NP-MRD: Showing NP-Card for Siccanochromene E (NP0066421)

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Record Information

Version

2.0

Created at

2022-04-28 10:40:55 UTC

Updated at

2022-04-28 10:40:55 UTC

NP-MRD ID

NP0066421

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Siccanochromene E

Description

Siccanochromene E belongs to the class of organic compounds known as xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring. Siccanochromene E is found in Helminthosporium siccans Drechsler and Lolium multifolium Lam.. Based on a literature review very few articles have been published on Siccanochromene E.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282212402D          

 25 28  0  0  1  0            999 V2000
    5.0352   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -1.1466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4149    1.6598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0647    2.1275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    1.9716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5953    1.3332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0097    1.8403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0647   -0.0552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946   -0.8348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    2.2834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1154    0.7243    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
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  4 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 15 22  1  1  0  0  0
 22 23  1  0  0  0  0
 10 24  1  1  0  0  0
  2 25  1  0  0  0  0
M  END

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
    6.7771   -0.9869   -0.0195 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3138   -0.9024    0.2104 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7942   -1.5531    1.3041 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4284   -1.5163    1.5829 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9131   -2.1701    2.6801 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6223   -0.8062    0.7246 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1034   -0.1293   -0.4020 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4818   -0.2038   -0.6262 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2741    0.5561   -1.2319 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9305    0.7848   -1.0124 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8123    2.3196   -0.8158 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1153    0.4750   -2.2670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3100    0.1262   -1.9685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8061    0.6251   -0.6457 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2911    0.5430   -0.5743 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8256    1.7869    0.1611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8681    0.6377   -1.9772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8727   -0.6878    0.0404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9741   -1.4422    0.9558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5298   -1.3787    0.6408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0534    0.0546    0.5195 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2920    0.7646    1.7910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6296    0.2317    2.8570 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4108    0.0676    0.1497 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1924   -0.6497    0.9337 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0332   -0.9480   -1.0984 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2259   -0.0769    0.4725 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1921   -1.8594    0.4911 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4263   -2.1208    1.9935 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9656   -2.2139    2.9753 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8794    0.3112   -1.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4682    2.5697    0.2011 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2699    2.7788   -1.6408 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8522    2.7792   -0.8580 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2138    1.3636   -2.9182 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6619   -0.3440   -2.7813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4198   -0.9677   -2.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9192    0.6069   -2.7629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5685    1.7391   -0.6429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5464    2.3646   -0.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4284    1.4526    1.0567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0168    2.4758    0.4304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9894    0.6698   -1.7984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6604    1.5908   -2.4760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7299   -0.2694   -2.5739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2599   -1.3953   -0.7331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7684   -0.3864    0.6261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1217   -1.1926    2.0269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2563   -2.5415    0.9161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9953   -1.9703    1.4026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3714   -1.9392   -0.3161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3912    0.6888    2.0635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1281    1.8671    1.7764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1297   -0.3988    3.4061 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7955   -1.1804    1.7998 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6 25  1  0
 25 24  2  0
 24 10  1  0
 10 11  1  1
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  1
 15 17  1  0
 15 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  1
 22 23  1  0
 10  9  1  0
  9  7  1  0
  7  8  2  0
  8  2  1  0
  7  6  1  0
 21 24  1  0
 21 14  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  5 30  1  0
 25 55  1  0
 11 32  1  0
 11 33  1  0
 11 34  1  0
 12 35  1  0
 12 36  1  0
 13 37  1  0
 13 38  1  0
 14 39  1  6
 16 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
 17 44  1  0
 17 45  1  0
 18 46  1  0
 18 47  1  0
 19 48  1  0
 19 49  1  0
 20 50  1  0
 20 51  1  0
 22 52  1  0
 22 53  1  0
 23 54  1  0
  8 31  1  0
M  END


  Mrv1652304282212402D          

 25 28  0  0  1  0            999 V2000
    5.0352   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -1.1466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4149    1.6598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0647    2.1275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    1.9716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5953    1.3332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0097    1.8403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0647   -0.0552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946   -0.8348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    2.2834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1154    0.7243    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
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  4 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 15 22  1  1  0  0  0
 22 23  1  0  0  0  0
 10 24  1  1  0  0  0
  2 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0066421

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC(O)=C2C=C3[C@](C)(CC[C@H]4C(C)(C)CCC[C@@]34CO)OC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O3/c1-14-10-16(24)15-12-19-21(4,25-17(15)11-14)9-6-18-20(2,3)7-5-8-22(18,19)13-23/h10-12,18,23-24H,5-9,13H2,1-4H3/t18-,21-,22-/m0/s1

