NP-MRD: Showing NP-Card for 4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione (NP0193123)

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Record Information

Version

2.0

Created at

2022-09-04 10:29:29 UTC

Updated at

2022-09-04 10:29:29 UTC

NP-MRD ID

NP0193123

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione

Description

4-(Furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]Hexadecane-6,11-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. 4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione is found in Tinospora malabarica. 4-(Furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]Hexadecane-6,11-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231514102D          

 29 33  0  0  0  0            999 V2000
   -2.0030    1.8448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2183    1.5898    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6053    2.1418    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.1794    1.8869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7925    2.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5771    2.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7486    1.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5939    1.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1340    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9590    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4561    1.2515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8892    0.4894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7941    2.0580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6011    2.2295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0136    1.5150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4615    0.9019    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  4 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
  7 23  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 11 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 25 29  1  0  0  0  0
M  END

     RDKit          3D

 55 59  0  0  0  0  0  0  0  0999 V2000
    6.9251   -0.0592   -0.7895 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3228    0.2672   -1.5743 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.9197   -1.0859   -0.7996 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.0490   -0.5371    0.6499 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0949   -1.6420    1.0678 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7528   -1.5715    0.3726 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1659   -0.2280    0.6448 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2873   -0.0325    0.3457 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0198   -0.3611    1.6638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6824   -1.1611   -0.5779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9687   -1.0147   -1.2872 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1934   -1.1373   -0.5034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8219   -0.1540    0.2391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9505   -0.7173    0.7985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0109   -1.9898    0.4154 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9878   -2.2521   -0.3486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9417    0.2360   -1.9940 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6169    1.3469   -1.2701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1205    2.4561   -1.6357 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7008    1.3154   -0.0745 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6470    2.3554   -0.3468 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6180    2.1333    0.3670 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7771    2.7590   -0.1816 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8899    1.9579    0.1157 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0605    2.3179   -0.0846 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3807    0.7387    0.6566 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0052    1.0144    2.0031 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0245    0.7072   -0.0693 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1768    0.6087   -1.5320 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8193   -0.4439    0.2384 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4794   -0.8139   -1.4076 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5101    0.8783   -0.8503 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8207   -0.5261    1.4835 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8971   -1.6397    2.1592 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5469   -2.6170    0.8184 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9865   -1.6867   -0.7159 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1610   -2.4131    0.7223 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3526   -0.0573    1.7538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2702   -0.4886    2.4755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5658   -1.3116    1.6186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6366    0.5025    1.9941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7369   -2.1156    0.0293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9005   -1.3843   -1.3320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0044   -1.8398   -2.0513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5295    0.8752    0.3867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6449   -0.1992    1.4301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7822   -3.2030   -0.8007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3515    1.7991    0.7211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0057    3.3853   -0.1172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4212    2.3866   -1.4535 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5821    2.1810    1.4518 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6665    0.6163    2.6114 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7761    1.5156   -1.8550 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7917   -0.2405   -1.8877 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2460    0.5699   -2.0892 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  0
  7 28  1  0
 28 29  1  6
 28 22  1  0
 22 21  1  0
 21 20  1  0
 20 18  1  0
 18 19  2  0
 18 17  1  0
 17 11  1  0
 11 10  1  0
 10  8  1  0
  8  9  1  1
 11 12  1  0
 12 16  2  0
 16 15  1  0
 15 14  1  0
 14 13  2  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  1
 26  4  1  0
  8  7  1  0
 13 12  1  0
 26 28  1  0
  8 20  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  1
  5 34  1  0
  5 35  1  0
  6 36  1  0
  6 37  1  0
  7 38  1  1
 29 53  1  0
 29 54  1  0
 29 55  1  0
 22 51  1  1
 21 49  1  0
 21 50  1  0
 20 48  1  1
 11 44  1  6
 10 42  1  0
 10 43  1  0
  9 39  1  0
  9 40  1  0
  9 41  1  0
 16 47  1  0
 14 46  1  0
 13 45  1  0
 27 52  1  0
M  END


  Mrv1533004231514102D          

 29 33  0  0  0  0            999 V2000
   -2.0030    1.8448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2183    1.5898    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6053    2.1418    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.1794    1.8869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7925    2.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5771    2.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7486    1.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5939    1.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1340    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9590    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4561    1.2515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8892    0.4894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7941    2.0580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6011    2.2295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0136    1.5150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4615    0.9019    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  4 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
  7 23  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 11 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 25 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0193123

