NP-MRD: Showing NP-Card for Chaetone E (NP0011209)

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Record Information

Version

2.0

Created at

2021-01-05 20:58:55 UTC

Updated at

2021-07-15 17:08:16 UTC

NP-MRD ID

NP0011209

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Chaetone E

Provided By

NPAtlas

Description

Chaetone E belongs to the class of organic compounds known as dibenzoxepines. Dibenzoxepines are compounds containing a dibenzoxepine moiety, which consists of two benzene connected by an oxazepine ring. Chaetone E is found in Chaetomium. Based on a literature review very few articles have been published on Chaetone E.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107443D          

 39 41  0  0  0  0            999 V2000
   -4.0587   -3.5861   -0.1460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8539   -2.8883   -0.2179 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6897   -1.5580    0.0632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7756   -0.8066    0.4528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5880    0.5470    0.7348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3503    1.1541    0.6354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1169    2.4838    0.9028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0987    3.3967    1.3102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2538    0.3804    0.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4541   -0.9584   -0.0375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4740   -1.8342   -0.4357 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8083   -1.7767   -0.9209 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6302   -0.6435   -0.5241 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9708   -0.9333   -0.6642 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9839   -0.0503   -0.3645 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4250   -0.3920   -0.5261 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8538   -0.0443   -1.8258 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6376    1.2102    0.1079 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3092    1.5455    0.2644 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9476    2.7976    0.7342 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3216    0.6329   -0.0467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0193    1.1588    0.1803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1107    2.3857    0.3380 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8302   -3.1984   -0.8520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8683   -4.6479   -0.4109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5153   -3.5654    0.8592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7436   -1.2746    0.5322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4288    1.1467    1.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8840    2.8964    1.9321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6089    3.8806    0.4501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6564    4.2419    1.9112 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7763   -1.8104   -2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3452   -2.7186   -0.6057 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2711   -1.9149   -1.0328 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0583    0.0646    0.2322 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5305   -1.4937   -0.4498 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4517    0.7430   -1.7788 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4058    1.9402    0.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6524    3.4893    0.9711 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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  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
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 10  3  1  0  0  0  0
 21 13  1  0  0  0  0
 22  9  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  4 27  1  0  0  0  0
  5 28  1  0  0  0  0
  8 29  1  0  0  0  0
  8 30  1  0  0  0  0
  8 31  1  0  0  0  0
 12 32  1  0  0  0  0
 12 33  1  0  0  0  0
 14 34  1  0  0  0  0
 16 35  1  0  0  0  0
 16 36  1  0  0  0  0
 17 37  1  0  0  0  0
 18 38  1  0  0  0  0
 20 39  1  0  0  0  0
M  END

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
   -4.0587   -3.5861   -0.1460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8539   -2.8883   -0.2179 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6897   -1.5580    0.0632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7756   -0.8066    0.4528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5880    0.5470    0.7348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3503    1.1541    0.6354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1169    2.4838    0.9028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0987    3.3967    1.3102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2538    0.3804    0.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4541   -0.9584   -0.0375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4740   -1.8342   -0.4357 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8083   -1.7767   -0.9209 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6302   -0.6435   -0.5241 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9708   -0.9333   -0.6642 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9839   -0.0503   -0.3645 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4250   -0.3920   -0.5261 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8538   -0.0443   -1.8258 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6376    1.2102    0.1079 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3092    1.5455    0.2644 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9476    2.7976    0.7342 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3216    0.6329   -0.0467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0193    1.1588    0.1803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1107    2.3857    0.3380 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8302   -3.1984   -0.8520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8683   -4.6479   -0.4109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5153   -3.5654    0.8592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7436   -1.2746    0.5322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4288    1.1467    1.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8840    2.8964    1.9321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6089    3.8806    0.4501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6564    4.2419    1.9112 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7763   -1.8104   -2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3452   -2.7186   -0.6057 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2711   -1.9149   -1.0328 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0583    0.0646    0.2322 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5305   -1.4937   -0.4498 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4517    0.7430   -1.7788 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4058    1.9402    0.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6524    3.4893    0.9711 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  6  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 15 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 22 23  2  0
 10  3  1  0
 21 13  1  0
 22  9  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  5 28  1  0
  8 29  1  0
  8 30  1  0
  8 31  1  0
 12 32  1  0
 12 33  1  0
 14 34  1  0
 16 35  1  0
 16 36  1  0
 17 37  1  0
 18 38  1  0
 20 39  1  0
M  END


