NP-MRD: Showing NP-Card for (3r,6s,9e,14r,15r)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2r)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one (NP0229481)

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Record Information

Version

2.0

Created at

2022-09-06 09:33:21 UTC

Updated at

2022-09-06 09:33:21 UTC

NP-MRD ID

NP0229481

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,6s,9e,14r,15r)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2r)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one

Description

Microtermolide A belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating. (3r,6s,9e,14r,15r)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2r)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one was first documented in 2015 (PMID: 26523486). Based on a literature review very few articles have been published on Microtermolide A (PMID: 27579840).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062211332D          

 32 32  0  0  1  0            999 V2000
    2.3431    2.6478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2742    1.8257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0267    1.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8472    1.4127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1824    0.6588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9893    0.4869    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5690    0.1071    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4353   -0.7857    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0918   -1.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6815   -1.1209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0143   -0.6356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5948   -1.9413    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8410   -2.2765    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7543   -3.0969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0005   -3.4321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4215   -3.5822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1738   -1.7912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4199   -2.1264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2604   -0.9708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5932   -0.4855    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -1.0011   -1.9763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0878   -2.7968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1009    0.1848    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5204    1.4905    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
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  4  5  1  0  0  0  0
  5  6  1  4  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
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 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
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 26 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 32  2  1  4  0  0  0
M  END

     RDKit          3D

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   -3.0925    0.0367    1.5947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3454    0.4398    2.8135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8669   -0.3004    4.0418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5069    1.1350   -1.0492 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9303    0.9526   -2.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2703    1.2665   -2.9326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6718    2.5834   -2.8059 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0394    2.5442   -0.7157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8229    3.6037   -1.2829 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2713   -3.2665   -2.2152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2169   -3.8692   -2.5782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6676   -3.3106   -0.9242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6358   -2.1280   -2.2605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6719    0.9625    1.0076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3031    0.5091   -0.4723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7319    2.3029    1.3665 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309062211332D          

 32 32  0  0  1  0            999 V2000
    2.3431    2.6478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.5932   -0.4855    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0229481

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC[C@@H](C)[C@H]1OC(=O)[C@H](N=C(O)[C@H](C)N=C(O)\C=C\C(=C)N=C(O)[C@@H]1CCO)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C23H37N3O6/c1-7-8-14(4)20-17(11-12-27)22(30)24-15(5)9-10-18(28)25-16(6)21(29)26-19(13(2)3)23(31)32-20/h9-10,13-14,16-17,19-20,27H,5,7-8,11-12H2,1-4,6H3,(H,24,30)(H,25,28)(H,26,29)/b10-9+/t14-,16+,17-,19-,20-/m1/s1

> <INCHI_KEY>
ODXMNBRNTDMSJW-ZAZPAPLLSA-N

> <FORMULA>
C23H37N3O6

> <MOLECULAR_WEIGHT>
451.564

> <EXACT_MASS>
451.268235923

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
48.195118464975764

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R,6S,9E,14R,15R)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-6-methyl-11-methylidene-15-[(2R)-pentan-2-yl]-3-(propan-2-yl)-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one

> <JCHEM_LOGP>
-1.5218897133389295

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
0.48943234238827227

> <JCHEM_PKA_STRONGEST_ACIDIC>
-2.02920104982305

> <JCHEM_PKA_STRONGEST_BASIC>
11.534160108744459

> <JCHEM_POLAR_SURFACE_AREA>
144.3

> <JCHEM_REFRACTIVITY>
122.3891

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3R,6S,9E,14R,15R)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2R)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       4.374   4.943   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.245   3.408   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.650   2.477   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.182   2.637   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.807   1.230   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       9.313   0.909   0.000  0.00  0.00           O+0
HETATM    7  N   UNK     0       6.662   0.200   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       6.413  -1.467   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.638  -2.399   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.005  -2.092   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.760  -1.187   0.000  0.00  0.00           O+0
HETATM   12  N   UNK     0       4.844  -3.624   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       3.436  -4.249   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.275  -5.781   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.868  -6.407   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.520  -6.687   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.191  -3.344   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.784  -3.969   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       2.353  -1.812   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.107  -0.906   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.300  -1.532   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.545  -0.626   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.462  -3.063   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.869  -3.689   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.031  -5.221   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.269   0.625   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.024   1.531   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.383   0.905   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -2.629   1.811   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       2.676   1.251   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       3.922   0.345   0.000  0.00  0.00           O+0
HETATM   32  N   UNK     0       2.838   2.782   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   32                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   17                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   13   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   26                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   20   27   30                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   26   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30    2                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₇N₃O₆

