NP-MRD: Showing NP-Card for 7-Hydroxycadalene (NP0076090)

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Record Information

Version

2.0

Created at

2022-04-28 21:15:54 UTC

Updated at

2022-04-28 21:15:54 UTC

NP-MRD ID

NP0076090

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-Hydroxycadalene

Description

7-Hydroxycadalene belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. 7-Hydroxycadalene is found in Alangium chinense, Bombax ceiba, Caesalpinia pulcherrima , Ceiba pentandra , Cornus capitata, Heterotheca grandiflora, Heterotheca subaxillaris, Platycarya strobilacea, Thespesia populnea, Thespesia populnea L.Soland.Ex Coor and Ulmus glabra. 7-Hydroxycadalene is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 34 35  0  0  0  0  0  0  0  0999 V2000
   -2.5911   -2.6611    1.1069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0871   -1.3261    0.6378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7044   -1.2779    0.3825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1499   -0.0845   -0.0693 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2301   -0.0422   -0.3588 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1332   -1.1488   -0.0249 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2998   -1.2328   -1.0081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8392   -0.6470    1.3266 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7083    1.1562   -0.8354 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9396    2.2998   -1.0420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3953    2.2075   -0.7438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2491    3.4262   -0.9405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9332    1.0317   -0.2648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3039    0.9413    0.0008 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8904   -0.2430    0.4547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2382   -0.3034    0.7057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1344   -3.4238    0.4222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1499   -2.8396    2.1034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6752   -2.6950    1.0811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1238   -2.1644    0.5460 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7214   -2.0920    0.2693 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5859   -0.2562   -1.3483 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9026   -1.8244   -1.8823 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1745   -1.7785   -0.5727 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3886   -1.4714    1.7586 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4852    0.2091    1.0132 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9907   -0.2445    1.8986 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7626    1.2988   -1.0682 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3660    3.2185   -1.4153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9589    3.5569   -0.1296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5647    4.3328   -0.9348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6752    3.3642   -1.9405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9485    1.7994   -0.1465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7546   -1.0858    1.0182 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0
  6  8  1  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 15  1  0
 15 16  1  0
 15 14  2  0
 14 13  1  0
 13 11  2  0
 11 12  1  0
 11 10  1  0
 10  9  2  0
  9  5  1  0
 13  4  1  0
  7 22  1  0
  7 23  1  0
  7 24  1  0
  6 21  1  0
  8 25  1  0
  8 26  1  0
  8 27  1  0
  3 20  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
 16 34  1  0
 14 33  1  0
 12 30  1  0
 12 31  1  0
 12 32  1  0
 10 29  1  0
  9 28  1  0
M  END


  Mrv1533004171523022D          

 16 17  0  0  0  0            999 V2000
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
  4 16  2  0  0  0  0
  9 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0076090

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=C2C=C(C)C(O)=CC2=C(C)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H18O/c1-9(2)12-6-5-10(3)13-8-15(16)11(4)7-14(12)13/h5-9,16H,1-4H3

> <INCHI_KEY>
RIWNMJBJRPCUBX-UHFFFAOYSA-N

> <FORMULA>
C15H18O

> <MOLECULAR_WEIGHT>
214.308

> <EXACT_MASS>
214.1357652

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
25.80831711588008

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,8-dimethyl-5-(propan-2-yl)naphthalen-2-ol

> <ALOGPS_LOGP>
4.78

> <JCHEM_LOGP>
4.931009180333334

> <ALOGPS_LOGS>
-4.22

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.134512836947984

> <JCHEM_PKA_STRONGEST_BASIC>
-5.484110545608545

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
68.7623

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.30e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-hydroxycadalene

> <JCHEM_VEBER_RULE>
1

$$$$

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       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   16                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   16                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15    4    9                                                  
MASTER        0    0    0    0    0    0    0    0   16    0   34    0
END

View in JSmol

Synonyms

Value	Source
7-Hydroxycadalene	ChEMBL

Chemical Formula

C₁₅H₁₈O

Average Mass

214.3080 Da

Monoisotopic Mass

214.13577 Da

IUPAC Name

3,8-dimethyl-5-(propan-2-yl)naphthalen-2-ol

Traditional Name

7-hydroxycadalene

CAS Registry Number

Not Available

SMILES

CC(C)C1=C2C=C(C)C(O)=CC2=C(C)C=C1

InChI Identifier

InChI=1S/C15H18O/c1-9(2)12-6-5-10(3)13-8-15(16)11(4)7-14(12)13/h5-9,16H,1-4H3

InChI Key

RIWNMJBJRPCUBX-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, 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
Alangium chinense	LOTUS Database	35616633
Bombax ceiba	LOTUS Database	35616633
Caesalpinia pulcherrima	Plant	KNApSAcK
Ceiba pentandra	Plant	KNApSAcK
Cornus capitata	LOTUS Database	35616633
Heterotheca grandiflora	LOTUS Database	35616633
Heterotheca subaxillaris	LOTUS Database	35616633
Platycarya strobilacea	LOTUS Database	35616633
Thespesia populnea	LOTUS Database	35616633
Thespesia populnea L.Soland.Ex Coor	Plant	KNApSAcK
Ulmus campestris	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Cadinane sesquiterpenoid
2-naphthol
Naphthalene
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	4.78	ALOGPS
logP	4.93	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	10.13	ChemAxon
pKa (Strongest Basic)	-5.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	68.76 m³·mol⁻¹	ChemAxon
Polarizability	25.81 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

608115

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 7-Hydroxycadalene (NP0076090)

MOL for NP0076090 (7-Hydroxycadalene)

3D MOL for NP0076090 (7-Hydroxycadalene)

3D SDF for NP0076090 (7-Hydroxycadalene)

3D-SDF for NP0076090 (7-Hydroxycadalene)

PDB for NP0076090 (7-Hydroxycadalene)

3D PDB for NP0076090 (7-Hydroxycadalene)

SMILES for NP0076090 (7-Hydroxycadalene)

INCHI for NP0076090 (7-Hydroxycadalene)

Structure for NP0076090 (7-Hydroxycadalene)

3D Structure for NP0076090 (7-Hydroxycadalene)