NP-MRD: Showing NP-Card for (1s,3z,7z,9s,11z,13r,14s,16r,17s,18r,19s)-21-hydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione (NP0272512)

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Record Information

Version

2.0

Created at

2022-09-08 19:09:36 UTC

Updated at

2022-09-08 19:09:36 UTC

NP-MRD ID

NP0272512

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3z,7z,9s,11z,13r,14s,16r,17s,18r,19s)-21-hydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione

Description

Prochaetoglobosin III 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. (1s,3z,7z,9s,11z,13r,14s,16r,17s,18r,19s)-21-hydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione is found in Chaetomium subaffine. (1s,3z,7z,9s,11z,13r,14s,16r,17s,18r,19s)-21-hydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione was first documented in 2010 (PMID: 20803114). Based on a literature review very few articles have been published on Prochaetoglobosin III (PMID: 30568921).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082221092D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309082221092D          

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    2.4257   -0.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6977   -0.4197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1676   -0.4471    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5970   -1.0429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0390   -1.7396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8149   -1.3054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0003   -1.1743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3401   -0.6796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2982   -1.2024    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0147    0.0652    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  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  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
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 19 27  1  0  0  0  0
 22 27  1  0  0  0  0
 17 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 31 29  1  1  0  0  0
  9 31  1  0  0  0  0
 16 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
  2 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0272512

> <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=C(C)/CC(=O)\C=C/C2=O)[C@@H]2O[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C32H36N2O4/c1-18-8-7-10-24-29-31(4,38-29)20(3)28-26(16-21-17-33-25-11-6-5-9-23(21)25)34-30(37)32(24,28)27(36)13-12-22(35)15-19(2)14-18/h5-7,9-14,17-18,20,24,26,28-29,33H,8,15-16H2,1-4H3,(H,34,37)/b10-7-,13-12-,19-14-/t18-,20-,24-,26-,28-,29-,31+,32+/m0/s1

> <INCHI_KEY>
ZIOWMHCMCYFIBL-YWPKHJSCSA-N

> <FORMULA>
C32H36N2O4

> <MOLECULAR_WEIGHT>
512.65

> <EXACT_MASS>
512.267507647

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
55.58683623162341

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3Z,7Z,9S,11Z,13R,14S,16R,17S,18R,19S)-21-hydroxy-19-[(1H-indol-3-yl)methyl]-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11,20-tetraene-2,5-dione

> <JCHEM_LOGP>
4.670222739470407

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.058909146665837

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.775357071014281

> <JCHEM_PKA_STRONGEST_BASIC>
5.4912243580169156

> <JCHEM_POLAR_SURFACE_AREA>
95.04999999999998

> <JCHEM_REFRACTIVITY>
150.02830000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3Z,7Z,9S,11Z,13R,14S,16R,17S,18R,19S)-21-hydroxy-19-(1H-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11,20-tetraene-2,5-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.448   2.087   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.032   1.661   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.800   2.995   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.101   3.820   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.611   5.280   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.635   3.947   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.053   3.345   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.029   2.154   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.339   0.645   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.834   1.016   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       9.328   1.387   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       8.902  -0.093   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.382  -0.519   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.476  -1.573   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.545  -2.682   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.981  -1.944   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.257  -3.302   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.930  -4.687   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.068  -5.963   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.593  -7.411   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       5.378  -8.358   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       4.102  -7.495   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.608  -7.866   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.539  -6.757   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.965  -5.277   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.460  -4.906   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.528  -6.015   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0       4.740  -3.033   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0       4.528  -1.508   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       3.169  -0.783   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       5.913  -0.835   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.848  -1.947   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       5.673  -3.247   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       3.388  -2.437   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.867  -2.192   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.635  -1.269   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -0.557  -2.244   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -0.027   0.122   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   38                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   31                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10   12                                                       
CONECT   12   11   10   13   14                                             
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   31                                                  
CONECT   17   16   18   28                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   27                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   19   22                                                  
CONECT   28   17   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29    9   16   32                                             
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36    2                                                       
MASTER        0    0    0    0    0    0    0    0   38    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₃₆N₂O₄

Average Mass

512.6500 Da

Monoisotopic Mass

512.26751 Da

IUPAC Name

(1S,3Z,7Z,9S,11Z,13R,14S,16R,17S,18R,19S)-21-hydroxy-19-[(1H-indol-3-yl)methyl]-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11,20-tetraene-2,5-dione

