MiMeDB: Showing metabocard for (2R,4bS,6aS,12bS,12cR,14aS)-9,10-diisopentenylpaxilline (MMDBc0009969)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 02:18:59 UTC

Update Date

2022-08-31 06:30:59 UTC

Metabolite ID

MMDBc0009969

Metabolite Identification

Common Name

(2R,4bS,6aS,12bS,12cR,14aS)-9,10-diisopentenylpaxilline

Description

21,22-Diprenylpaxilline belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. 21,22-Diprenylpaxilline is a primary metabolite. Primary metabolites are metabolically or physiologically essential metabolites. They are directly involved in an organism’s growth, development or reproduction. Based on a literature review very few articles have been published on 21,22-Diprenylpaxilline.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152104192D          

 45 50  0  0  1  0            999 V2000
    7.3717   -2.3883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5361   -1.2291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7896    3.3573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2035    2.0541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1287    0.3368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4520    1.8417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5578    0.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8988    0.6634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9578   -1.0851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6251    2.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8746   -0.2643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7083    1.3773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0549   -1.4234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0530    1.3773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8054    1.0390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3025   -1.0851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4530   -0.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2866    1.2333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5304   -1.1156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7976   -0.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2885   -1.5675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8727    2.5365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1222    0.0741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0390    0.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7241   -0.9410    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7005   -0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9456   -0.4026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4669    0.0741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6174    0.7509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0452   -0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3837    0.8949    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3959    0.2125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0379    0.7509    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7904    1.0893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8885    0.2182    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6410   -0.1202    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2193   -0.2643    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8111    0.9254    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6240   -0.5523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5428    1.4276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5500   -0.7467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6313    1.2333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9717   -0.6026    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1211    1.5717    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 15 14  1  0  0  0  0
 16 13  1  0  0  0  0
 21  1  1  0  0  0  0
 21  2  1  0  0  0  0
 21  9  2  0  0  0  0
 22  3  1  0  0  0  0
 22  4  1  0  0  0  0
 22 10  2  0  0  0  0
 23 11  1  0  0  0  0
 23 17  2  0  0  0  0
 24 12  1  0  0  0  0
 24 18  2  0  0  0  0
 24 23  1  0  0  0  0
 25 13  1  0  0  0  0
 25 19  1  0  0  0  0
 26 17  1  0  0  0  0
 27 19  1  0  0  0  0
 27 26  1  0  0  0  0
 28 20  2  0  0  0  0
 29 18  1  0  0  0  0
 29 26  2  0  0  0  0
 30 20  1  0  0  0  0
 31 14  1  0  0  0  0
 31 28  1  0  0  0  0
 32 27  2  0  0  0  0
 33 30  1  0  0  0  0
 34  5  1  0  0  0  0
 34  6  1  0  0  0  0
 33 34  1  1  0  0  0
 35  7  1  1  0  0  0
 35 15  1  0  0  0  0
 36  8  1  6  0  0  0
 36 25  1  0  0  0  0
 36 32  1  0  0  0  0
 36 35  1  0  0  0  0
 37 16  1  0  0  0  0
 37 28  1  0  0  0  0
 37 35  1  0  0  0  0
 38 29  1  0  0  0  0
 38 32  1  0  0  0  0
 39 30  2  0  0  0  0
 40 34  1  0  0  0  0
 37 41  1  6  0  0  0
 42 31  1  0  0  0  0
 42 33  1  0  0  0  0
 25 43  1  1  0  0  0
 31 44  1  6  0  0  0
 33 45  1  6  0  0  0
M  END


