NP-MRD: Showing NP-Card for (1s,2r,4s,5r,10s,12s,14r,15r,18r)-5-[(2r)-2-hydroxy-1-[(s)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]octadec-8-ene-7,16-dione (NP0155896)

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Record Information

Version

2.0

Created at

2022-09-02 13:01:55 UTC

Updated at

2022-09-02 13:01:55 UTC

NP-MRD ID

NP0155896

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,4s,5r,10s,12s,14r,15r,18r)-5-[(2r)-2-hydroxy-1-[(s)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]octadec-8-ene-7,16-dione

Description

(1S,2R,4S,5R,10S,12S,14R,15R,18R)-5-[(2R)-2-hydroxy-1-[(S)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]Octadec-8-ene-7,16-dione 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. (1s,2r,4s,5r,10s,12s,14r,15r,18r)-5-[(2r)-2-hydroxy-1-[(s)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]octadec-8-ene-7,16-dione is found in Podocarpus macrophyllus. Based on a literature review very few articles have been published on (1S,2R,4S,5R,10S,12S,14R,15R,18R)-5-[(2R)-2-hydroxy-1-[(S)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]Octadec-8-ene-7,16-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022215012D          

 29 34  0  0  1  0            999 V2000
   -1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9186   -2.6518    0.0000 S   0  3  2  0  0  0  0  0  0  0  0  0
   -1.2248   -1.8857    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -0.1021   -2.7696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4083   -2.1214    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0565   -2.6318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2399   -1.6111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9186   -1.4732    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6124   -0.7071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1227   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8165    0.7071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9393   -0.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2455   -0.9429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0620   -1.0607    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7558   -0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3889   -0.5304    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2054   -0.6482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6951   -1.2964    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1848   -1.9446    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9537   -2.2436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1106   -2.9362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7495   -3.4582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3167   -3.1607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0413   -2.3571    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2248   -2.2393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7351   -1.5911    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3682   -1.8268    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  6  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  1  0  0  0
  8  5  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 19 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 25 24  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 28 27  1  1  0  0  0
 13 28  1  0  0  0  0
 26 28  1  0  0  0  0
  8 28  1  0  0  0  0
 29 25  1  6  0  0  0
 14 29  1  0  0  0  0
 20 29  1  0  0  0  0
M  CHG  2   2   1   3  -1
M  END

     RDKit          3D

 53 58  0  0  0  0  0  0  0  0999 V2000
    5.0975    0.9796    2.0764 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2935    0.0239    0.7957 S   0  0  0  0  0  3  0  0  0  0  0  0
    5.5554   -0.6313   -0.1184 O   0  0  0  0  0  1  0  0  0  0  0  0
    3.5346    1.2375   -0.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8090    0.5847   -1.4182 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8978   -0.2069   -2.1701 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3977    1.5595   -2.2917 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7653   -0.3974   -1.0558 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3574   -1.3490   -0.1315 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5505   -2.4109    0.2787 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0158   -3.5252    0.5988 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1246   -2.1470    0.3139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3400   -0.9723   -0.0201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8155   -0.7376    0.0011 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2270   -0.7414   -1.4588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6069   -1.8375    0.6522 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9800   -1.4311    1.0540 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7798   -0.9072   -0.0804 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3953   -0.1052    0.9779 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4301    1.0153    0.7782 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5007    2.0135    1.9427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6250    1.7809   -0.4679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7368    2.1537   -0.9180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3481    2.0009   -1.0315 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3688    1.6962   -0.0899 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0058    1.4202   -0.5827 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8555    1.1309    0.5315 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5088    0.1521   -0.4431 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9947    0.5815    0.6823 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3948    1.7666    2.4097 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3802    0.2864    2.8947 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0494    1.4250    1.7091 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4037    1.7851   -0.7521 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9871    2.0035    0.2657 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8595    0.3242   -2.1349 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5883   -0.2937   -3.2321 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9655   -1.2322   -1.7650 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3548    1.2330   -3.2182 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5152   -0.9900   -1.9563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5730   -2.9631    0.6242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3189   -1.8334   -1.7408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4292   -0.3630   -2.1235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2097   -0.3091   -1.6589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1306   -2.2218    1.5922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6937   -2.7271   -0.0008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5249   -2.1821    1.6564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2827    0.2116    1.6050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3792    1.8053    2.5886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5417    3.0587    1.5698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6024    1.9410    2.5892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3025    2.5917    0.5977 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3752    2.1633   -1.3143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4941    0.5242    1.6639 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  6
  2  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  6
  5  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 28  1  0
 28 27  1  1
 27 26  1  0
 26 25  1  0
 25 24  1  0
 24 22  1  0
 22 23  2  0
 22 20  1  0
 20 21  1  1
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 14  1  0
 14 15  1  6
 14 29  1  0
 28  8  1  0
 26 28  1  0
 29 25  1  0
 14 13  1  0
 29 20  1  0
 17 19  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
  4 34  1  0
  6 35  1  0
  6 36  1  0
  6 37  1  0
  7 38  1  0
  8 39  1  6
 12 40  1  0
 26 52  1  6
 25 51  1  1
 21 48  1  0
 21 49  1  0
 21 50  1  0
 19 47  1  1
 17 46  1  1
 16 44  1  0
 16 45  1  0
 15 41  1  0
 15 42  1  0
 15 43  1  0
 29 53  1  1
M  CHG  2   2   1   3  -1
M  END


