NP-MRD: Showing NP-Card for pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol (NP0184853)

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Record Information

Version

1.0

Created at

2022-09-04 00:05:16 UTC

Updated at

2022-09-04 00:05:17 UTC

NP-MRD ID

NP0184853

Secondary Accession Numbers

None

Natural Product Identification

Common Name

pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol

Description

Pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]Octacosa-1(24),2,4,6,10(28),11,13,15,17,19(27),20,22,25-tridecaene-5,13,16,24-tetrol belongs to the class of organic compounds known as 1-hydroxy-4-unsubstituted benzenoids. These are phenols that are unsubstituted at the 4-position. pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol is found in Herbertus dicranus and Herbertus sakuraii. Based on a literature review very few articles have been published on pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]Octacosa-1(24),2,4,6,10(28),11,13,15,17,19(27),20,22,25-tridecaene-5,13,16,24-tetrol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042202052D          

 32 36  0  0  0  0            999 V2000
   -1.6373   -0.2899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8806   -0.6186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7868   -1.4382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0301   -1.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6328   -1.2759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5391   -0.4563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2176   -0.1276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8902    0.3957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5504    0.9960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4472    1.0707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1645    0.2971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6236   -0.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4264   -0.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6736   -1.0308    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8248    0.4804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3042    1.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4084   -0.1973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0478   -0.9610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4216   -1.7082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2567   -1.6603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6646   -0.9381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2419   -0.2187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6609    0.4920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9876   -2.4574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3282   -3.0012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4466   -3.1127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6655   -3.4179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9941   -2.9271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0217   -2.0758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8006   -1.8020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9152   -0.9850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4692   -2.2761    0.0000 C   0  0  0  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
  2  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 10 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 24 19  1  4  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 26 32  1  0  0  0  0
M  END

     RDKit          3D

 54 58  0  0  0  0  0  0  0  0999 V2000
    6.2165   -3.1364   -0.9475 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2397   -2.2079   -0.5724 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5277   -1.1979    0.2994 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5580   -0.3341    0.6317 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1914   -0.3314    0.1701 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9409   -1.3817   -0.7268 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9779   -2.2695   -1.0519 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7349   -1.6852   -1.5264 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7663   -2.6819   -1.1177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6542   -2.2504   -0.8156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5693   -3.2579   -1.1124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9281   -3.1267   -0.9505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3634   -1.8876   -0.4564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7414   -1.7607   -0.2758 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4802   -0.8819   -0.1622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0824   -1.0581   -0.3392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0792    0.4766    0.2412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5957    1.2690    1.2725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8614    2.5913    1.3229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6739    3.1582    0.3311 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2113    2.4388   -0.7101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8924    1.1003   -0.7303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4433    0.3929   -1.8114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1108    3.6322    2.1335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7631    3.6530    2.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1700    2.6135    1.7095 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5107    1.4391    2.3627 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4306    0.5490    1.8281 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1470    0.6463    0.6226 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7680    1.8342   -0.0135 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2193    2.3600   -1.2930 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8383    2.7559    0.5012 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3111   -3.9910   -0.3755 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5406   -1.1486    0.6817 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9018    0.4483    1.3234 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7717   -3.1024   -1.7586 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0925   -1.9508   -2.5927 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1923   -0.7206   -1.8064 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7404   -3.4779   -1.9394 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1091   -3.2675   -0.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2299   -4.2456   -1.5039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6334   -3.9070   -1.1798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2492   -1.0208    0.1157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3432   -0.2459   -0.0501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1139    0.7219    2.2090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9200    4.2403    0.3750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8440    2.8980   -1.4627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0142    0.7997   -2.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6799    4.4446    2.5717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4912    4.5472    2.9687 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0876    1.0305    3.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4249   -0.3387    2.5611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8688    3.2053   -1.6142 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6907    3.6200   -0.2623 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  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 19 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  1  0
 30 32  2  0
  6  7  2  0
  7  2  1  0
 29  5  1  0
 16 10  1  0
 22 17  1  0
 32 26  1  0
  1 33  1  0
  3 34  1  0
  4 35  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 11 41  1  0
 12 42  1  0
 14 43  1  0
 16 44  1  0
 18 45  1  0
 20 46  1  0
 21 47  1  0
 23 48  1  0
 24 49  1  0
 25 50  1  0
 27 51  1  0
 28 52  1  0
 31 53  1  0
 32 54  1  0
  7 36  1  0
M  END