  Mrv1652306242107443D          

 39 41  0  0  0  0            999 V2000
   -4.0587   -3.5861   -0.1460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8539   -2.8883   -0.2179 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6897   -1.5580    0.0632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7756   -0.8066    0.4528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5880    0.5470    0.7348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3503    1.1541    0.6354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1169    2.4838    0.9028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0987    3.3967    1.3102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2538    0.3804    0.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4541   -0.9584   -0.0375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4740   -1.8342   -0.4357 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8083   -1.7767   -0.9209 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6302   -0.6435   -0.5241 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9708   -0.9333   -0.6642 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9839   -0.0503   -0.3645 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4250   -0.3920   -0.5261 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8538   -0.0443   -1.8258 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6376    1.2102    0.1079 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3092    1.5455    0.2644 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9476    2.7976    0.7342 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3216    0.6329   -0.0467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0193    1.1588    0.1803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1107    2.3857    0.3380 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8302   -3.1984   -0.8520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8683   -4.6479   -0.4109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5153   -3.5654    0.8592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7436   -1.2746    0.5322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4288    1.1467    1.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8840    2.8964    1.9321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6089    3.8806    0.4501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6564    4.2419    1.9112 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7763   -1.8104   -2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3452   -2.7186   -0.6057 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2711   -1.9149   -1.0328 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0583    0.0646    0.2322 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5305   -1.4937   -0.4498 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4517    0.7430   -1.7788 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4058    1.9402    0.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6524    3.4893    0.9711 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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  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
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 10  3  1  0  0  0  0
 21 13  1  0  0  0  0
 22  9  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  4 27  1  0  0  0  0
  5 28  1  0  0  0  0
  8 29  1  0  0  0  0
  8 30  1  0  0  0  0
  8 31  1  0  0  0  0
 12 32  1  0  0  0  0
 12 33  1  0  0  0  0
 14 34  1  0  0  0  0
 16 35  1  0  0  0  0
 16 36  1  0  0  0  0
 17 37  1  0  0  0  0
 18 38  1  0  0  0  0
 20 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0011209

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=C([H])C(=C1[H])C([H])([H])O[H])C([H])([H])OC1=C(C(OC([H])([H])[H])=C([H])C([H])=C1OC([H])([H])[H])C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H16O6/c1-21-12-3-4-13(22-2)17-15(12)16(20)14-10(8-23-17)5-9(7-18)6-11(14)19/h3-6,18-19H,7-8H2,1-2H3

> <INCHI_KEY>
DOKRMVDLGJSCQD-UHFFFAOYSA-N

> <FORMULA>
C17H16O6

> <MOLECULAR_WEIGHT>
316.309

> <EXACT_MASS>
316.094688235

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
33.170777789402976

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
15-hydroxy-13-(hydroxymethyl)-4,7-dimethoxy-9-oxatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3(8),4,6,11,13-hexaen-2-one

