NP-MRD: Showing NP-Card for Monaspyranoindole (NP0007628)

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Record Information

Version

2.0

Created at

2020-12-09 04:27:20 UTC

Updated at

2021-07-15 16:58:06 UTC

NP-MRD ID

NP0007628

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Monaspyranoindole

Provided By

NPAtlas

Description

Monaspyranoindole belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position. Monaspyranoindole is found in Monascus and Monascus pilosus. Monaspyranoindole was first documented in 2008 (PMID: 18310957). Based on a literature review very few articles have been published on Monaspyranoindole.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118423D          

 30 32  0  0  0  0            999 V2000
   -2.2845   -1.6772    1.0157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9829   -0.4864    0.1284 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5217   -0.8221   -1.2571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5561    0.6433    0.6623 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0318    1.8045    0.0847 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6030    2.0336    0.4796 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1754    0.8103    0.2255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4922   -0.3798    0.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4265   -1.3666   -0.1603 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6347   -0.7790   -0.1296 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9089   -1.3197   -0.2952 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0251   -0.5129   -0.2219 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9074    0.8445    0.0164 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6555    1.4010    0.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5302    0.5756    0.1075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7482   -2.5499    0.5885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3564   -1.8706    1.1219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8337   -1.4579    2.0131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5405   -1.9439   -1.3759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7861   -0.3786   -1.9786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5217   -0.4340   -1.4358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1779    1.8048   -1.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6295    2.6523    0.4907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5674    2.3295    1.5446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2092    2.8639   -0.1374 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2031   -2.3838   -0.3209 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0202   -2.3800   -0.4825 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0206   -0.9231   -0.3492 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8150    1.4525    0.0679 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5202    2.4499    0.3702 H   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  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
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  8  2  1  0  0  0  0
 15 10  1  0  0  0  0
 15  7  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  3 19  1  0  0  0  0
  3 20  1  0  0  0  0
  3 21  1  0  0  0  0
  5 22  1  0  0  0  0
  5 23  1  0  0  0  0
  6 24  1  0  0  0  0
  6 25  1  0  0  0  0
  9 26  1  0  0  0  0
 11 27  1  0  0  0  0
 12 28  1  0  0  0  0
 13 29  1  0  0  0  0
 14 30  1  0  0  0  0
M  END

     RDKit          3D

 30 32  0  0  0  0  0  0  0  0999 V2000
   -2.2845   -1.6772    1.0157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9829   -0.4864    0.1284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5217   -0.8221   -1.2571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5561    0.6433    0.6623 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0318    1.8045    0.0847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6030    2.0336    0.4796 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1754    0.8103    0.2255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4922   -0.3798    0.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4265   -1.3666   -0.1603 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6347   -0.7790   -0.1296 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9089   -1.3197   -0.2952 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0251   -0.5129   -0.2219 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9074    0.8445    0.0164 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6555    1.4010    0.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5302    0.5756    0.1075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7482   -2.5499    0.5885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3564   -1.8706    1.1219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8337   -1.4579    2.0131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5405   -1.9439   -1.3759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7861   -0.3786   -1.9786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5217   -0.4340   -1.4358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1779    1.8048   -1.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6295    2.6523    0.4907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5674    2.3295    1.5446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2092    2.8639   -0.1374 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2031   -2.3838   -0.3209 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0202   -2.3800   -0.4825 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0206   -0.9231   -0.3492 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8150    1.4525    0.0679 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5202    2.4499    0.3702 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  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
  8  2  1  0
 15 10  1  0
 15  7  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  3 20  1  0
  3 21  1  0
  5 22  1  0
  5 23  1  0
  6 24  1  0
  6 25  1  0
  9 26  1  0
 11 27  1  0
 12 28  1  0
 13 29  1  0
 14 30  1  0
M  END


  Mrv1652306242118423D          

 30 32  0  0  0  0            999 V2000
   -2.2845   -1.6772    1.0157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9829   -0.4864    0.1284 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5217   -0.8221   -1.2571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5561    0.6433    0.6623 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0318    1.8045    0.0847 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6030    2.0336    0.4796 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1754    0.8103    0.2255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4922   -0.3798    0.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4265   -1.3666   -0.1603 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6347   -0.7790   -0.1296 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9089   -1.3197   -0.2952 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0251   -0.5129   -0.2219 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9074    0.8445    0.0164 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6555    1.4010    0.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5302    0.5756    0.1075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7482   -2.5499    0.5885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3564   -1.8706    1.1219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8337   -1.4579    2.0131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5405   -1.9439   -1.3759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7861   -0.3786   -1.9786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5217   -0.4340   -1.4358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1779    1.8048   -1.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6295    2.6523    0.4907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5674    2.3295    1.5446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2092    2.8639   -0.1374 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2031   -2.3838   -0.3209 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0202   -2.3800   -0.4825 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0206   -0.9231   -0.3492 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8150    1.4525    0.0679 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5202    2.4499    0.3702 H   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  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
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  8  2  1  0  0  0  0
 15 10  1  0  0  0  0
 15  7  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  3 19  1  0  0  0  0
  3 20  1  0  0  0  0
  3 21  1  0  0  0  0
  5 22  1  0  0  0  0
  5 23  1  0  0  0  0
  6 24  1  0  0  0  0
  6 25  1  0  0  0  0
  9 26  1  0  0  0  0
 11 27  1  0  0  0  0
 12 28  1  0  0  0  0
 13 29  1  0  0  0  0
 14 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0007628

