NP-MRD: Showing NP-Card for (1r,5r,5as,9as,9bs)-1,9b-dihydroxy-6,6,9a-trimethyl-1h,3h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-5-yl (2e,4e,6e)-octa-2,4,6-trienoate (NP0190095)

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Record Information

Version

2.0

Created at

2022-09-04 06:42:36 UTC

Updated at

2022-09-04 06:42:36 UTC

NP-MRD ID

NP0190095

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,5r,5as,9as,9bs)-1,9b-dihydroxy-6,6,9a-trimethyl-1h,3h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-5-yl (2e,4e,6e)-octa-2,4,6-trienoate

Description

MEGxm0_000040 belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. (1r,5r,5as,9as,9bs)-1,9b-dihydroxy-6,6,9a-trimethyl-1h,3h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-5-yl (2e,4e,6e)-octa-2,4,6-trienoate is found in Aspergillus pseudodeflectus. Based on a literature review very few articles have been published on MEGxm0_000040.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042208422D          

 28 30  0  0  1  0            999 V2000
    6.0967    0.9592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2721    0.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8821    1.7119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0575    1.7377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6675    2.4647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8429    2.4905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4529    3.2175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6283    3.2432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2383    3.9702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1937    2.5420    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837    1.8150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4083    1.7892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983    1.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5995    0.8656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6601    0.0428    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8963   -0.2691    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6996   -1.0703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3637    0.3610    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0047   -0.3819    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    0.3867    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6853   -0.4252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1045   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3245    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4416    1.4457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4930    1.9471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491    1.1137    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 11 10  1  6  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  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 28 25  1  6  0  0  0
 11 28  1  0  0  0  0
 20 28  1  0  0  0  0
M  END

     RDKit          3D

 60 62  0  0  0  0  0  0  0  0999 V2000
    9.1817   -0.9537    1.8678 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2639    0.0473    1.3083 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9717   -0.2965    1.1882 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0476    0.6563    0.6440 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8322    0.5221    0.4651 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4668    0.3722    0.2637 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9541   -0.8119    0.6656 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6061   -1.1568    0.5491 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695   -2.3061    1.0177 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5425   -0.4470   -0.0040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7673   -0.9195   -0.0328 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0152   -1.6408   -1.3581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1963   -1.8318   -1.8608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7435   -2.4742   -3.0746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1282   -2.4000   -2.9748 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4468   -1.2873   -2.2095 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7076   -1.5128   -1.6184 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4189   -1.2719   -1.1430 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6775   -2.0343   -0.0452 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9241    0.1494   -0.7916 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2909    0.6854   -2.0285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0319    0.9926   -0.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5407    2.3936   -0.0844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0776    2.4474    0.2962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6355    1.2080    1.0668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1994    1.4770    1.4476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4175    1.2690    2.3901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8847   -0.0680    0.3362 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.7743   -0.5304    2.6914 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8209   -1.4612    1.1230 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5915   -1.7819    2.3442 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5571    1.0330    0.9945 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6995   -1.2887    1.5121 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4786    1.6099    0.3784 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8278    1.7988   -0.0684 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7100    1.0192   -0.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6664   -1.5112    1.1023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7393   -1.8554    0.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1354   -1.9911   -1.8650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3929   -2.0603   -4.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4761   -3.5689   -3.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4929   -0.3469   -2.8024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5635   -2.2840   -0.9833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3496   -1.6601    0.5830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7401    1.7014   -2.2424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4908    0.0598   -2.9478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2166    0.8443   -1.9825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8412    1.0312   -1.0657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5121    0.5742    0.6268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1709    2.8545    0.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7298    2.9878   -0.9990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9833    3.2933    1.0329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4020    2.7293   -0.5188 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1960    0.7263    2.1315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2229    2.4302    2.0785 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4434    1.7618    0.6017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6905    0.2243    2.6691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3309    1.8468    2.3015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8035    1.6939    3.2139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5135   -0.6878    1.0679 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  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  1
 18 20  1  0
 20 21  1  6
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 28 11  1  0
 18 13  1  0
 28 20  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  3 33  1  0
  4 34  1  0
  5 35  1  0
  6 36  1  0
  7 37  1  0
 11 38  1  1
 12 39  1  0
 14 40  1  0
 14 41  1  0
 16 42  1  6
 17 43  1  0
 19 44  1  0
 21 45  1  0
 21 46  1  0
 21 47  1  0
 22 48  1  0
 22 49  1  0
 23 50  1  0
 23 51  1  0
 24 52  1  0
 24 53  1  0
 26 54  1  0
 26 55  1  0
 26 56  1  0
 27 57  1  0
 27 58  1  0
 27 59  1  0
 28 60  1  1
M  END


  Mrv1652309042208422D          

 28 30  0  0  1  0            999 V2000
    6.0967    0.9592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2721    0.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8821    1.7119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0575    1.7377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6675    2.4647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8429    2.4905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4529    3.2175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6283    3.2432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2383    3.9702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1937    2.5420    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837    1.8150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4083    1.7892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983    1.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5995    0.8656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6601    0.0428    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8963   -0.2691    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6996   -1.0703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3637    0.3610    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0047   -0.3819    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    0.3867    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6853   -0.4252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1045   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3245    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4416    1.4457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4930    1.9471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491    1.1137    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 11 10  1  6  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  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 28 25  1  6  0  0  0
 11 28  1  0  0  0  0
 20 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0190095