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CSSC1CCC2C3(C)C(CC4C(=O)OC(CC24C)C2=COC=C2)OC(=O)C13O

> <INCHI_IDENTIFIER>
InChI=1S/C21H26O6S2/c1-19-9-13(11-6-7-25-10-11)26-17(22)12(19)8-15-20(2)14(19)4-5-16(29-28-3)21(20,24)18(23)27-15/h6-7,10,12-16,24H,4-5,8-9H2,1-3H3

> <INCHI_KEY>
URMGJVOOVFNXOK-UHFFFAOYSA-N

> <FORMULA>
C21H26O6S2

> <MOLECULAR_WEIGHT>
438.55

> <EXACT_MASS>
438.117080905

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
44.59670498796818

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione

> <ALOGPS_LOGP>
3.73

> <JCHEM_LOGP>
2.910475713666666

> <ALOGPS_LOGS>
-3.89

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.457127267718718

> <JCHEM_PKA_STRONGEST_BASIC>
-2.888596480014417

> <JCHEM_POLAR_SURFACE_AREA>
85.97

> <JCHEM_REFRACTIVITY>
109.58559999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.61e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0      -3.739   3.444   0.000  0.00  0.00           C+0
HETATM    2  S   UNK     0      -2.274   2.968   0.000  0.00  0.00           S+0
HETATM    3  S   UNK     0      -1.130   3.998   0.000  0.00  0.00           S+0
HETATM    4  C   UNK     0       0.335   3.522   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.479   4.553   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.944   4.077   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.264   2.570   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.842   3.079   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.454  -0.000   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.121  -2.310   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.453  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.120   0.000   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.655  -0.476   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.250   0.770   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.790   0.770   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.655   2.016   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.851   2.336   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.120   1.540   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.526   0.914   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.788   2.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.949   3.842   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      10.455   4.162   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      11.225   2.828   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.195   1.684   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   21                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   23                                                  
CONECT    8    7    9   10   15                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   25                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    8   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    4   22   23                                             
CONECT   22   21                                                            
CONECT   23   21    7   17   24                                             
CONECT   24   23                                                            
CONECT   25   11   26   29                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   25                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Value	Source
4-(Furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulphanyl)-5,10-dioxatetracyclo[7.6.1.0,.0,]hexadecane-6,11-dione	Generator
4-(Furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulphanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione	Generator

Chemical Formula

C₂₁H₂₆O₆S₂

Average Mass

438.5500 Da

Monoisotopic Mass

438.11708 Da

IUPAC Name

4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione

Traditional Name

4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione

CAS Registry Number

Not Available

SMILES

CSSC1CCC2C3(C)C(CC4C(=O)OC(CC24C)C2=COC=C2)OC(=O)C13O

InChI Identifier

InChI=1S/C21H26O6S2/c1-19-9-13(11-6-7-25-10-11)26-17(22)12(19)8-15-20(2)14(19)4-5-16(29-28-3)21(20,24)18(23)27-15/h6-7,10,12-16,24H,4-5,8-9H2,1-3H3

InChI Key

URMGJVOOVFNXOK-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
Tinospora malabarica	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
Delta valerolactone
Delta_valerolactone
Dicarboxylic acid or derivatives
Gamma butyrolactone
Pyran
Oxane
Cyclic alcohol
Heteroaromatic compound
Furan
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Dialkyldisulfide
Lactone
Organic disulfide
Sulfenyl compound
Oxacycle
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Organosulfur compound
Organooxygen compound
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	3.73	ALOGPS
logP	2.91	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	11.46	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	85.97 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	109.59 m³·mol⁻¹	ChemAxon
Polarizability	44.6 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

73826770

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione (NP0193123)

MOL for NP0193123 (4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione)

3D MOL for NP0193123 (4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione)

3D SDF for NP0193123 (4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione)

3D-SDF for NP0193123 (4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione)

PDB for NP0193123 (4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione)

3D PDB for NP0193123 (4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione)

SMILES for NP0193123 (4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione)

INCHI for NP0193123 (4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione)

Structure for NP0193123 (4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione)

3D Structure for NP0193123 (4-(furan-3-yl)-12-hydroxy-2,16-dimethyl-13-(methyldisulfanyl)-5,10-dioxatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadecane-6,11-dione)