NP-MRD: Showing NP-Card for Cephalosporolide C (NP0005601)

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Record Information

Version

2.0

Created at

2020-12-09 02:48:41 UTC

Updated at

2021-07-15 16:52:28 UTC

NP-MRD ID

NP0005601

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Cephalosporolide C

Provided By

NPAtlas

Description

(4S,5S,10R)-4,5-dihydroxy-10-methyloxecane-2,7-dione belongs to the class of organic compounds known as lactones. These are cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. Cephalosporolide C is found in Cordyceps. Based on a literature review very few articles have been published on (4S,5S,10R)-4,5-dihydroxy-10-methyloxecane-2,7-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118213D          

 31 31  0  0  0  0            999 V2000
    3.5539   -0.7902   -0.1324 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0660   -0.5031   -0.3893 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9548    0.9047   -0.8517 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8994    1.7113   -0.1729 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4313    1.4987   -0.7814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4798    1.2409   -1.9706 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7179    1.5778   -0.0402 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3932    0.2088   -0.2004 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7707    0.3040   -0.0830 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8018   -0.7497    0.8101 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7802   -1.4923    1.4561 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7646   -1.6612    0.1661 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4395   -1.7460    1.0240 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4632   -2.6676    1.8682 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4074   -0.7982    0.7999 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1659   -0.4620   -0.9747 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8079   -0.2561    0.8222 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6313   -1.8837    0.0059 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7913   -1.1669   -1.2396 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9273    1.4679   -0.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7506    0.9684   -1.9608 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1501    2.7995   -0.3485 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8976    1.5886    0.9279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5347    1.7616    1.0532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3946    2.3311   -0.4446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1353   -0.1647   -1.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0735    1.0787    0.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2763   -0.1589    1.5868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6472   -1.0173    1.4519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4828   -1.2707   -0.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2221   -2.6534   -0.0298 H   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  2  0  0  0  0
  5  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
 10 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
 15  2  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  2 19  1  6  0  0  0
  3 20  1  0  0  0  0
  3 21  1  0  0  0  0
  4 22  1  0  0  0  0
  4 23  1  0  0  0  0
  7 24  1  0  0  0  0
  7 25  1  0  0  0  0
  8 26  1  6  0  0  0
  9 27  1  0  0  0  0
 10 28  1  1  0  0  0
 11 29  1  0  0  0  0
 12 30  1  0  0  0  0
 12 31  1  0  0  0  0
M  END

     RDKit          3D

 31 31  0  0  0  0  0  0  0  0999 V2000
    3.5539   -0.7902   -0.1324 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0660   -0.5031   -0.3893 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9548    0.9047   -0.8517 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8994    1.7113   -0.1729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4313    1.4987   -0.7814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4798    1.2409   -1.9706 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7179    1.5778   -0.0402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3932    0.2088   -0.2004 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7707    0.3040   -0.0830 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8018   -0.7497    0.8101 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7802   -1.4923    1.4561 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7646   -1.6612    0.1661 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4395   -1.7460    1.0240 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4632   -2.6676    1.8682 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4074   -0.7982    0.7999 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1659   -0.4620   -0.9747 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8079   -0.2561    0.8222 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6313   -1.8837    0.0059 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7913   -1.1669   -1.2396 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9273    1.4679   -0.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7506    0.9684   -1.9608 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1501    2.7995   -0.3485 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8976    1.5886    0.9279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5347    1.7616    1.0532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3946    2.3311   -0.4446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1353   -0.1647   -1.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0735    1.0787    0.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2763   -0.1589    1.5868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6472   -1.0173    1.4519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4828   -1.2707   -0.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2221   -2.6534   -0.0298 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  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15  2  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  6
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  7 24  1  0
  7 25  1  0
  8 26  1  6
  9 27  1  0
 10 28  1  1
 11 29  1  0
 12 30  1  0
 12 31  1  0
M  END


  Mrv1652306242118213D          

 31 31  0  0  0  0            999 V2000
    3.5539   -0.7902   -0.1324 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0660   -0.5031   -0.3893 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9548    0.9047   -0.8517 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8994    1.7113   -0.1729 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4313    1.4987   -0.7814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4798    1.2409   -1.9706 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7179    1.5778   -0.0402 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3932    0.2088   -0.2004 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7707    0.3040   -0.0830 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8018   -0.7497    0.8101 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7802   -1.4923    1.4561 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7646   -1.6612    0.1661 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4395   -1.7460    1.0240 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4632   -2.6676    1.8682 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4074   -0.7982    0.7999 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1659   -0.4620   -0.9747 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8079   -0.2561    0.8222 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6313   -1.8837    0.0059 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7913   -1.1669   -1.2396 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9273    1.4679   -0.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7506    0.9684   -1.9608 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1501    2.7995   -0.3485 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8976    1.5886    0.9279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5347    1.7616    1.0532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3946    2.3311   -0.4446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1353   -0.1647   -1.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0735    1.0787    0.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2763   -0.1589    1.5868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6472   -1.0173    1.4519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4828   -1.2707   -0.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2221   -2.6534   -0.0298 H   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  2  0  0  0  0
  5  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
 10 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
 15  2  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  2 19  1  6  0  0  0
  3 20  1  0  0  0  0
  3 21  1  0  0  0  0
  4 22  1  0  0  0  0
  4 23  1  0  0  0  0
  7 24  1  0  0  0  0
  7 25  1  0  0  0  0
  8 26  1  6  0  0  0
  9 27  1  0  0  0  0
 10 28  1  1  0  0  0
 11 29  1  0  0  0  0
 12 30  1  0  0  0  0
 12 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0005601

