NP-MRD: Showing NP-Card for 9-Hydroxyxeniolide F (NP0080424)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-29 01:26:54 UTC

Updated at

2022-04-29 01:26:54 UTC

NP-MRD ID

NP0080424

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9-Hydroxyxeniolide F

Description

9-Hydroxyxeniolide-F belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety. 9-Hydroxyxeniolide F is found in Xenia sp. 9-Hydroxyxeniolide F was first documented in 2007 (PMID: 17987497). Based on a literature review very few articles have been published on 9-hydroxyxeniolide-F (PMID: 33669051).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 54  0  0  0  0  0  0  0  0999 V2000
   -3.2523   -2.3100   -0.2250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6318   -1.3526   -0.8904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4261   -0.4574   -1.7566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0152    0.7165   -1.0833 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1711    1.0930   -1.8112 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4324    0.5250    0.3266 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2979    1.6117    0.6227 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3406    0.5942    1.3207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3919   -0.1774    2.3805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2413    1.5323    1.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0509    1.0582    0.3562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7158   -0.3748    0.4201 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7546   -0.5691    0.4693 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6521    0.3308    0.1965 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0654   -0.0089    0.2878 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9537    0.9685    0.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3907    0.6589    0.0868 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8651   -0.1741   -1.0851 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2205    1.9151    0.2477 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5696   -0.1015    1.2659 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1515   -1.9352    0.8492 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1777   -2.1667    1.4741 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2090   -2.9101    0.4030 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4797   -2.5403   -0.7782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1620   -1.2176   -0.7608 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6890   -2.9961    0.4316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3195   -2.4954   -0.2697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7760   -0.0722   -2.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2386   -1.0203   -2.3062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3658    1.6385   -1.1278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9301    1.3381   -2.7404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0876   -0.3631    0.4517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8328    2.3126    1.1059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6101   -0.1244    3.1207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1912   -0.8816    2.5618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5985    2.4642    0.5715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8699    1.9646    2.0990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1831    1.6128    0.8389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0187    1.4224   -0.6956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2041   -0.8287    1.3418 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4002    1.3437   -0.1191 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5159   -0.9291    0.5349 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6248    1.9493   -0.2726 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3921    0.1186   -2.0399 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9556   -0.0245   -1.1833 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7040   -1.2492   -0.8681 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5650    2.7793    0.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6627    2.1568   -0.7491 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9974    1.7685    1.0273 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5103    0.0002    1.5710 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2108   -2.6309   -1.6536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2523   -3.3257   -0.9560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7722   -0.6369   -1.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 17  1  0
 17 19  1  0
 17 20  1  1
 17 16  1  0
 16 15  2  0
 15 14  1  0
 14 13  2  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  8  1  0
  8  9  2  3
  8  6  1  0
  6  7  1  0
  6  4  1  0
  4  5  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 25  1  0
 25 24  1  0
 24 23  1  0
 23 21  1  0
 21 22  2  0
 21 13  1  0
 25 12  1  0
 18 44  1  0
 18 45  1  0
 18 46  1  0
 19 47  1  0
 19 48  1  0
 19 49  1  0
 20 50  1  0
 16 43  1  0
 15 42  1  0
 14 41  1  0
 12 40  1  1
 11 38  1  0
 11 39  1  0
 10 36  1  0
 10 37  1  0
  9 34  1  0
  9 35  1  0
  6 32  1  6
  7 33  1  0
  4 30  1  1
  5 31  1  0
  3 28  1  0
  3 29  1  0
  1 26  1  0
  1 27  1  0
 25 53  1  6
 24 51  1  0
 24 52  1  0
M  END


  Mrv1652304292203262D          

 25 26  0  0  1  0            999 V2000
    1.7751    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9626    0.5558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4323    1.1877    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4323    2.0127    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9626    2.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5501    3.3592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7751    2.7880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4895    2.3755    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7717    1.6002    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4895    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1215    0.2947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5967    1.6002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1215    2.9058    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822    2.4252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9966    2.0127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9966    1.1877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7111    0.7752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822    0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822   -0.0498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9966   -0.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7111   -0.0498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4256   -0.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1401   -0.8748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8381    0.2522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0131   -1.1767    0.0000 C   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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  1 10  1  0  0  0  0
 10 11  2  0  0  0  0
  9 12  1  6  0  0  0
  8 13  1  1  0  0  0
  4 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
  3 18  1  6  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0080424

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(O)\C=C\C=C1\[C@H]2CCC(=C)[C@@H](O)[C@H](O)CC(=C)[C@@H]2COC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O5/c1-12-7-8-14-15(6-5-9-20(3,4)24)19(23)25-11-16(14)13(2)10-17(21)18(12)22/h5-6,9,14,16-18,21-22,24H,1-2,7-8,10-11H2,3-4H3/b9-5+,15-6-/t14-,16+,17-,18-/m1/s1

