NP-MRD: Showing NP-Card for (3r)-3-hydroxy-3-methyl-5-oxo-5-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid (NP0310795)

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Record Information

Version

2.0

Created at

2022-09-11 06:21:58 UTC

Updated at

2022-09-11 06:21:58 UTC

NP-MRD ID

NP0310795

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r)-3-hydroxy-3-methyl-5-oxo-5-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid

Description

CHEMBL3403681 belongs to the class of organic compounds known as saccharolipids. Saccharolipids are compounds in which fatty acids are linked directly to a sugar backbone, forming structures that are compatible with membrane bilayers. In the saccharolipids, a sugar substitutes for the glycerol backbone that is present in glycerolipids and glycerophospholipids. The most familiar saccharolipids contain an acylated glucosamine. In contrast to others glycolipids, the fatty acid is not glycosidically linked to the sugar moiety. (3r)-3-hydroxy-3-methyl-5-oxo-5-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid is found in Ailanthus altissima. Based on a literature review very few articles have been published on CHEMBL3403681.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112208212D          

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M  END

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M  END


  Mrv1652309112208212D          

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  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  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  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 26 31  2  0  0  0  0
 31 32  1  0  0  0  0
 17 32  1  0  0  0  0
 32 33  2  0  0  0  0
 20 33  1  0  0  0  0
 25 33  1  0  0  0  0
 15 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  6  0  0  0
 36 38  1  0  0  0  0
 13 38  1  0  0  0  0
 38 39  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0310795

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@](O)(CC(O)=O)CC(=O)OC[C@H]1O[C@@H](OC2=CN=C3C=CC(=O)N4C5=C(C=CC=C5)C2=C34)[C@H](O)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C26H26N2O11/c1-26(36,8-18(30)31)9-19(32)37-11-16-22(33)23(34)24(35)25(39-16)38-15-10-27-13-6-7-17(29)28-14-5-3-2-4-12(14)20(15)21(13)28/h2-7,10,16,22-25,33-36H,8-9,11H2,1H3,(H,30,31)/t16-,22-,23+,24-,25-,26-/m1/s1

> <INCHI_KEY>
LEQPGBPPUCRECO-HFWDXPBASA-N

> <FORMULA>
C26H26N2O11

> <MOLECULAR_WEIGHT>
542.497

> <EXACT_MASS>
542.153659665

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
52.18665746641546

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R)-3-hydroxy-3-methyl-5-oxo-5-{[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0^{5,16}.0^{10,15}]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid

> <JCHEM_LOGP>
-1.2301993651963186

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.200531117559752

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.8347196002825097

> <JCHEM_PKA_STRONGEST_BASIC>
2.9866969002708514

> <JCHEM_POLAR_SURFACE_AREA>
197.86999999999998

> <JCHEM_REFRACTIVITY>
129.26750000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3R)-3-hydroxy-3-methyl-5-oxo-5-{[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0^{5,16}.0^{10,15}]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       0.265 -11.665   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.730 -11.189   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.194 -10.713   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       2.206 -12.653   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.175 -13.798   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.651 -15.262   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -0.331 -13.478   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.254  -9.724   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.284  -8.580   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.791  -8.900   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       1.808  -7.115   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.839  -5.971   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.363  -4.506   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.393  -3.361   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.918  -1.897   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.948  -0.752   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.472   0.712   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.966   1.032   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       1.490   2.497   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       2.520   3.641   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.459   5.479   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.705   6.384   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.112   5.758   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.357   6.663   0.000  0.00  0.00           O+0
HETATM   25  N   UNK     0       5.273   4.226   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       6.518   3.321   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.025   3.641   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.055   2.497   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.579   1.032   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.073   0.712   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.043   1.857   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.503   1.857   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.027   3.321   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.411  -1.577   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       0.935  -0.112   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       0.381  -2.721   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -1.126  -2.401   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       0.857  -4.186   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -0.174  -5.330   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4    8                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    2    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   38                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   34                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   32                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   33                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   33                                                  
CONECT   26   25   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   26   32                                                  
CONECT   32   31   17   33                                                  
CONECT   33   32   20   25                                                  
CONECT   34   15   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   13   39                                                  
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₂₆N₂O₁₁

