NP-MRD: Showing NP-Card for 5beta-hydroxyasperilin (NP0044103)

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Record Information

Version

2.0

Created at

2021-11-12 23:50:15 UTC

Updated at

2021-11-26 17:45:28 UTC

NP-MRD ID

NP0044103

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5beta-hydroxyasperilin

Description

5beta-hydroxyasperilin is found in Eriocephalus africanus and Telekia speciosa.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
    4.1426    1.1856    0.3917 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2843    0.2272    0.1123 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4893   -0.8901   -0.7905 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5104   -1.1295   -1.4695 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3450   -1.7023   -0.8043 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6371   -1.3654    0.3766 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1968   -1.7037    0.3455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6878   -0.7646   -0.3689 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5886   -1.0689   -1.8681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1176   -1.0711    0.0223 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5671   -2.1661   -0.7392 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0540    0.0780   -0.2802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7631    1.2523    0.6463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3006    1.2119    0.9267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8638    1.6379    2.1050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4097    0.6909   -0.1448 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8666    1.3404   -1.3242 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0183    1.0501   -0.0031 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9150    0.0894    0.6686 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1308    1.2474   -0.0369 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8968    1.9917    1.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1168   -1.9586    1.1949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1860   -1.8821    1.3846 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0981   -2.7131   -0.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9051   -2.0940   -2.0925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2574   -0.3347   -2.3687 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4426   -0.8583   -2.2133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2186   -1.3486    1.0859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9842   -1.8246   -1.5502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0776   -0.2808   -0.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0165    0.3680   -1.3379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3571    1.1036    1.5935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0983    2.2130    0.2286 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1891    1.6305    2.3595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5279    2.0142    2.8736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1237    2.2689   -1.1335 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4642    1.3142   -1.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0712    2.0239    0.5678 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0230    0.2177    1.7667 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 17  1  6
 16  8  1  0
  8  9  1  6
  8  7  1  0
  7  6  1  0
  6 19  1  0
 19 18  1  0
 19  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  2  0
  3  5  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  3
 18 16  1  0
 14 16  1  0
  5  6  1  0
 17 36  1  0
  9 25  1  0
  9 26  1  0
  9 27  1  0
  7 23  1  0
  7 24  1  0
  6 22  1  1
 19 39  1  1
 18 37  1  0
 18 38  1  0
  1 20  1  0
  1 21  1  0
 10 28  1  1
 11 29  1  0
 12 30  1  0
 12 31  1  0
 13 32  1  0
 13 33  1  0
 15 34  1  0
 15 35  1  0
M  END


  Mrv1652311132100502D          

 21 23  0  0  1  0            999 V2000
    1.3556   -3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -2.3479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3556   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0734   -1.5229    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0734   -2.3479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6411   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8580   -2.6029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1129   -3.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3429   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1679   -1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8580   -1.2680    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -1.9354    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1596   -0.7025    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  2  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  6 13  1  0  0  0  0
  7 14  1  1  0  0  0
  6 15  1  1  0  0  0
  3 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  2 20  1  0  0  0  0
 20 21  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0044103

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12C[C@@]3(C)[C@H](O)CCC(=C)[C@@]3(O)C[C@]1([H])C(=C)C(=O)O2

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O4/c1-8-4-5-12(16)14(3)7-11-10(6-15(8,14)18)9(2)13(17)19-11/h10-12,16,18H,1-2,4-7H2,3H3/t10-,11-,12-,14+,15+/m1/s1

> <INCHI_KEY>
GPTBAALURMUXBS-FPVZYODXSA-N

> <FORMULA>
C15H20O4

> <MOLECULAR_WEIGHT>
264.321

> <EXACT_MASS>
264.136159124

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
27.470348840768402

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aR,4aS,8R,8aS,9aR)-4a,8-dihydroxy-8a-methyl-3,5-dimethylidene-dodecahydronaphtho[2,3-b]furan-2-one

> <ALOGPS_LOGP>
0.95

> <JCHEM_LOGP>
1.1237719499999999

> <ALOGPS_LOGS>
-1.74

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.751516048755768

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.695522349913215

> <JCHEM_PKA_STRONGEST_BASIC>
-2.97446490685207

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
69.087

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.82e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3aR,4aS,8R,8aS,9aR)-4a,8-dihydroxy-8a-methyl-3,5-dimethylidene-hexahydro-3aH-naphtho[2,3-b]furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 13-NOV-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   13-NOV-21         0                                  
HETATM    1  O   UNK     0       2.530  -5.923   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       2.530  -4.383   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.530  -2.843   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.530  -1.303   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.197  -2.073   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.137  -2.843   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.137  -4.383   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.197  -5.153   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.602  -4.859   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.077  -6.323   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.507  -3.613   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -4.047  -3.613   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      -1.602  -2.367   0.000  0.00  0.00           O+0
HETATM   14  H   UNK     0       1.197  -3.613   0.000  0.00  0.00           H+0
HETATM   15  H   UNK     0      -0.298  -1.311   0.000  0.00  0.00           H+0
HETATM   16  C   UNK     0       3.864  -2.073   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.864  -0.533   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.198  -2.843   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.198  -4.383   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.864  -5.153   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.864  -6.693   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    8   20                                             
CONECT    3    2    4    5   16                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   13   15                                             
CONECT    7    6    8    9   14                                             
CONECT    8    7    2                                                       
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    6                                                       
CONECT   14    7                                                            
CONECT   15    6                                                            
CONECT   16    3   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19    2   21                                                  
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₀O₄

Average Mass

264.3210 Da

Monoisotopic Mass

264.13616 Da

IUPAC Name

(3aR,4aS,8R,8aS,9aR)-4a,8-dihydroxy-8a-methyl-3,5-dimethylidene-dodecahydronaphtho[2,3-b]furan-2-one

Traditional Name

(3aR,4aS,8R,8aS,9aR)-4a,8-dihydroxy-8a-methyl-3,5-dimethylidene-hexahydro-3aH-naphtho[2,3-b]furan-2-one

CAS Registry Number

Not Available

SMILES

[H][C@@]12C[C@@]3(C)[C@H](O)CCC(=C)[C@@]3(O)C[C@]1([H])C(=C)C(=O)O2

InChI Identifier

InChI=1S/C15H20O4/c1-8-4-5-12(16)14(3)7-11-10(6-15(8,14)18)9(2)13(17)19-11/h10-12,16,18H,1-2,4-7H2,3H3/t10-,11-,12-,14+,15+/m1/s1

InChI Key

GPTBAALURMUXBS-FPVZYODXSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Eriocephalus africanus	Plant	KNApSAcK
Telekia speciosa	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	0.95	ALOGPS
logP	1.12	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	13.7	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	69.09 m³·mol⁻¹	ChemAxon
Polarizability	27.47 Å³	ChemAxon
Number of Rings	3	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

Not Available

References

General References

Showing NP-Card for 5beta-hydroxyasperilin (NP0044103)

MOL for NP0044103 (5beta-hydroxyasperilin)

3D MOL for NP0044103 (5beta-hydroxyasperilin)

3D SDF for NP0044103 (5beta-hydroxyasperilin)

3D-SDF for NP0044103 (5beta-hydroxyasperilin)

PDB for NP0044103 (5beta-hydroxyasperilin)

3D PDB for NP0044103 (5beta-hydroxyasperilin)

SMILES for NP0044103 (5beta-hydroxyasperilin)

INCHI for NP0044103 (5beta-hydroxyasperilin)

Structure for NP0044103 (5beta-hydroxyasperilin)

3D Structure for NP0044103 (5beta-hydroxyasperilin)