> <ALOGPS_LOGP>
2.26

> <JCHEM_LOGP>
2.2898972686666674

> <ALOGPS_LOGS>
-3.52

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.004533327031695

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.690403047950886

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8923794879975135

> <JCHEM_POLAR_SURFACE_AREA>
85.22

> <JCHEM_REFRACTIVITY>
83.3745

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.52e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
15-hydroxy-13-(hydroxymethyl)-4,7-dimethoxy-9-oxatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3(8),4,6,11,13-hexaen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
   -4.0587   -3.5861   -0.1460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8539   -2.8883   -0.2179 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6897   -1.5580    0.0632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7756   -0.8066    0.4528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5880    0.5470    0.7348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3503    1.1541    0.6354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1169    2.4838    0.9028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0987    3.3967    1.3102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2538    0.3804    0.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4541   -0.9584   -0.0375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4740   -1.8342   -0.4357 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8083   -1.7767   -0.9209 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6302   -0.6435   -0.5241 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9708   -0.9333   -0.6642 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9839   -0.0503   -0.3645 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4250   -0.3920   -0.5261 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8538   -0.0443   -1.8258 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6376    1.2102    0.1079 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3092    1.5455    0.2644 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9476    2.7976    0.7342 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3216    0.6329   -0.0467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0193    1.1588    0.1803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1107    2.3857    0.3380 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8302   -3.1984   -0.8520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8683   -4.6479   -0.4109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5153   -3.5654    0.8592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7436   -1.2746    0.5322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4288    1.1467    1.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8840    2.8964    1.9321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6089    3.8806    0.4501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6564    4.2419    1.9112 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7763   -1.8104   -2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3452   -2.7186   -0.6057 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2711   -1.9149   -1.0328 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0583    0.0646    0.2322 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5305   -1.4937   -0.4498 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4517    0.7430   -1.7788 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4058    1.9402    0.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6524    3.4893    0.9711 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
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  6  7  1  0
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  6  9  1  0
  9 10  2  0
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 21 22  1  0
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 10  3  1  0
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 17 37  1  0
 18 38  1  0
 20 39  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      -4.059  -3.586  -0.146  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.854  -2.888  -0.218  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.690  -1.558   0.063  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.776  -0.807   0.453  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.588   0.547   0.735  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.350   1.154   0.635  0.00  0.00           C+0
HETATM    7  O   UNK     0      -2.117   2.484   0.903  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.099   3.397   1.310  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.254   0.380   0.239  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.454  -0.958  -0.038  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.474  -1.834  -0.436  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.808  -1.777  -0.921  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.630  -0.644  -0.524  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.971  -0.933  -0.664  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.984  -0.050  -0.365  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.425  -0.392  -0.526  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.854  -0.044  -1.826  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.638   1.210   0.108  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.309   1.546   0.264  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.948   2.798   0.734  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.322   0.633  -0.047  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.019   1.159   0.180  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.111   2.386   0.338  0.00  0.00           O+0
HETATM   24  H   UNK     0      -4.830  -3.198  -0.852  0.00  0.00           H+0
HETATM   25  H   UNK     0      -3.868  -4.648  -0.411  0.00  0.00           H+0
HETATM   26  H   UNK     0      -4.515  -3.565   0.859  0.00  0.00           H+0
HETATM   27  H   UNK     0      -4.744  -1.275   0.532  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.429   1.147   1.040  0.00  0.00           H+0
HETATM   29  H   UNK     0      -3.884   2.896   1.932  0.00  0.00           H+0
HETATM   30  H   UNK     0      -3.609   3.881   0.450  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.656   4.242   1.911  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.776  -1.810  -2.045  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.345  -2.719  -0.606  0.00  0.00           H+0
HETATM   34  H   UNK     0       3.271  -1.915  -1.033  0.00  0.00           H+0
HETATM   35  H   UNK     0       6.058   0.065   0.232  0.00  0.00           H+0
HETATM   36  H   UNK     0       5.531  -1.494  -0.450  0.00  0.00           H+0
HETATM   37  H   UNK     0       6.452   0.743  -1.779  0.00  0.00           H+0
HETATM   38  H   UNK     0       4.406   1.940   0.357  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.652   3.489   0.971  0.00  0.00           H+0
CONECT    1    2   24   25   26                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5   27                                                  
CONECT    5    4    6   28                                                  
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7   29   30   31                                             
CONECT    9    6   10   22                                                  
CONECT   10    9   11    3                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   32   33                                             
CONECT   13   12   14   21                                                  
CONECT   14   13   15   34                                                  
CONECT   15   14   16   18                                                  
CONECT   16   15   17   35   36                                             
CONECT   17   16   37                                                       
CONECT   18   15   19   38                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19   39                                                       
CONECT   21   19   22   13                                                  
CONECT   22   21   23    9                                                  
CONECT   23   22                                                            
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    4                                                            
CONECT   28    5                                                            
CONECT   29    8                                                            
CONECT   30    8                                                            
CONECT   31    8                                                            
CONECT   32   12                                                            
CONECT   33   12                                                            
CONECT   34   14                                                            
CONECT   35   16                                                            
CONECT   36   16                                                            
CONECT   37   17                                                            
CONECT   38   18                                                            
CONECT   39   20                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   82    0
END