  Mrv1652305152104192D          

 45 50  0  0  1  0            999 V2000
    7.3717   -2.3883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5361   -1.2291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7896    3.3573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2035    2.0541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1287    0.3368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4520    1.8417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5578    0.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8988    0.6634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9578   -1.0851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6251    2.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8746   -0.2643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7083    1.3773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0549   -1.4234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0530    1.3773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8054    1.0390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3025   -1.0851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4530   -0.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2866    1.2333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5304   -1.1156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7976   -0.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2885   -1.5675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8727    2.5365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1222    0.0741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0390    0.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7241   -0.9410    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7005   -0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9456   -0.4026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4669    0.0741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6174    0.7509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0452   -0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3837    0.8949    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3959    0.2125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0379    0.7509    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7904    1.0893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8885    0.2182    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6410   -0.1202    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2193   -0.2643    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8111    0.9254    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6240   -0.5523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5428    1.4276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5500   -0.7467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6313    1.2333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9717   -0.6026    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1211    1.5717    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 15 14  1  0  0  0  0
 16 13  1  0  0  0  0
 21  1  1  0  0  0  0
 21  2  1  0  0  0  0
 21  9  2  0  0  0  0
 22  3  1  0  0  0  0
 22  4  1  0  0  0  0
 22 10  2  0  0  0  0
 23 11  1  0  0  0  0
 23 17  2  0  0  0  0
 24 12  1  0  0  0  0
 24 18  2  0  0  0  0
 24 23  1  0  0  0  0
 25 13  1  0  0  0  0
 25 19  1  0  0  0  0
 26 17  1  0  0  0  0
 27 19  1  0  0  0  0
 27 26  1  0  0  0  0
 28 20  2  0  0  0  0
 29 18  1  0  0  0  0
 29 26  2  0  0  0  0
 30 20  1  0  0  0  0
 31 14  1  0  0  0  0
 31 28  1  0  0  0  0
 32 27  2  0  0  0  0
 33 30  1  0  0  0  0
 34  5  1  0  0  0  0
 34  6  1  0  0  0  0
 33 34  1  1  0  0  0
 35  7  1  1  0  0  0
 35 15  1  0  0  0  0
 36  8  1  6  0  0  0
 36 25  1  0  0  0  0
 36 32  1  0  0  0  0
 36 35  1  0  0  0  0
 37 16  1  0  0  0  0
 37 28  1  0  0  0  0
 37 35  1  0  0  0  0
 38 29  1  0  0  0  0
 38 32  1  0  0  0  0
 39 30  2  0  0  0  0
 40 34  1  0  0  0  0
 37 41  1  6  0  0  0
 42 31  1  0  0  0  0
 42 33  1  0  0  0  0
 25 43  1  1  0  0  0
 31 44  1  6  0  0  0
 33 45  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0009969

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]12CC3=C(NC4=C3C=C(CC=C(C)C)C(CC=C(C)C)=C4)[C@]1(C)[C@@]1(C)CC[C@]3([H])O[C@@]([H])(C(=O)C=C3[C@]1(O)CC2)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C37H49NO4/c1-21(2)9-11-23-17-26-27-19-25-13-16-37(41)28-20-30(39)33(34(5,6)40)42-31(28)14-15-35(37,7)36(25,8)32(27)38-29(26)18-24(23)12-10-22(3)4/h9-10,17-18,20,25,31,33,38,40-41H,11-16,19H2,1-8H3/t25-,31-,33-,35+,36+,37+/m0/s1

> <INCHI_KEY>
YMPSZJNRZBHLRI-OGYDQXLWSA-N

> <FORMULA>
C37H49NO4

> <MOLECULAR_WEIGHT>
571.802

> <EXACT_MASS>
571.366159062

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
91

> <JCHEM_AVERAGE_POLARIZABILITY>
70.14274313239147

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,5S,7R,11S,14S)-11-hydroxy-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-19,20-bis(3-methylbut-2-en-1-yl)-6-oxa-23-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{16,24}.0^{17,22}]tetracosa-9,16(24),17(22),18,20-pentaen-8-one

