NP-MRD: Showing NP-Card for (5s,10s)-7,9-dibromo-n-[(2s)-3-{2,6-dibromo-4-[(5s)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide (NP0181608)

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Record Information

Version

2.0

Created at

2022-09-03 20:09:20 UTC

Updated at

2022-09-03 20:09:20 UTC

NP-MRD ID

NP0181608

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5s,10s)-7,9-dibromo-n-[(2s)-3-{2,6-dibromo-4-[(5s)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide

Description

(5S,10S)-7,9-dibromo-N-[(2S)-3-{2,6-dibromo-4-[(5S)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]Deca-2,6,8-triene-3-carboxamide belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring. (5s,10s)-7,9-dibromo-n-[(2s)-3-{2,6-dibromo-4-[(5s)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide is found in Aplysina fistularis. Based on a literature review very few articles have been published on (5S,10S)-7,9-dibromo-N-[(2S)-3-{2,6-dibromo-4-[(5S)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]Deca-2,6,8-triene-3-carboxamide.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032222092D          

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M  END

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  Mrv1652309032222092D          

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M  END
> <DATABASE_ID>
NP0181608

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(Br)[C@@H](O)[C@]2(CC(=NO2)C(=O)NC[C@H](O)COC2=C(Br)C=C(C=C2Br)[C@H]2CN=C(O)O2)C=C1Br

> <INCHI_IDENTIFIER>
InChI=1S/C22H21Br4N3O8/c1-34-18-13(25)4-22(19(31)16(18)26)5-14(29-37-22)20(32)27-6-10(30)8-35-17-11(23)2-9(3-12(17)24)15-7-28-21(33)36-15/h2-4,10,15,19,30-31H,5-8H2,1H3,(H,27,32)(H,28,33)/t10-,15+,19+,22+/m0/s1

> <INCHI_KEY>
WZKUTASMIUOUPM-HUOCMSNQSA-N

> <FORMULA>
C22H21Br4N3O8

> <MOLECULAR_WEIGHT>
775.039

> <EXACT_MASS>
770.806217

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
60.01680559636651

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5S,10S)-7,9-dibromo-N-[(2S)-3-{2,6-dibromo-4-[(5S)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide

> <JCHEM_LOGP>
3.0793251819999985

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.912583943880918

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.76644542355548

> <JCHEM_PKA_STRONGEST_BASIC>
0.19456838513528285

> <JCHEM_POLAR_SURFACE_AREA>
151.42999999999998

> <JCHEM_REFRACTIVITY>
146.8482

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(5S,10S)-7,9-dibromo-N-[(2S)-3-{2,6-dibromo-4-[(5S)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0     -10.398   8.052   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -8.867   7.891   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -8.240   6.484   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.709   6.323   0.000  0.00  0.00           C+0
HETATM    5 Br   UNK     0      -5.803   7.569   0.000  0.00  0.00          Br+0
HETATM    6  C   UNK     0      -6.082   4.916   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -4.551   4.755   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -6.987   3.671   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -8.519   3.832   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -9.145   5.238   0.000  0.00  0.00           C+0
HETATM   11 Br   UNK     0     -10.677   5.399   0.000  0.00  0.00          Br+0
HETATM   12  C   UNK     0      -5.481   3.350   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.320   1.819   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.986   1.049   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -3.986  -0.491   0.000  0.00  0.00           O+0
HETATM   16  N   UNK     0      -2.653   1.819   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      -1.319   1.049   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.015   1.819   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.015   3.359   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.348   1.049   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.682   1.819   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.016   1.049   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.349   1.819   0.000  0.00  0.00           C+0
HETATM   24 Br   UNK     0       5.349   3.359   0.000  0.00  0.00          Br+0
HETATM   25  C   UNK     0       6.683   1.049   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.683  -0.491   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.017  -1.261   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.424  -0.635   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0      10.454  -1.779   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0       9.684  -3.113   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      10.310  -4.520   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       8.178  -2.793   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       5.349  -1.261   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.016  -0.491   0.000  0.00  0.00           C+0
HETATM   35 Br   UNK     0       2.682  -1.261   0.000  0.00  0.00          Br+0
HETATM   36  N   UNK     0      -6.727   1.192   0.000  0.00  0.00           N+0
HETATM   37  O   UNK     0      -7.757   2.337   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   12   37                                             
CONECT    9    8   10                                                       
CONECT   10    9    3   11                                                  
CONECT   11   10                                                            
CONECT   12    8   13                                                       
CONECT   13   12   14   36                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   34                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   33                                                  
CONECT   27   26   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   27                                                       
CONECT   33   26   34                                                       
CONECT   34   33   22   35                                                  
CONECT   35   34                                                            
CONECT   36   13   37                                                       
CONECT   37   36    8                                                       
MASTER        0    0    0    0    0    0    0    0   37    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₁Br₄N₃O₈

