NP-MRD: Showing NP-Card for 4-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2h-naphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-2h-pyrrol-3-one (NP0291023)

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Record Information

Version

2.0

Created at

2022-09-09 21:57:31 UTC

Updated at

2022-09-09 21:57:32 UTC

NP-MRD ID

NP0291023

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2h-naphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-2h-pyrrol-3-one

Description

4-{[1,6-Dimethyl-2-(prop-1-en-1-yl)-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-3,4-dihydro-2H-pyrrol-3-one belongs to the class of organic compounds known as pyrrolines. Pyrrolines are compounds containing a pyrroline ring, which is a five-member unsaturated aliphatic ring with one nitrogen atom and four carbon atoms. 4-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2h-naphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-2h-pyrrol-3-one is found in Cordyceps farinosa. 4-{[1,6-Dimethyl-2-(prop-1-en-1-yl)-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-3,4-dihydro-2H-pyrrol-3-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241511222D          

 27 29  0  0  0  0            999 V2000
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8163   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0416   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4788   -3.0781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3018   -3.1356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8321   -2.5036    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5014   -3.9361    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8017   -4.3733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7442   -5.1963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4282   -5.6576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0027   -5.5579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1698   -3.8430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3693   -4.0426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2171   -2.4072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 21 25  1  0  0  0  0
 17 25  1  0  0  0  0
 25 26  2  0  0  0  0
 16 27  1  4  0  0  0
M  END

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
    1.3617    4.1007   -0.2827 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3072    3.0844   -0.5203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2901    2.2803    0.2819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9464    1.3967    1.1634 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4198    1.7393    1.2952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3295    1.2296    0.5209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8669    0.2557   -0.5452 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0028   -0.4982   -1.1428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1595   -1.9296   -0.7301 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9448   -1.9352    0.5871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9042   -2.7334   -0.6276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6647   -1.8364   -0.7686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9203   -0.6819    0.1431 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7192   -0.0449    0.7837 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4710   -0.8648    2.0558 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4716   -0.1710   -0.0754 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2875   -0.5346   -1.4503 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7414    0.0131    0.2378 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4069    0.3957    1.4644 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8747    0.7303    2.5784 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8239    0.3468    1.2597 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0395   -0.6074    0.1765 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3624   -0.3183   -0.4427 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7530   -1.2590   -1.5467 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3912    0.9790   -0.9265 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8727   -0.2604   -0.7099 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8492   -0.2114   -1.9563 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0327    4.7670    0.5825 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4154    4.7770   -1.1523 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3256    3.6644   -0.0328 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0037    3.0366   -1.6144 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4958    2.8146    1.3105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6127    1.4664    2.2470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6880    2.4374    2.0702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3475    1.5180    0.6624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3336    0.8513   -1.2980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0458   -0.3908   -2.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9399    0.0233   -0.7823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8090   -2.4282   -1.4745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9503   -0.9222    1.0244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4414   -2.6330    1.2885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9715   -2.2875    0.4582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8214   -3.5830   -1.2978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8336   -3.1463    0.3980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7108   -1.5070   -1.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7662   -2.4052   -0.5409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5631   -1.1114    1.0063 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4884   -1.4049    1.9896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3174   -1.6227    2.1938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5591   -0.1989    2.9067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0737    0.2373   -2.0313 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5658    0.8505    1.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9364   -1.6358    0.5573 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1369   -0.4342    0.3809 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6622   -0.8346   -2.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9837   -1.3371   -2.3137 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0118   -2.2596   -1.1514 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8230    1.0337   -1.8324 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
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  6
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 22 26  1  0
 26 27  2  0
 14  4  1  0
 26 18  1  0
 13  7  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  3 32  1  0
  4 33  1  1
  5 34  1  0
  6 35  1  0
  7 36  1  6
  8 37  1  0
  8 38  1  0
  9 39  1  6
 10 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 12 45  1  0
 12 46  1  0
 13 47  1  1
 15 48  1  0
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 15 50  1  0
 17 51  1  0
 21 52  1  0
 22 53  1  1
 23 54  1  1
 24 55  1  0
 24 56  1  0
 24 57  1  0
 25 58  1  0
M  END


  Mrv1533004241511222D          

 27 29  0  0  0  0            999 V2000
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8163   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0416   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4788   -3.0781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3018   -3.1356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8321   -2.5036    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5014   -3.9361    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8017   -4.3733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7442   -5.1963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4282   -5.6576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0027   -5.5579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1698   -3.8430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3693   -4.0426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2171   -2.4072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 21 25  1  0  0  0  0
 17 25  1  0  0  0  0
 25 26  2  0  0  0  0
 16 27  1  4  0  0  0
M  END
> <DATABASE_ID>
NP0291023

