34,38)/b10-7+/t15-,17-,20+,21-,23-,25-,26-,29-,31+,32+/m0/s1

InChI Key

MRENMDHAGXAXRK-QFHPAQOTSA-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 chaetoglobosins. These are cytochalasans with a structure in which the hydrogenated isoindole bears an (indol-3-yl)methyl group.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Cytochalasans

Sub Class

Chaetoglobosins

Direct Parent

Chaetoglobosins

Alternative Parents

Substituents

Chaetoglobosin skeleton
Isoindolone
3-alkylindole
Indole
Indole or derivatives
Isoindoline
Isoindole or derivatives
Oxepane
Benzenoid
Substituted pyrrole
2-pyrrolidone
Pyrrolidone
Heteroaromatic compound
Pyrrole
Pyrrolidine
Carboxamide group
Ketone
Lactam
Secondary carboxylic acid amide
Carboxylic acid derivative
Azacycle
Oxacycle
Organoheterocyclic compound
Dialkyl ether
Enol
Oxirane
Ether
Organonitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organic nitrogen compound
Organooxygen compound
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

indoles (CHEBI:68733 )
macrocycle (CHEBI:68733 )
cytochalasan alkaloid (CHEBI:68733 )

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	3.69	ChemAxon
pKa (Strongest Acidic)	2.75	ChemAxon
pKa (Strongest Basic)	5.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	115.28 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	149.02 m³·mol⁻¹	ChemAxon
Polarizability	57.31 Å³	ChemAxon
Number of Rings	7	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

C00041429

Chemspider ID

9744792

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11570022

PDB ID

Not Available

ChEBI ID

68733

Good Scents ID

Not Available

References

General References

Ding G, Song YC, Chen JR, Xu C, Ge HM, Wang XT, Tan RX: Chaetoglobosin U, a cytochalasan alkaloid from endophytic Chaetomium globosum IFB-E019. J Nat Prod. 2006 Feb;69(2):302-4. doi: 10.1021/np050515+. [PubMed:16499339 ]
LOTUS database [Link]

Showing NP-Card for (1s,4r,8r,9s,11e,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0¹,¹⁸.0⁴,⁸.0¹⁴,¹⁶]henicosa-6,11,20-triene-2,5-dione (NP0252710)

MOL for NP0252710 ((1s,4r,8r,9s,11e,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0¹,¹⁸.0⁴,⁸.0¹⁴,¹⁶]henicosa-6,11,20-triene-2,5-dione)

3D MOL for NP0252710 ((1s,4r,8r,9s,11e,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0¹,¹⁸.0⁴,⁸.0¹⁴,¹⁶]henicosa-6,11,20-triene-2,5-dione)

3D SDF for NP0252710 ((1s,4r,8r,9s,11e,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0¹,¹⁸.0⁴,⁸.0¹⁴,¹⁶]henicosa-6,11,20-triene-2,5-dione)

3D-SDF for NP0252710 ((1s,4r,8r,9s,11e,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0¹,¹⁸.0⁴,⁸.0¹⁴,¹⁶]henicosa-6,11,20-triene-2,5-dione)

PDB for NP0252710 ((1s,4r,8r,9s,11e,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0¹,¹⁸.0⁴,⁸.0¹⁴,¹⁶]henicosa-6,11,20-triene-2,5-dione)

3D PDB for NP0252710 ((1s,4r,8r,9s,11e,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0¹,¹⁸.0⁴,⁸.0¹⁴,¹⁶]henicosa-6,11,20-triene-2,5-dione)

SMILES for NP0252710 ((1s,4r,8r,9s,11e,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0¹,¹⁸.0⁴,⁸.0¹⁴,¹⁶]henicosa-6,11,20-triene-2,5-dione)

INCHI for NP0252710 ((1s,4r,8r,9s,11e,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0¹,¹⁸.0⁴,⁸.0¹⁴,¹⁶]henicosa-6,11,20-triene-2,5-dione)

Structure for NP0252710 ((1s,4r,8r,9s,11e,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0¹,¹⁸.0⁴,⁸.0¹⁴,¹⁶]henicosa-6,11,20-triene-2,5-dione)

3D Structure for NP0252710 ((1s,4r,8r,9s,11e,13r,14s,16r,17s,18r,19s)-6,21-dihydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azapentacyclo[11.8.0.0¹,¹⁸.0⁴,⁸.0¹⁴,¹⁶]henicosa-6,11,20-triene-2,5-dione)