NP-MRD: Showing NP-Card for 3-{3-[(6r,7r)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-5h-furan-2-one (NP0296920)

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Record Information

Version

2.0

Created at

2022-09-10 06:48:44 UTC

Updated at

2022-09-10 06:48:45 UTC

NP-MRD ID

NP0296920

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-{3-[(6r,7r)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-5h-furan-2-one

Description

Cis-Geralcin D belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom. Based on a literature review very few articles have been published on Cis-Geralcin D.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 46  0  0  0  0  0  0  0  0999 V2000
   -5.8877    1.0862   -0.9502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0542    0.4224   -2.0532 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9436   -0.4252   -1.4583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0225    0.4285   -0.6184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9016   -0.3879   -0.0105 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1241    0.4819    0.7321 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1658    0.0844    0.8159 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1761    0.9383    0.3317 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8145    2.0388   -0.1583 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6102    0.6211    0.3659 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4504    1.7394   -0.2277 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8958    1.3780   -0.1736 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8169    2.0681    0.4685 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1305    1.3997    0.2932 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8692    0.2729   -0.5020 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5371    0.2312   -0.7999 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8903   -0.6229   -1.4946 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5576   -1.1583    1.3709 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1800   -2.1684    1.7302 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4833   -3.3641    2.2892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5775   -2.1758    1.6118 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4558   -1.5346    0.7421 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6201   -1.1456    1.4175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2864    1.8098   -0.4016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7054    1.6251   -1.5124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3548    0.2963   -0.3571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7723   -0.1887   -2.6306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6326    1.1918   -2.7143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3681   -1.2273   -0.8205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4119   -0.8921   -2.2849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6352    1.2312   -1.2729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5602    0.9208    0.2168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2745   -0.7356   -0.8619 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9108    0.5035    1.4269 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8382   -0.3011   -0.2302 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2629    2.6437    0.3831 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1483    1.9606   -1.2700 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7108    2.9823    1.0505 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6030    1.1628    1.2654 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7872    2.0732   -0.3263 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4531   -3.0542    2.7321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1751   -3.8924    2.9777 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7053   -4.0586    1.4380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7955   -2.3034   -0.0060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0781   -1.9561    1.7569 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 22  5  1  0
 16 12  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  6
 20 41  1  0
 20 42  1  0
 20 43  1  0
 22 44  1  6
 23 45  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 13 38  1  0
 14 39  1  0
 14 40  1  0
M  END


  Mrv1652309102208482D          

 23 24  0  0  1  0            999 V2000
   -4.2703   11.2330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7092   10.6282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9524    9.8399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3912    9.2351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6344    8.4467    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0296    7.8856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0913    7.0629    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3768    6.6504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6623    7.0629    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3768    5.8254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6623    5.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6623    4.5879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9949    4.1030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2498    3.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0748    3.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3298    4.1030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1144    4.3579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7729    6.5982    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5613    6.8413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1224    6.2366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8627    7.6093    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4502    8.3238    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9149    9.0054    0.0000 O   0  0  0  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  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  2  0  0  0  0
  7 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
  5 22  1  0  0  0  0
 22 23  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0296920

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC[C@H]1ON(N=C(C)O[C@H]1O)C(=O)CCC1=CCOC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H22N2O6/c1-3-4-5-12-15(20)22-10(2)16-17(23-12)13(18)7-6-11-8-9-21-14(11)19/h8,12,15,20H,3-7,9H2,1-2H3/t12-,15-/m1/s1

> <INCHI_KEY>
UJHUXJYJBBLUDC-IUODEOHRSA-N

> <FORMULA>
C15H22N2O6

> <MOLECULAR_WEIGHT>
326.349

> <EXACT_MASS>
326.147786436

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
33.184766705511954

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-{3-[(6R,7R)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-2H-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-2,5-dihydrofuran-2-one

> <JCHEM_LOGP>
1.7043660369999998

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.39361456355789

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.256924021911995

> <JCHEM_PKA_STRONGEST_BASIC>
-2.713039832794804

> <JCHEM_POLAR_SURFACE_AREA>
97.66

> <JCHEM_REFRACTIVITY>
79.88550000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-{3-[(6R,7R)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-5H-furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      -7.971  20.968   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.924  19.839   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.378  18.368   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.330  17.239   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.784  15.767   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -5.655  14.720   0.000  0.00  0.00           O+0
HETATM    7  N   UNK     0      -5.770  13.184   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      -4.437  12.414   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.103  13.184   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -4.437  10.874   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.103  10.104   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.103   8.564   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.857   7.659   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.333   6.194   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -3.873   6.194   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -4.349   7.659   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -5.814   8.135   0.000  0.00  0.00           O+0
HETATM   18  N   UNK     0      -7.043  12.317   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0      -8.514  12.771   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -9.562  11.642   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -9.077  14.204   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -8.307  15.538   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -9.175  16.810   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   22                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   18                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   16                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   12   17                                                  
CONECT   17   16                                                            
CONECT   18    7   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21    5   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₂N₂O₆

Average Mass

326.3490 Da

Monoisotopic Mass

326.14779 Da

IUPAC Name

3-{3-[(6R,7R)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-2H-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-2,5-dihydrofuran-2-one

Traditional Name

3-{3-[(6R,7R)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

CCCC[C@H]1ON(N=C(C)O[C@H]1O)C(=O)CCC1=CCOC1=O

InChI Identifier

InChI=1S/C15H22N2O6/c1-3-4-5-12-15(20)22-10(2)16-17(23-12)13(18)7-6-11-8-9-21-14(11)19/h8,12,15,20H,3-7,9H2,1-2H3/t12-,15-/m1/s1

InChI Key

UJHUXJYJBBLUDC-IUODEOHRSA-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 butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dihydrofurans

Sub Class

Furanones

Direct Parent

Butenolides

Alternative Parents

Substituents

2-furanone
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Hemiacetal
Lactone
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Azacycle
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Carbonyl group
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	1.7	ChemAxon
pKa (Strongest Acidic)	11.26	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	97.66 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	79.89 m³·mol⁻¹	ChemAxon
Polarizability	33.18 Å³	ChemAxon
Number of Rings	2	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

29419765

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71716366

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-{3-[(6r,7r)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-5h-furan-2-one (NP0296920)

MOL for NP0296920 (3-{3-[(6r,7r)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-5h-furan-2-one)

3D MOL for NP0296920 (3-{3-[(6r,7r)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-5h-furan-2-one)

3D SDF for NP0296920 (3-{3-[(6r,7r)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-5h-furan-2-one)

3D-SDF for NP0296920 (3-{3-[(6r,7r)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-5h-furan-2-one)

PDB for NP0296920 (3-{3-[(6r,7r)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-5h-furan-2-one)

3D PDB for NP0296920 (3-{3-[(6r,7r)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-5h-furan-2-one)

SMILES for NP0296920 (3-{3-[(6r,7r)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-5h-furan-2-one)

INCHI for NP0296920 (3-{3-[(6r,7r)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-5h-furan-2-one)

Structure for NP0296920 (3-{3-[(6r,7r)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-5h-furan-2-one)

3D Structure for NP0296920 (3-{3-[(6r,7r)-7-butyl-6-hydroxy-4-methyl-6,7-dihydro-1,5,2,3-dioxadiazepin-2-yl]-3-oxopropyl}-5h-furan-2-one)