NP-MRD: Showing NP-Card for (3r,4r,6r)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4(9),5,7,11(15),12,17(22),18,20-decaen-3-yl}-2-methyloxane-2,3-diol (NP0279386)

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Record Information

Version

2.0

Created at

2022-09-09 04:45:29 UTC

Updated at

2022-09-09 04:45:30 UTC

NP-MRD ID

NP0279386

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,4r,6r)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4(9),5,7,11(15),12,17(22),18,20-decaen-3-yl}-2-methyloxane-2,3-diol

Description

Holyrine B belongs to the class of organic compounds known as indolocarbazoles. These are polycyclic aromatic compounds containing an indole fused to a carbazole. (3r,4r,6r)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4(9),5,7,11(15),12,17(22),18,20-decaen-3-yl}-2-methyloxane-2,3-diol was first documented in 2022 (PMID: 34730069). Based on a literature review very few articles have been published on holyrine B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092206452D          

 34 40  0  0  1  0            999 V2000
    2.9817   -6.9615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8062   -6.9328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6914   -7.7497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6347   -6.1258    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2478   -5.5737    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0762   -4.7668    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3226   -4.4312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5689   -4.7668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9015   -4.2819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9877   -3.4614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7414   -3.1258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4088   -3.6107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2158   -3.4392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5908   -7.1877    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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    2.9731    1.7289   -0.0549 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.9988   -2.6924    0.7179 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9318   -4.0662    0.9322 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7045   -4.6931    0.9512 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6192   -2.5656    0.5412 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6683   -1.6385    0.3313 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2203   -0.4522    0.1791 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7216    0.8095   -0.0551 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.5377    3.1324   -0.6445 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.3253   -1.9540    0.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309092206452D          

 34 40  0  0  1  0            999 V2000
    2.9817   -6.9615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8062   -6.9328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6914   -7.7497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.3733   -1.9401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.9885   -6.8906    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0279386

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(O)O[C@H](C[C@@H](N)[C@H]1O)N1C2=C(C=CC=C2)C2=C1C1=C(C3=C2C(O)=NC3)C2=CC=CC=C2N1

> <INCHI_IDENTIFIER>
InChI=1S/C26H24N4O4/c1-26(33)24(31)15(27)10-18(34-26)30-17-9-5-3-7-13(17)20-21-14(11-28-25(21)32)19-12-6-2-4-8-16(12)29-22(19)23(20)30/h2-9,15,18,24,29,31,33H,10-11,27H2,1H3,(H,28,32)/t15-,18-,24-,26?/m1/s1

> <INCHI_KEY>
LPTYIIOZCJOTKS-FNMALOSOSA-N

> <FORMULA>
C26H24N4O4

> <MOLECULAR_WEIGHT>
456.502

> <EXACT_MASS>
456.179755269

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
49.400279374118874

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,4R,6R)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0^{2,10}.0^{4,9}.0^{11,15}.0^{17,22}]tricosa-1(16),2(10),4(9),5,7,11(15),12,17,19,21-decaen-3-yl}-2-methyloxane-2,3-diol

> <JCHEM_LOGP>
1.3102033872469774

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA>
11.257898887523856

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.854604176832245

> <JCHEM_PKA_STRONGEST_BASIC>
9.439376315682257

> <JCHEM_POLAR_SURFACE_AREA>
129.01999999999998

> <JCHEM_REFRACTIVITY>
126.73260000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4R,6R)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0^{2,10}.0^{4,9}.0^{11,15}.0^{17,22}]tricosa-1(16),2(10),4(9),5,7,11(15),12,17,19,21-decaen-3-yl}-2-methyloxane-2,3-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       5.566 -12.995   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.105 -12.941   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       6.891 -14.466   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.785 -11.435   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.929 -10.404   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       7.609  -8.898   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       6.202  -8.272   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.795  -8.898   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.549  -7.993   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.710  -6.461   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.117  -5.835   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.363  -6.740   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.869  -6.420   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.639  -5.086   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.179  -5.086   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.949  -6.420   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.456  -6.740   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      13.702  -5.835   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      15.109  -6.461   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      15.270  -7.993   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.024  -8.898   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.617  -8.272   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0      11.210  -8.898   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0      10.179  -7.754   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.639  -7.754   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.655  -3.622   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0       9.409  -2.716   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0       8.164  -3.622   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.699  -3.146   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       9.394 -10.880   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.714 -12.387   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0      11.179 -12.862   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0       8.570 -13.417   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       8.890 -14.923   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   33                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   30                                                  
CONECT    6    5    7   25                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    7   13                                                  
CONECT   13   12   14   25                                                  
CONECT   14   13   15   28                                                  
CONECT   15   14   16   26                                                  
CONECT   16   15   17   24                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   16   25                                                  
CONECT   25   24   13    6                                                  
CONECT   26   15   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   14   29                                                  
CONECT   29   28                                                            
CONECT   30    5   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31    2   34                                                  
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₂₄N₄O₄

