NP-MRD: Showing NP-Card for Z-stachyline A (NP0035743)

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Record Information

Version

2.0

Created at

2021-06-20 19:06:13 UTC

Updated at

2021-06-30 00:06:56 UTC

NP-MRD ID

NP0035743

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Z-stachyline A

Provided By

JEOL Database JEOL Logo

Description

Stachyline A belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring. Z-stachyline A is found in Stachylidium sp. Z-stachyline A was first documented in 2011 (PMID: 21162532). Based on a literature review very few articles have been published on Stachyline A.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202121063D          

 34 34  0  0  0  0            999 V2000
   -0.6052   -2.4517   -2.8109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0186   -3.3295   -1.9778 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6040   -4.5894   -2.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1057   -3.1624   -0.4727 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5666   -4.2664    0.1402 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4099   -1.8535    0.1636 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8394   -1.8039    0.0494 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4619   -0.6825    0.5226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8402   -0.6441    0.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6036    0.4438    0.7319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9937    1.5122    1.3976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7989    2.7013    1.8598 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5538    3.9032    0.9808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9809    5.0206    1.3183 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5804    5.0101    2.6567 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6109    1.4701    1.6195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8493    0.3792    1.1863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6540   -2.6346   -3.8809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0674   -1.5328   -2.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6630   -4.6398   -2.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5441   -4.6379   -3.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0977   -5.4749   -2.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1689   -3.2498   -0.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5170   -4.0589    0.0600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1493   -1.8658    1.2293 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0545   -0.9886   -0.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3257   -1.4699   -0.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6747    0.4439    0.5439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5793    2.9036    2.9120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8701    2.4745    1.8021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8974    3.8148   -0.0643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1872    5.8969    2.7637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1166    2.2931    2.1341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7837    0.3931    1.3884 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0  0  0  0
 17  8  2  0  0  0  0
  7  6  1  0  0  0  0
 11 16  2  0  0  0  0
  6  4  1  0  0  0  0
  8  9  1  0  0  0  0
  4  2  1  0  0  0  0
  9 10  2  0  0  0  0
  2  3  1  0  0  0  0
 10 11  1  0  0  0  0
 13 14  2  0  0  0  0
 11 12  1  0  0  0  0
 14 15  1  0  0  0  0
 16 17  1  0  0  0  0
  4  5  1  0  0  0  0
 12 13  1  0  0  0  0
  2  1  2  3  0  0  0
 13 31  1  0  0  0  0
 10 28  1  0  0  0  0
 16 33  1  0  0  0  0
 17 34  1  0  0  0  0
  9 27  1  0  0  0  0
 12 29  1  0  0  0  0
 12 30  1  0  0  0  0
  6 25  1  0  0  0  0
  6 26  1  0  0  0  0
  4 23  1  6  0  0  0
  3 20  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
 15 32  1  0  0  0  0
  5 24  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
M  END

     RDKit          3D

 34 34  0  0  0  0  0  0  0  0999 V2000
   -0.6052   -2.4517   -2.8109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0186   -3.3295   -1.9778 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6040   -4.5894   -2.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1057   -3.1624   -0.4727 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5666   -4.2664    0.1402 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4099   -1.8535    0.1636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8394   -1.8039    0.0494 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4619   -0.6825    0.5226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8402   -0.6441    0.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6036    0.4438    0.7319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9937    1.5122    1.3976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7989    2.7013    1.8598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5538    3.9032    0.9808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9809    5.0206    1.3183 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5804    5.0101    2.6567 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6109    1.4701    1.6195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8493    0.3792    1.1863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6540   -2.6346   -3.8809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0674   -1.5328   -2.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6630   -4.6398   -2.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5441   -4.6379   -3.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0977   -5.4749   -2.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1689   -3.2498   -0.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5170   -4.0589    0.0600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1493   -1.8658    1.2293 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0545   -0.9886   -0.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3257   -1.4699   -0.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6747    0.4439    0.5439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5793    2.9036    2.9120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8701    2.4745    1.8021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8974    3.8148   -0.0643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1872    5.8969    2.7637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1166    2.2931    2.1341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7837    0.3931    1.3884 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
 17  8  2  0
  7  6  1  0
 11 16  2  0
  6  4  1  0
  8  9  1  0
  4  2  1  0
  9 10  2  0
  2  3  1  0
 10 11  1  0
 13 14  2  0
 11 12  1  0
 14 15  1  0
 16 17  1  0
  4  5  1  0
 12 13  1  0
  2  1  2  3
 13 31  1  0
 10 28  1  0
 16 33  1  0
 17 34  1  0
  9 27  1  0
 12 29  1  0
 12 30  1  0
  6 25  1  0
  6 26  1  0
  4 23  1  6
  3 20  1  0
  3 21  1  0
  3 22  1  0
 15 32  1  0
  5 24  1  0
  1 18  1  0
  1 19  1  0
M  END