RDKit          3D

39 41  0  0  0  0  0  0  0  0999 V2000
   -4.0587   -3.5861   -0.1460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8539   -2.8883   -0.2179 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6897   -1.5580    0.0632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7756   -0.8066    0.4528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5880    0.5470    0.7348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3503    1.1541    0.6354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1169    2.4838    0.9028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0987    3.3967    1.3102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2538    0.3804    0.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4541   -0.9584   -0.0375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4740   -1.8342   -0.4357 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8083   -1.7767   -0.9209 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6302   -0.6435   -0.5241 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9708   -0.9333   -0.6642 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9839   -0.0503   -0.3645 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4250   -0.3920   -0.5261 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8538   -0.0443   -1.8258 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6376    1.2102    0.1079 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3092    1.5455    0.2644 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9476    2.7976    0.7342 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3216    0.6329   -0.0467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0193    1.1588    0.1803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1107    2.3857    0.3380 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8302   -3.1984   -0.8520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8683   -4.6479   -0.4109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5153   -3.5654    0.8592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7436   -1.2746    0.5322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4288    1.1467    1.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8840    2.8964    1.9321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6089    3.8806    0.4501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6564    4.2419    1.9112 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7763   -1.8104   -2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3452   -2.7186   -0.6057 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2711   -1.9149   -1.0328 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0583    0.0646    0.2322 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5305   -1.4937   -0.4498 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4517    0.7430   -1.7788 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4058    1.9402    0.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6524    3.4893    0.9711 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  6  9  1  0
  9 10  2  0
 10 11  1  0
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 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 15 18  2  0
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 10  3  1  0
 21 13  1  0
 22  9  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  5 28  1  0
  8 29  1  0
  8 30  1  0
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 16 35  1  0
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 17 37  1  0
 18 38  1  0
 20 39  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₇H₁₆O₆

Average Mass

316.3090 Da

Monoisotopic Mass

316.09469 Da

IUPAC Name

15-hydroxy-13-(hydroxymethyl)-4,7-dimethoxy-9-oxatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3(8),4,6,11,13-hexaen-2-one

Traditional Name

15-hydroxy-13-(hydroxymethyl)-4,7-dimethoxy-9-oxatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3(8),4,6,11,13-hexaen-2-one

CAS Registry Number

Not Available

SMILES

COC1=C2OCC3=CC(CO)=CC(O)=C3C(=O)C2=C(OC)C=C1

InChI Identifier

InChI=1S/C17H16O6/c1-21-12-3-4-13(22-2)17-15(12)16(20)14-10(8-23-17)5-9(7-18)6-11(14)19/h3-6,18-19H,7-8H2,1-2H3

InChI Key

DOKRMVDLGJSCQD-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
Chaetomium	NPAtlas	23096258

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dibenzoxepines. Dibenzoxepines are compounds containing a dibenzoxepine moiety, which consists of two benzene connected by an oxazepine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzoxepines

Sub Class

Dibenzoxepines

Direct Parent

Dibenzoxepines

Alternative Parents

Substituents

Dibenzoxepine
Anisole
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Vinylogous acid
Ketone
Ether
Oxacycle
Organooxygen compound
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Primary alcohol
Aromatic alcohol
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	2.26	ALOGPS
logP	2.29	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	8.69	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	83.37 m³·mol⁻¹	ChemAxon
Polarizability	33.17 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

NPA003744

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78435591

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139584131

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Chaetone E (NP0011209)

MOL for NP0011209 (Chaetone E)

3D MOL for NP0011209 (Chaetone E)

3D SDF for NP0011209 (Chaetone E)

3D-SDF for NP0011209 (Chaetone E)

PDB for NP0011209 (Chaetone E)

3D PDB for NP0011209 (Chaetone E)

SMILES for NP0011209 (Chaetone E)

INCHI for NP0011209 (Chaetone E)

Structure for NP0011209 (Chaetone E)

3D Structure for NP0011209 (Chaetone E)