NP-MRD: Showing NP-Card for 7-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,7h,8h,11h,11ah-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde (NP0302228)

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Record Information

Version

2.0

Created at

2022-09-10 15:38:21 UTC

Updated at

2022-09-10 15:38:21 UTC

NP-MRD ID

NP0302228

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,7h,8h,11h,11ah-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde

Description

Galanal A 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). Galanal A is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Galanal A has been detected, but not quantified in, herbs and spices. 7-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,7h,8h,11h,11ah-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde is found in Aframomum alboviolaceum, Alpinia galanga and Zingiber mioga. This could make galanal a a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
   -3.3630   -1.7155   -0.3784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8057   -0.3002   -0.1138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2752    0.5522   -1.2346 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3738    0.1009    1.2213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3212    0.6576    2.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3172    1.4904    1.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5263    0.6977    0.3773 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1705    1.5899   -0.7703 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7650    0.1302    0.9901 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7747    1.1826    1.3303 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5727    1.7262    0.2571 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2903    1.1051   -0.6411 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0128    1.9164   -1.6317 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9045    3.1494   -1.5645 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4561   -0.3542   -0.7697 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7705   -1.1969    0.2031 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4435   -1.1626    1.4299 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2839   -1.0724    0.3332 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9822   -2.2696    1.2321 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8166   -3.3734    0.7787 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7014   -1.4372   -0.9994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6983   -1.0365   -1.2440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3241   -0.5004   -0.0087 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4117   -1.7361    0.0126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3707   -1.9429   -1.4532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7705   -2.4573    0.2035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4347    1.6174   -0.9768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6768    0.4313   -2.1327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3109    0.1904   -1.5151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1856    0.8474    1.0213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8717   -0.7289    1.7653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8110   -0.1043    2.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8182    1.3484    2.8574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9248    2.2370    0.7781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7586    2.0696    2.0948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0893    2.0039   -1.2635 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5395    1.1773   -1.4869 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3099    2.5034   -0.3306 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3616   -0.1351    2.0284 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3975    0.7713    2.1852 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2480    2.0336    1.8184 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6291    2.8199    0.1235 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6047    1.4393   -2.3748 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5660   -0.5314   -0.6168 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3041   -0.5914   -1.8370 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9353   -2.2660   -0.1520 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2854   -1.6708    1.4113 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9108   -2.1459    2.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3212   -1.0608   -1.8534 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7444   -2.5608   -1.1428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7697   -0.2668   -2.0685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3397   -1.8789   -1.6392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2123   -1.2927    0.7926 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  7 23  1  0
 23 22  1  0
 22 21  1  0
 21 18  1  0
 18 19  1  1
 19 20  2  0
 18  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 15  1  0
 15 16  1  0
 16 17  1  0
 12 13  1  0
 13 14  2  0
 23  2  1  0
 16 18  1  0
  9  7  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  0
  4 31  1  0
  5 32  1  0
  5 33  1  0
  6 34  1  0
  6 35  1  0
  8 36  1  0
  8 37  1  0
  8 38  1  0
 23 53  1  1
 22 51  1  0
 22 52  1  0
 21 49  1  0
 21 50  1  0
 19 48  1  0
  9 39  1  1
 10 40  1  0
 10 41  1  0
 11 42  1  0
 15 44  1  0
 15 45  1  0
 16 46  1  6
 17 47  1  0
 13 43  1  0
M  END


  Mrv0541 02241217292D          

 23 25  0  0  0  0            999 V2000
   -1.1485   -0.4919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9020    0.3283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6408    0.0003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3796    0.4098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2974    1.2307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5586    1.5586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9020    1.1485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1640    1.5586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4098    1.1485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6563    0.3283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0818   -0.0818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1640   -0.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3276   -1.5586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1485   -1.5586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5586   -0.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3943   -0.0818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1331    0.2461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5586   -2.2974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3796   -2.2974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2307    0.9027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4765    1.6408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1331    2.2152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1485    2.2974    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  7  1  0  0  0  0
  2 11  1  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
  6 22  1  0  0  0  0
  6 23  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
 10 11  1  0  0  0  0
 10 16  1  0  0  0  0
 10 20  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 18  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 19  2  0  0  0  0
 20 21  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0302228

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CCCC2(C)C1CCC1(C=O)C2CC=C(CC1O)C=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O3/c1-18(2)8-4-9-19(3)15(18)7-10-20(13-22)16(19)6-5-14(12-21)11-17(20)23/h5,12-13,15-17,23H,4,6-11H2,1-3H3

