NP-MRD: Showing NP-Card for 10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one (NP0230102)

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Record Information

Version

2.0

Created at

2022-09-06 10:26:48 UTC

Updated at

2022-09-06 10:26:48 UTC

NP-MRD ID

NP0230102

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one

Description

10-Hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]Octadec-12-en-5-one belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17. 10-Hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]Octadec-12-en-5-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171519062D          

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M  END

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M  END


  Mrv1533004171519062D          

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    4.9059   -4.8711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8833   -4.9835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5462   -4.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0063   -4.6354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1961   -4.4798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6563   -5.1037    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9258   -3.7004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3859   -4.3243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3600   -0.0661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  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
  7  9  1  0  0  0  0
  4  9  1  0  0  0  0
  6 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
 10 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  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
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
 19 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 13 33  1  0  0  0  0
 18 33  1  0  0  0  0
 33 34  1  0  0  0  0
  2 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0230102

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CC1CC(C(O)O1)C1CC=C2C1(C)CCC1C3(C)CCC(=O)OC(C)(C)C3CC(O)C21C

> <INCHI_IDENTIFIER>
InChI=1S/C30H46O5/c1-17(2)14-18-15-19(26(33)34-18)20-8-9-21-28(20,5)12-10-22-29(6)13-11-25(32)35-27(3,4)23(29)16-24(31)30(21,22)7/h9,14,18-20,22-24,26,31,33H,8,10-13,15-16H2,1-7H3

> <INCHI_KEY>
UCTXLRQSPUCMBO-UHFFFAOYSA-N

> <FORMULA>
C30H46O5

> <MOLECULAR_WEIGHT>
486.693

> <EXACT_MASS>
486.334524581

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
56.90656365627414

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one

> <ALOGPS_LOGP>
4.95

> <JCHEM_LOGP>
4.403239141999999

> <ALOGPS_LOGS>
-5.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.625618735268397

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.155931202315825

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9632018087117906

> <JCHEM_POLAR_SURFACE_AREA>
75.99000000000001

> <JCHEM_REFRACTIVITY>
137.61390000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.04e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -3.117   2.213   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.087   0.673   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.738  -0.071   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.708  -1.610   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.445  -2.491   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.892  -3.965   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.431  -3.995   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -3.312  -5.258   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      -2.936  -2.540   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.038  -5.192   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.409  -6.666   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.855  -7.547   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.082  -6.617   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.578  -5.162   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.924  -3.768   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.585  -3.998   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.098  -4.288   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.602  -5.743   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.115  -6.033   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.503  -4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.938  -4.732   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.468  -4.563   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.554  -5.655   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      11.009  -5.151   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       9.378  -7.185   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.072  -8.001   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.158  -9.093   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.249  -9.303   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.620  -7.488   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.612  -8.653   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.099  -8.362   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       3.092  -9.527   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       3.595  -6.907   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.587  -8.072   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -4.405  -0.123   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   35                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   10                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7    4                                                       
CONECT   10    6   11   14                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   33                                                  
CONECT   14   13   10   15   16                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   33                                                  
CONECT   19   18   20   21   29                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   26   19   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   13   18   34                                             
CONECT   34   33                                                            
CONECT   35    2                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₆O₅

Average Mass

486.6930 Da

Monoisotopic Mass

486.33452 Da

IUPAC Name

10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one

Traditional Name

10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one

CAS Registry Number

Not Available

SMILES

CC(C)=CC1CC(C(O)O1)C1CC=C2C1(C)CCC1C3(C)CCC(=O)OC(C)(C)C3CC(O)C21C

InChI Identifier

InChI=1S/C30H46O5/c1-17(2)14-18-15-19(26(33)34-18)20-8-9-21-28(20,5)12-10-22-29(6)13-11-25(32)35-27(3,4)23(29)16-24(31)30(21,22)7/h9,14,18-20,22-24,26,31,33H,8,10-13,15-16H2,1-7H3

InChI Key

UCTXLRQSPUCMBO-UHFFFAOYSA-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 limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Limonoids

Alternative Parents

Substituents

Limonoid skeleton
Caprolactone
Oxepane
Cyclic alcohol
Tetrahydrofuran
Carboxylic acid ester
Hemiacetal
Lactone
Secondary alcohol
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
Organooxygen compound
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	4.95	ALOGPS
logP	4.4	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	12.16	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	137.61 m³·mol⁻¹	ChemAxon
Polarizability	56.91 Å³	ChemAxon
Number of Rings	5	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one (NP0230102)

MOL for NP0230102 (10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one)

3D MOL for NP0230102 (10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one)

3D SDF for NP0230102 (10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one)

3D-SDF for NP0230102 (10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one)

PDB for NP0230102 (10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one)

3D PDB for NP0230102 (10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one)

SMILES for NP0230102 (10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one)

INCHI for NP0230102 (10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one)

Structure for NP0230102 (10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one)

3D Structure for NP0230102 (10-hydroxy-15-[2-hydroxy-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-5-one)