Average Mass

456.5020 Da

Monoisotopic Mass

456.17976 Da

IUPAC Name

(3R,4R,6R)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0^{2,10}.0^{4,9}.0^{11,15}.0^{17,22}]tricosa-1(16),2(10),4(9),5,7,11(15),12,17,19,21-decaen-3-yl}-2-methyloxane-2,3-diol

Traditional Name

(3R,4R,6R)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0^{2,10}.0^{4,9}.0^{11,15}.0^{17,22}]tricosa-1(16),2(10),4(9),5,7,11(15),12,17,19,21-decaen-3-yl}-2-methyloxane-2,3-diol

CAS Registry Number

Not Available

SMILES

CC1(O)O[C@H](C[C@@H](N)[C@H]1O)N1C2=C(C=CC=C2)C2=C1C1=C(C3=C2C(O)=NC3)C2=CC=CC=C2N1

InChI Identifier

InChI=1S/C26H24N4O4/c1-26(33)24(31)15(27)10-18(34-26)30-17-9-5-3-7-13(17)20-21-14(11-28-25(21)32)19-12-6-2-4-8-16(12)29-22(19)23(20)30/h2-9,15,18,24,29,31,33H,10-11,27H2,1H3,(H,28,32)/t15-,18-,24-,26?/m1/s1

InChI Key

LPTYIIOZCJOTKS-FNMALOSOSA-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 indolocarbazoles. These are polycyclic aromatic compounds containing an indole fused to a carbazole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Carbazoles

Direct Parent

Indolocarbazoles

Alternative Parents

Substituents

Indolocarbazole
Pyrrolo[2,3-a]carbazole
Pyrroloindole
N-alkylindole
Isoindolone
Indole
Isoindoline
Isoindole or derivatives
Oxane
Substituted pyrrole
Benzenoid
Pyrrole
Heteroaromatic compound
Secondary carboxylic acid amide
Secondary alcohol
1,2-aminoalcohol
Amino acid or derivatives
Carboxamide group
Lactam
Hemiacetal
Oxacycle
Azacycle
Carboxylic acid derivative
Primary amine
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Primary aliphatic amine
Organonitrogen compound
Organooxygen compound
Alcohol
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	1.31	ChemAxon
pKa (Strongest Acidic)	7.85	ChemAxon
pKa (Strongest Basic)	9.44	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	129.02 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	126.73 m³·mol⁻¹	ChemAxon
Polarizability	49.4 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

C00028350

Chemspider ID

10364815

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15403381

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Rahul S, Sarkar A: Microbial based natural compounds as potential inhibitors for SARS-CoV-2 Papain-like protease (PLpro): a molecular docking and dynamic simulation study. J Biomol Struct Dyn. 2022;40(24):13848-13858. doi: 10.1080/07391102.2021.1997815. Epub 2021 Nov 3. [PubMed:34730069 ]
LOTUS database [Link]

Showing NP-Card for (3r,4r,6r)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4(9),5,7,11(15),12,17(22),18,20-decaen-3-yl}-2-methyloxane-2,3-diol (NP0279386)

MOL for NP0279386 ((3r,4r,6r)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4(9),5,7,11(15),12,17(22),18,20-decaen-3-yl}-2-methyloxane-2,3-diol)

3D MOL for NP0279386 ((3r,4r,6r)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4(9),5,7,11(15),12,17(22),18,20-decaen-3-yl}-2-methyloxane-2,3-diol)

3D SDF for NP0279386 ((3r,4r,6r)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4(9),5,7,11(15),12,17(22),18,20-decaen-3-yl}-2-methyloxane-2,3-diol)

3D-SDF for NP0279386 ((3r,4r,6r)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4(9),5,7,11(15),12,17(22),18,20-decaen-3-yl}-2-methyloxane-2,3-diol)

PDB for NP0279386 ((3r,4r,6r)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4(9),5,7,11(15),12,17(22),18,20-decaen-3-yl}-2-methyloxane-2,3-diol)

3D PDB for NP0279386 ((3r,4r,6r)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4(9),5,7,11(15),12,17(22),18,20-decaen-3-yl}-2-methyloxane-2,3-diol)

SMILES for NP0279386 ((3r,4r,6r)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4(9),5,7,11(15),12,17(22),18,20-decaen-3-yl}-2-methyloxane-2,3-diol)

INCHI for NP0279386 ((3r,4r,6r)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4(9),5,7,11(15),12,17(22),18,20-decaen-3-yl}-2-methyloxane-2,3-diol)

Structure for NP0279386 ((3r,4r,6r)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4(9),5,7,11(15),12,17(22),18,20-decaen-3-yl}-2-methyloxane-2,3-diol)

3D Structure for NP0279386 ((3r,4r,6r)-4-amino-6-{12-hydroxy-3,13,23-triazahexacyclo[14.7.0.0²,¹⁰.0⁴,⁹.0¹¹,¹⁵.0¹⁷,²²]tricosa-1(16),2(10),4(9),5,7,11(15),12,17(22),18,20-decaen-3-yl}-2-methyloxane-2,3-diol)