NP-MRD: Showing NP-Card for 16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione (NP0231448)

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Record Information

Version

2.0

Created at

2022-09-06 12:18:46 UTC

Updated at

2022-09-06 12:18:46 UTC

NP-MRD ID

NP0231448

Secondary Accession Numbers

None

Natural Product Identification

Common Name

16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione

Description

16-Acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]Hexadeca-10,12,14-triene-3,6-dione belongs to the class of organic compounds known as pyrroloindoles. Pyrroloindoles are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. 16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione is found in Penicillium javanicum. 16-Acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]Hexadeca-10,12,14-triene-3,6-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 04121518232D          

 31 34  0  0  0  0            999 V2000
    0.3825   -0.9221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0066   -1.4617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8513   -2.2720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7859   -1.1911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4100   -1.7306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2547   -2.5409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8788   -3.0805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7235   -3.8908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6581   -2.8098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5884   -3.6319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3807   -3.2079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9826   -2.6436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6320   -1.8969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2338   -1.3326    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.1311   -0.5140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7887   -0.0158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3708   -0.1937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9565   -1.7306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7358   -1.4600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3599   -1.9996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2046   -2.8098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4253   -3.0805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8012   -2.5409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8134   -1.9996    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1893   -1.4600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3446   -0.6497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3333   -3.3904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0800   -3.0398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5865   -3.7410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6839   -4.1372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2125   -4.8142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
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  9 10  1  0  0  0  0
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 27 30  1  0  0  0  0
 30 31  2  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv0541 04121518232D          

 31 34  0  0  0  0            999 V2000
    0.3825   -0.9221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0066   -1.4617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8513   -2.2720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7859   -1.1911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4100   -1.7306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8788   -3.0805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6581   -2.8098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0231448

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC1OC(=O)C2(O)CC3(C(N(C(C)=O)C4=CC=CC=C34)N2C1=O)C(C)(C)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C24H30N2O5/c1-7-22(5,6)23-13-24(30)21(29)31-18(12-14(2)3)19(28)26(24)20(23)25(15(4)27)17-11-9-8-10-16(17)23/h7-11,14,18,20,30H,1,12-13H2,2-6H3

> <INCHI_KEY>
KQOPIDROORHFNV-UHFFFAOYSA-N

> <FORMULA>
C24H30N2O5

> <MOLECULAR_WEIGHT>
426.513

> <EXACT_MASS>
426.215472074

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
45.49541183463883

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione

> <ALOGPS_LOGP>
2.45

> <JCHEM_LOGP>
3.2218248253333344

> <ALOGPS_LOGS>
-3.92

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.294874488984853

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.665678907759174

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9211997847470306

> <JCHEM_POLAR_SURFACE_AREA>
87.15

> <JCHEM_REFRACTIVITY>
113.64250000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.17e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-APR-15         0                                  
HETATM    1  C   UNK     0       0.714  -1.721   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.879  -2.729   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.589  -4.241   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.334  -2.223   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.499  -3.231   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.209  -4.743   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.374  -5.750   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       5.084  -7.263   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       6.828  -5.245   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.698  -6.780   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       8.177  -5.988   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.301  -4.935   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.646  -3.541   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       9.770  -2.488   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       9.578  -0.960   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      10.805  -0.029   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.159  -0.362   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.119  -3.231   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.573  -2.725   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.738  -3.733   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.449  -5.245   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.994  -5.750   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.829  -4.743   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0       7.118  -3.733   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0       5.953  -2.725   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.243  -1.213   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       9.955  -6.329   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.349  -5.674   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.561  -6.983   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.610  -7.723   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.730  -8.987   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   25                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11   24                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   23   27                                             
CONECT   13   12   14   24                                                  
CONECT   14   13   15   18                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   14   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   12   18                                                  
CONECT   24   13    9   25                                                  
CONECT   25   24    5   26                                                  
CONECT   26   25                                                            
CONECT   27   12   28   29   30                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   27   31                                                       
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₀N₂O₅

Average Mass

426.5130 Da

Monoisotopic Mass

426.21547 Da

IUPAC Name

16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione

Traditional Name

16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione

CAS Registry Number

Not Available

SMILES

CC(C)CC1OC(=O)C2(O)CC3(C(N(C(C)=O)C4=CC=CC=C34)N2C1=O)C(C)(C)C=C

InChI Identifier

InChI=1S/C24H30N2O5/c1-7-22(5,6)23-13-24(30)21(29)31-18(12-14(2)3)19(28)26(24)20(23)25(15(4)27)17-11-9-8-10-16(17)23/h7-11,14,18,20,30H,1,12-13H2,2-6H3

InChI Key

KQOPIDROORHFNV-UHFFFAOYSA-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
Penicillium javanicum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrroloindoles. Pyrroloindoles are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyrroloindoles

Direct Parent

Pyrroloindoles

Alternative Parents

Substituents

Pyrroloindole
Alpha-amino acid or derivatives
Indole
Morpholine
Oxazinane
Benzenoid
Acetamide
Tertiary carboxylic acid amide
Pyrrolidine
Pyrrole
Carboxamide group
Carboxylic acid ester
Lactam
Lactone
Oxacycle
Azacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Alkanolamine
Organopnictogen compound
Organic oxygen compound
Organic oxide
Organic nitrogen compound
Carbonyl group
Hydrocarbon derivative
Organonitrogen compound
Organooxygen 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	2.45	ALOGPS
logP	3.22	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	10.67	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	87.15 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	113.64 m³·mol⁻¹	ChemAxon
Polarizability	45.5 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

73210892

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione (NP0231448)

MOL for NP0231448 (16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione)

3D MOL for NP0231448 (16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione)

3D SDF for NP0231448 (16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione)

3D-SDF for NP0231448 (16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione)

PDB for NP0231448 (16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione)

3D PDB for NP0231448 (16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione)

SMILES for NP0231448 (16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione)

INCHI for NP0231448 (16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione)

Structure for NP0231448 (16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione)

3D Structure for NP0231448 (16-acetyl-7-hydroxy-9-(2-methylbut-3-en-2-yl)-4-(2-methylpropyl)-5-oxa-2,16-diazatetracyclo[7.7.0.0²,⁷.0¹⁰,¹⁵]hexadeca-10,12,14-triene-3,6-dione)