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]1([H])C([H])([H])C(=O)O[C@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])C(=O)C([H])([H])[C@]1([H])O[H]

> <INCHI_IDENTIFIER>
InChI=1S/C10H16O5/c1-6-2-3-7(11)4-8(12)9(13)5-10(14)15-6/h6,8-9,12-13H,2-5H2,1H3/t6-,8+,9+/m1/s1

> <INCHI_KEY>
JTOYXZZLKBAIEJ-YEPSODPASA-N

> <FORMULA>
C10H16O5

> <MOLECULAR_WEIGHT>
216.233

> <EXACT_MASS>
216.099773615

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
21.190905748100946

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4S,5S,10R)-4,5-dihydroxy-10-methyloxecane-2,7-dione

> <ALOGPS_LOGP>
-0.84

> <JCHEM_LOGP>
-0.5400552839999999

> <ALOGPS_LOGS>
-0.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.995576895323111

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.628019379573612

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2323644259973046

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
51.0963

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.10e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4S,5S,10R)-4,5-dihydroxy-10-methyloxecane-2,7-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 31 31  0  0  0  0  0  0  0  0999 V2000
    3.5539   -0.7902   -0.1324 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0660   -0.5031   -0.3893 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9548    0.9047   -0.8517 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8994    1.7113   -0.1729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4313    1.4987   -0.7814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4798    1.2409   -1.9706 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7179    1.5778   -0.0402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3932    0.2088   -0.2004 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7707    0.3040   -0.0830 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8018   -0.7497    0.8101 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7802   -1.4923    1.4561 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7646   -1.6612    0.1661 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4395   -1.7460    1.0240 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4632   -2.6676    1.8682 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4074   -0.7982    0.7999 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1659   -0.4620   -0.9747 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8079   -0.2561    0.8222 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6313   -1.8837    0.0059 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7913   -1.1669   -1.2396 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9273    1.4679   -0.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7506    0.9684   -1.9608 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1501    2.7995   -0.3485 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8976    1.5886    0.9279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5347    1.7616    1.0532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3946    2.3311   -0.4446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1353   -0.1647   -1.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0735    1.0787    0.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2763   -0.1589    1.5868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6472   -1.0173    1.4519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4828   -1.2707   -0.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2221   -2.6534   -0.0298 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  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15  2  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  6
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  7 24  1  0
  7 25  1  0
  8 26  1  6
  9 27  1  0
 10 28  1  1
 11 29  1  0
 12 30  1  0
 12 31  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       3.554  -0.790  -0.132  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.066  -0.503  -0.389  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.955   0.905  -0.852  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.899   1.711  -0.173  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.431   1.499  -0.781  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.480   1.241  -1.971  0.00  0.00           O+0
HETATM    7  C   UNK     0      -1.718   1.578  -0.040  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.393   0.209  -0.200  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.771   0.304  -0.083  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.802  -0.750   0.810  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.780  -1.492   1.456  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.765  -1.661   0.166  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.440  -1.746   1.024  0.00  0.00           C+0
HETATM   14  O   UNK     0       0.463  -2.668   1.868  0.00  0.00           O+0
HETATM   15  O   UNK     0       1.407  -0.798   0.800  0.00  0.00           O+0
HETATM   16  H   UNK     0       4.166  -0.462  -0.975  0.00  0.00           H+0
HETATM   17  H   UNK     0       3.808  -0.256   0.822  0.00  0.00           H+0
HETATM   18  H   UNK     0       3.631  -1.884   0.006  0.00  0.00           H+0
HETATM   19  H   UNK     0       1.791  -1.167  -1.240  0.00  0.00           H+0
HETATM   20  H   UNK     0       2.927   1.468  -0.734  0.00  0.00           H+0
HETATM   21  H   UNK     0       1.751   0.968  -1.961  0.00  0.00           H+0
HETATM   22  H   UNK     0       1.150   2.800  -0.349  0.00  0.00           H+0
HETATM   23  H   UNK     0       0.898   1.589   0.928  0.00  0.00           H+0
HETATM   24  H   UNK     0      -1.535   1.762   1.053  0.00  0.00           H+0
HETATM   25  H   UNK     0      -2.395   2.331  -0.445  0.00  0.00           H+0
HETATM   26  H   UNK     0      -2.135  -0.165  -1.210  0.00  0.00           H+0
HETATM   27  H   UNK     0      -4.074   1.079   0.443  0.00  0.00           H+0
HETATM   28  H   UNK     0      -1.276  -0.159   1.587  0.00  0.00           H+0
HETATM   29  H   UNK     0      -3.647  -1.017   1.452  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.483  -1.271  -0.851  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.222  -2.653  -0.030  0.00  0.00           H+0
CONECT    1    2   16   17   18                                             
CONECT    2    1    3   15   19                                             
CONECT    3    2    4   20   21                                             
CONECT    4    3    5   22   23                                             
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   24   25                                             
CONECT    8    7    9   10   26                                             
CONECT    9    8   27                                                       
CONECT   10    8   11   12   28                                             
CONECT   11   10   29                                                       
CONECT   12   10   13   30   31                                             
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    2                                                       
CONECT   16    1                                                            
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    2                                                            
CONECT   20    3                                                            
CONECT   21    3                                                            
CONECT   22    4                                                            
CONECT   23    4                                                            
CONECT   24    7                                                            
CONECT   25    7                                                            
CONECT   26    8                                                            
CONECT   27    9                                                            
CONECT   28   10                                                            
CONECT   29   11                                                            
CONECT   30   12                                                            
CONECT   31   12                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   62    0
END