  Mrv1652306202121063D          

 34 34  0  0  0  0            999 V2000
   -0.6052   -2.4517   -2.8109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0186   -3.3295   -1.9778 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6040   -4.5894   -2.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1057   -3.1624   -0.4727 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5666   -4.2664    0.1402 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4099   -1.8535    0.1636 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8394   -1.8039    0.0494 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4619   -0.6825    0.5226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8402   -0.6441    0.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6036    0.4438    0.7319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9937    1.5122    1.3976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7989    2.7013    1.8598 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5538    3.9032    0.9808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9809    5.0206    1.3183 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5804    5.0101    2.6567 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6109    1.4701    1.6195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8493    0.3792    1.1863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6540   -2.6346   -3.8809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0674   -1.5328   -2.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6630   -4.6398   -2.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5441   -4.6379   -3.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0977   -5.4749   -2.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1689   -3.2498   -0.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5170   -4.0589    0.0600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1493   -1.8658    1.2293 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0545   -0.9886   -0.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3257   -1.4699   -0.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6747    0.4439    0.5439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5793    2.9036    2.9120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8701    2.4745    1.8021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8974    3.8148   -0.0643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1872    5.8969    2.7637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1166    2.2931    2.1341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7837    0.3931    1.3884 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0  0  0  0
 17  8  2  0  0  0  0
  7  6  1  0  0  0  0
 11 16  2  0  0  0  0
  6  4  1  0  0  0  0
  8  9  1  0  0  0  0
  4  2  1  0  0  0  0
  9 10  2  0  0  0  0
  2  3  1  0  0  0  0
 10 11  1  0  0  0  0
 13 14  2  0  0  0  0
 11 12  1  0  0  0  0
 14 15  1  0  0  0  0
 16 17  1  0  0  0  0
  4  5  1  0  0  0  0
 12 13  1  0  0  0  0
  2  1  2  3  0  0  0
 13 31  1  0  0  0  0
 10 28  1  0  0  0  0
 16 33  1  0  0  0  0
 17 34  1  0  0  0  0
  9 27  1  0  0  0  0
 12 29  1  0  0  0  0
 12 30  1  0  0  0  0
  6 25  1  0  0  0  0
  6 26  1  0  0  0  0
  4 23  1  6  0  0  0
  3 20  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
 15 32  1  0  0  0  0
  5 24  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0035743

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O\N=C(\[H])C([H])([H])C1=C([H])C([H])=C(OC([H])([H])[C@@]([H])(O[H])C(=C([H])[H])C([H])([H])[H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C13H17NO3/c1-10(2)13(15)9-17-12-5-3-11(4-6-12)7-8-14-16/h3-6,8,13,15-16H,1,7,9H2,2H3/b14-8-/t13-/m1/s1

> <INCHI_KEY>
RYDLTTLOGVZOMQ-HRYODUOUSA-N

> <FORMULA>
C13H17NO3

> <MOLECULAR_WEIGHT>
235.283

> <EXACT_MASS>
235.120843411

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
25.87422495351095

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-1-{4-[(2Z)-2-(hydroxyimino)ethyl]phenoxy}-3-methylbut-3-en-2-ol

