NP-MRD: Showing NP-Card for Epiguadalupol (NP0064456)

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Record Information

Version

2.0

Created at

2022-04-28 08:41:26 UTC

Updated at

2022-04-28 08:41:26 UTC

NP-MRD ID

NP0064456

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Epiguadalupol

Description

(1R,3S,9aS)-1,4,7,9a-tetramethyl-2,3,5,6,9,9a-hexahydro-1H-benzo[7]annulen-3-ol belongs to the class of organic compounds known as secondary alcohols. Secondary alcohols are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl). Epiguadalupol is found in Laurencia snyderae. Based on a literature review very few articles have been published on (1R,3S,9aS)-1,4,7,9a-tetramethyl-2,3,5,6,9,9a-hexahydro-1H-benzo[7]annulen-3-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 41  0  0  0  0  0  0  0  0999 V2000
    4.1905   -0.1320    0.8114 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7244   -0.0378    0.5656 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0036   -0.8089    1.3626 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5572   -1.0232    1.4653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1844   -0.7926    0.1518 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4858   -1.6249   -0.8945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1619    0.6511   -0.0954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2580    1.3906   -0.2398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1843    2.8645   -0.4909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6383    0.7972   -0.1610 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1167    0.4411   -1.3990 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5730   -0.3540    0.8089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5693   -1.3637    0.3261 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1009   -2.0003   -0.9380 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0065    1.5472   -0.2292 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3029    0.8826   -0.5080 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6822    0.8644    0.8355 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6117   -0.7221   -0.0309 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3963   -0.6034    1.7982 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5808   -1.4019    2.0834 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3690   -2.0824    1.7817 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1588   -0.3491    2.2404 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2337   -1.3075   -1.9326 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5715   -1.6887   -0.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1345   -2.6873   -0.7290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1318    3.3579   -0.2349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3992    3.3564    0.1211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0193    3.0391   -1.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3327    1.5486    0.2696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3814    1.2745   -1.8702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5634   -0.8535    0.8035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3756    0.0154    1.8140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5225   -2.1695    1.0864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7952   -1.4978   -1.8537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8429   -3.0755   -1.0231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2192   -1.9803   -0.8517 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7909    2.2356   -1.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1120    2.1250    0.7137 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3824    0.4529   -1.5282 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0754    1.7121   -0.5094 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 12  1  0
 12 10  1  0
 10 11  1  0
 10  8  1  0
  8  9  1  0
  8  7  2  0
  7 15  1  0
 15 16  1  0
 16  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  6
  5 13  1  0
  5  7  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 13 33  1  1
 12 31  1  0
 12 32  1  0
 10 29  1  1
 11 30  1  0
  9 26  1  0
  9 27  1  0
  9 28  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  0
 16 40  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  6 23  1  0
  6 24  1  0
  6 25  1  0
M  END


  Mrv1652304282210412D          

 16 17  0  0  1  0            999 V2000
   -0.8374   -0.4033    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8374   -1.2283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1230   -1.6408    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5915   -1.2283    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5915   -0.4033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1230    0.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1230    0.8342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2365    0.1111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0408   -0.0725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3988   -0.8158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0408   -1.5591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2365   -1.7427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2238   -0.8158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5299   -2.0510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1230   -2.4658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5519    0.0092    0.0000 O   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
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  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
  4 12  1  0  0  0  0
 10 13  1  0  0  0  0
  4 14  1  6  0  0  0
  3 15  1  6  0  0  0
  1 16  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0064456

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@H](O)C(C)=C2CCC(C)=CC[C@@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O/c1-10-5-6-13-12(3)14(16)9-11(2)15(13,4)8-7-10/h7,11,14,16H,5-6,8-9H2,1-4H3/t11-,14+,15+/m1/s1

> <INCHI_KEY>
PYNBPBFJIFSMEA-UGFHNGPFSA-N

> <FORMULA>
C15H24O

> <MOLECULAR_WEIGHT>
220.356

> <EXACT_MASS>
220.182715393

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
26.497452788556302

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,3S,9aS)-1,4,7,9a-tetramethyl-2,3,5,6,9,9a-hexahydro-1H-benzo[7]annulen-3-ol

> <ALOGPS_LOGP>
4.57

> <JCHEM_LOGP>
3.1869068296666665

> <ALOGPS_LOGS>
-3.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.418433754548946

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3035770757602911

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
69.7738

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.96e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,4R,4aS)-1,4,4a,7-tetramethyl-2,3,4,5,8,9-hexahydrobenzo[7]annulen-2-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -1.563  -0.753   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.563  -2.293   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.230  -3.063   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.104  -2.293   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.104  -0.753   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.230   0.017   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.230   1.557   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.308   0.207   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.810  -0.135   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.478  -1.523   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.810  -2.910   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.308  -3.253   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.018  -1.523   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.989  -3.828   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.230  -4.603   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.897   0.017   0.000  0.00  0.00           O+0
CONECT    1    2    6   16                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   15                                                  
CONECT    4    3    5   12   14                                             
CONECT    5    4    6    8                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    5    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11    4                                                       
CONECT   13   10                                                            
CONECT   14    4                                                            
CONECT   15    3                                                            
CONECT   16    1                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₄O

Average Mass

220.3560 Da

Monoisotopic Mass

220.18272 Da

IUPAC Name

(1R,3S,9aS)-1,4,7,9a-tetramethyl-2,3,5,6,9,9a-hexahydro-1H-benzo[7]annulen-3-ol

Traditional Name

(2S,4R,4aS)-1,4,4a,7-tetramethyl-2,3,4,5,8,9-hexahydrobenzo[7]annulen-2-ol

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@H](O)C(C)=C2CCC(C)=CC[C@@]12C

InChI Identifier

InChI=1S/C15H24O/c1-10-5-6-13-12(3)14(16)9-11(2)15(13,4)8-7-10/h7,11,14,16H,5-6,8-9H2,1-4H3/t11-,14+,15+/m1/s1

InChI Key

PYNBPBFJIFSMEA-UGFHNGPFSA-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
Laurencia snyderae	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as secondary alcohols. Secondary alcohols are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl).

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Secondary alcohols

Alternative Parents

Hydrocarbon derivatives

Substituents

Secondary alcohol
Hydrocarbon derivative
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic 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	4.57	ALOGPS
logP	3.19	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	18.42	ChemAxon
pKa (Strongest Basic)	-1.3	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	0	ChemAxon
Refractivity	69.77 m³·mol⁻¹	ChemAxon
Polarizability	26.5 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

162948436

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Epiguadalupol (NP0064456)

MOL for NP0064456 (Epiguadalupol)

3D MOL for NP0064456 (Epiguadalupol)

3D SDF for NP0064456 (Epiguadalupol)

3D-SDF for NP0064456 (Epiguadalupol)

PDB for NP0064456 (Epiguadalupol)

3D PDB for NP0064456 (Epiguadalupol)

SMILES for NP0064456 (Epiguadalupol)

INCHI for NP0064456 (Epiguadalupol)

Structure for NP0064456 (Epiguadalupol)

3D Structure for NP0064456 (Epiguadalupol)