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Showing NP-Card for 16α, 17-epoxy gibberellin A9 (NP0339985)

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Record Information
Version2.0
Created at2024-09-12 00:40:35 UTC
Updated at2024-09-12 00:40:35 UTC
NP-MRD IDNP0339985
Secondary Accession NumbersNone
Natural Product Identification
Common Name16α, 17-epoxy gibberellin A9
Description16α, 17-Epoxy gibberellin A9 belongs to the class of organic compounds known as c19-gibberellin 6-carboxylic acids. These are c19-gibberellins with a carboxyl group at the 6-position. Based on a literature review very few articles have been published on 16α, 17-epoxy gibberellin A9.
Structure
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MOLSDFPDBSMILESInChI

MOL for NP0339985 (16α, 17-epoxy gibberellin A9)


  Mrv2104 05252301372D          

 28 33  0  0  1  0            999 V2000
   -1.2313    4.0601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8302    2.7927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8273    0.7221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9729    0.7520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0268    3.4524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5161    2.0487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6484    1.8520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8440    2.7891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3559    2.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2794    1.4558    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6162    1.5447    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4940    2.8945    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2693    2.5621    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6482    3.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2329    2.6630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7932    3.3610    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0934    2.2935    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5511    2.2747    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1830    1.6106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4272    3.9767    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0234    4.2437    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -2.0526    2.7563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1109    2.8807    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9613    1.8840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0271    1.1072    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1402    0.8709    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3090    3.0837    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5528    2.4928    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 16  1  1  1  0  0  0
  2  5  1  0  0  0  0
  2  6  1  0  0  0  0
  3  4  1  0  0  0  0
 10  3  1  0  0  0  0
 11  4  1  0  0  0  0
 16  5  1  0  0  0  0
  6 19  1  0  0  0  0
 10  7  1  0  0  0  0
 17  7  1  6  0  0  0
 17  8  1  0  0  0  0
 18  8  1  0  0  0  0
 18  9  1  0  0  0  0
  9 23  1  0  0  0  0
 10 25  1  1  0  0  0
 10 18  1  0  0  0  0
 11 26  1  6  0  0  0
 17 11  1  0  0  0  0
 11 19  1  0  0  0  0
 12 27  1  1  0  0  0
 12 13  1  0  0  0  0
 12 14  1  6  0  0  0
 12 17  1  0  0  0  0
 13 28  1  6  0  0  0
 13 16  1  0  0  0  0
 13 19  1  0  0  0  0
 14 20  2  0  0  0  0
 14 21  1  0  0  0  0
 16 15  1  0  0  0  0
 15 22  2  0  0  0  0
 15 24  1  0  0  0  0
 18 23  1  6  0  0  0
 19 24  1  0  0  0  0
M  CHG  1  21  -1
M  END
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3D MOL for NP0339985 (16α, 17-epoxy gibberellin A9)

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3D SDF for NP0339985 (16α, 17-epoxy gibberellin A9)

  Mrv2104 05252301372D          

 28 33  0  0  1  0            999 V2000
   -1.2313    4.0601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8302    2.7927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8273    0.7221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9729    0.7520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0268    3.4524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5161    2.0487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6484    1.8520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8440    2.7891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3559    2.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2794    1.4558    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6162    1.5447    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4940    2.8945    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2693    2.5621    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6482    3.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2329    2.6630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7932    3.3610    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0934    2.2935    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5511    2.2747    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1830    1.6106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4272    3.9767    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0234    4.2437    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -2.0526    2.7563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1109    2.8807    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9613    1.8840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0271    1.1072    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1402    0.8709    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3090    3.0837    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5528    2.4928    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 16  1  1  1  0  0  0
  2  5  1  0  0  0  0
  2  6  1  0  0  0  0
  3  4  1  0  0  0  0
 10  3  1  0  0  0  0
 11  4  1  0  0  0  0
 16  5  1  0  0  0  0
  6 19  1  0  0  0  0
 10  7  1  0  0  0  0
 17  7  1  6  0  0  0
 17  8  1  0  0  0  0
 18  8  1  0  0  0  0
 18  9  1  0  0  0  0
  9 23  1  0  0  0  0
 10 25  1  1  0  0  0
 10 18  1  0  0  0  0
 11 26  1  6  0  0  0
 17 11  1  0  0  0  0
 11 19  1  0  0  0  0
 12 27  1  1  0  0  0
 12 13  1  0  0  0  0
 12 14  1  6  0  0  0
 12 17  1  0  0  0  0
 13 28  1  6  0  0  0
 13 16  1  0  0  0  0
 13 19  1  0  0  0  0
 14 20  2  0  0  0  0
 14 21  1  0  0  0  0
 16 15  1  0  0  0  0
 15 22  2  0  0  0  0
 15 24  1  0  0  0  0
 18 23  1  6  0  0  0
 19 24  1  0  0  0  0
M  CHG  1  21  -1
M  END
> <DATABASE_ID>
NP0339985

