NP-MRD: Showing NP-Card for ATCC 20928B (NP0061512)

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Record Information

Version

2.0

Created at

2022-04-28 06:17:05 UTC

Updated at

2022-04-28 06:17:06 UTC

NP-MRD ID

NP0061512

Secondary Accession Numbers

None

Natural Product Identification

Common Name

ATCC 20928B

Description

(2S,2'S,4'aS,6'S,8'aS)-4,6'-dihydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,5',6',7',8',8'a-octahydro-2'H,3H-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde belongs to the class of organic compounds known as benzofurans. These are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. ATCC 20928B is found in Memnoniella echinata (ATCC 20298). Based on a literature review very few articles have been published on (2S,2'S,4'aS,6'S,8'aS)-4,6'-dihydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,5',6',7',8',8'a-octahydro-2'H,3H-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282208172D          

 28 31  0  0  1  0            999 V2000
    3.4920    1.1478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0422    0.4562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4163   -0.2791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2401   -0.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6899    0.3688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3158    1.1041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5137    0.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9635    1.0167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6142   -1.0582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4380   -1.1019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8325   -0.8621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0977   -0.4871    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2273    0.3277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4061   -0.0373    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6708   -0.4113    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6270   -1.2352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3186   -1.6850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0540   -1.3109    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7456   -1.7607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0209    0.0384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0229    0.8623    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7582    1.2363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4498    0.7866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6687    1.3121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4945   -0.6370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8457    0.0534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9898    0.5457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1179    1.8832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  2  0  0  0  0
  3 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
  2 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  1  0  0  0
 15 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
 14 23  1  0  0  0  0
 21 24  1  1  0  0  0
 20 25  1  0  0  0  0
 20 26  1  0  0  0  0
 14 27  1  1  0  0  0
  1 28  1  0  0  0  0
M  END

     RDKit          3D

 60 63  0  0  0  0  0  0  0  0999 V2000
    0.2162   -2.8419   -1.5761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2419   -1.4012   -1.7870 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6714   -1.4394   -2.1932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6527   -1.2976   -1.0763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2309   -0.0963   -0.2845 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2901    0.4488    0.6060 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6136   -0.3674    1.8049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5734    0.5465   -0.2295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8872    1.8378    0.9819 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7518    2.2304    2.0335 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4557    2.0158    1.3145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5699    0.8498    1.2831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9027   -0.2873    0.3843 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8531   -1.5686    1.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1455   -0.4803   -0.7109 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6961    0.7986   -1.2458 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1135    0.8808   -0.8139 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1097    1.8165   -0.9816 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9023    2.9941   -1.6835 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3836    1.6259   -0.4512 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465    0.4661    0.2598 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0017    0.2396    0.8368 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8133    1.3171    0.5309 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6295   -0.4540    0.4121 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9239   -1.6862    1.1726 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3529   -2.6634    0.5225 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3680   -0.2579   -0.1170 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2689   -1.0730   -0.0487 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3950   -3.3380   -2.5759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5668   -3.4598   -1.0963 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1790   -2.8380   -1.0686 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3274   -1.0927   -2.7192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8932   -0.6335   -2.9356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8800   -2.3986   -2.7138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8402   -2.2003   -0.5097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6397   -1.0218   -1.5550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0521    0.7139   -1.0598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8259   -0.4295    2.5647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0344   -1.3530    1.5048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4774    0.1526    2.3191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2421    1.3259    0.2049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3361    0.8744   -1.2625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0992   -0.4279   -0.2053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2076    2.5031    0.1240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0255    3.1765    1.9386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0632    2.8693    0.6792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4269    2.4836    2.3492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3829    0.5019    2.3458 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4581    1.2164    0.9771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6219   -1.3358    2.3005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0460   -2.2531    0.9090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7818   -2.1228    1.2243 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1208    1.6914   -1.0340 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7396    0.7239   -2.3741 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9841    3.1469   -2.0741 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1797    2.3449   -0.5698 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4397   -0.6805    0.3864 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9229    0.1337    1.9416 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0502    1.3018   -0.4302 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7694   -1.7283    2.2533 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6  8  1  0
  6  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  2  0
 24 27  2  0
 27 28  1  0
 15  2  1  0
 15 28  1  1
 13  5  1  0
 27 17  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  6
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  6
  7 38  1  0
  7 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
  8 43  1  0
  9 44  1  6
 10 45  1  0
 11 46  1  0
 11 47  1  0
 12 48  1  0
 12 49  1  0
 14 50  1  0
 14 51  1  0
 14 52  1  0
 16 53  1  0
 16 54  1  0
 19 55  1  0
 20 56  1  0
 22 57  1  0
 22 58  1  0
 23 59  1  0
 25 60  1  0
M  END


  Mrv1652304282208172D          

 28 31  0  0  1  0            999 V2000
    3.4920    1.1478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0422    0.4562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4163   -0.2791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2401   -0.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6899    0.3688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3158    1.1041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5137    0.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9635    1.0167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6142   -1.0582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4380   -1.1019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8325   -0.8621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0977   -0.4871    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2273    0.3277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4061   -0.0373    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6708   -0.4113    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6270   -1.2352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3186   -1.6850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0540   -1.3109    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7456   -1.7607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0209    0.0384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0229    0.8623    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7582    1.2363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4498    0.7866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6687    1.3121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4945   -0.6370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8457    0.0534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9898    0.5457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1179    1.8832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  2  0  0  0  0
  3 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
  2 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  1  0  0  0
 15 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
 14 23  1  0  0  0  0
 21 24  1  1  0  0  0
 20 25  1  0  0  0  0
 20 26  1  0  0  0  0
 14 27  1  1  0  0  0
  1 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0061512

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC[C@H]2C(C)(C)[C@@H](O)CC[C@]2(C)[C@]11CC2=C(O)C=C(CO)C(C=O)=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O5/c1-13-5-6-18-21(2,3)19(27)7-8-22(18,4)23(13)10-15-17(26)9-14(11-24)16(12-25)20(15)28-23/h9,12-13,18-19,24,26-27H,5-8,10-11H2,1-4H3/t13-,18-,19-,22-,23-/m0/s1

> <INCHI_KEY>
QKXGRPHIBLICSC-ZQFQKCGKSA-N

> <FORMULA>
C23H32O5

> <MOLECULAR_WEIGHT>
388.504

> <EXACT_MASS>
388.22497413

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
43.18068374252338

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,2'S,4'aS,6'S,8'aS)-4,6'-dihydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,5',6',7',8',8'a-octahydro-2'H,3H-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde

> <ALOGPS_LOGP>
3.48

> <JCHEM_LOGP>
3.3967217333333326

> <ALOGPS_LOGS>
-4.27

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.871037548068411

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.433841411840949

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8351378704898197

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
107.94429999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.11e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,2'S,4'aS,6'S,8'aS)-4,6'-dihydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'H,3H-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       6.518   2.143   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.679   0.852   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.377  -0.521   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.915  -0.603   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.754   0.688   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.056   2.061   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.292   0.607   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      11.132   1.898   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.613  -1.975   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      10.151  -2.057   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       5.287  -1.609   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.916  -0.909   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.158   0.612   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.625  -0.070   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.252  -0.768   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.170  -2.306   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.461  -3.145   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.834  -2.447   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.125  -3.287   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.039   0.072   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.043   1.610   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.415   2.308   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.706   1.468   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -1.248   2.449   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -0.923  -1.189   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.579   0.100   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.714   1.019   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.820   3.515   0.000  0.00  0.00           O+0
CONECT    1    2    6   28                                                  
CONECT    2    1    3   13                                                  
CONECT    3    2    4   11                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7                                                            
CONECT    9    4   10                                                       
CONECT   10    9                                                            
CONECT   11    3   12                                                       
CONECT   12   11   13   14   18                                             
CONECT   13   12    2                                                       
CONECT   14   12   15   23   27                                             
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   12   19                                                  
CONECT   19   18                                                            
CONECT   20   15   21   25   26                                             
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22   14                                                       
CONECT   24   21                                                            
CONECT   25   20                                                            
CONECT   26   20                                                            
CONECT   27   14                                                            
CONECT   28    1                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₂O₅

Average Mass

388.5040 Da

Monoisotopic Mass

388.22497 Da

IUPAC Name

(2S,2'S,4'aS,6'S,8'aS)-4,6'-dihydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,5',6',7',8',8'a-octahydro-2'H,3H-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde

Traditional Name

(2S,2'S,4'aS,6'S,8'aS)-4,6'-dihydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethyl-3',4',4'a,6',7',8'-hexahydro-2'H,3H-spiro[1-benzofuran-2,1'-naphthalene]-7-carbaldehyde

CAS Registry Number

Not Available

SMILES

C[C@H]1CC[C@H]2C(C)(C)[C@@H](O)CC[C@]2(C)[C@]11CC2=C(O)C=C(CO)C(C=O)=C2O1

InChI Identifier

InChI=1S/C23H32O5/c1-13-5-6-18-21(2,3)19(27)7-8-22(18,4)23(13)10-15-17(26)9-14(11-24)16(12-25)20(15)28-23/h9,12-13,18-19,24,26-27H,5-8,10-11H2,1-4H3/t13-,18-,19-,22-,23-/m0/s1

InChI Key

QKXGRPHIBLICSC-ZQFQKCGKSA-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
Memnoniella echinata (ATCC 20298)	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzofurans. These are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzofurans

Sub Class

Not Available

Direct Parent

Benzofurans

Alternative Parents

Substituents

Coumaran
Benzofuran
1-hydroxy-2-unsubstituted benzenoid
Aryl-aldehyde
Alkyl aryl ether
Benzenoid
Cyclic alcohol
Secondary alcohol
Oxacycle
Ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic alcohol
Primary alcohol
Organooxygen compound
Aldehyde
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	3.48	ALOGPS
logP	3.4	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	7.43	ChemAxon
pKa (Strongest Basic)	-0.84	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	107.94 m³·mol⁻¹	ChemAxon
Polarizability	43.18 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

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

163009174

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for ATCC 20928B (NP0061512)

MOL for NP0061512 (ATCC 20928B)

3D MOL for NP0061512 (ATCC 20928B)

3D SDF for NP0061512 (ATCC 20928B)

3D-SDF for NP0061512 (ATCC 20928B)

PDB for NP0061512 (ATCC 20928B)

3D PDB for NP0061512 (ATCC 20928B)

SMILES for NP0061512 (ATCC 20928B)

INCHI for NP0061512 (ATCC 20928B)

Structure for NP0061512 (ATCC 20928B)

3D Structure for NP0061512 (ATCC 20928B)