  Mrv1652309042202052D          

 32 36  0  0  0  0            999 V2000
   -1.6373   -0.2899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8806   -0.6186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7868   -1.4382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0301   -1.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6328   -1.2759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5391   -0.4563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2176   -0.1276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8902    0.3957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5504    0.9960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4472    1.0707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1645    0.2971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6236   -0.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4264   -0.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6736   -1.0308    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8248    0.4804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3042    1.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4084   -0.1973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0478   -0.9610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4216   -1.7082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2567   -1.6603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6646   -0.9381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2419   -0.2187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6609    0.4920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9876   -2.4574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3282   -3.0012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4466   -3.1127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6655   -3.4179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9941   -2.9271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0217   -2.0758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8006   -1.8020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9152   -0.9850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4692   -2.2761    0.0000 C   0  0  0  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
  2  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 10 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 24 19  1  4  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 26 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0184853

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C2C(CCC3=CC=C(O)C(=C3)C3=CC(=CC=C3O)C=CC3=CC=C2C(O)=C3)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C28H22O4/c29-21-8-10-22-20(16-21)7-3-18-6-12-27(31)25(14-18)24-13-17(5-11-26(24)30)1-2-19-4-9-23(22)28(32)15-19/h1-2,4-6,8-16,29-32H,3,7H2

> <INCHI_KEY>
AANIEYOTXCALEB-UHFFFAOYSA-N

> <FORMULA>
C28H22O4

> <MOLECULAR_WEIGHT>
422.48

> <EXACT_MASS>
422.151809188

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
44.97601940850533

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
pentacyclo[20.2.2.1^{10,14}.1^{15,19}.0^{2,7}]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol

> <JCHEM_LOGP>
6.956393164666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.242395526479346

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.694935930084855

> <JCHEM_PKA_STRONGEST_BASIC>
-5.495219704536088

> <JCHEM_POLAR_SURFACE_AREA>
80.92

> <JCHEM_REFRACTIVITY>
127.989

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
pentacyclo[20.2.2.1^{10,14}.1^{15,19}.0^{2,7}]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol

> <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  O   UNK     0      -3.056  -0.541   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -1.644  -1.155   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.469  -2.685   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.056  -3.298   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.181  -2.382   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.006  -0.852   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.406  -0.238   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.662   0.739   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.894   1.859   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.568   1.999   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.040   0.555   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.897  -0.711   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.396  -0.455   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.857  -1.924   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       7.140   0.897   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.168   2.151   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.229  -0.368   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.556  -1.794   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.254  -3.189   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.812  -3.099   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.574  -1.751   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.785  -0.408   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.567   0.918   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       7.444  -4.587   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.213  -5.602   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.567  -5.810   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.109  -6.380   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.856  -5.464   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.907  -3.875   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.361  -3.364   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       3.575  -1.839   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.609  -4.249   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   29                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6    2                                                       
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15   10                                                       
CONECT   17   15   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17   23                                                  
CONECT   23   22                                                            
CONECT   24   19   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   32                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28    5   30                                                  
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   26                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₂₂O₄

Average Mass

422.4800 Da

Monoisotopic Mass

422.15181 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

OC1=CC=C2C(CCC3=CC=C(O)C(=C3)C3=CC(=CC=C3O)C=CC3=CC=C2C(O)=C3)=C1

InChI Identifier

InChI=1S/C28H22O4/c29-21-8-10-22-20(16-21)7-3-18-6-12-27(31)25(14-18)24-13-17(5-11-26(24)30)1-2-19-4-9-23(22)28(32)15-19/h1-2,4-6,8-16,29-32H,3,7H2

InChI Key

AANIEYOTXCALEB-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
Herbertus dicranus	LOTUS Database	35616633
Herbertus sakuraii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-hydroxy-4-unsubstituted benzenoids. These are phenols that are unsubstituted at the 4-position.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenols

Sub Class

1-hydroxy-4-unsubstituted benzenoids

Direct Parent

1-hydroxy-4-unsubstituted benzenoids

Alternative Parents

Substituents

1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Polyol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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

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

85355066

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol (NP0184853)

MOL for NP0184853 (pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

3D MOL for NP0184853 (pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

3D SDF for NP0184853 (pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

3D-SDF for NP0184853 (pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

PDB for NP0184853 (pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

3D PDB for NP0184853 (pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

SMILES for NP0184853 (pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

INCHI for NP0184853 (pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

Structure for NP0184853 (pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)

3D Structure for NP0184853 (pentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol)