NP-MRD: Showing NP-Card for 2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal (NP0196423)

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Record Information

Version

2.0

Created at

2022-09-04 14:30:40 UTC

Updated at

2022-09-04 14:30:40 UTC

NP-MRD ID

NP0196423

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal

Description

AC1MVGS5 belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units. 2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal is found in Iris domestica, Iris foetidissima and Tigridia pavonia. AC1MVGS5 is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004241506152D          

 34 35  0  0  0  0            999 V2000
   -4.7808    4.4748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0271    4.1392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9408    3.3187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1872    2.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1009    2.1627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3473    1.8272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2610    1.0067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5074    0.6711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4211   -0.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6674   -0.4849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5812   -1.3054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0396   -1.0396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820    3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9195    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7445    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1570    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9195    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6533   -1.1265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3730   -1.0669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6798    2.3121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3596    4.6242    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  2  0  0  0  0
  7  8  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  4  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  4  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 15 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
  6 33  1  0  0  0  0
  2 34  1  0  0  0  0
M  END


  Mrv1533004241506152D          

 34 35  0  0  0  0            999 V2000
   -4.7808    4.4748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0271    4.1392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9408    3.3187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1872    2.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1009    2.1627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3473    1.8272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2610    1.0067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5074    0.6711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4211   -0.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6674   -0.4849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5812   -1.3054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0396   -1.0396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820    3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9195    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7445    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1570    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9195    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6820   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6533   -1.1265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3730   -1.0669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6798    2.3121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3596    4.6242    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  2  0  0  0  0
  7  8  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  4  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  4  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 15 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
  6 33  1  0  0  0  0
  2 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0196423

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCCC(C)=CC=CC(=C)C1CCC2(C1O)C(CCCO)C(CCC2(C)O)=C(C)C=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H46O4/c1-21(2)10-7-11-22(3)12-8-13-23(4)26-16-18-30(28(26)33)27(14-9-19-31)25(24(5)20-32)15-17-29(30,6)34/h8,10,12-13,20,26-28,31,33-34H,4,7,9,11,14-19H2,1-3,5-6H3

> <INCHI_KEY>
CKYPHBIOFUNLLX-UHFFFAOYSA-N

> <FORMULA>
C30H46O4

> <MOLECULAR_WEIGHT>
470.694

> <EXACT_MASS>
470.339609961

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
56.04924959164488

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal

> <ALOGPS_LOGP>
4.67

> <JCHEM_LOGP>
4.547189546000001

> <ALOGPS_LOGS>
-4.77

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.782520653147689

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.072390327126811

> <JCHEM_PKA_STRONGEST_BASIC>
-1.9850966987698362

> <JCHEM_POLAR_SURFACE_AREA>
77.76

> <JCHEM_REFRACTIVITY>
144.5719

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.95e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -8.924   8.353   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.517   7.727   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.356   6.195   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.949   5.569   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.788   4.037   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.382   3.411   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.221   1.879   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.814   1.253   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.653  -0.279   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.246  -0.905   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.085  -2.437   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.465   2.016   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.370   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.465  -0.476   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.941  -1.941   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.140   2.104   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.370   3.437   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.140   4.771   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.370   6.105   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.140   7.438   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.680   2.104   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.450   3.437   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.680   4.771   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.990   3.437   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.760   4.771   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.450   0.770   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.680  -0.564   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.140  -0.564   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.086  -2.103   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.563  -1.992   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -3.136   4.316   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -6.271   8.632   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   34                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   33                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   16                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   18   30                                             
CONECT   16   15   12   17                                                  
CONECT   17   16                                                            
CONECT   18   15   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   18   24   28                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26                                                            
CONECT   28   23   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   15   31   32                                             
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33    6                                                            
CONECT   34    2                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₆O₄

Average Mass

470.6940 Da

Monoisotopic Mass

470.33961 Da

IUPAC Name

2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal

Traditional Name

2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal

CAS Registry Number

Not Available

SMILES

CC(C)=CCCC(C)=CC=CC(=C)C1CCC2(C1O)C(CCCO)C(CCC2(C)O)=C(C)C=O

InChI Identifier

InChI=1S/C30H46O4/c1-21(2)10-7-11-22(3)12-8-13-23(4)26-16-18-30(28(26)33)27(14-9-19-31)25(24(5)20-32)15-17-29(30,6)34/h8,10,12-13,20,26-28,31,33-34H,4,7,9,11,14-19H2,1-3,5-6H3

InChI Key

CKYPHBIOFUNLLX-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Iris domestica	LOTUS Database	35616633
Iris foetidissima	LOTUS Database	35616633
Tigridia pavonia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Sesterterpenoids

Alternative Parents

Substituents

Sesterterpenoid
Tertiary alcohol
Enal
Cyclic alcohol
Alpha,beta-unsaturated aldehyde
Secondary alcohol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Aldehyde
Alcohol
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	4.67	ALOGPS
logP	4.55	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	14.07	ChemAxon
pKa (Strongest Basic)	-2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	77.76 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	144.57 m³·mol⁻¹	ChemAxon
Polarizability	56.05 Å³	ChemAxon
Number of Rings	2	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

3732651

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal (NP0196423)

MOL for NP0196423 (2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

3D MOL for NP0196423 (2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

3D SDF for NP0196423 (2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

3D-SDF for NP0196423 (2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

PDB for NP0196423 (2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

3D PDB for NP0196423 (2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

SMILES for NP0196423 (2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

INCHI for NP0196423 (2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

Structure for NP0196423 (2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

3D Structure for NP0196423 (2-[2-(6,10-dimethylundeca-1,3,5,9-tetraen-2-yl)-1,10-dihydroxy-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)