NP-MRD: Showing NP-Card for 5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosane-2,8,12,18-tetrone (NP0207927)

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Record Information

Version

2.0

Created at

2022-09-05 04:43:05 UTC

Updated at

2022-09-05 04:43:05 UTC

NP-MRD ID

NP0207927

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosane-2,8,12,18-tetrone

Description

5,6,15,16-Tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]Docosane-2,8,12,18-tetrone belongs to the class of organic compounds known as epipolythiodioxopiperazines. Epipolythiodioxopiperazines are compounds containing an epipolythiodioxopiperazine moiety, which consists of a 2,3-dithia-5,7-diazabicyclo[2.2.2]Octane-6,8-dione ring system. One distinct characteristics of Epipolythiodioxopiperazines is the presence of unique di- or polysulfide bridges. Based on a literature review very few articles have been published on 5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]Docosane-2,8,12,18-tetrone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052206432D          

 30 35  0  0  0  0            999 V2000
    9.7877   -1.0292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4956   -0.2577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0177    0.3811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7256    1.1526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2477    1.7914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9113    1.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6192    2.0570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3892    0.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6813   -0.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9917   -0.6117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2463   -0.1866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5274    0.1186    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    6.8028    0.8203    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    6.0783    1.1227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3653    1.5874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6545    1.1422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8431    1.2910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5662    2.0681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3085    0.6626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5854   -0.1145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0508   -0.7429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3968   -0.2633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6737   -1.0404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9314    0.3651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7875    0.2590    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3602   -0.4655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1176   -1.2541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9535    1.4101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1896    2.2006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5337    0.6825    0.0000 N   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  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  2  9  1  0  0  0  0
  9 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  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  0  0  0  0
 14 25  1  0  0  0  0
 25 26  1  0  0  0  0
 11 26  1  0  0  0  0
 26 27  2  0  0  0  0
 14 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
  8 30  1  0  0  0  0
 11 30  1  0  0  0  0
M  END

     RDKit          3D

 50 55  0  0  0  0  0  0  0  0999 V2000
    3.7436   -0.7327   -2.0781 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0097   -0.7840   -0.8936 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2826   -0.1551   -0.4188 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9886    0.3663    0.9873 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8415    1.4130    1.3206 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5334    0.7986    1.0292 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2497    1.3681   -0.2284 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7111   -0.4594    1.1684 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1580   -1.4308    0.1309 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9398   -2.0812   -0.4451 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8311   -1.4065    0.2270 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0078   -2.4354    1.5104 S   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3361   -0.9646    2.3650 S   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0420    0.4580    1.2399 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0184    1.5402    1.4291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2261    0.8443    0.7864 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2963    1.7593    0.3843 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5547    2.7700    0.9767 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0513    1.3141   -0.8514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9385   -0.2148   -0.9374 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.4887   -0.7248    0.2129 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4749   -0.6375   -1.1187 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2915   -1.8506   -0.4442 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5628    0.3669   -0.5100 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2761   -0.1084   -0.1036 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2565   -0.9340   -0.6627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3082   -1.2339   -1.8789 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3737    0.7965    1.2869 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7235    1.9589    1.6100 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3097   -0.2450    0.9527 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0351   -0.9882   -0.3056 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6593    0.6179   -1.0878 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1626   -0.4415    1.7040 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6624    2.1957    0.7449 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3584    1.5104    1.8382 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0747    1.8251   -0.5148 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9437   -0.8860    2.1649 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7848   -2.2595    0.5740 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9178   -1.8125   -1.5411 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9191   -3.1825   -0.3032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7155    2.4248    0.8754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1960    1.7159    2.5104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5083    0.0313    1.4435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1025    1.5316   -0.6631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6271    1.7687   -1.7565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5548   -0.5519   -1.7936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9556   -1.5744    0.1134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2876   -0.7990   -2.2137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6764   -1.7851    0.4608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4759    1.3038   -1.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 19  1  0
 19 17  1  0
 17 18  2  0
 17 16  1  0
 16 15  1  0
 14 15  1  1
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  6
 10  9  1  0
  9  8  1  0
  8  6  1  0
  6  7  1  0
  6  4  1  0
  4  5  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  0
  8 30  1  0
 30 28  1  0
 28 29  2  0
 11 26  1  0
 26 27  2  0
 26 25  1  0
 25 24  1  0
 24 22  1  0
 22 23  1  0
 22 20  1  0
 24 16  1  0
 28 14  1  0
 25 14  1  0
 30 11  1  0
  2  9  1  0
 21 47  1  0
 20 46  1  6
 19 44  1  0
 19 45  1  0
 16 43  1  1
 15 41  1  0
 15 42  1  0
 10 39  1  0
 10 40  1  0
  9 38  1  1
  8 37  1  1
  6 35  1  1
  7 36  1  0
  4 33  1  1
  5 34  1  0
  3 31  1  0
  3 32  1  0
 24 50  1  6
 22 48  1  6
 23 49  1  0
M  END


  Mrv1652309052206432D          

 30 35  0  0  0  0            999 V2000
    9.7877   -1.0292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4956   -0.2577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0177    0.3811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7256    1.1526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2477    1.7914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9113    1.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6192    2.0570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3892    0.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6813   -0.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9917   -0.6117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2463   -0.1866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5274    0.1186    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    6.8028    0.8203    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    6.0783    1.1227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3653    1.5874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6545    1.1422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8431    1.2910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5662    2.0681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3085    0.6626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5854   -0.1145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0508   -0.7429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3968   -0.2633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6737   -1.0404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9314    0.3651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7875    0.2590    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3602   -0.4655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1176   -1.2541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9535    1.4101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1896    2.2006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5337    0.6825    0.0000 N   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  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  2  9  1  0  0  0  0
  9 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  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  0  0  0  0
 14 25  1  0  0  0  0
 25 26  1  0  0  0  0
 11 26  1  0  0  0  0
 26 27  2  0  0  0  0
 14 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
  8 30  1  0  0  0  0
 11 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0207927

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1CC(=O)C2CC34SSC5(CC6C(C(O)C(O)CC6=O)N5C3=O)C(=O)N4C2C1O

> <INCHI_IDENTIFIER>
InChI=1S/C18H20N2O8S2/c21-7-1-9(23)13(25)11-5(7)3-17-15(27)20-12-6(8(22)2-10(24)14(12)26)4-18(20,30-29-17)16(28)19(11)17/h5-6,9-14,23-26H,1-4H2

> <INCHI_KEY>
YNFKMTRYYNDXHU-UHFFFAOYSA-N

> <FORMULA>
C18H20N2O8S2

> <MOLECULAR_WEIGHT>
456.48

> <EXACT_MASS>
456.06610796

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
41.77955885224208

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{14,19}]docosane-2,8,12,18-tetrone

> <JCHEM_LOGP>
-1.936202140666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.400090526557918

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.842704965656011

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2462527138032318

> <JCHEM_POLAR_SURFACE_AREA>
155.68

> <JCHEM_REFRACTIVITY>
102.48140000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{14,19}]docosane-2,8,12,18-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  O   UNK     0      18.270  -1.921   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      17.725  -0.481   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      18.700   0.711   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      18.154   2.152   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      19.129   3.344   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      16.634   2.399   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      16.089   3.840   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      15.660   1.207   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      16.205  -0.233   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.918  -1.142   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.526  -0.348   0.000  0.00  0.00           C+0
HETATM   12  S   UNK     0      12.184   0.221   0.000  0.00  0.00           S+0
HETATM   13  S   UNK     0      12.699   1.531   0.000  0.00  0.00           S+0
HETATM   14  C   UNK     0      11.346   2.096   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.015   2.963   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.688   2.132   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.174   2.410   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.657   3.861   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.176   1.237   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.693  -0.214   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.695  -1.387   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.207  -0.491   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.724  -1.942   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       9.205   0.681   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0      10.803   0.484   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0      11.872  -0.869   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      11.420  -2.341   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      12.980   2.632   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      13.420   4.108   0.000  0.00  0.00           O+0
HETATM   30  N   UNK     0      14.063   1.274   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   30                                                  
CONECT    9    8    2   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   26   30                                             
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   25   28                                             
CONECT   15   14   16                                                       
CONECT   16   15   17   24                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   16   25                                                  
CONECT   25   24   14   26                                                  
CONECT   26   25   11   27                                                  
CONECT   27   26                                                            
CONECT   28   14   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28    8   11                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₀N₂O₈S₂

Average Mass

456.4800 Da

Monoisotopic Mass

456.06611 Da

IUPAC Name

5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{14,19}]docosane-2,8,12,18-tetrone

Traditional Name

5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0^{1,13}.0^{3,11}.0^{4,9}.0^{14,19}]docosane-2,8,12,18-tetrone

CAS Registry Number

Not Available

SMILES

OC1CC(=O)C2CC34SSC5(CC6C(C(O)C(O)CC6=O)N5C3=O)C(=O)N4C2C1O

InChI Identifier

InChI=1S/C18H20N2O8S2/c21-7-1-9(23)13(25)11-5(7)3-17-15(27)20-12-6(8(22)2-10(24)14(12)26)4-18(20,30-29-17)16(28)19(11)17/h5-6,9-14,23-26H,1-4H2

InChI Key

YNFKMTRYYNDXHU-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as epipolythiodioxopiperazines. Epipolythiodioxopiperazines are compounds containing an epipolythiodioxopiperazine moiety, which consists of a 2,3-dithia-5,7-diazabicyclo[2.2.2]Octane-6,8-dione ring system. One distinct characteristics of Epipolythiodioxopiperazines is the presence of unique di- or polysulfide bridges.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazinanes

Sub Class

Piperazines

Direct Parent

Epipolythiodioxopiperazines

Alternative Parents

Substituents

Epipolythiodioxopiperazine
Alpha-amino acid or derivatives
Indole or derivatives
N-alkylpiperazine
Dithiazinane
Tertiary carboxylic acid amide
Pyrrolidine
Cyclic alcohol
Secondary alcohol
Organic disulfide
Lactam
Ketone
Carboxamide group
Azacycle
Polyol
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
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	-1.9	ChemAxon
pKa (Strongest Acidic)	12.84	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	155.68 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	102.48 m³·mol⁻¹	ChemAxon
Polarizability	41.78 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

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

163064875

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosane-2,8,12,18-tetrone (NP0207927)

MOL for NP0207927 (5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosane-2,8,12,18-tetrone)

3D MOL for NP0207927 (5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosane-2,8,12,18-tetrone)

3D SDF for NP0207927 (5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosane-2,8,12,18-tetrone)

3D-SDF for NP0207927 (5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosane-2,8,12,18-tetrone)

PDB for NP0207927 (5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosane-2,8,12,18-tetrone)

3D PDB for NP0207927 (5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosane-2,8,12,18-tetrone)

SMILES for NP0207927 (5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosane-2,8,12,18-tetrone)

INCHI for NP0207927 (5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosane-2,8,12,18-tetrone)

Structure for NP0207927 (5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosane-2,8,12,18-tetrone)

3D Structure for NP0207927 (5,6,15,16-tetrahydroxy-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosane-2,8,12,18-tetrone)