  Mrv1652309022215012D          

 29 34  0  0  1  0            999 V2000
   -1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9186   -2.6518    0.0000 S   0  3  2  0  0  0  0  0  0  0  0  0
   -1.2248   -1.8857    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -0.1021   -2.7696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4083   -2.1214    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0565   -2.6318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2399   -1.6111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9186   -1.4732    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6124   -0.7071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1227   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8165    0.7071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9393   -0.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2455   -0.9429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0620   -1.0607    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7558   -0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3889   -0.5304    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2054   -0.6482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6951   -1.2964    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1848   -1.9446    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9537   -2.2436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1106   -2.9362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7495   -3.4582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3167   -3.1607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0413   -2.3571    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2248   -2.2393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7351   -1.5911    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3682   -1.8268    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  6  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  1  0  0  0
  8  5  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 19 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 25 24  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 28 27  1  1  0  0  0
 13 28  1  0  0  0  0
 26 28  1  0  0  0  0
  8 28  1  0  0  0  0
 29 25  1  6  0  0  0
 14 29  1  0  0  0  0
 20 29  1  0  0  0  0
M  CHG  2   2   1   3  -1
M  END
> <DATABASE_ID>
NP0155896

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[S@+]([O-])C[C@](C)(O)[C@H]1OC(=O)C=C2[C@@]11O[C@@H]1[C@H]1OC(=O)[C@@]3(C)[C@H]4O[C@H]4C[C@@]2(C)[C@@H]13

> <INCHI_IDENTIFIER>
InChI=1S/C20H24O8S/c1-17-6-8-13(25-8)19(3)12(17)11(27-16(19)22)14-20(28-14)9(17)5-10(21)26-15(20)18(2,23)7-29(4)24/h5,8,11-15,23H,6-7H2,1-4H3/t8-,11-,12+,13-,14+,15+,17+,18-,19+,20-,29-/m0/s1

> <INCHI_KEY>
SZWRHPLVENMBBZ-CSBGMMFISA-N

> <FORMULA>
C20H24O8S

> <MOLECULAR_WEIGHT>
424.46

> <EXACT_MASS>
424.119188907

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
41.64939172790886

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,4S,5R,10S,12S,14R,15R,18R)-5-[(2R)-2-hydroxy-1-[(S)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0^{2,4}.0^{4,9}.0^{12,14}.0^{15,18}]octadec-8-ene-7,16-dione

> <ALOGPS_LOGP>
0.71

> <JCHEM_LOGP>
-1.0950431659999982

> <ALOGPS_LOGS>
-1.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.423045208001113

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4885600260203127

> <JCHEM_POLAR_SURFACE_AREA>
114.96

> <JCHEM_REFRACTIVITY>
99.28639999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.13e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,4S,5R,10S,12S,14R,15R,18R)-5-[(2R)-2-hydroxy-1-[(S)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0^{2,4}.0^{4,9}.0^{12,14}.0^{15,18}]octadec-8-ene-7,16-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.667  -6.160   0.000  0.00  0.00           C+0
HETATM    2  S   UNK     0      -1.715  -4.950   0.000  0.00  0.00           S+1
HETATM    3  O   UNK     0      -2.286  -3.520   0.000  0.00  0.00           O-1
HETATM    4  C   UNK     0      -0.191  -5.170   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.762  -3.960   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.972  -4.913   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.448  -3.007   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.715  -2.750   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.143  -1.320   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.096  -0.110   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.524   1.320   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.620  -0.330   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.192  -1.760   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.716  -1.980   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.144  -0.550   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.193  -0.990   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.717  -1.210   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.764  -2.420   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.812  -3.630   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.247  -4.188   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.673  -5.481   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.866  -6.455   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       6.191  -5.900   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.811  -4.400   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.286  -4.180   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.239  -2.970   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.287  -3.410   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7    8                                             
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    5    9   28                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   28                                                  
CONECT   14   13   15   16   29                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17   19                                                       
CONECT   19   18   17   20                                                  
CONECT   20   19   21   22   29                                             
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   29                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26   28                                                       
CONECT   28   27   13   26    8                                             
CONECT   29   25   14   20                                                  
MASTER        0    0    0    0    0    0    0    0   29    0   68    0
END

View in JSmol

Synonyms

Value	Source
(1S,2R,4S,5R,10S,12S,14R,15R,18R)-5-[(2R)-2-Hydroxy-1-[(S)-methanesulphinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0,.0,.0,.0,]octadec-8-ene-7,16-dione	Generator

Chemical Formula

C₂₀H₂₄O₈S

Average Mass

424.4600 Da

Monoisotopic Mass

424.11919 Da

IUPAC Name

(1S,2R,4S,5R,10S,12S,14R,15R,18R)-5-[(2R)-2-hydroxy-1-[(S)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0^{2,4}.0^{4,9}.0^{12,14}.0^{15,18}]octadec-8-ene-7,16-dione

Traditional Name

(1S,2R,4S,5R,10S,12S,14R,15R,18R)-5-[(2R)-2-hydroxy-1-[(S)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0^{2,4}.0^{4,9}.0^{12,14}.0^{15,18}]octadec-8-ene-7,16-dione

CAS Registry Number

Not Available

SMILES

C[S@+]([O-])C[C@](C)(O)[C@H]1OC(=O)C=C2[C@@]11O[C@@H]1[C@H]1OC(=O)[C@@]3(C)[C@H]4O[C@H]4C[C@@]2(C)[C@@H]13

InChI Identifier

InChI=1S/C20H24O8S/c1-17-6-8-13(25-8)19(3)12(17)11(27-16(19)22)14-20(28-14)9(17)5-10(21)26-15(20)18(2,23)7-29(4)24/h5,8,11-15,23H,6-7H2,1-4H3/t8-,11-,12+,13-,14+,15+,17+,18-,19+,20-,29-/m0/s1

InChI Key

SZWRHPLVENMBBZ-CSBGMMFISA-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
Podocarpus macrophyllus	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
Dihydropyranone
Oxepane
Dicarboxylic acid or derivatives
Gamma butyrolactone
Pyran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Lactone
Sulfoxide
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Oxacycle
Sulfinyl compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Alcohol
Organic oxygen compound
Organosulfur compound
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	0.71	ALOGPS
logP	-1.1	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	13.42	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	114.96 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	99.29 m³·mol⁻¹	ChemAxon
Polarizability	41.65 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

62985866

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131878333

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,4s,5r,10s,12s,14r,15r,18r)-5-[(2r)-2-hydroxy-1-[(s)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]octadec-8-ene-7,16-dione (NP0155896)

MOL for NP0155896 ((1s,2r,4s,5r,10s,12s,14r,15r,18r)-5-[(2r)-2-hydroxy-1-[(s)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]octadec-8-ene-7,16-dione)

3D MOL for NP0155896 ((1s,2r,4s,5r,10s,12s,14r,15r,18r)-5-[(2r)-2-hydroxy-1-[(s)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]octadec-8-ene-7,16-dione)

3D SDF for NP0155896 ((1s,2r,4s,5r,10s,12s,14r,15r,18r)-5-[(2r)-2-hydroxy-1-[(s)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]octadec-8-ene-7,16-dione)

3D-SDF for NP0155896 ((1s,2r,4s,5r,10s,12s,14r,15r,18r)-5-[(2r)-2-hydroxy-1-[(s)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]octadec-8-ene-7,16-dione)

PDB for NP0155896 ((1s,2r,4s,5r,10s,12s,14r,15r,18r)-5-[(2r)-2-hydroxy-1-[(s)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]octadec-8-ene-7,16-dione)

3D PDB for NP0155896 ((1s,2r,4s,5r,10s,12s,14r,15r,18r)-5-[(2r)-2-hydroxy-1-[(s)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]octadec-8-ene-7,16-dione)

SMILES for NP0155896 ((1s,2r,4s,5r,10s,12s,14r,15r,18r)-5-[(2r)-2-hydroxy-1-[(s)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]octadec-8-ene-7,16-dione)

INCHI for NP0155896 ((1s,2r,4s,5r,10s,12s,14r,15r,18r)-5-[(2r)-2-hydroxy-1-[(s)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]octadec-8-ene-7,16-dione)

Structure for NP0155896 ((1s,2r,4s,5r,10s,12s,14r,15r,18r)-5-[(2r)-2-hydroxy-1-[(s)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]octadec-8-ene-7,16-dione)

3D Structure for NP0155896 ((1s,2r,4s,5r,10s,12s,14r,15r,18r)-5-[(2r)-2-hydroxy-1-[(s)-methanesulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.0²,⁴.0⁴,⁹.0¹²,¹⁴.0¹⁵,¹⁸]octadec-8-ene-7,16-dione)