NP-MRD: Showing NP-Card for (5s,7r,8r,10r,11r,12r,15r,16s,18z,25s)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0⁵,¹⁶.0⁷,¹⁵.0⁸,¹²]octacosa-1,3,13,18,20-pentaene-27,28-dione (NP0141771)

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Record Information

Version

2.0

Created at

2022-09-01 20:10:00 UTC

Updated at

2022-09-01 20:10:00 UTC

NP-MRD ID

NP0141771

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5s,7r,8r,10r,11r,12r,15r,16s,18z,25s)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0⁵,¹⁶.0⁷,¹⁵.0⁸,¹²]octacosa-1,3,13,18,20-pentaene-27,28-dione

Description

30-Oxo-28-N-methylikarugamycin belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides. (5s,7r,8r,10r,11r,12r,15r,16s,18z,25s)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0⁵,¹⁶.0⁷,¹⁵.0⁸,¹²]octacosa-1,3,13,18,20-pentaene-27,28-dione is found in Streptomyces zhaozhouensis. (5s,7r,8r,10r,11r,12r,15r,16s,18z,25s)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0⁵,¹⁶.0⁷,¹⁵.0⁸,¹²]octacosa-1,3,13,18,20-pentaene-27,28-dione was first documented in 2019 (PMID: 30542952). Based on a literature review very few articles have been published on 30-oxo-28-N-methylikarugamycin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309012222102D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309012222102D          

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   -0.5507   -0.7945    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3727   -0.7249    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9746   -1.2892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6972   -0.8912    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4440   -1.2419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4399   -1.1964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8291   -1.9238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8379   -0.4737    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6564   -0.3709    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
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  2  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  4  0  0  0
 16 17  1  0  0  0  0
 17 18  1  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
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  4  0  0  0
 25 23  1  4  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
  9 27  1  0  0  0  0
 27 28  1  6  0  0  0
 29 28  1  6  0  0  0
  8 29  1  0  0  0  0
 29 30  1  0  0  0  0
  5 30  1  0  0  0  0
 30 31  1  1  0  0  0
 31 32  1  0  0  0  0
  4 32  1  0  0  0  0
 32 33  1  1  0  0  0
 22 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 19 36  1  6  0  0  0
 36 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0141771

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@@H]2[C@H]3C[C@H]4C=CC(O)=C5C(=O)[C@H](CCCN=C(O)\C=C/C[C@@H]4[C@H]3C=C[C@H]2[C@@H]1C(C)=O)N(C)C5=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H38N2O5/c1-16-14-22-21(27(16)17(2)33)11-10-20-19-6-4-8-26(35)31-13-5-7-24-29(36)28(30(37)32(24)3)25(34)12-9-18(19)15-23(20)22/h4,8-12,16,18-24,27,34H,5-7,13-15H2,1-3H3,(H,31,35)/b8-4-,12-9?,28-25?/t16-,18-,19+,20-,21-,22+,23+,24+,27+/m1/s1

> <INCHI_KEY>
XRGRHICYOPBQHL-VHJCOEOQSA-N

> <FORMULA>
C30H38N2O5

> <MOLECULAR_WEIGHT>
506.643

> <EXACT_MASS>
506.278072332

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
54.7894297252101

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5S,7R,8R,10R,11R,12R,15R,16S,18Z,25S)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0^{5,16}.0^{7,15}.0^{8,12}]octacosa-1,3,13,18,20-pentaene-27,28-dione

> <ALOGPS_LOGP>
3.14

> <JCHEM_LOGP>
2.7031961177427455

> <ALOGPS_LOGS>
-4.89

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.240403030039849

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.90369151126089

> <JCHEM_PKA_STRONGEST_BASIC>
6.57660688334818

> <JCHEM_POLAR_SURFACE_AREA>
107.27000000000001

> <JCHEM_REFRACTIVITY>
145.8935

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.53e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5S,7R,8R,10R,11R,12R,15R,16S,18Z,25S)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0^{5,16}.0^{7,15}.0^{8,12}]octacosa-1,3,13,18,20-pentaene-27,28-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 01-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-SEP-22         0                                  
HETATM    1  C   UNK     0      -7.298   0.622   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.798   0.972   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -5.352   2.446   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -4.745  -0.151   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.217   0.041   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.337   1.305   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.803   1.175   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.299  -0.376   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.326  -0.665   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.023   0.078   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.054   1.617   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.264   2.414   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.613   1.671   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.644   0.131   0.000  0.00  0.00           O+0
HETATM   15  N   UNK     0       3.930   2.468   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       5.279   1.725   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.597   2.522   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.946   1.779   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.977   0.239   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.659  -0.558   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.310   0.185   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.691  -2.097   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.373  -2.894   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.404  -4.434   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       4.024  -2.151   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.706  -2.948   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.357  -2.205   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.098  -2.710   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.028  -1.483   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -2.562  -1.353   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -3.686  -2.406   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -5.035  -1.664   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -6.429  -2.318   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       8.288  -2.233   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       9.014  -3.591   0.000  0.00  0.00           O+0
HETATM   36  N   UNK     0       9.031  -0.884   0.000  0.00  0.00           N+0
HETATM   37  C   UNK     0      10.559  -0.692   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   32                                                  
CONECT    5    4    6   30                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   29                                                  
CONECT    9    8   10   27                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   36                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   34                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26    9   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28    8   30                                                  
CONECT   30   29    5   31                                                  
CONECT   31   30   32                                                       
CONECT   32   31    4   33                                                  
CONECT   33   32                                                            
CONECT   34   22   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   19   37                                                  
CONECT   37   36                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₃₈N₂O₅