RDKit          3D

31 31  0  0  0  0  0  0  0  0999 V2000
    3.5539   -0.7902   -0.1324 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0660   -0.5031   -0.3893 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9548    0.9047   -0.8517 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8994    1.7113   -0.1729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4313    1.4987   -0.7814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4798    1.2409   -1.9706 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7179    1.5778   -0.0402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3932    0.2088   -0.2004 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7707    0.3040   -0.0830 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8018   -0.7497    0.8101 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7802   -1.4923    1.4561 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7646   -1.6612    0.1661 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4395   -1.7460    1.0240 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4632   -2.6676    1.8682 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4074   -0.7982    0.7999 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1659   -0.4620   -0.9747 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8079   -0.2561    0.8222 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6313   -1.8837    0.0059 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7913   -1.1669   -1.2396 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9273    1.4679   -0.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7506    0.9684   -1.9608 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1501    2.7995   -0.3485 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8976    1.5886    0.9279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5347    1.7616    1.0532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3946    2.3311   -0.4446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1353   -0.1647   -1.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0735    1.0787    0.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2763   -0.1589    1.5868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6472   -1.0173    1.4519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4828   -1.2707   -0.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2221   -2.6534   -0.0298 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  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15  2  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  6
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  7 24  1  0
  7 25  1  0
  8 26  1  6
  9 27  1  0
 10 28  1  1
 11 29  1  0
 12 30  1  0
 12 31  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Cephalosporolide C	MeSH
Bassianolone	MeSH

Chemical Formula

C₁₀H₁₆O₅

Average Mass

216.2330 Da

Monoisotopic Mass

216.09977 Da

IUPAC Name

(4S,5S,10R)-4,5-dihydroxy-10-methyloxecane-2,7-dione

Traditional Name

(4S,5S,10R)-4,5-dihydroxy-10-methyloxecane-2,7-dione

CAS Registry Number

Not Available

SMILES

C[C@@H]1CCC(=O)C[C@H](O)[C@@H](O)CC(=O)O1

InChI Identifier

InChI=1S/C10H16O5/c1-6-2-3-7(11)4-8(12)9(13)5-10(14)15-6/h6,8-9,12-13H,2-5H2,1H3/t6-,8+,9+/m1/s1

InChI Key

JTOYXZZLKBAIEJ-YEPSODPASA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Cordyceps	NPAtlas	15568800

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lactones. These are cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Not Available

Direct Parent

Lactones

Alternative Parents

Substituents

1,2-diol
Carboxylic acid ester
Ketone
Lactone
Cyclic ketone
Secondary alcohol
Carboxylic acid derivative
Oxacycle
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Alcohol
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	-0.84	ALOGPS
logP	-0.54	ChemAxon
logS	-0.01	ALOGPS
pKa (Strongest Acidic)	13.63	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	51.1 m³·mol⁻¹	ChemAxon
Polarizability	21.19 Å³	ChemAxon
Number of Rings	1	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

NPAtlas ID

NPA016752

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

24702832

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44575720

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Cephalosporolide C (NP0005601)

MOL for NP0005601 (Cephalosporolide C)

3D MOL for NP0005601 (Cephalosporolide C)

3D SDF for NP0005601 (Cephalosporolide C)

3D-SDF for NP0005601 (Cephalosporolide C)

PDB for NP0005601 (Cephalosporolide C)

3D PDB for NP0005601 (Cephalosporolide C)

SMILES for NP0005601 (Cephalosporolide C)

INCHI for NP0005601 (Cephalosporolide C)

Structure for NP0005601 (Cephalosporolide C)

3D Structure for NP0005601 (Cephalosporolide C)