> <ALOGPS_LOGP>
2.19

> <JCHEM_LOGP>
1.6484625263333332

> <ALOGPS_LOGS>
-2.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.839209423561773

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.871039406354774

> <JCHEM_PKA_STRONGEST_BASIC>
2.26667492156886

> <JCHEM_POLAR_SURFACE_AREA>
62.05

> <JCHEM_REFRACTIVITY>
66.1323

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.97e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-1-{4-[(2Z)-2-(hydroxyimino)ethyl]phenoxy}-3-methylbut-3-en-2-ol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 34 34  0  0  0  0  0  0  0  0999 V2000
   -0.6052   -2.4517   -2.8109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0186   -3.3295   -1.9778 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6040   -4.5894   -2.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1057   -3.1624   -0.4727 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5666   -4.2664    0.1402 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4099   -1.8535    0.1636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8394   -1.8039    0.0494 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4619   -0.6825    0.5226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8402   -0.6441    0.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6036    0.4438    0.7319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9937    1.5122    1.3976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7989    2.7013    1.8598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5538    3.9032    0.9808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9809    5.0206    1.3183 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5804    5.0101    2.6567 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6109    1.4701    1.6195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8493    0.3792    1.1863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6540   -2.6346   -3.8809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0674   -1.5328   -2.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6630   -4.6398   -2.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5441   -4.6379   -3.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0977   -5.4749   -2.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1689   -3.2498   -0.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5170   -4.0589    0.0600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1493   -1.8658    1.2293 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0545   -0.9886   -0.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3257   -1.4699   -0.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6747    0.4439    0.5439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5793    2.9036    2.9120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8701    2.4745    1.8021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8974    3.8148   -0.0643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1872    5.8969    2.7637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1166    2.2931    2.1341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7837    0.3931    1.3884 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
 17  8  2  0
  7  6  1  0
 11 16  2  0
  6  4  1  0
  8  9  1  0
  4  2  1  0
  9 10  2  0
  2  3  1  0
 10 11  1  0
 13 14  2  0
 11 12  1  0
 14 15  1  0
 16 17  1  0
  4  5  1  0
 12 13  1  0
  2  1  2  3
 13 31  1  0
 10 28  1  0
 16 33  1  0
 17 34  1  0
  9 27  1  0
 12 29  1  0
 12 30  1  0
  6 25  1  0
  6 26  1  0
  4 23  1  6
  3 20  1  0
  3 21  1  0
  3 22  1  0
 15 32  1  0
  5 24  1  0
  1 18  1  0
  1 19  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.605  -2.452  -2.811  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.019  -3.329  -1.978  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.604  -4.589  -2.526  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.106  -3.162  -0.473  0.00  0.00           C+0
HETATM    5  O   UNK     0      -0.567  -4.266   0.140  0.00  0.00           O+0
HETATM    6  C   UNK     0      -0.410  -1.853   0.164  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.839  -1.804   0.049  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.462  -0.683   0.523  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.840  -0.644   0.301  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.604   0.444   0.732  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.994   1.512   1.398  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.799   2.701   1.860  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.554   3.903   0.981  0.00  0.00           C+0
HETATM   14  N   UNK     0      -3.981   5.021   1.318  0.00  0.00           N+0
HETATM   15  O   UNK     0      -3.580   5.010   2.657  0.00  0.00           O+0
HETATM   16  C   UNK     0      -2.611   1.470   1.619  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.849   0.379   1.186  0.00  0.00           C+0
HETATM   18  H   UNK     0      -0.654  -2.635  -3.881  0.00  0.00           H+0
HETATM   19  H   UNK     0      -1.067  -1.533  -2.465  0.00  0.00           H+0
HETATM   20  H   UNK     0       1.663  -4.640  -2.252  0.00  0.00           H+0
HETATM   21  H   UNK     0       0.544  -4.638  -3.619  0.00  0.00           H+0
HETATM   22  H   UNK     0       0.098  -5.475  -2.129  0.00  0.00           H+0
HETATM   23  H   UNK     0       1.169  -3.250  -0.218  0.00  0.00           H+0
HETATM   24  H   UNK     0      -1.517  -4.059   0.060  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.149  -1.866   1.229  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.055  -0.989  -0.325  0.00  0.00           H+0
HETATM   27  H   UNK     0      -4.326  -1.470  -0.213  0.00  0.00           H+0
HETATM   28  H   UNK     0      -5.675   0.444   0.544  0.00  0.00           H+0
HETATM   29  H   UNK     0      -4.579   2.904   2.912  0.00  0.00           H+0
HETATM   30  H   UNK     0      -5.870   2.474   1.802  0.00  0.00           H+0
HETATM   31  H   UNK     0      -4.897   3.815  -0.064  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.187   5.897   2.764  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.117   2.293   2.134  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.784   0.393   1.388  0.00  0.00           H+0
CONECT    1    2   18   19                                                  
CONECT    2    4    3    1                                                  
CONECT    3    2   20   21   22                                             
CONECT    4    6    2    5   23                                             
CONECT    5    4   24                                                       
CONECT    6    7    4   25   26                                             
CONECT    7    8    6                                                       
CONECT    8    7   17    9                                                  
CONECT    9    8   10   27                                                  
CONECT   10    9   11   28                                                  
CONECT   11   16   10   12                                                  
CONECT   12   11   13   29   30                                             
CONECT   13   14   12   31                                                  
CONECT   14   13   15                                                       
CONECT   15   14   32                                                       
CONECT   16   11   17   33                                                  
CONECT   17    8   16   34                                                  
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    3                                                            
CONECT   21    3                                                            
CONECT   22    3                                                            
CONECT   23    4                                                            
CONECT   24    5                                                            
CONECT   25    6                                                            
CONECT   26    6                                                            
CONECT   27    9                                                            
CONECT   28   10                                                            
CONECT   29   12                                                            
CONECT   30   12                                                            
CONECT   31   13                                                            
CONECT   32   15                                                            
CONECT   33   16                                                            
CONECT   34   17                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   68    0
END

