NP-MRD: Showing NP-Card for (1r,11s,18s,20r,21r,22s)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,14-tetraen-9-one (NP0217279)

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Record Information

Version

2.0

Created at

2022-09-05 17:34:50 UTC

Updated at

2022-09-05 17:34:51 UTC

NP-MRD ID

NP0217279

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,11s,18s,20r,21r,22s)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,14-tetraen-9-one

Description

(1R,11S,18S,20R,21R,22S)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]Tetracosa-2(7),3,5,14-tetraen-9-one belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton. (1r,11s,18s,20r,21r,22s)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,14-tetraen-9-one is found in Strychnos nux-vomica and Strychnos wallichiana. Based on a literature review very few articles have been published on (1R,11S,18S,20R,21R,22S)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]Tetracosa-2(7),3,5,14-tetraen-9-one.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309052219342D          

 28 34  0  0  1  0            999 V2000
   -0.6609   -2.2598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0194   -2.7265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7637   -2.3707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8277   -1.5482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5721   -1.1924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2524   -1.6591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1884   -2.4816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4441   -2.8374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3801   -3.6599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9720   -2.7945    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3502   -3.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9011   -4.2394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1942   -3.5862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7191   -2.9059    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5744   -2.8617    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1451   -2.2028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9862   -1.3824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3080   -0.9051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7972   -0.0597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8838   -0.1070    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0068    0.0282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5493   -0.6787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0947   -1.3602    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8249   -0.8853    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7536   -1.0765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6949   -1.5950    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2947   -2.2513    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4630   -2.1268    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  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  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  1  0  0  0
  6 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  1  0  0  0  0
 24 25  1  1  0  0  0
 26 25  1  1  0  0  0
 18 26  1  0  0  0  0
 26 27  1  0  0  0  0
 14 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 10  1  6  0  0  0
 23 28  1  0  0  0  0
M  END


  Mrv1652309052219342D          

 28 34  0  0  1  0            999 V2000
   -0.6609   -2.2598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0194   -2.7265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7637   -2.3707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8277   -1.5482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5721   -1.1924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2524   -1.6591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1884   -2.4816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4441   -2.8374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3801   -3.6599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9720   -2.7945    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3502   -3.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9011   -4.2394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1942   -3.5862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7191   -2.9059    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5744   -2.8617    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1451   -2.2028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9862   -1.3824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3080   -0.9051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7972   -0.0597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8838   -0.1070    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0068    0.0282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5493   -0.6787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0947   -1.3602    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8249   -0.8853    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7536   -1.0765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6949   -1.5950    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2947   -2.2513    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4630   -2.1268    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  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  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  1  0  0  0
  6 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  1  0  0  0  0
 24 25  1  1  0  0  0
 26 25  1  1  0  0  0
 18 26  1  0  0  0  0
 26 27  1  0  0  0  0
 14 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 10  1  6  0  0  0
 23 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0217279

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2C(N3[C@H]4[C@@H]5[C@H](CC3=O)OCC=C3CN6CC[C@]24[C@@H]6C[C@H]53)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C22H24N2O4/c1-27-14-3-2-13-19(20(14)26)24-17(25)9-15-18-12-8-16-22(13,21(18)24)5-6-23(16)10-11(12)4-7-28-15/h2-4,12,15-16,18,21,26H,5-10H2,1H3/t12-,15-,16-,18-,21-,22+/m0/s1

> <INCHI_KEY>
YNTZDAWFDSBXFV-UFZWUQRGSA-N

> <FORMULA>
C22H24N2O4

> <MOLECULAR_WEIGHT>
380.444

> <EXACT_MASS>
380.173607261

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
39.921451877740495

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,11S,18S,20R,21R,22S)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0^{1,18}.0^{2,7}.0^{8,22}.0^{11,21}.0^{15,20}]tetracosa-2,4,6,14-tetraen-9-one

> <JCHEM_LOGP>
0.0019371223193722946

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
17.24553641698858

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.346138407641101

> <JCHEM_PKA_STRONGEST_BASIC>
8.68884993043396

> <JCHEM_POLAR_SURFACE_AREA>
62.24

> <JCHEM_REFRACTIVITY>
102.95179999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,11S,18S,20R,21R,22S)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0^{1,18}.0^{2,7}.0^{8,22}.0^{11,21}.0^{15,20}]tetracosa-2,4,6,14-tetraen-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.234  -4.218   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.036  -5.090   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.426  -4.425   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.545  -2.890   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.935  -2.226   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.204  -3.097   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.085  -4.632   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.696  -5.296   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.576  -6.832   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0       5.548  -5.216   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       6.254  -6.622   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.415  -7.914   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       7.829  -6.694   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.809  -5.424   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      10.406  -5.342   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      11.471  -4.112   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.174  -2.580   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.908  -1.690   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.955  -0.111   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       7.250  -0.200   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       5.613   0.053   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.759  -1.267   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.777  -2.539   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.140  -1.653   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.873  -2.009   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.764  -2.977   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.017  -4.202   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.464  -3.970   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   23                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8                                                            
CONECT   10    7   11   28                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   27                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   26                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    6   24   28                                             
CONECT   24   23   20   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   18   27                                                  
CONECT   27   26   14   28                                                  
CONECT   28   27   10   23                                                  
MASTER        0    0    0    0    0    0    0    0   28    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₄N₂O₄

Average Mass

380.4440 Da

Monoisotopic Mass

380.17361 Da

IUPAC Name

(1R,11S,18S,20R,21R,22S)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0^{1,18}.0^{2,7}.0^{8,22}.0^{11,21}.0^{15,20}]tetracosa-2,4,6,14-tetraen-9-one

Traditional Name

(1R,11S,18S,20R,21R,22S)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0^{1,18}.0^{2,7}.0^{8,22}.0^{11,21}.0^{15,20}]tetracosa-2,4,6,14-tetraen-9-one

CAS Registry Number

Not Available

SMILES

COC1=CC=C2C(N3[C@H]4[C@@H]5[C@H](CC3=O)OCC=C3CN6CC[C@]24[C@@H]6C[C@H]53)=C1O

InChI Identifier

InChI=1S/C22H24N2O4/c1-27-14-3-2-13-19(20(14)26)24-17(25)9-15-18-12-8-16-22(13,21(18)24)5-6-23(16)10-11(12)4-7-28-15/h2-4,12,15-16,18,21,26H,5-10H2,1H3/t12-,15-,16-,18-,21-,22+/m0/s1

InChI Key

YNTZDAWFDSBXFV-UFZWUQRGSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Strychnos nux-vomica	LOTUS Database	35616633
Strychnos wallichiana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Strychnos alkaloids

Sub Class

Not Available

Direct Parent

Strychnos alkaloids

Alternative Parents

Substituents

Strychnan skeleton
Akuammicine-skeleton
Stemmadenine-skeleton
Carbazole
Quinolidine
Indole or derivatives
Indolizidine
Anisole
Phenol ether
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Delta-lactam
Phenol
Piperidinone
Aralkylamine
Benzenoid
Piperidine
N-alkylpyrrolidine
Pyrrolidine
Tertiary carboxylic acid amide
Tertiary amine
Tertiary aliphatic amine
Carboxamide group
Lactam
Amino acid or derivatives
Azacycle
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Ether
Dialkyl ether
Hydrocarbon derivative
Organic oxygen compound
Organopnictogen compound
Organonitrogen compound
Carbonyl group
Organooxygen compound
Organic oxide
Organic nitrogen compound
Amine
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	0.0019	ChemAxon
pKa (Strongest Acidic)	9.35	ChemAxon
pKa (Strongest Basic)	8.69	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	62.24 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	102.95 m³·mol⁻¹	ChemAxon
Polarizability	39.92 Å³	ChemAxon
Number of Rings	7	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

10296827

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

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METLIN ID

Not Available

PubChem Compound

21680051

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for (1r,11s,18s,20r,21r,22s)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,14-tetraen-9-one (NP0217279)

MOL for NP0217279 ((1r,11s,18s,20r,21r,22s)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,14-tetraen-9-one)

3D MOL for NP0217279 ((1r,11s,18s,20r,21r,22s)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,14-tetraen-9-one)

3D SDF for NP0217279 ((1r,11s,18s,20r,21r,22s)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,14-tetraen-9-one)

3D-SDF for NP0217279 ((1r,11s,18s,20r,21r,22s)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,14-tetraen-9-one)

PDB for NP0217279 ((1r,11s,18s,20r,21r,22s)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,14-tetraen-9-one)

3D PDB for NP0217279 ((1r,11s,18s,20r,21r,22s)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,14-tetraen-9-one)

SMILES for NP0217279 ((1r,11s,18s,20r,21r,22s)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,14-tetraen-9-one)

INCHI for NP0217279 ((1r,11s,18s,20r,21r,22s)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,14-tetraen-9-one)

Structure for NP0217279 ((1r,11s,18s,20r,21r,22s)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,14-tetraen-9-one)

3D Structure for NP0217279 ((1r,11s,18s,20r,21r,22s)-6-hydroxy-5-methoxy-12-oxa-8,17-diazaheptacyclo[15.5.2.0¹,¹⁸.0²,⁷.0⁸,²².0¹¹,²¹.0¹⁵,²⁰]tetracosa-2,4,6,14-tetraen-9-one)