NP-MRD: Showing NP-Card for (1'r,2s,3r,4s,11'r,12's)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]hexadecane]-2',4',6',8'-tetraen-3-ol (NP0296060)

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Record Information

Version

2.0

Created at

2022-09-10 05:25:09 UTC

Updated at

2022-09-10 05:25:09 UTC

NP-MRD ID

NP0296060

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1'r,2s,3r,4s,11'r,12's)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]hexadecane]-2',4',6',8'-tetraen-3-ol

Description

(1'R,2S,3R,4S,11'R,12'S)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]Hexadecane]-2',4',6',8'-tetraen-3-ol belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. (1'r,2s,3r,4s,11'r,12's)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]hexadecane]-2',4',6',8'-tetraen-3-ol is found in Agaricus blazei. Based on a literature review very few articles have been published on (1'R,2S,3R,4S,11'R,12'S)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]Hexadecane]-2',4',6',8'-tetraen-3-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102207252D          

 30 34  0  0  1  0            999 V2000
    5.5132   -0.3392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9812    0.2913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1691    0.1459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8891   -0.6301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0770   -0.7756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5450   -0.1450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8250    0.6310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6371    0.7764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9172    1.5524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2930    1.2615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3645    1.1235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2009    0.3401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7182   -0.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3136    0.6945    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3534   -0.1296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0225   -0.6123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7329   -0.2905    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1387    0.3695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7453    1.0947    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4878    1.8785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1536    2.3656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5995    2.9769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7036    2.9806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8227    1.8829    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6064    2.1405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7753    2.9480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5703    1.0975    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0575    0.4317    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9331    1.2393    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7110    2.0339    0.0000 C   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
  3  4  2  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  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 17 16  1  6  0  0  0
  6 17  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
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 24 27  1  0  0  0  0
 19 27  1  0  0  0  0
 27 28  1  1  0  0  0
 19 29  1  0  0  0  0
 14 29  1  0  0  0  0
 29 30  1  6  0  0  0
M  END

     RDKit          3D

 64 68  0  0  0  0  0  0  0  0999 V2000
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    5.1014    1.2628    2.0541 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0390    0.9394    1.1884 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6899    1.7944    0.1594 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7065   -1.1812    2.4822 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9341   -2.3020   -0.4818 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6424   -1.4358   -2.2778 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3380   -0.3163   -3.3028 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3799    0.7255   -2.4238 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6735    0.0306   -1.1498 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2684    0.2905   -0.1583 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5212   -0.1658   -0.3003 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3867    0.9483   -0.3248 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6630    1.2833    0.9685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5729    2.0593    1.6537 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9477    2.0817    1.0481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8748   -0.0055    1.7128 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2821   -0.5369    1.5279 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3534   -1.7319    2.2642 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8845   -0.9086    0.9952 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5150   -2.1061    0.7590 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8238   -0.9961   -1.4952 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8540   -0.3166   -2.4016 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3545    2.4800    0.9063 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5023    2.6929    2.6574 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0183    3.2944    1.8732 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.9057   -2.2003    2.1098 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6566   -0.8202    2.9260 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9767   -2.5694    1.3446 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5427   -3.3138   -0.3847 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2940   -2.3669   -3.3450 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0915   -0.7254   -3.1073 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5858   -2.1933   -2.1567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7509   -2.3978   -2.7843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2360    0.0788   -3.7621 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3207   -0.6904   -4.1059 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2772    1.0646   -2.9583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2986    1.6127   -2.2920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3212    2.9880    1.1391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9541    2.3332    2.6717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6899    1.3973    1.8547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8011    3.1278    0.7018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6921    1.5717    0.4033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3087    2.0707    2.1092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6352    0.0821    2.7949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3665   -0.8197    0.4503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0313    0.1810    1.8586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9671   -2.3491    1.7824 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6702    0.7685   -2.4900 H   0  0  0  0  0  0  0  0  0  0  0  0
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 21 24  1  0
 24 25  1  0
 25 26  1  0
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  7  8  2  0
  8  9  1  0
  8  3  1  0
 17  6  1  0
 27 19  1  0
 17 12  1  0
 29 14  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
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 13 41  1  0
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 16 48  1  0
 22 49  1  0
 22 50  1  0
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 30 63  1  0
 30 64  1  0
  9 36  1  0
  9 37  1  0
  9 38  1  0
M  END


  Mrv1652309102207252D          

 30 34  0  0  1  0            999 V2000
    5.5132   -0.3392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9812    0.2913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1691    0.1459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8891   -0.6301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0770   -0.7756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5450   -0.1450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8250    0.6310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6371    0.7764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9172    1.5524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2930    1.2615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3645    1.1235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3534   -0.1296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1387    0.3695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7453    1.0947    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4878    1.8785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1536    2.3656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5995    2.9769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7036    2.9806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8227    1.8829    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6064    2.1405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7753    2.9480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5703    1.0975    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0575    0.4317    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9331    1.2393    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7110    2.0339    0.0000 C   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
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 14 29  1  0  0  0  0
 29 30  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0296060

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2C(C=CC3(C)[C@@H]4CC[C@]23O[C@@]2(OC(C)(C)[C@@H](CO)[C@H]2O)[C@H]4C)=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C25H34O5/c1-14-16-9-11-23(5)17-10-12-24(23,18(16)7-8-20(14)28-6)30-25(15(17)2)21(27)19(13-26)22(3,4)29-25/h7-9,11,15,17,19,21,26-27H,10,12-13H2,1-6H3/t15-,17+,19-,21+,23?,24-,25-/m0/s1