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=CC1C=CC2CC(C)CCC2C1(C)C(O)=C1C(=O)NC(C(C)O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H31NO4/c1-5-6-15-9-8-14-11-12(2)7-10-16(14)22(15,4)20(26)17-19(25)18(13(3)24)23-21(17)27/h5-6,8-9,12-16,18,24,26H,7,10-11H2,1-4H3,(H,23,27)

> <INCHI_KEY>
MOMBVLIMWZDBMW-UHFFFAOYSA-N

> <FORMULA>
C22H31NO4

> <MOLECULAR_WEIGHT>
373.493

> <EXACT_MASS>
373.225308482

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
41.672647045419666

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-{[1,6-dimethyl-2-(prop-1-en-1-yl)-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl](hydroxy)methylidene}-5-(1-hydroxyethyl)pyrrolidine-2,4-dione

> <ALOGPS_LOGP>
2.90

> <JCHEM_LOGP>
2.8624925773333327

> <ALOGPS_LOGS>
-4.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
10.421546120585782

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.6854050382587245

> <JCHEM_PKA_STRONGEST_BASIC>
-0.9501460514195715

> <JCHEM_POLAR_SURFACE_AREA>
86.63000000000001

> <JCHEM_REFRACTIVITY>
107.75369999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.47e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2H-naphthalen-1-yl](hydroxy)methylidene}-5-(1-hydroxyethyl)pyrrolidine-2,4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.390  -4.440   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.944  -4.440   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.760  -5.746   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.297  -5.853   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.287  -4.673   0.000  0.00  0.00           O+0
HETATM   20  N   UNK     0       4.669  -7.347   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       3.363  -8.163   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.256  -9.700   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.533 -10.561   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.872 -10.375   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.184  -7.174   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.689  -7.546   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       0.405  -4.493   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   14                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   13                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    7   14                                                  
CONECT   14   13    4   15   16                                             
CONECT   15   14                                                            
CONECT   16   14   17   27                                                  
CONECT   17   16   18   25                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   25                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   21   17   26                                                  
CONECT   26   25                                                            
CONECT   27   16                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₁NO₄

Average Mass

373.4930 Da

Monoisotopic Mass

373.22531 Da

IUPAC Name

3-{[1,6-dimethyl-2-(prop-1-en-1-yl)-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl](hydroxy)methylidene}-5-(1-hydroxyethyl)pyrrolidine-2,4-dione

Traditional Name

3-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2H-naphthalen-1-yl](hydroxy)methylidene}-5-(1-hydroxyethyl)pyrrolidine-2,4-dione

CAS Registry Number

Not Available

SMILES

CC=CC1C=CC2CC(C)CCC2C1(C)C(O)=C1C(=O)NC(C(C)O)C1=O

InChI Identifier

InChI=1S/C22H31NO4/c1-5-6-15-9-8-14-11-12(2)7-10-16(14)22(15,4)20(26)17-19(25)18(13(3)24)23-21(17)27/h5-6,8-9,12-16,18,24,26H,7,10-11H2,1-4H3,(H,23,27)

InChI Key

MOMBVLIMWZDBMW-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Cordyceps farinosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrrolines. Pyrrolines are compounds containing a pyrroline ring, which is a five-member unsaturated aliphatic ring with one nitrogen atom and four carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrrolines

Sub Class

Not Available

Direct Parent

Pyrrolines

Alternative Parents

Substituents

Pyrroline
Vinylogous acid
Cyclic carboximidic acid
Ketone
Secondary alcohol
Lactim
Cyclic ketone
Enol
Azacycle
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Organic oxide
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	2.9	ALOGPS
logP	2.86	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	4.69	ChemAxon
pKa (Strongest Basic)	-0.95	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.63 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	107.75 m³·mol⁻¹	ChemAxon
Polarizability	41.67 Å³	ChemAxon
Number of Rings	3	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

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2h-naphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-2h-pyrrol-3-one (NP0291023)

MOL for NP0291023 (4-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2h-naphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-2h-pyrrol-3-one)

3D MOL for NP0291023 (4-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2h-naphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-2h-pyrrol-3-one)

3D SDF for NP0291023 (4-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2h-naphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-2h-pyrrol-3-one)

3D-SDF for NP0291023 (4-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2h-naphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-2h-pyrrol-3-one)

PDB for NP0291023 (4-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2h-naphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-2h-pyrrol-3-one)

3D PDB for NP0291023 (4-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2h-naphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-2h-pyrrol-3-one)

SMILES for NP0291023 (4-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2h-naphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-2h-pyrrol-3-one)

INCHI for NP0291023 (4-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2h-naphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-2h-pyrrol-3-one)

Structure for NP0291023 (4-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2h-naphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-2h-pyrrol-3-one)

3D Structure for NP0291023 (4-{[1,6-dimethyl-2-(prop-1-en-1-yl)-4a,5,6,7,8,8a-hexahydro-2h-naphthalen-1-yl](hydroxy)methylidene}-5-hydroxy-2-(1-hydroxyethyl)-2h-pyrrol-3-one)