> <INCHI_KEY>
DFVRPHGROBFFBS-KORXDNNLSA-N

> <FORMULA>
C20H28O5

> <MOLECULAR_WEIGHT>
348.439

> <EXACT_MASS>
348.193674002

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
37.81585313518835

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4Z,4aS,8R,9R,11aR)-8,9-dihydroxy-4-[(2E)-4-hydroxy-4-methylpent-2-en-1-ylidene]-7,11-dimethylidene-dodecahydrocyclonona[c]pyran-3-one

> <ALOGPS_LOGP>
1.88

> <JCHEM_LOGP>
1.5931333993333316

> <ALOGPS_LOGS>
-2.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.044236681673734

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.49733582514812

> <JCHEM_PKA_STRONGEST_BASIC>
-1.5252954722369338

> <JCHEM_POLAR_SURFACE_AREA>
86.99

> <JCHEM_REFRACTIVITY>
97.863

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.38e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4Z,4aS,8R,9R,11aR)-8,9-dihydroxy-4-[(2E)-4-hydroxy-4-methylpent-2-en-1-ylidene]-7,11-dimethylidene-octahydrocyclonona[c]pyran-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       3.313   0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.797   1.037   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.807   2.217   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.807   3.757   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.797   4.937   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.027   6.271   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.313   5.204   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.647   4.434   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.174   2.987   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.647   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.827   0.550   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.714   2.987   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       5.827   5.424   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.527   4.527   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.860   3.757   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.860   2.217   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -3.194   1.447   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -0.527   1.447   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.527  -0.093   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.860  -0.863   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.194  -0.093   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.528  -0.863   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.861  -1.633   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -5.298   0.471   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -3.758  -2.197   0.000  0.00  0.00           C+0
CONECT    1    2   10                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   18                                                  
CONECT    4    3    5   14                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10   12                                                  
CONECT   10    9    1   11                                                  
CONECT   11   10                                                            
CONECT   12    9                                                            
CONECT   13    8                                                            
CONECT   14    4   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16    3   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

View in JSmol

Synonyms

Value	Source
9-Hydroxyxeniolide F	MeSH

Chemical Formula

C₂₀H₂₈O₅

Average Mass

348.4390 Da

Monoisotopic Mass

348.19367 Da

IUPAC Name

(4Z,4aS,8R,9R,11aR)-8,9-dihydroxy-4-[(2E)-4-hydroxy-4-methylpent-2-en-1-ylidene]-7,11-dimethylidene-dodecahydrocyclonona[c]pyran-3-one

Traditional Name

(4Z,4aS,8R,9R,11aR)-8,9-dihydroxy-4-[(2E)-4-hydroxy-4-methylpent-2-en-1-ylidene]-7,11-dimethylidene-octahydrocyclonona[c]pyran-3-one

CAS Registry Number

Not Available

SMILES

CC(C)(O)\C=C\C=C1\[C@H]2CCC(=C)[C@@H](O)[C@H](O)CC(=C)[C@@H]2COC1=O

InChI Identifier

InChI=1S/C20H28O5/c1-12-7-8-14-15(6-5-9-20(3,4)24)19(23)25-11-16(14)13(2)10-17(21)18(12)22/h5-6,9,14,16-18,21-22,24H,1-2,7-8,10-11H2,3-4H3/b9-5+,15-6-/t14-,16+,17-,18-/m1/s1

InChI Key

DFVRPHGROBFFBS-KORXDNNLSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Xenia sp.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Delta valerolactones

Direct Parent

Delta valerolactones

Alternative Parents

Substituents

Delta valerolactone
Delta_valerolactone
Oxane
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Carboxylic acid ester
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	1.88	ALOGPS
logP	1.59	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	13.5	ChemAxon
pKa (Strongest Basic)	-1.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	97.86 m³·mol⁻¹	ChemAxon
Polarizability	37.82 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

9285981

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11110845

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Shen YC, Chen YH, Cheng YB, Kuo YH, Khalil AT: Two new xeniolides from a Taiwanese Xenia soft coral. Nat Prod Res. 2007 Nov;21(13):1171-7. doi: 10.1080/14786410600906020. [PubMed:17987497 ]
Lin YC, Chen YJ, Chen SR, Lien WJ, Chang HW, Yang YL, Liaw CC, Su JH, Chen CY, Cheng YB: Targeted Isolation of Xenicane Diterpenoids from Taiwanese Soft Coral Asterospicularia laurae. Mar Drugs. 2021 Feb 25;19(3). pii: md19030123. doi: 10.3390/md19030123. [PubMed:33669051 ]

Showing NP-Card for 9-Hydroxyxeniolide F (NP0080424)

MOL for NP0080424 (9-Hydroxyxeniolide F)

3D MOL for NP0080424 (9-Hydroxyxeniolide F)

3D SDF for NP0080424 (9-Hydroxyxeniolide F)

3D-SDF for NP0080424 (9-Hydroxyxeniolide F)

PDB for NP0080424 (9-Hydroxyxeniolide F)

3D PDB for NP0080424 (9-Hydroxyxeniolide F)

SMILES for NP0080424 (9-Hydroxyxeniolide F)

INCHI for NP0080424 (9-Hydroxyxeniolide F)

Structure for NP0080424 (9-Hydroxyxeniolide F)

3D Structure for NP0080424 (9-Hydroxyxeniolide F)