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C\C=C\C=C\C(=O)O[C@@H]1C=C2CO[C@@H](O)[C@]2(O)[C@@]2(C)CCCC(C)(C)[C@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O5/c1-5-6-7-8-9-11-18(24)28-17-14-16-15-27-20(25)23(16,26)22(4)13-10-12-21(2,3)19(17)22/h5-9,11,14,17,19-20,25-26H,10,12-13,15H2,1-4H3/b6-5+,8-7+,11-9+/t17-,19+,20-,22+,23+/m1/s1

> <INCHI_KEY>
BIBMODCOJDZAGU-UFVLLNNXSA-N

> <FORMULA>
C23H32O5

> <MOLECULAR_WEIGHT>
388.504

> <EXACT_MASS>
388.22497413

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
43.353734797065705

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,5R,5aS,9aS,9bS)-1,9b-dihydroxy-6,6,9a-trimethyl-1H,3H,5H,5aH,6H,7H,8H,9H,9aH,9bH-naphtho[1,2-c]furan-5-yl (2E,4E,6E)-octa-2,4,6-trienoate

> <JCHEM_LOGP>
3.8298468849999985

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.004623523378935

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.13007929692271

> <JCHEM_PKA_STRONGEST_BASIC>
-4.0459269202890615

> <JCHEM_POLAR_SURFACE_AREA>
75.99000000000001

> <JCHEM_REFRACTIVITY>
111.38669999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,5R,5aS,9aS,9bS)-1,9b-dihydroxy-6,6,9a-trimethyl-1H,3H,5H,5aH,7H,8H,9H-naphtho[1,2-c]furan-5-yl (2E,4E,6E)-octa-2,4,6-trienoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      11.380   1.790   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.841   1.839   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.113   3.196   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.574   3.244   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.846   4.601   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.307   4.649   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.579   6.006   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.040   6.054   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.312   7.411   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       2.228   4.745   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.956   3.388   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.495   3.340   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.223   1.983   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.719   1.616   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.832   0.080   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.406  -0.502   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.039  -1.998   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.412   0.674   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.742  -0.713   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.873   0.722   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.146  -0.794   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.062  -0.587   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.522  -0.539   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.206   0.818   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.606   2.127   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.824   2.699   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.920   3.635   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.145   2.079   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   28                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   13   19   20                                             
CONECT   19   18                                                            
CONECT   20   18   21   22   28                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25   11   20                                                  
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₂O₅

Average Mass

388.5040 Da

Monoisotopic Mass

388.22497 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C\C=C\C=C\C=C\C(=O)O[C@@H]1C=C2CO[C@@H](O)[C@]2(O)[C@@]2(C)CCCC(C)(C)[C@H]12

InChI Identifier

InChI=1S/C23H32O5/c1-5-6-7-8-9-11-18(24)28-17-14-16-15-27-20(25)23(16,26)22(4)13-10-12-21(2,3)19(17)22/h5-9,11,14,17,19-20,25-26H,10,12-13,15H2,1-4H3/b6-5+,8-7+,11-9+/t17-,19+,20-,22+,23+/m1/s1

InChI Key

BIBMODCOJDZAGU-UFVLLNNXSA-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
Aspergillus pseudodeflectus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four 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

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
Fatty acid ester
Fatty acyl
Oxolane
Tertiary alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Hemiacetal
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Organooxygen compound
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Hydrocarbon derivative
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

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

8843372

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10668020

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,5r,5as,9as,9bs)-1,9b-dihydroxy-6,6,9a-trimethyl-1h,3h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-5-yl (2e,4e,6e)-octa-2,4,6-trienoate (NP0190095)

MOL for NP0190095 ((1r,5r,5as,9as,9bs)-1,9b-dihydroxy-6,6,9a-trimethyl-1h,3h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-5-yl (2e,4e,6e)-octa-2,4,6-trienoate)

3D MOL for NP0190095 ((1r,5r,5as,9as,9bs)-1,9b-dihydroxy-6,6,9a-trimethyl-1h,3h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-5-yl (2e,4e,6e)-octa-2,4,6-trienoate)

3D SDF for NP0190095 ((1r,5r,5as,9as,9bs)-1,9b-dihydroxy-6,6,9a-trimethyl-1h,3h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-5-yl (2e,4e,6e)-octa-2,4,6-trienoate)

3D-SDF for NP0190095 ((1r,5r,5as,9as,9bs)-1,9b-dihydroxy-6,6,9a-trimethyl-1h,3h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-5-yl (2e,4e,6e)-octa-2,4,6-trienoate)

PDB for NP0190095 ((1r,5r,5as,9as,9bs)-1,9b-dihydroxy-6,6,9a-trimethyl-1h,3h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-5-yl (2e,4e,6e)-octa-2,4,6-trienoate)

3D PDB for NP0190095 ((1r,5r,5as,9as,9bs)-1,9b-dihydroxy-6,6,9a-trimethyl-1h,3h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-5-yl (2e,4e,6e)-octa-2,4,6-trienoate)

SMILES for NP0190095 ((1r,5r,5as,9as,9bs)-1,9b-dihydroxy-6,6,9a-trimethyl-1h,3h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-5-yl (2e,4e,6e)-octa-2,4,6-trienoate)

INCHI for NP0190095 ((1r,5r,5as,9as,9bs)-1,9b-dihydroxy-6,6,9a-trimethyl-1h,3h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-5-yl (2e,4e,6e)-octa-2,4,6-trienoate)

Structure for NP0190095 ((1r,5r,5as,9as,9bs)-1,9b-dihydroxy-6,6,9a-trimethyl-1h,3h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-5-yl (2e,4e,6e)-octa-2,4,6-trienoate)

3D Structure for NP0190095 ((1r,5r,5as,9as,9bs)-1,9b-dihydroxy-6,6,9a-trimethyl-1h,3h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-5-yl (2e,4e,6e)-octa-2,4,6-trienoate)