> <INCHI_KEY>
XJWNZCLHCHZSKX-NYVOZVTQSA-N

> <FORMULA>
C22H30O3

> <MOLECULAR_WEIGHT>
342.479

> <EXACT_MASS>
342.219494826

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
39.365841694693884

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5aS,7aS,11aS)-11a-(hydroxymethyl)-3,5a,8,8-tetramethyl-6,7,7a,8,9,10,11,11a-octahydro-5aH-5-oxatetraphen-1-ol

> <ALOGPS_LOGP>
5.04

> <JCHEM_LOGP>
4.436243514333333

> <ALOGPS_LOGS>
-4.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.04657967486806

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.455285710214717

> <JCHEM_PKA_STRONGEST_BASIC>
-2.778427682595688

> <JCHEM_POLAR_SURFACE_AREA>
49.69

> <JCHEM_REFRACTIVITY>
100.8488

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.21e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5aS,7aS,11aS)-11a-(hydroxymethyl)-3,5a,8,8-tetramethyl-6,7,7a,9,10,11-hexahydro-5-oxatetraphen-1-ol

> <JCHEM_VEBER_RULE>
0

$$$$

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       9.399  -0.394   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.903   1.061   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.895   2.225   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.383   1.934   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.879   0.479   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.887  -0.685   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.383  -2.140   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.366   0.188   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.358   1.352   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.862   2.807   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.375   3.098   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.854   3.971   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.342   3.680   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.838   2.225   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.846   1.061   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.342  -0.394   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.830  -0.685   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.179   0.479   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.326   1.934   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.111   2.489   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.018   3.435   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.854  -0.103   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       3.350  -1.558   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.366   4.262   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.415   1.352   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   11                                                  
CONECT    5    4    6    8                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    5    9                                                       
CONECT    9    8   10   15                                                  
CONECT   10    9   11   12   24                                             
CONECT   11   10    4                                                       
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14    9   16   22                                             
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14   20   21                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   15   23                                                       
CONECT   23   22                                                            
CONECT   24   10                                                            
CONECT   25    2                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₀O₃

Average Mass

342.4790 Da

Monoisotopic Mass

342.21949 Da

IUPAC Name

(5aS,7aS,11aS)-11a-(hydroxymethyl)-3,5a,8,8-tetramethyl-6,7,7a,8,9,10,11,11a-octahydro-5aH-5-oxatetraphen-1-ol

Traditional Name

(5aS,7aS,11aS)-11a-(hydroxymethyl)-3,5a,8,8-tetramethyl-6,7,7a,9,10,11-hexahydro-5-oxatetraphen-1-ol

CAS Registry Number

Not Available

SMILES

CC1=CC(O)=C2C=C3[C@](C)(CC[C@H]4C(C)(C)CCC[C@@]34CO)OC2=C1

InChI Identifier

InChI=1S/C22H30O3/c1-14-10-16(24)15-12-19-21(4,25-17(15)11-14)9-6-18-20(2,3)7-5-8-22(18,19)13-23/h10-12,18,23-24H,5-9,13H2,1-4H3/t18-,21-,22-/m0/s1

InChI Key

XJWNZCLHCHZSKX-NYVOZVTQSA-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
Helminthosporium siccans Drechsler	Fungi	KNApSAcK
Lolium multifolium Lam.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Xanthenes

Alternative Parents

Substituents

Naphthopyran
Xanthene
Naphthalene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyran
Benzenoid
Oxacycle
Ether
Primary alcohol
Organooxygen compound
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	5.04	ALOGPS
logP	4.44	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	9.46	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	49.69 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	100.85 m³·mol⁻¹	ChemAxon
Polarizability	39.37 Å³	ChemAxon
Number of Rings	4	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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00023936

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

12315535

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Siccanochromene E (NP0066421)

MOL for NP0066421 (Siccanochromene E)

3D MOL for NP0066421 (Siccanochromene E)

3D SDF for NP0066421 (Siccanochromene E)

3D-SDF for NP0066421 (Siccanochromene E)

PDB for NP0066421 (Siccanochromene E)

3D PDB for NP0066421 (Siccanochromene E)

SMILES for NP0066421 (Siccanochromene E)

INCHI for NP0066421 (Siccanochromene E)

Structure for NP0066421 (Siccanochromene E)

3D Structure for NP0066421 (Siccanochromene E)