NP-MRD: Showing NP-Card for EI-1941-1 (NP0004679)

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Record Information

Version

2.0

Created at

2020-12-09 02:06:20 UTC

Updated at

2021-07-15 16:49:50 UTC

NP-MRD ID

NP0004679

Secondary Accession Numbers

None

Natural Product Identification

Common Name

EI-1941-1

Provided By

NPAtlas

Description

EI-1941-1 is found in Farrowia and Farrowia sp. E-1941. EI-1941-1 was first documented in 2003 (PMID: 12870812). Based on a literature review very few articles have been published on 6,8-dihydroxy-10-propyl-4,9-dioxatricyclo[5.4.0.0³,⁵]Undec-1(7)-en-2-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118083D          

 33 35  0  0  0  0            999 V2000
    4.8630    0.2406   -0.2586 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4892    0.7758    0.0599 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5295   -0.3870    0.0247 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1073    0.0445    0.3339 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2807   -1.2255    0.2585 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1443   -0.8973    0.2268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5115    0.2961   -0.2030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5666    1.3189   -0.6523 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8353    2.5154    0.0014 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7525    1.0021   -0.5574 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9415    0.6883   -0.2599 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2678    0.8618   -1.5965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8740   -0.2772    0.3516 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7359   -0.5115    1.7537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5169   -1.5348    0.7653 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1031   -1.8988    0.6701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7111   -3.0625    0.9662 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6265    0.7661    0.3460 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0764    0.3255   -1.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9426   -0.8472   -0.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4942    1.1449    1.1221 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2316    1.5741   -0.6419 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8331   -1.0850    0.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5033   -0.8905   -0.9570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0415    0.4956    1.3669 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5768   -1.8496    1.1294 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5647   -1.7189   -0.7093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7894    1.5109   -1.7434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9690    3.2737   -0.6198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0195    1.6561    0.2999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7382    0.0875   -1.9751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9559   -0.0222    0.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2329   -2.3699    0.8504 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  1  0  0  0  0
  6  7  2  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
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 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  2  0  0  0  0
 10  4  1  0  0  0  0
 15 13  1  0  0  0  0
 16  6  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  2 21  1  0  0  0  0
  2 22  1  0  0  0  0
  3 23  1  0  0  0  0
  3 24  1  0  0  0  0
  4 25  1  1  0  0  0
  5 26  1  0  0  0  0
  5 27  1  0  0  0  0
  8 28  1  6  0  0  0
  9 29  1  0  0  0  0
 11 30  1  1  0  0  0
 12 31  1  0  0  0  0
 13 32  1  1  0  0  0
 15 33  1  1  0  0  0
M  END

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
    4.8630    0.2406   -0.2586 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4892    0.7758    0.0599 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5295   -0.3870    0.0247 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1073    0.0445    0.3339 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2807   -1.2255    0.2585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1443   -0.8973    0.2268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5115    0.2961   -0.2030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5666    1.3189   -0.6523 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8353    2.5154    0.0014 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7525    1.0021   -0.5574 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9415    0.6883   -0.2599 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2678    0.8618   -1.5965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8740   -0.2772    0.3516 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7359   -0.5115    1.7537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5169   -1.5348    0.7653 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1031   -1.8988    0.6701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7111   -3.0625    0.9662 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6265    0.7661    0.3460 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0764    0.3255   -1.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9426   -0.8472   -0.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4942    1.1449    1.1221 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2316    1.5741   -0.6419 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8331   -1.0850    0.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5033   -0.8905   -0.9570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0415    0.4956    1.3669 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5768   -1.8496    1.1294 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5647   -1.7189   -0.7093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7894    1.5109   -1.7434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9690    3.2737   -0.6198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0195    1.6561    0.2999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7382    0.0875   -1.9751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9559   -0.0222    0.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2329   -2.3699    0.8504 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  2  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
  7 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 10  4  1  0
 15 13  1  0
 16  6  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  2 22  1  0
  3 23  1  0
  3 24  1  0
  4 25  1  1
  5 26  1  0
  5 27  1  0
  8 28  1  6
  9 29  1  0
 11 30  1  1
 12 31  1  0
 13 32  1  1
 15 33  1  1
M  END