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12C[C@]3(C[C@@]11CO1)[C@@]([H])(CC2)C12CCC[C@@](C)(C(=O)O1)[C@@]2([H])[C@]3([H])C([O-])=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H24O5/c1-16-5-2-6-19(24-15(16)22)11-4-3-10-7-17(11,8-18(10)9-23-18)12(13(16)19)14(20)21/h10-13H,2-9H2,1H3,(H,20,21)/p-1/t10-,11-,12-,13-,16-,17+,18-,19?/m1/s1

> <INCHI_KEY>
PXYCXLNQKAEBRB-HFDQALKSSA-M

> <FORMULA>
C19H23O5

> <MOLECULAR_WEIGHT>
331.389

> <EXACT_MASS>
331.155097421

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
0.0

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
-1

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,2'R,5'R,8'S,9'S,10'R,11'R)-11'-methyl-16'-oxo-15'-oxaspiro[oxirane-2,6'-pentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane]-9'-carboxylate

> <JCHEM_LOGP>
1.9383630439999993

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.225505659842585

> <JCHEM_PKA_STRONGEST_BASIC>
-4.204175914594416

> <JCHEM_POLAR_SURFACE_AREA>
78.96

> <JCHEM_REFRACTIVITY>
93.33859999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,2'R,5'R,8'S,9'S,10'R,11'R)-11'-methyl-16'-oxo-15'-oxaspiro[oxirane-2,6'-pentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane]-9'-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

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3D-SDF for NP0339985 (16α, 17-epoxy gibberellin A9)
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PDB for NP0339985 (16α, 17-epoxy gibberellin A9)
HEADER    PROTEIN                                 25-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-MAY-23         0                                  
HETATM    1  C   UNK     0      -2.298   7.579   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.550   5.213   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.411   1.348   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.816   1.404   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.050   6.445   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.963   3.824   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.077   3.457   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.442   5.206   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.264   3.907   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.255   2.718   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.150   2.883   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.922   5.403   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.503   4.783   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.210   6.916   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.301   4.971   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.481   6.274   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.041   4.281   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.762   4.246   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.342   3.006   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.664   7.423   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       0.044   7.922   0.000  0.00  0.00           O-1
HETATM   22  O   UNK     0      -3.832   5.145   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       5.807   5.377   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -1.795   3.517   0.000  0.00  0.00           O+0
HETATM   25  H   UNK     0       5.651   2.067   0.000  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.262   1.626   0.000  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.577   5.756   0.000  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.032   4.653   0.000  0.00  0.00           H+0
CONECT    1   16                                                            
CONECT    2    5    6                                                       
CONECT    3    4   10                                                       
CONECT    4    3   11                                                       
CONECT    5    2   16                                                       
CONECT    6    2   19                                                       
CONECT    7   10   17                                                       
CONECT    8   17   18                                                       
CONECT    9   18   23                                                       
CONECT   10    3    7   25   18                                             
CONECT   11    4   26   17   19                                             
CONECT   12   27   13   14   17                                             
CONECT   13   12   28   16   19                                             
CONECT   14   12   20   21                                                  
CONECT   15   16   22   24                                                  
CONECT   16    1    5   13   15                                             
CONECT   17    7    8   11   12                                             
CONECT   18    8    9   10   23                                             
CONECT   19    6   11   13   24                                             
CONECT   20   14                                                            
CONECT   21   14                                                            
CONECT   22   15                                                            
CONECT   23    9   18                                                       
CONECT   24   15   19                                                       
CONECT   25   10                                                            
CONECT   26   11                                                            
CONECT   27   12                                                            
CONECT   28   13                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   66    0
END