Average Mass

506.6430 Da

Monoisotopic Mass

506.27807 Da

IUPAC Name

(5S,7R,8R,10R,11R,12R,15R,16S,18Z,25S)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0^{5,16}.0^{7,15}.0^{8,12}]octacosa-1,3,13,18,20-pentaene-27,28-dione

Traditional Name

(5S,7R,8R,10R,11R,12R,15R,16S,18Z,25S)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0^{5,16}.0^{7,15}.0^{8,12}]octacosa-1,3,13,18,20-pentaene-27,28-dione

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@@H]2[C@H]3C[C@H]4C=CC(O)=C5C(=O)[C@H](CCCN=C(O)\C=C/C[C@@H]4[C@H]3C=C[C@H]2[C@@H]1C(C)=O)N(C)C5=O

InChI Identifier

InChI=1S/C30H38N2O5/c1-16-14-22-21(27(16)17(2)33)11-10-20-19-6-4-8-26(35)31-13-5-7-24-29(36)28(30(37)32(24)3)25(34)12-9-18(19)15-23(20)22/h4,8-12,16,18-24,27,34H,5-7,13-15H2,1-3H3,(H,31,35)/b8-4-,12-9?,28-25?/t16-,18-,19+,20-,21-,22+,23+,24+,27+/m1/s1

InChI Key

XRGRHICYOPBQHL-VHJCOEOQSA-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
Streptomyces zhaozhouensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolactams

Sub Class

Not Available

Direct Parent

Macrolactams

Alternative Parents

Substituents

Macrolactam
Monoterpenoid
11-noriridane monoterpenoid
N-alkylpyrrolidine
3-pyrrolidone
2-pyrrolidone
Pyrrolidone
Vinylogous acid
Cyclic carboximidic acid
Tertiary carboxylic acid amide
Pyrrolidine
Lactam
Ketone
Carboxamide group
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Enol
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	3.14	ALOGPS
logP	2.7	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	4.9	ChemAxon
pKa (Strongest Basic)	6.58	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	107.27 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	145.89 m³·mol⁻¹	ChemAxon
Polarizability	54.79 Å³	ChemAxon
Number of Rings	5	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

139585104

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Dhaneesha M, Hasin O, Sivakumar KC, Ravinesh R, Naman CB, Carmeli S, Sajeevan TP: DNA Binding and Molecular Dynamic Studies of Polycyclic Tetramate Macrolactams (PTM) with Potential Anticancer Activity Isolated from a Sponge-Associated Streptomyces zhaozhouensis subsp. mycale subsp. nov. Mar Biotechnol (NY). 2019 Feb;21(1):124-137. doi: 10.1007/s10126-018-9866-9. Epub 2018 Dec 13. [PubMed:30542952 ]
LOTUS database [Link]

Showing NP-Card for (5s,7r,8r,10r,11r,12r,15r,16s,18z,25s)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0⁵,¹⁶.0⁷,¹⁵.0⁸,¹²]octacosa-1,3,13,18,20-pentaene-27,28-dione (NP0141771)

MOL for NP0141771 ((5s,7r,8r,10r,11r,12r,15r,16s,18z,25s)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0⁵,¹⁶.0⁷,¹⁵.0⁸,¹²]octacosa-1,3,13,18,20-pentaene-27,28-dione)

3D MOL for NP0141771 ((5s,7r,8r,10r,11r,12r,15r,16s,18z,25s)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0⁵,¹⁶.0⁷,¹⁵.0⁸,¹²]octacosa-1,3,13,18,20-pentaene-27,28-dione)

3D SDF for NP0141771 ((5s,7r,8r,10r,11r,12r,15r,16s,18z,25s)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0⁵,¹⁶.0⁷,¹⁵.0⁸,¹²]octacosa-1,3,13,18,20-pentaene-27,28-dione)

3D-SDF for NP0141771 ((5s,7r,8r,10r,11r,12r,15r,16s,18z,25s)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0⁵,¹⁶.0⁷,¹⁵.0⁸,¹²]octacosa-1,3,13,18,20-pentaene-27,28-dione)

PDB for NP0141771 ((5s,7r,8r,10r,11r,12r,15r,16s,18z,25s)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0⁵,¹⁶.0⁷,¹⁵.0⁸,¹²]octacosa-1,3,13,18,20-pentaene-27,28-dione)

3D PDB for NP0141771 ((5s,7r,8r,10r,11r,12r,15r,16s,18z,25s)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0⁵,¹⁶.0⁷,¹⁵.0⁸,¹²]octacosa-1,3,13,18,20-pentaene-27,28-dione)

SMILES for NP0141771 ((5s,7r,8r,10r,11r,12r,15r,16s,18z,25s)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0⁵,¹⁶.0⁷,¹⁵.0⁸,¹²]octacosa-1,3,13,18,20-pentaene-27,28-dione)

INCHI for NP0141771 ((5s,7r,8r,10r,11r,12r,15r,16s,18z,25s)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0⁵,¹⁶.0⁷,¹⁵.0⁸,¹²]octacosa-1,3,13,18,20-pentaene-27,28-dione)

Structure for NP0141771 ((5s,7r,8r,10r,11r,12r,15r,16s,18z,25s)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0⁵,¹⁶.0⁷,¹⁵.0⁸,¹²]octacosa-1,3,13,18,20-pentaene-27,28-dione)

3D Structure for NP0141771 ((5s,7r,8r,10r,11r,12r,15r,16s,18z,25s)-11-acetyl-2,20-dihydroxy-10,26-dimethyl-21,26-diazapentacyclo[23.2.1.0⁵,¹⁶.0⁷,¹⁵.0⁸,¹²]octacosa-1,3,13,18,20-pentaene-27,28-dione)