  Mrv1652306242118083D          

 33 35  0  0  0  0            999 V2000
    4.8630    0.2406   -0.2586 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4892    0.7758    0.0599 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5295   -0.3870    0.0247 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1073    0.0445    0.3339 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2807   -1.2255    0.2585 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1443   -0.8973    0.2268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5115    0.2961   -0.2030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5666    1.3189   -0.6523 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8353    2.5154    0.0014 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7525    1.0021   -0.5574 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9415    0.6883   -0.2599 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2678    0.8618   -1.5965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8740   -0.2772    0.3516 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7359   -0.5115    1.7537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5169   -1.5348    0.7653 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1031   -1.8988    0.6701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7111   -3.0625    0.9662 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6265    0.7661    0.3460 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0764    0.3255   -1.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9426   -0.8472   -0.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4942    1.1449    1.1221 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2316    1.5741   -0.6419 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8331   -1.0850    0.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5033   -0.8905   -0.9570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0415    0.4956    1.3669 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5768   -1.8496    1.1294 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5647   -1.7189   -0.7093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7894    1.5109   -1.7434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9690    3.2737   -0.6198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0195    1.6561    0.2999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7382    0.0875   -1.9751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9559   -0.0222    0.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2329   -2.3699    0.8504 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  1  0  0  0  0
  6  7  2  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
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 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  2  0  0  0  0
 10  4  1  0  0  0  0
 15 13  1  0  0  0  0
 16  6  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  2 21  1  0  0  0  0
  2 22  1  0  0  0  0
  3 23  1  0  0  0  0
  3 24  1  0  0  0  0
  4 25  1  1  0  0  0
  5 26  1  0  0  0  0
  5 27  1  0  0  0  0
  8 28  1  6  0  0  0
  9 29  1  0  0  0  0
 11 30  1  1  0  0  0
 12 31  1  0  0  0  0
 13 32  1  1  0  0  0
 15 33  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0004679

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]1([H])O[C@]([H])(C([H])([H])C([H])([H])C([H])([H])[H])C([H])([H])C2=C1[C@@]([H])(O[H])[C@]1([H])O[C@]1([H])C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C12H16O5/c1-2-3-5-4-6-7(12(15)16-5)9(14)11-10(17-11)8(6)13/h5,9-12,14-15H,2-4H2,1H3/t5-,9-,10-,11+,12+/m1/s1

> <INCHI_KEY>
DJMYUSHSKVTQAD-UHFFFAOYSA-N

> <FORMULA>
C12H16O5

> <MOLECULAR_WEIGHT>
240.255

> <EXACT_MASS>
240.099773615

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
24.358199623865108

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,5S,6R,8S,10R)-6,8-dihydroxy-10-propyl-4,9-dioxatricyclo[5.4.0.0^{3,5}]undec-1(7)-en-2-one

> <ALOGPS_LOGP>
-0.25

> <JCHEM_LOGP>
0.3299320199999999

> <ALOGPS_LOGS>
-0.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.413199866118127