Average Mass

451.5640 Da

Monoisotopic Mass

451.26824 Da

IUPAC Name

(3R,6S,9E,14R,15R)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-6-methyl-11-methylidene-15-[(2R)-pentan-2-yl]-3-(propan-2-yl)-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one

Traditional Name

(3R,6S,9E,14R,15R)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2R)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one

CAS Registry Number

Not Available

SMILES

CCC[C@@H](C)[C@H]1OC(=O)[C@H](N=C(O)[C@H](C)N=C(O)\C=C\C(=C)N=C(O)[C@@H]1CCO)C(C)C

InChI Identifier

InChI=1S/C23H37N3O6/c1-7-8-14(4)20-17(11-12-27)22(30)24-15(5)9-10-18(28)25-16(6)21(29)26-19(13(2)3)23(31)32-20/h9-10,13-14,16-17,19-20,27H,5,7-8,11-12H2,1-4,6H3,(H,24,30)(H,25,28)(H,26,29)/b10-9+/t14-,16+,17-,19-,20-/m1/s1

InChI Key

ODXMNBRNTDMSJW-ZAZPAPLLSA-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 cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Peptidomimetics

Sub Class

Depsipeptides

Direct Parent

Cyclic depsipeptides

Alternative Parents

Substituents

Cyclic depsipeptide
Macrolide lactam
Alpha-amino acid ester
Macrolactam
Macrolide
Alpha-amino acid or derivatives
Carboxamide group
Carboxylic acid ester
Lactam
Lactone
Secondary carboxylic acid amide
Carboxylic acid derivative
Oxacycle
Azacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organopnictogen compound
Organic oxygen compound
Primary alcohol
Organooxygen compound
Carbonyl group
Organonitrogen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	-1.5	ChemAxon
pKa (Strongest Acidic)	-2	ChemAxon
pKa (Strongest Basic)	11.53	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	144.3 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	122.39 m³·mol⁻¹	ChemAxon
Polarizability	48.2 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

75574816

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

60149579

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Yang Z, Ma M, Yang CH, Gao Y, Zhang Q, Chen Y: Determination of the Absolute Configurations of Microtermolides A and B. J Nat Prod. 2016 Sep 23;79(9):2408-12. doi: 10.1021/acs.jnatprod.5b01143. Epub 2016 Aug 31. [PubMed:27579840 ]
Yang Z, Yang G, Ma M, Li J, Liu J, Wang J, Jiang S, Zhang Q, Chen Y: Total Synthesis and Determination of the Absolute Configuration of Vinylamycin. Org Lett. 2015 Dec 4;17(23):5725-7. doi: 10.1021/acs.orglett.5b02809. Epub 2015 Nov 2. [PubMed:26523486 ]
LOTUS database [Link]

Showing NP-Card for (3r,6s,9e,14r,15r)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2r)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one (NP0229481)

MOL for NP0229481 ((3r,6s,9e,14r,15r)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2r)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one)

3D MOL for NP0229481 ((3r,6s,9e,14r,15r)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2r)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one)

3D SDF for NP0229481 ((3r,6s,9e,14r,15r)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2r)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one)

3D-SDF for NP0229481 ((3r,6s,9e,14r,15r)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2r)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one)

PDB for NP0229481 ((3r,6s,9e,14r,15r)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2r)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one)

3D PDB for NP0229481 ((3r,6s,9e,14r,15r)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2r)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one)

SMILES for NP0229481 ((3r,6s,9e,14r,15r)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2r)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one)

INCHI for NP0229481 ((3r,6s,9e,14r,15r)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2r)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one)

Structure for NP0229481 ((3r,6s,9e,14r,15r)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2r)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one)

3D Structure for NP0229481 ((3r,6s,9e,14r,15r)-5,8,13-trihydroxy-14-(2-hydroxyethyl)-3-isopropyl-6-methyl-11-methylidene-15-[(2r)-pentan-2-yl]-1-oxa-4,7,12-triazacyclopentadeca-4,7,9,12-tetraen-2-one)