Traditional Name

(1S,3Z,7Z,9S,11Z,13R,14S,16R,17S,18R,19S)-21-hydroxy-19-(1H-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11,20-tetraene-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=C(C)/CC(=O)\C=C/C2=O)[C@@H]2O[C@]12C

InChI Identifier

InChI=1S/C32H36N2O4/c1-18-8-7-10-24-29-31(4,38-29)20(3)28-26(16-21-17-33-25-11-6-5-9-23(21)25)34-30(37)32(24,28)27(36)13-12-22(35)15-19(2)14-18/h5-7,9-14,17-18,20,24,26,28-29,33H,8,15-16H2,1-4H3,(H,34,37)/b10-7-,13-12-,19-14-/t18-,20-,24-,26-,28-,29-,31+,32+/m0/s1

InChI Key

ZIOWMHCMCYFIBL-YWPKHJSCSA-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
Chaetomium subaffine	LOTUS Database	35616633

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
Macrolactam
Isoindolone
3-alkylindole
Indole
Indole or derivatives
Isoindoline
Isoindole or derivatives
Oxepane
Benzenoid
Substituted pyrrole
2-pyrrolidone
Pyrrolidone
Heteroaromatic compound
Pyrrole
Pyrrolidine
Cyclic ketone
Carboxamide group
Ketone
Lactam
Secondary carboxylic acid amide
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Azacycle
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
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	4.67	ChemAxon
pKa (Strongest Acidic)	2.78	ChemAxon
pKa (Strongest Basic)	5.49	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	95.05 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	150.03 m³·mol⁻¹	ChemAxon
Polarizability	55.59 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

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

101618659

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Mori M, Tsuge S, Fukasawa W, Jeelani G, Nakada-Tsukui K, Nonaka K, Matsumoto A, Omura S, Nozaki T, Shiomi K: Discovery of Antiamebic Compounds That Inhibit Cysteine Synthase From the Enteric Parasitic Protist Entamoeba histolytica by Screening of Microbial Secondary Metabolites. Front Cell Infect Microbiol. 2018 Dec 5;8:409. doi: 10.3389/fcimb.2018.00409. eCollection 2018. [PubMed:30568921 ]
Thohinung S, Kanokmedhakul S, Kanokmedhakul K, Kukongviriyapan V, Tusskorn O, Soytong K: Cytotoxic 10-(indol-3-yl)-[13]cytochalasans from the fungus Chaetomium elatum ChE01. Arch Pharm Res. 2010 Aug;33(8):1135-41. doi: 10.1007/s12272-010-0801-5. Epub 2010 Aug 28. [PubMed:20803114 ]
LOTUS database [Link]

Showing NP-Card for (1s,3z,7z,9s,11z,13r,14s,16r,17s,18r,19s)-21-hydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione (NP0272512)

MOL for NP0272512 ((1s,3z,7z,9s,11z,13r,14s,16r,17s,18r,19s)-21-hydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

3D MOL for NP0272512 ((1s,3z,7z,9s,11z,13r,14s,16r,17s,18r,19s)-21-hydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

3D SDF for NP0272512 ((1s,3z,7z,9s,11z,13r,14s,16r,17s,18r,19s)-21-hydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

3D-SDF for NP0272512 ((1s,3z,7z,9s,11z,13r,14s,16r,17s,18r,19s)-21-hydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

PDB for NP0272512 ((1s,3z,7z,9s,11z,13r,14s,16r,17s,18r,19s)-21-hydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

3D PDB for NP0272512 ((1s,3z,7z,9s,11z,13r,14s,16r,17s,18r,19s)-21-hydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

SMILES for NP0272512 ((1s,3z,7z,9s,11z,13r,14s,16r,17s,18r,19s)-21-hydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

INCHI for NP0272512 ((1s,3z,7z,9s,11z,13r,14s,16r,17s,18r,19s)-21-hydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

Structure for NP0272512 ((1s,3z,7z,9s,11z,13r,14s,16r,17s,18r,19s)-21-hydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)

3D Structure for NP0272512 ((1s,3z,7z,9s,11z,13r,14s,16r,17s,18r,19s)-21-hydroxy-19-(1h-indol-3-ylmethyl)-7,9,16,17-tetramethyl-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraene-2,5-dione)