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3D PDB for NP0339985 (16α, 17-epoxy gibberellin A9)
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SMILES for NP0339985 (16α, 17-epoxy gibberellin A9)
[H][C@@]12C[C@]3(C[C@@]11CO1)[C@@]([H])(CC2)C12CCC[C@@](C)(C(=O)O1)[C@@]2([H])[C@]3([H])C([O-])=O
Download
INCHI for NP0339985 (16α, 17-epoxy gibberellin A9)
InChI=1S/C19H24O5/c1-16-5-2-6-19(24-15(16)22)11-4-3-10-7-17(11,8-18(10)9-23-18)12(13(16)19)14(20)21/h10-13H,2-9H2,1H3,(H,20,21)/p-1/t10-,11-,12-,13-,16-,17+,18-,19?/m1/s1
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View in JSmol
SynonymsNot Available
Chemical FormulaC19H23O5
Average Mass331.3890 Da
Monoisotopic Mass331.15510 Da
IUPAC Name(2S,2'R,5'R,8'S,9'S,10'R,11'R)-11'-methyl-16'-oxo-15'-oxaspiro[oxirane-2,6'-pentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane]-9'-carboxylate
Traditional Name(2S,2'R,5'R,8'S,9'S,10'R,11'R)-11'-methyl-16'-oxo-15'-oxaspiro[oxirane-2,6'-pentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane]-9'-carboxylate
CAS Registry NumberNot Available
SMILES
[H][C@@]12C[C@]3(C[C@@]11CO1)[C@@]([H])(CC2)C12CCC[C@@](C)(C(=O)O1)[C@@]2([H])[C@]3([H])C([O-])=O
InChI Identifier
InChI=1S/C19H24O5/c1-16-5-2-6-19(24-15(16)22)11-4-3-10-7-17(11,8-18(10)9-23-18)12(13(16)19)14(20)21/h10-13H,2-9H2,1H3,(H,20,21)/p-1/t10-,11-,12-,13-,16-,17+,18-,19?/m1/s1
InChI KeyPXYCXLNQKAEBRB-HFDQALKSSA-M
Experimental Spectra
Not Available
Predicted Spectra
Not Available
Chemical Shift Submissions
Not Available
Species
Species of OriginNot Available
Chemical Taxonomy
Description Belongs to the class of organic compounds known as c19-gibberellin 6-carboxylic acids. These are c19-gibberellins with a carboxyl group at the 6-position.
KingdomOrganic compounds  
Super ClassLipids and lipid-like molecules  
ClassPrenol lipids  
Sub ClassDiterpenoids  
Direct ParentC19-gibberellin 6-carboxylic acids  
Alternative Parents
Substituents
  • 20-norgibberellane-6-carboxylic acid
    • 

  • Diterpene lactone
    • 

  • Caprolactone
    • 

  • Oxepane
    • 

  • Heterocyclic fatty acid
    • 

  • Fatty acid ester
    • 

  • Branched fatty acid
    • 

  • Fatty acyl
    • 

  • Gamma butyrolactone
    • 

  • Dicarboxylic acid or derivatives
    • 

  • Tetrahydrofuran
    • 

  • Lactone
    • 

  • Carboxylic acid ester
    • 

  • Oxacycle
    • 

  • Organoheterocyclic compound
    • 

  • Ether
    • 

  • Oxirane
    • 

  • Dialkyl ether
    • 

  • Carboxylic acid
    • 

  • Carboxylic acid derivative
    • 

  • Organic oxygen compound
    • 

  • Organic oxide
    • 

  • Hydrocarbon derivative
    • 

  • Organooxygen compound
    • 

  • Organic anion
    • 

  • Aliphatic heteropolycyclic compound
Molecular FrameworkAliphatic heteropolycyclic compounds
External DescriptorsNot Available
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP1.94ChemAxon
pKa (Strongest Acidic)4.23ChemAxon
pKa (Strongest Basic)-4.2ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.96 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity93.34 m³·mol⁻¹ChemAxon
Polarizability0 ųChemAxon
Number of Rings6ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem CompoundNot Available
PDB IDNot Available
ChEBI IDNot Available
Good Scents IDNot Available
References
General ReferencesNot Available