> <INCHI_KEY>
UDKRLAJJSYRYRU-UHFFFAOYSA-N

> <FORMULA>
C20H30O3

> <MOLECULAR_WEIGHT>
318.4504

> <EXACT_MASS>
318.219494826

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
36.0123243201233

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-hydroxy-4,4,11b-trimethyl-1H,2H,3H,4H,4aH,5H,6H,6aH,7H,8H,11H,11aH,11bH-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde

> <ALOGPS_LOGP>
4.04

> <JCHEM_LOGP>
3.014821592666667

> <ALOGPS_LOGS>
-4.14

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.445364803023022

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0413974351577293

> <JCHEM_POLAR_SURFACE_AREA>
54.37

> <JCHEM_REFRACTIVITY>
91.67259999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.30e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-hydroxy-4,4,11b-trimethyl-1H,2H,3H,4aH,5H,6H,7H,8H,11H,11aH-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -2.144  -0.918   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.684   0.613   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.063   0.001   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.442   0.765   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.288   2.297   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.909   2.909   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.684   2.144   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.306   2.909   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.765   2.144   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.225   0.613   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.153  -0.153   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.306  -1.684   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.612  -2.909   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.144  -2.909   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.909  -1.684   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.603  -0.153   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.982   0.459   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.909  -4.288   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.442  -4.288   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.297   1.685   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.756   3.063   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -3.982   4.135   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.144   4.288   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7   11                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   22   23                                             
CONECT    7    2    6    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   16   20                                             
CONECT   11    2   10   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   10   15   17                                                  
CONECT   17   16                                                            
CONECT   18   14   19                                                       
CONECT   19   18                                                            
CONECT   20   10   21                                                       
CONECT   21   20                                                            
CONECT   22    6                                                            
CONECT   23    6                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₀O₃

Average Mass

318.4504 Da

Monoisotopic Mass

318.21949 Da

IUPAC Name

7-hydroxy-4,4,11b-trimethyl-1H,2H,3H,4H,4aH,5H,6H,6aH,7H,8H,11H,11aH,11bH-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde

Traditional Name

7-hydroxy-4,4,11b-trimethyl-1H,2H,3H,4aH,5H,6H,7H,8H,11H,11aH-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde

CAS Registry Number

Not Available

SMILES

CC1(C)CCCC2(C)C1CCC1(C=O)C2CC=C(CC1O)C=O

InChI Identifier

InChI=1S/C20H30O3/c1-18(2)8-4-9-19(3)15(18)7-10-20(13-22)16(19)6-5-14(12-21)11-17(20)23/h5,12-13,15-17,23H,4,6-11H2,1-3H3

InChI Key

UDKRLAJJSYRYRU-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

Species Name	Source	Reference
Aframomum alboviolaceum	LOTUS Database	35616633
Alpinia galanga	LOTUS Database	35616633
Zingiber mioga	LOTUS Database	35616633

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

Substituents

Secondary alcohol
Organic oxide
Hydrocarbon derivative
Carbonyl group
Aldehyde
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	4.04	ALOGPS
logP	3.01	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	14.45	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	54.37 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	91.67 m³·mol⁻¹	ChemAxon
Polarizability	36.01 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

HMDB ID

HMDB0035311

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB013980

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

14330184

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,7h,8h,11h,11ah-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde (NP0302228)

MOL for NP0302228 (7-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,7h,8h,11h,11ah-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde)

3D MOL for NP0302228 (7-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,7h,8h,11h,11ah-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde)

3D SDF for NP0302228 (7-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,7h,8h,11h,11ah-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde)

3D-SDF for NP0302228 (7-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,7h,8h,11h,11ah-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde)

PDB for NP0302228 (7-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,7h,8h,11h,11ah-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde)

3D PDB for NP0302228 (7-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,7h,8h,11h,11ah-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde)

SMILES for NP0302228 (7-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,7h,8h,11h,11ah-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde)

INCHI for NP0302228 (7-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,7h,8h,11h,11ah-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde)

Structure for NP0302228 (7-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,7h,8h,11h,11ah-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde)

3D Structure for NP0302228 (7-hydroxy-4,4,11b-trimethyl-1h,2h,3h,4ah,5h,6h,7h,8h,11h,11ah-cyclohepta[a]naphthalene-6a,9-dicarbaldehyde)