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]N1C2=C([H])C([H])=C([H])C([H])=C2C2=C1C(OC([H])([H])C2([H])[H])(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C13H15NO/c1-13(2)12-10(7-8-15-13)9-5-3-4-6-11(9)14-12/h3-6,14H,7-8H2,1-2H3

> <INCHI_KEY>
DEFSXUNWUSCNII-UHFFFAOYSA-N

> <FORMULA>
C13H15NO

> <MOLECULAR_WEIGHT>
201.269

> <EXACT_MASS>
201.115364107

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
23.183365611987462

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,1-dimethyl-1H,3H,4H,9H-pyrano[3,4-b]indole

> <ALOGPS_LOGP>
3.31

> <JCHEM_LOGP>
2.604825868333333

> <ALOGPS_LOGS>
-3.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.914631624079739

> <JCHEM_PKA_STRONGEST_BASIC>
-4.205243642016865

> <JCHEM_POLAR_SURFACE_AREA>
25.02

> <JCHEM_REFRACTIVITY>
60.9557

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.37e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,1-dimethyl-3H,4H,9H-pyrano[3,4-b]indole

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 30 32  0  0  0  0  0  0  0  0999 V2000
   -2.2845   -1.6772    1.0157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9829   -0.4864    0.1284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5217   -0.8221   -1.2571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5561    0.6433    0.6623 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0318    1.8045    0.0847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6030    2.0336    0.4796 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1754    0.8103    0.2255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4922   -0.3798    0.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4265   -1.3666   -0.1603 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6347   -0.7790   -0.1296 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9089   -1.3197   -0.2952 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0251   -0.5129   -0.2219 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9074    0.8445    0.0164 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6555    1.4010    0.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5302    0.5756    0.1075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7482   -2.5499    0.5885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3564   -1.8706    1.1219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8337   -1.4579    2.0131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5405   -1.9439   -1.3759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7861   -0.3786   -1.9786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5217   -0.4340   -1.4358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1779    1.8048   -1.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6295    2.6523    0.4907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5674    2.3295    1.5446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2092    2.8639   -0.1374 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2031   -2.3838   -0.3209 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0202   -2.3800   -0.4825 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0206   -0.9231   -0.3492 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8150    1.4525    0.0679 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5202    2.4499    0.3702 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  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
  8  2  1  0
 15 10  1  0
 15  7  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  3 20  1  0
  3 21  1  0
  5 22  1  0
  5 23  1  0
  6 24  1  0
  6 25  1  0
  9 26  1  0
 11 27  1  0
 12 28  1  0
 13 29  1  0
 14 30  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -2.285  -1.677   1.016  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.983  -0.486   0.128  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.522  -0.822  -1.257  0.00  0.00           C+0
HETATM    4  O   UNK     0      -2.556   0.643   0.662  0.00  0.00           O+0
HETATM    5  C   UNK     0      -2.032   1.805   0.085  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.603   2.034   0.480  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.175   0.810   0.226  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.492  -0.380   0.061  0.00  0.00           C+0
HETATM    9  N   UNK     0       0.427  -1.367  -0.160  0.00  0.00           N+0
HETATM   10  C   UNK     0       1.635  -0.779  -0.130  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.909  -1.320  -0.295  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.025  -0.513  -0.222  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.907   0.845   0.016  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.656   1.401   0.183  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.530   0.576   0.108  0.00  0.00           C+0
HETATM   16  H   UNK     0      -1.748  -2.550   0.589  0.00  0.00           H+0
HETATM   17  H   UNK     0      -3.356  -1.871   1.122  0.00  0.00           H+0
HETATM   18  H   UNK     0      -1.834  -1.458   2.013  0.00  0.00           H+0
HETATM   19  H   UNK     0      -2.541  -1.944  -1.376  0.00  0.00           H+0
HETATM   20  H   UNK     0      -1.786  -0.379  -1.979  0.00  0.00           H+0
HETATM   21  H   UNK     0      -3.522  -0.434  -1.436  0.00  0.00           H+0
HETATM   22  H   UNK     0      -2.178   1.805  -1.017  0.00  0.00           H+0
HETATM   23  H   UNK     0      -2.630   2.652   0.491  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.567   2.329   1.545  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.209   2.864  -0.137  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.203  -2.384  -0.321  0.00  0.00           H+0
HETATM   27  H   UNK     0       3.020  -2.380  -0.483  0.00  0.00           H+0
HETATM   28  H   UNK     0       5.021  -0.923  -0.349  0.00  0.00           H+0
HETATM   29  H   UNK     0       4.815   1.452   0.068  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.520   2.450   0.370  0.00  0.00           H+0
CONECT    1    2   16   17   18                                             
CONECT    2    1    3    4    8                                             
CONECT    3    2   19   20   21                                             
CONECT    4    2    5                                                       
CONECT    5    4    6   22   23                                             
CONECT    6    5    7   24   25                                             
CONECT    7    6    8   15                                                  
CONECT    8    7    9    2                                                  
CONECT    9    8   10   26                                                  
CONECT   10    9   11   15                                                  
CONECT   11   10   12   27                                                  
CONECT   12   11   13   28                                                  
CONECT   13   12   14   29                                                  
CONECT   14   13   15   30                                                  
CONECT   15   14   10    7                                                  
CONECT   16    1                                                            
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    3                                                            
CONECT   20    3                                                            
CONECT   21    3                                                            
CONECT   22    5                                                            
CONECT   23    5                                                            
CONECT   24    6                                                            
CONECT   25    6                                                            
CONECT   26    9                                                            
CONECT   27   11                                                            
CONECT   28   12                                                            
CONECT   29   13                                                            
CONECT   30   14                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