Average Mass

775.0390 Da

Monoisotopic Mass

770.80622 Da

IUPAC Name

(5S,10S)-7,9-dibromo-N-[(2S)-3-{2,6-dibromo-4-[(5S)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide

Traditional Name

(5S,10S)-7,9-dibromo-N-[(2S)-3-{2,6-dibromo-4-[(5S)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide

CAS Registry Number

Not Available

SMILES

COC1=C(Br)[C@@H](O)[C@]2(CC(=NO2)C(=O)NC[C@H](O)COC2=C(Br)C=C(C=C2Br)[C@H]2CN=C(O)O2)C=C1Br

InChI Identifier

InChI=1S/C22H21Br4N3O8/c1-34-18-13(25)4-22(19(31)16(18)26)5-14(29-37-22)20(32)27-6-10(30)8-35-17-11(23)2-9(3-12(17)24)15-7-28-21(33)36-15/h2-4,10,15,19,30-31H,5-8H2,1H3,(H,27,32)(H,28,33)/t10-,15+,19+,22+/m0/s1

InChI Key

WZKUTASMIUOUPM-HUOCMSNQSA-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
Aplysina fistularis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenol ethers

Sub Class

Not Available

Direct Parent

Phenol ethers

Alternative Parents

Substituents

Phenoxy compound
Phenol ether
Alkyl aryl ether
Bromobenzene
Halobenzene
Aryl bromide
Aryl halide
Monocyclic benzene moiety
Isoxazoline
Oxazoline
Bromohydrin
Carboxamide group
Halohydrin
Oxime ether
Secondary alcohol
Secondary carboxylic acid amide
Organoheterocyclic compound
Haloalkene
Organic 1,3-dipolar compound
Bromoalkene
Propargyl-type 1,3-dipolar organic compound
Vinyl halide
Vinyl bromide
Carboxylic acid derivative
Azacycle
Ether
Oxacycle
Organopnictogen compound
Organohalogen compound
Organic nitrogen compound
Carbonyl group
Alcohol
Hydrocarbon derivative
Organic oxide
Organobromide
Organonitrogen compound
Organooxygen compound
Organic oxygen 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	3.08	ChemAxon
pKa (Strongest Acidic)	2.77	ChemAxon
pKa (Strongest Basic)	0.19	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	151.43 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	146.85 m³·mol⁻¹	ChemAxon
Polarizability	60.02 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

163090008

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (5s,10s)-7,9-dibromo-n-[(2s)-3-{2,6-dibromo-4-[(5s)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide (NP0181608)

MOL for NP0181608 ((5s,10s)-7,9-dibromo-n-[(2s)-3-{2,6-dibromo-4-[(5s)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

3D MOL for NP0181608 ((5s,10s)-7,9-dibromo-n-[(2s)-3-{2,6-dibromo-4-[(5s)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

3D SDF for NP0181608 ((5s,10s)-7,9-dibromo-n-[(2s)-3-{2,6-dibromo-4-[(5s)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

3D-SDF for NP0181608 ((5s,10s)-7,9-dibromo-n-[(2s)-3-{2,6-dibromo-4-[(5s)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

PDB for NP0181608 ((5s,10s)-7,9-dibromo-n-[(2s)-3-{2,6-dibromo-4-[(5s)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

3D PDB for NP0181608 ((5s,10s)-7,9-dibromo-n-[(2s)-3-{2,6-dibromo-4-[(5s)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

SMILES for NP0181608 ((5s,10s)-7,9-dibromo-n-[(2s)-3-{2,6-dibromo-4-[(5s)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

INCHI for NP0181608 ((5s,10s)-7,9-dibromo-n-[(2s)-3-{2,6-dibromo-4-[(5s)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

Structure for NP0181608 ((5s,10s)-7,9-dibromo-n-[(2s)-3-{2,6-dibromo-4-[(5s)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)

3D Structure for NP0181608 ((5s,10s)-7,9-dibromo-n-[(2s)-3-{2,6-dibromo-4-[(5s)-2-hydroxy-4,5-dihydro-1,3-oxazol-5-yl]phenoxy}-2-hydroxypropyl]-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide)