NP-MRD: Showing NP-Card for 2-[(1r,2s,5s,6r,7e,10s)-1,10-dihydroxy-2-[(2z,4e)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal (NP0164871)

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Record Information

Version

2.0

Created at

2022-09-02 23:50:16 UTC

Updated at

2022-09-02 23:50:16 UTC

NP-MRD ID

NP0164871

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(1r,2s,5s,6r,7e,10s)-1,10-dihydroxy-2-[(2z,4e)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal

Description

28-Deacetylbelamcandal, also known as iridotectoral b, belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units. 2-[(1r,2s,5s,6r,7e,10s)-1,10-dihydroxy-2-[(2z,4e)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal is found in Iris domestica, Iris japonica and Iris tectorum. Based on a literature review very few articles have been published on 28-Deacetylbelamcandal.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309032201502D          

 35 36  0  0  1  0            999 V2000
   -4.2633   -0.4481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5097   -0.7837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8422   -0.2987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0886   -0.6343    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
    0.1725   -1.6410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  2  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  1  0  0  0  0  0  0  0  0  0
    1.6820    1.1270    0.0000 C   0  0  2  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  1  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
    0.9824   -0.7392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7846   -1.0799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4234   -1.6041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0909   -2.0891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0046   -2.9095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6721   -3.3945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5858   -4.2149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4257   -3.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  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
  9  6  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 12 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  6  0  0  0
 12 28  1  0  0  0  0
  9 28  1  0  0  0  0
 28 29  1  6  0  0  0
  2 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
M  END


  Mrv1652309032201502D          

 35 36  0  0  1  0            999 V2000
   -4.2633   -0.4481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5097   -0.7837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8422   -0.2987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0886   -0.6343    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
    0.1725   -1.6410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  2  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  1  0  0  0  0  0  0  0  0  0
    1.6820    1.1270    0.0000 C   0  0  2  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  1  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
    0.9824   -0.7392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7846   -1.0799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4234   -1.6041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0909   -2.0891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0046   -2.9095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6721   -3.3945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5858   -4.2149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4257   -3.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  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
  9  6  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 12 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  6  0  0  0
 12 28  1  0  0  0  0
  9 28  1  0  0  0  0
 28 29  1  6  0  0  0
  2 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0164871

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCCC(=C)\C=C\C=C(/CO)[C@@H]1CC[C@@]2([C@@H]1O)[C@H](CCCO)\C(CC[C@]2(C)O)=C(/C)C=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H46O5/c1-21(2)9-6-10-22(3)11-7-12-24(20-33)26-15-17-30(28(26)34)27(13-8-18-31)25(23(4)19-32)14-16-29(30,5)35/h7,9,11-12,19,26-28,31,33-35H,3,6,8,10,13-18,20H2,1-2,4-5H3/b11-7+,24-12+,25-23+/t26-,27+,28+,29-,30-/m0/s1

> <INCHI_KEY>
XVFORSWJIMCHND-MYCBEMGISA-N

> <FORMULA>
C30H46O5

> <MOLECULAR_WEIGHT>
486.693

> <EXACT_MASS>
486.334524581

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
57.54530341500555

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(1R,2S,5S,6R,7E,10S)-1,10-dihydroxy-2-[(2Z,4E)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal

> <ALOGPS_LOGP>
3.62

> <JCHEM_LOGP>
3.2664183893333334

> <ALOGPS_LOGS>
-4.46

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.661207055695119

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.039182514639023

> <JCHEM_PKA_STRONGEST_BASIC>
-1.9850966922058157

> <JCHEM_POLAR_SURFACE_AREA>
97.99000000000001

> <JCHEM_REFRACTIVITY>
146.3466

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.70e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(1R,2S,5S,6R,7E,10S)-1,10-dihydroxy-2-[(2Z,4E)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -7.958  -0.836   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.551  -1.463   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.305  -0.558   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.899  -1.184   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.653  -0.279   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.246  -0.905   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.085  -2.437   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.322  -3.063   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.465   2.016   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.370   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.140   2.104   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.370   3.437   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.140   4.771   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.370   6.105   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.140   7.438   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.680   2.104   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.450   3.437   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.680   4.771   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.990   3.437   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       7.760   4.771   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       5.450   0.770   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.680  -0.564   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.140  -0.564   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.086  -2.103   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       1.834  -1.380   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       1.465  -0.476   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       1.465  -2.016   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -6.390  -2.994   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -7.636  -3.900   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -7.475  -5.431   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -8.721  -6.336   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -8.560  -7.868   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -10.128  -5.710   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   30                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10   28                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   25   28                                             
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   13   19   23                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21                                                            
CONECT   23   18   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   12   26   27                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   12    9   29                                                  
CONECT   29   28                                                            
CONECT   30    2   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   72    0
END

View in JSmol

Synonyms

Value	Source
Iridotectoral b	MeSH

Chemical Formula

C₃₀H₄₆O₅

Average Mass

486.6930 Da

Monoisotopic Mass

486.33452 Da

IUPAC Name

2-[(1R,2S,5S,6R,7E,10S)-1,10-dihydroxy-2-[(2Z,4E)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal

Traditional Name

2-[(1R,2S,5S,6R,7E,10S)-1,10-dihydroxy-2-[(2Z,4E)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal

CAS Registry Number

Not Available

SMILES

CC(C)=CCCC(=C)\C=C\C=C(/CO)[C@@H]1CC[C@@]2([C@@H]1O)[C@H](CCCO)\C(CC[C@]2(C)O)=C(/C)C=O

InChI Identifier

InChI=1S/C30H46O5/c1-21(2)9-6-10-22(3)11-7-12-24(20-33)26-15-17-30(28(26)34)27(13-8-18-31)25(23(4)19-32)14-16-29(30,5)35/h7,9,11-12,19,26-28,31,33-35H,3,6,8,10,13-18,20H2,1-2,4-5H3/b11-7+,24-12+,25-23+/t26-,27+,28+,29-,30-/m0/s1

InChI Key

XVFORSWJIMCHND-MYCBEMGISA-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 japonica	LOTUS Database	35616633
Iris tectorum	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
Fatty alcohol
Fatty acyl
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	3.62	ALOGPS
logP	3.27	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	14.04	ChemAxon
pKa (Strongest Basic)	-2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	97.99 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	146.35 m³·mol⁻¹	ChemAxon
Polarizability	57.55 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

C00049347

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

101615676

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(1r,2s,5s,6r,7e,10s)-1,10-dihydroxy-2-[(2z,4e)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal (NP0164871)

MOL for NP0164871 (2-[(1r,2s,5s,6r,7e,10s)-1,10-dihydroxy-2-[(2z,4e)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

3D MOL for NP0164871 (2-[(1r,2s,5s,6r,7e,10s)-1,10-dihydroxy-2-[(2z,4e)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

3D SDF for NP0164871 (2-[(1r,2s,5s,6r,7e,10s)-1,10-dihydroxy-2-[(2z,4e)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

3D-SDF for NP0164871 (2-[(1r,2s,5s,6r,7e,10s)-1,10-dihydroxy-2-[(2z,4e)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

PDB for NP0164871 (2-[(1r,2s,5s,6r,7e,10s)-1,10-dihydroxy-2-[(2z,4e)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

3D PDB for NP0164871 (2-[(1r,2s,5s,6r,7e,10s)-1,10-dihydroxy-2-[(2z,4e)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

SMILES for NP0164871 (2-[(1r,2s,5s,6r,7e,10s)-1,10-dihydroxy-2-[(2z,4e)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

INCHI for NP0164871 (2-[(1r,2s,5s,6r,7e,10s)-1,10-dihydroxy-2-[(2z,4e)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

Structure for NP0164871 (2-[(1r,2s,5s,6r,7e,10s)-1,10-dihydroxy-2-[(2z,4e)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)

3D Structure for NP0164871 (2-[(1r,2s,5s,6r,7e,10s)-1,10-dihydroxy-2-[(2z,4e)-1-hydroxy-10-methyl-6-methylideneundeca-2,4,9-trien-2-yl]-6-(3-hydroxypropyl)-10-methylspiro[4.5]decan-7-ylidene]propanal)