> <INCHI_KEY>
ZQFUYFFDPNJAJG-RCGBAFMHSA-N

> <FORMULA>
C25H34O5

> <MOLECULAR_WEIGHT>
414.542

> <EXACT_MASS>
414.240624195

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
46.50422852507609

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1'R,2S,3R,4S,11'R,12'S)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0^{1,10}.0^{2,7}]hexadecane]-2',4',6',8'-tetraen-3-ol

> <JCHEM_LOGP>
3.832984241666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.389738273738942

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.87589675681346

> <JCHEM_PKA_STRONGEST_BASIC>
-2.672008261041399

> <JCHEM_POLAR_SURFACE_AREA>
68.15

> <JCHEM_REFRACTIVITY>
115.79030000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1'R,2S,3R,4S,11'R,12'S)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0^{1,10}.0^{2,7}]hexadecane]-2',4',6',8'-tetraen-3-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      10.291  -0.633   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.298   0.544   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.782   0.272   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.260  -1.176   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.744  -1.448   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.751  -0.271   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.273   1.178   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.789   1.449   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.312   2.898   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.280   2.355   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.547   2.097   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.242   0.635   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.341  -0.614   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.585   1.296   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.660  -0.242   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.909  -1.143   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.235  -0.542   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.992   0.690   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.258   2.043   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.777   3.507   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.020   4.416   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.986   5.557   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.047   5.564   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.269   3.515   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.732   3.996   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.047   5.503   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.798   2.049   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.707   0.806   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.742   2.313   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.327   3.797   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   17                                             
CONECT   13   12                                                            
CONECT   14   12   15   29                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16    6   12   18                                             
CONECT   18   17   19                                                       
CONECT   19   18   20   27   29                                             
CONECT   20   19   21                                                       
CONECT   21   20   22   23   24                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   19   28                                                  
CONECT   28   27                                                            
CONECT   29   19   14   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₄O₅

Average Mass

414.5420 Da

Monoisotopic Mass

414.24062 Da

IUPAC Name

(1'R,2S,3R,4S,11'R,12'S)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0^{1,10}.0^{2,7}]hexadecane]-2',4',6',8'-tetraen-3-ol

Traditional Name

(1'R,2S,3R,4S,11'R,12'S)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0^{1,10}.0^{2,7}]hexadecane]-2',4',6',8'-tetraen-3-ol

CAS Registry Number

Not Available

SMILES

COC1=CC=C2C(C=CC3(C)[C@@H]4CC[C@]23O[C@@]2(OC(C)(C)[C@@H](CO)[C@H]2O)[C@H]4C)=C1C

InChI Identifier

InChI=1S/C25H34O5/c1-14-16-9-11-23(5)17-10-12-24(23,18(16)7-8-20(14)28-6)30-25(15(17)2)21(27)19(13-26)22(3,4)29-25/h7-9,11,15,17,19,21,26-27H,10,12-13H2,1-6H3/t15-,17+,19-,21+,23?,24-,25-/m0/s1

InChI Key

ZQFUYFFDPNJAJG-RCGBAFMHSA-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
Agaricus blazei	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
Anisole
Ketal
Oxepane
Alkyl aryl ether
Benzenoid
Pyran
Oxane
Tetrahydrofuran
Secondary alcohol
Oxacycle
Ether
Acetal
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
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	3.83	ChemAxon
pKa (Strongest Acidic)	12.88	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	68.15 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	115.79 m³·mol⁻¹	ChemAxon
Polarizability	46.5 Å³	ChemAxon
Number of Rings	5	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

163195099

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1'r,2s,3r,4s,11'r,12's)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]hexadecane]-2',4',6',8'-tetraen-3-ol (NP0296060)

MOL for NP0296060 ((1'r,2s,3r,4s,11'r,12's)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]hexadecane]-2',4',6',8'-tetraen-3-ol)

3D MOL for NP0296060 ((1'r,2s,3r,4s,11'r,12's)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]hexadecane]-2',4',6',8'-tetraen-3-ol)

3D SDF for NP0296060 ((1'r,2s,3r,4s,11'r,12's)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]hexadecane]-2',4',6',8'-tetraen-3-ol)

3D-SDF for NP0296060 ((1'r,2s,3r,4s,11'r,12's)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]hexadecane]-2',4',6',8'-tetraen-3-ol)

PDB for NP0296060 ((1'r,2s,3r,4s,11'r,12's)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]hexadecane]-2',4',6',8'-tetraen-3-ol)

3D PDB for NP0296060 ((1'r,2s,3r,4s,11'r,12's)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]hexadecane]-2',4',6',8'-tetraen-3-ol)

SMILES for NP0296060 ((1'r,2s,3r,4s,11'r,12's)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]hexadecane]-2',4',6',8'-tetraen-3-ol)

INCHI for NP0296060 ((1'r,2s,3r,4s,11'r,12's)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]hexadecane]-2',4',6',8'-tetraen-3-ol)

Structure for NP0296060 ((1'r,2s,3r,4s,11'r,12's)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]hexadecane]-2',4',6',8'-tetraen-3-ol)

3D Structure for NP0296060 ((1'r,2s,3r,4s,11'r,12's)-4-(hydroxymethyl)-5'-methoxy-5,5,6',10',12'-pentamethyl-14'-oxaspiro[oxolane-2,13'-tetracyclo[9.3.2.0¹,¹⁰.0²,⁷]hexadecane]-2',4',6',8'-tetraen-3-ol)