Average Mass

542.4970 Da

Monoisotopic Mass

542.15366 Da

IUPAC Name

(3R)-3-hydroxy-3-methyl-5-oxo-5-{[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0^{5,16}.0^{10,15}]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@](O)(CC(O)=O)CC(=O)OC[C@H]1O[C@@H](OC2=CN=C3C=CC(=O)N4C5=C(C=CC=C5)C2=C34)[C@H](O)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C26H26N2O11/c1-26(36,8-18(30)31)9-19(32)37-11-16-22(33)23(34)24(35)25(39-16)38-15-10-27-13-6-7-17(29)28-14-5-3-2-4-12(14)20(15)21(13)28/h2-7,10,16,22-25,33-36H,8-9,11H2,1H3,(H,30,31)/t16-,22-,23+,24-,25-,26-/m1/s1

InChI Key

LEQPGBPPUCRECO-HFWDXPBASA-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
Ailanthus altissima	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as saccharolipids. Saccharolipids are compounds in which fatty acids are linked directly to a sugar backbone, forming structures that are compatible with membrane bilayers. In the saccharolipids, a sugar substitutes for the glycerol backbone that is present in glycerolipids and glycerophospholipids. The most familiar saccharolipids contain an acylated glucosamine. In contrast to others glycolipids, the fatty acid is not glycosidically linked to the sugar moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Saccharolipids

Sub Class

Not Available

Direct Parent

Saccharolipids

Alternative Parents

Substituents

Saccharolipid
Indolo[3,2-1de][1,5]naphthyridine
Beta-carboline
Pyridoindole
Glycosyl compound
O-glycosyl compound
Diazanaphthalene
Naphthyridine
Indole
Indole or derivatives
Indolizine
Pyrrolopyridine
Alkaloid or derivatives
Fatty acid ester
Pyridinone
Fatty acyl
Dicarboxylic acid or derivatives
Monosaccharide
Oxane
Pyridine
Benzenoid
Tertiary alcohol
Pyrrole
Heteroaromatic compound
Secondary alcohol
Carboxylic acid ester
Lactam
Organoheterocyclic compound
Polyol
Azacycle
Carboxylic acid derivative
Carboxylic acid
Acetal
Oxacycle
Organonitrogen compound
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organic nitrogen compound
Alcohol
Organic oxide
Organooxygen compound
Organopnictogen 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	-1.2	ChemAxon
pKa (Strongest Acidic)	3.83	ChemAxon
pKa (Strongest Basic)	2.99	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	197.87 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	129.27 m³·mol⁻¹	ChemAxon
Polarizability	52.19 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	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

58987957

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

118729953

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r)-3-hydroxy-3-methyl-5-oxo-5-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid (NP0310795)

MOL for NP0310795 ((3r)-3-hydroxy-3-methyl-5-oxo-5-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid)

3D MOL for NP0310795 ((3r)-3-hydroxy-3-methyl-5-oxo-5-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid)

3D SDF for NP0310795 ((3r)-3-hydroxy-3-methyl-5-oxo-5-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid)

3D-SDF for NP0310795 ((3r)-3-hydroxy-3-methyl-5-oxo-5-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid)

PDB for NP0310795 ((3r)-3-hydroxy-3-methyl-5-oxo-5-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid)

3D PDB for NP0310795 ((3r)-3-hydroxy-3-methyl-5-oxo-5-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid)

SMILES for NP0310795 ((3r)-3-hydroxy-3-methyl-5-oxo-5-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid)

INCHI for NP0310795 ((3r)-3-hydroxy-3-methyl-5-oxo-5-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid)

Structure for NP0310795 ((3r)-3-hydroxy-3-methyl-5-oxo-5-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid)

3D Structure for NP0310795 ((3r)-3-hydroxy-3-methyl-5-oxo-5-{[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-({2-oxo-1,6-diazatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁵]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-8-yl}oxy)oxan-2-yl]methoxy}pentanoic acid)