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.698093785118056

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5378721539086246

> <JCHEM_POLAR_SURFACE_AREA>
79.28999999999999

> <JCHEM_REFRACTIVITY>
57.898900000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.48e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,5S,6R,8S,10R)-6,8-dihydroxy-10-propyl-4,9-dioxatricyclo[5.4.0.0^{3,5}]undec-1(7)-en-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
    4.8630    0.2406   -0.2586 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4892    0.7758    0.0599 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5295   -0.3870    0.0247 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1073    0.0445    0.3339 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2807   -1.2255    0.2585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1443   -0.8973    0.2268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5115    0.2961   -0.2030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5666    1.3189   -0.6523 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8353    2.5154    0.0014 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7525    1.0021   -0.5574 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9415    0.6883   -0.2599 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2678    0.8618   -1.5965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8740   -0.2772    0.3516 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7359   -0.5115    1.7537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5169   -1.5348    0.7653 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1031   -1.8988    0.6701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7111   -3.0625    0.9662 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6265    0.7661    0.3460 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0764    0.3255   -1.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9426   -0.8472   -0.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4942    1.1449    1.1221 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2316    1.5741   -0.6419 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8331   -1.0850    0.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5033   -0.8905   -0.9570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0415    0.4956    1.3669 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5768   -1.8496    1.1294 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5647   -1.7189   -0.7093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7894    1.5109   -1.7434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9690    3.2737   -0.6198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0195    1.6561    0.2999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7382    0.0875   -1.9751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9559   -0.0222    0.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2329   -2.3699    0.8504 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  2  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
  7 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 10  4  1  0
 15 13  1  0
 16  6  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  2 22  1  0
  3 23  1  0
  3 24  1  0
  4 25  1  1
  5 26  1  0
  5 27  1  0
  8 28  1  6
  9 29  1  0
 11 30  1  1
 12 31  1  0
 13 32  1  1
 15 33  1  1
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       4.863   0.241  -0.259  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.489   0.776   0.060  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.530  -0.387   0.025  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.107   0.045   0.334  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.281  -1.226   0.259  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.144  -0.897   0.227  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.512   0.296  -0.203  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.567   1.319  -0.652  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.835   2.515   0.001  0.00  0.00           O+0
HETATM   10  O   UNK     0       0.753   1.002  -0.557  0.00  0.00           O+0
HETATM   11  C   UNK     0      -2.942   0.688  -0.260  0.00  0.00           C+0
HETATM   12  O   UNK     0      -3.268   0.862  -1.597  0.00  0.00           O+0
HETATM   13  C   UNK     0      -3.874  -0.277   0.352  0.00  0.00           C+0
HETATM   14  O   UNK     0      -3.736  -0.511   1.754  0.00  0.00           O+0
HETATM   15  C   UNK     0      -3.517  -1.535   0.765  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.103  -1.899   0.670  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.711  -3.063   0.966  0.00  0.00           O+0
HETATM   18  H   UNK     0       5.627   0.766   0.346  0.00  0.00           H+0
HETATM   19  H   UNK     0       5.076   0.326  -1.345  0.00  0.00           H+0
HETATM   20  H   UNK     0       4.943  -0.847  -0.008  0.00  0.00           H+0
HETATM   21  H   UNK     0       3.494   1.145   1.122  0.00  0.00           H+0
HETATM   22  H   UNK     0       3.232   1.574  -0.642  0.00  0.00           H+0
HETATM   23  H   UNK     0       2.833  -1.085   0.836  0.00  0.00           H+0
HETATM   24  H   UNK     0       2.503  -0.891  -0.957  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.042   0.496   1.367  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.577  -1.850   1.129  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.565  -1.719  -0.709  0.00  0.00           H+0
HETATM   28  H   UNK     0      -0.789   1.511  -1.743  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.969   3.274  -0.620  0.00  0.00           H+0
HETATM   30  H   UNK     0      -3.019   1.656   0.300  0.00  0.00           H+0
HETATM   31  H   UNK     0      -3.738   0.088  -1.975  0.00  0.00           H+0
HETATM   32  H   UNK     0      -4.956  -0.022   0.135  0.00  0.00           H+0
HETATM   33  H   UNK     0      -4.233  -2.370   0.850  0.00  0.00           H+0
CONECT    1    2   18   19   20                                             
CONECT    2    1    3   21   22                                             
CONECT    3    2    4   23   24                                             
CONECT    4    3    5   10   25                                             
CONECT    5    4    6   26   27                                             
CONECT    6    5    7   16                                                  
CONECT    7    6    8   11                                                  
CONECT    8    7    9   10   28                                             
CONECT    9    8   29                                                       
CONECT   10    8    4                                                       
CONECT   11    7   12   13   30                                             
CONECT   12   11   31                                                       
CONECT   13   11   14   15   32                                             
CONECT   14   13   15                                                       
CONECT   15   14   16   13   33                                             
CONECT   16   15   17    6                                                  
CONECT   17   16                                                            
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    2                                                            
CONECT   22    2                                                            
CONECT   23    3                                                            
CONECT   24    3                                                            
CONECT   25    4                                                            
CONECT   26    5                                                            
CONECT   27    5                                                            
CONECT   28    8                                                            
CONECT   29    9                                                            
CONECT   30   11                                                            
CONECT   31   12                                                            
CONECT   32   13                                                            
CONECT   33   15                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

RDKit          3D

33 35  0  0  0  0  0  0  0  0999 V2000
    4.8630    0.2406   -0.2586 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4892    0.7758    0.0599 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5295   -0.3870    0.0247 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1073    0.0445    0.3339 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2807   -1.2255    0.2585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1443   -0.8973    0.2268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5115    0.2961   -0.2030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5666    1.3189   -0.6523 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8353    2.5154    0.0014 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7525    1.0021   -0.5574 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9415    0.6883   -0.2599 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2678    0.8618   -1.5965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8740   -0.2772    0.3516 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7359   -0.5115    1.7537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5169   -1.5348    0.7653 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1031   -1.8988    0.6701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7111   -3.0625    0.9662 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6265    0.7661    0.3460 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0764    0.3255   -1.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9426   -0.8472   -0.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4942    1.1449    1.1221 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2316    1.5741   -0.6419 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8331   -1.0850    0.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5033   -0.8905   -0.9570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0415    0.4956    1.3669 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5768   -1.8496    1.1294 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5647   -1.7189   -0.7093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7894    1.5109   -1.7434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9690    3.2737   -0.6198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0195    1.6561    0.2999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7382    0.0875   -1.9751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9559   -0.0222    0.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2329   -2.3699    0.8504 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  2  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
  7 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 10  4  1  0
 15 13  1  0
 16  6  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  2 22  1  0
  3 23  1  0
  3 24  1  0
  4 25  1  1
  5 26  1  0
  5 27  1  0
  8 28  1  6
  9 29  1  0
 11 30  1  1
 12 31  1  0
 13 32  1  1
 15 33  1  1
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₂H₁₆O₅

Average Mass

240.2550 Da

Monoisotopic Mass

240.09977 Da

IUPAC Name

(3S,5S,6R,8S,10R)-6,8-dihydroxy-10-propyl-4,9-dioxatricyclo[5.4.0.0^{3,5}]undec-1(7)-en-2-one

Traditional Name

(3S,5S,6R,8S,10R)-6,8-dihydroxy-10-propyl-4,9-dioxatricyclo[5.4.0.0^{3,5}]undec-1(7)-en-2-one

CAS Registry Number

Not Available

SMILES

CCCC1CC2=C(C(O)O1)C(O)C1OC1C2=O

InChI Identifier

InChI=1S/C12H16O5/c1-2-3-5-4-6-7(12(15)16-5)9(14)11-10(17-11)8(6)13/h5,9-12,14-15H,2-4H2,1H3

InChI Key

DJMYUSHSKVTQAD-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, 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
Farrowia	NPAtlas	12870812
Farrowia sp. E-1941	Fungi	KNApSAcK

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as cyclohexenones. These are compounds containing a cylohexenone moiety, which is a six-membered aliphatic ring that carries a ketone and has one endocyclic double bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Cyclohexenones

Alternative Parents

Substituents

Cyclohexenone
Pyran
Secondary alcohol
Hemiacetal
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxide
Hydrocarbon derivative
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	-0.25	ALOGPS
logP	0.33	ChemAxon
logS	-0.51	ALOGPS
pKa (Strongest Acidic)	11.7	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	79.29 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	57.9 m³·mol⁻¹	ChemAxon
Polarizability	24.36 Å³	ChemAxon
Number of Rings	3	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

NPAtlas ID

NPA001518

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

8306495

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10130980

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Koizumi F, Matsuda Y, Nakanishi S: EI-1941-1 and -2, novel interleukin-1beta converting enzyme inhibitors produced by Farrowia sp. E-1941. I. Biochemical characterization of EI-1941-1 and -2. J Antibiot (Tokyo). 2003 May;56(5):464-9. doi: 10.7164/antibiotics.56.464. [PubMed:12870812 ]

Showing NP-Card for EI-1941-1 (NP0004679)

MOL for NP0004679 (EI-1941-1)

3D MOL for NP0004679 (EI-1941-1)

3D SDF for NP0004679 (EI-1941-1)

3D-SDF for NP0004679 (EI-1941-1)

PDB for NP0004679 (EI-1941-1)

3D PDB for NP0004679 (EI-1941-1)

SMILES for NP0004679 (EI-1941-1)

INCHI for NP0004679 (EI-1941-1)

Structure for NP0004679 (EI-1941-1)

3D Structure for NP0004679 (EI-1941-1)