RDKit          3D

30 32  0  0  0  0  0  0  0  0999 V2000
   -2.2845   -1.6772    1.0157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9829   -0.4864    0.1284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5217   -0.8221   -1.2571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5561    0.6433    0.6623 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0318    1.8045    0.0847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6030    2.0336    0.4796 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1754    0.8103    0.2255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4922   -0.3798    0.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4265   -1.3666   -0.1603 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6347   -0.7790   -0.1296 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9089   -1.3197   -0.2952 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0251   -0.5129   -0.2219 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9074    0.8445    0.0164 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6555    1.4010    0.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5302    0.5756    0.1075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7482   -2.5499    0.5885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3564   -1.8706    1.1219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8337   -1.4579    2.0131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5405   -1.9439   -1.3759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7861   -0.3786   -1.9786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5217   -0.4340   -1.4358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1779    1.8048   -1.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6295    2.6523    0.4907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5674    2.3295    1.5446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2092    2.8639   -0.1374 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2031   -2.3838   -0.3209 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0202   -2.3800   -0.4825 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0206   -0.9231   -0.3492 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8150    1.4525    0.0679 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5202    2.4499    0.3702 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  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
  8  2  1  0
 15 10  1  0
 15  7  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  3 20  1  0
  3 21  1  0
  5 22  1  0
  5 23  1  0
  6 24  1  0
  6 25  1  0
  9 26  1  0
 11 27  1  0
 12 28  1  0
 13 29  1  0
 14 30  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₃H₁₅NO

Average Mass

201.2690 Da

Monoisotopic Mass

201.11536 Da

IUPAC Name

1,1-dimethyl-1H,3H,4H,9H-pyrano[3,4-b]indole

Traditional Name

1,1-dimethyl-3H,4H,9H-pyrano[3,4-b]indole

CAS Registry Number

Not Available

SMILES

CC1(C)OCCC2=C1NC1=CC=CC=C21

InChI Identifier

InChI=1S/C13H15NO/c1-13(2)12-10(7-8-15-13)9-5-3-4-6-11(9)14-12/h3-6,14H,7-8H2,1-2H3

InChI Key

DEFSXUNWUSCNII-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, 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
Monascus	NPAtlas	18310957
Monascus pilosus	LOTUS Database	35616633

Species Where Detected

Species Name	Source	Reference
Monascus pilosus BCRC38072	KNApSAcK Database	22123792

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

3-alkylindoles

Alternative Parents

Substituents

3-alkylindole
Benzenoid
Heteroaromatic compound
Pyrrole
Oxacycle
Azacycle
Ether
Dialkyl ether
Organic nitrogen compound
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen 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	3.31	ALOGPS
logP	2.6	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	15.91	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	25.02 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	60.96 m³·mol⁻¹	ChemAxon
Polarizability	23.18 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA008481

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00030791

Chemspider ID

15260734

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

12230454

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Cheng MJ, Wu MD, Chen IS, Yuan GF: Secondary metabolites from the mycelia of the fungus Monascus pilosus BCRC 38072. Chem Pharm Bull (Tokyo). 2008 Mar;56(3):394-7. doi: 10.1248/cpb.56.394. [PubMed:18310957 ]

Showing NP-Card for Monaspyranoindole (NP0007628)

MOL for NP0007628 (Monaspyranoindole)

3D MOL for NP0007628 (Monaspyranoindole)

3D SDF for NP0007628 (Monaspyranoindole)

3D-SDF for NP0007628 (Monaspyranoindole)

PDB for NP0007628 (Monaspyranoindole)

3D PDB for NP0007628 (Monaspyranoindole)

SMILES for NP0007628 (Monaspyranoindole)

INCHI for NP0007628 (Monaspyranoindole)

Structure for NP0007628 (Monaspyranoindole)

3D Structure for NP0007628 (Monaspyranoindole)