> <ALOGPS_LOGP>
6.40

> <JCHEM_LOGP>
7.080217259333334

> <ALOGPS_LOGS>
-6.40

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.265814194166133

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.558853001280657

> <JCHEM_PKA_STRONGEST_BASIC>
-3.178614806490442

> <JCHEM_POLAR_SURFACE_AREA>
82.55000000000001

> <JCHEM_REFRACTIVITY>
171.70209999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.28e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5S,7R,11S,14S)-11-hydroxy-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-19,20-bis(3-methylbut-2-en-1-yl)-6-oxa-23-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{16,24}.0^{17,22}]tetracosa-9,16(24),17(22),18,20-pentaen-8-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0      13.760  -4.458   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.201  -2.294   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.674   6.267   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.580   3.834   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.107   0.629   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.844   3.438   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.641   1.308   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.278   1.238   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.855  -2.025   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.234   4.103   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.699  -0.493   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.389   2.571   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.702  -2.657   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.832   2.571   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.237   1.939   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.298  -2.025   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.046  -0.762   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.735   2.302   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.457  -2.082   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.489  -0.762   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.605  -2.926   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.829   4.735   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.295   0.138   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      13.140   1.671   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.952  -1.757   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.641  -0.131   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.232  -0.752   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.738   0.138   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.486   1.402   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.084  -0.131   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.583   1.671   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.206   0.397   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -0.071   1.402   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -1.475   2.033   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.392   0.407   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.796  -0.224   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       4.143  -0.493   0.000  0.00  0.00           C+0
HETATM   38  N   UNK     0       8.981   1.727   0.000  0.00  0.00           N+0
HETATM   39  O   UNK     0      -1.165  -1.031   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      -2.880   2.665   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       2.893  -1.394   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       1.178   2.302   0.000  0.00  0.00           O+0
HETATM   43  H   UNK     0       5.547  -1.125   0.000  0.00  0.00           H+0
HETATM   44  H   UNK     0       1.334   0.770   0.000  0.00  0.00           H+0
HETATM   45  H   UNK     0      -0.226   2.934   0.000  0.00  0.00           H+0
CONECT    1   21                                                            
CONECT    2   21                                                            
CONECT    3   22                                                            
CONECT    4   22                                                            
CONECT    5   34                                                            
CONECT    6   34                                                            
CONECT    7   35                                                            
CONECT    8   36                                                            
CONECT    9   11   21                                                       
CONECT   10   12   22                                                       
CONECT   11    9   23                                                       
CONECT   12   10   24                                                       
CONECT   13   16   25                                                       
CONECT   14   15   31                                                       
CONECT   15   14   35                                                       
CONECT   16   13   37                                                       
CONECT   17   23   26                                                       
CONECT   18   24   29                                                       
CONECT   19   25   27                                                       
CONECT   20   28   30                                                       
CONECT   21    1    2    9                                                  
CONECT   22    3    4   10                                                  
CONECT   23   11   17   24                                                  
CONECT   24   12   18   23                                                  
CONECT   25   13   19   36   43                                             
CONECT   26   17   27   29                                                  
CONECT   27   19   26   32                                                  
CONECT   28   20   31   37                                                  
CONECT   29   18   26   38                                                  
CONECT   30   20   33   39                                                  
CONECT   31   14   28   42   44                                             
CONECT   32   27   36   38                                                  
CONECT   33   30   34   42   45                                             
CONECT   34    5    6   33   40                                             
CONECT   35    7   15   36   37                                             
CONECT   36    8   25   32   35                                             
CONECT   37   16   28   35   41                                             
CONECT   38   29   32                                                       
CONECT   39   30                                                            
CONECT   40   34                                                            
CONECT   41   37                                                            
CONECT   42   31   33                                                       
CONECT   43   25                                                            
CONECT   44   31                                                            
CONECT   45   33                                                            
MASTER        0    0    0    0    0    0    0    0   45    0  100    0
END

Synonyms

Not Available

Molecular Formula

C₃₇H₄₉NO₄

Average Mass

571.802

Monoisotopic Mass

571.366159062

IUPAC Name

(1S,2R,5S,7R,11S,14S)-11-hydroxy-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-19,20-bis(3-methylbut-2-en-1-yl)-6-oxa-23-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{16,24}.0^{17,22}]tetracosa-9,16(24),17(22),18,20-pentaen-8-one

Traditional Name

CAS Registry Number

Not Available

SMILES

[H][C@]12CC3=C(NC4=C3C=C(CC=C(C)C)C(CC=C(C)C)=C4)[C@]1(C)[C@@]1(C)CC[C@]3([H])O[C@@]([H])(C(=O)C=C3[C@]1(O)CC2)C(C)(C)O

InChI Identifier

InChI=1S/C37H49NO4/c1-21(2)9-11-23-17-26-27-19-25-13-16-37(41)28-20-30(39)33(34(5,6)40)42-31(28)14-15-35(37,7)36(25,8)32(27)38-29(26)18-24(23)12-10-22(3)4/h9-10,17-18,20,25,31,33,38,40-41H,11-16,19H2,1-8H3/t25-,31-,33-,35+,36+,37+/m0/s1

InChI Key

YMPSZJNRZBHLRI-OGYDQXLWSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
3-alkylindole
Indole
Indole or derivatives
Dihydropyranone
Pyran
Benzenoid
Heteroaromatic compound
Tertiary alcohol
Pyrrole
Cyclic alcohol
Cyclic ketone
Ketone
Oxacycle
Azacycle
Dialkyl ether
Ether
Alcohol
Organic oxide
Organopnictogen compound
Organic oxygen compound
Hydrocarbon derivative
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.00023 g/L	ALOGPS
logP	6.4	ALOGPS
logP	7.08	ChemAxon
logS	-6.4	ALOGPS
pKa (Strongest Acidic)	13.56	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	82.55 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	171.7 m³·mol⁻¹	ChemAxon
Polarizability	70.14 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_4_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Not Available

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	2	Human feces; Human sputum; Human	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

30771021

KEGG Compound ID

C20561

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71745339

PDB ID

Not Available

ChEBI ID

181405

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for (2R,4bS,6aS,12bS,12cR,14aS)-9,10-diisopentenylpaxilline (MMDBc0009969)

MOL for #<Metabolite:0x00007f4706fa5a38>

3D MOL for #<Metabolite:0x00007f4706fa5a38>

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3D-SDF for #<Metabolite:0x00007f4706fa5a38>

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Structure for #<Metabolite:0x00007f4706fa5a38>

3D Structure for #<Metabolite:0x00007f4706fa5a38>