RDKit          3D

34 34  0  0  0  0  0  0  0  0999 V2000
   -0.6052   -2.4517   -2.8109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0186   -3.3295   -1.9778 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6040   -4.5894   -2.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1057   -3.1624   -0.4727 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5666   -4.2664    0.1402 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4099   -1.8535    0.1636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8394   -1.8039    0.0494 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4619   -0.6825    0.5226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8402   -0.6441    0.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6036    0.4438    0.7319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9937    1.5122    1.3976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7989    2.7013    1.8598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5538    3.9032    0.9808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9809    5.0206    1.3183 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5804    5.0101    2.6567 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6109    1.4701    1.6195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8493    0.3792    1.1863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6540   -2.6346   -3.8809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0674   -1.5328   -2.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6630   -4.6398   -2.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5441   -4.6379   -3.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0977   -5.4749   -2.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1689   -3.2498   -0.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5170   -4.0589    0.0600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1493   -1.8658    1.2293 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0545   -0.9886   -0.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3257   -1.4699   -0.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6747    0.4439    0.5439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5793    2.9036    2.9120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8701    2.4745    1.8021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8974    3.8148   -0.0643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1872    5.8969    2.7637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1166    2.2931    2.1341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7837    0.3931    1.3884 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
 17  8  2  0
  7  6  1  0
 11 16  2  0
  6  4  1  0
  8  9  1  0
  4  2  1  0
  9 10  2  0
  2  3  1  0
 10 11  1  0
 13 14  2  0
 11 12  1  0
 14 15  1  0
 16 17  1  0
  4  5  1  0
 12 13  1  0
  2  1  2  3
 13 31  1  0
 10 28  1  0
 16 33  1  0
 17 34  1  0
  9 27  1  0
 12 29  1  0
 12 30  1  0
  6 25  1  0
  6 26  1  0
  4 23  1  6
  3 20  1  0
  3 21  1  0
  3 22  1  0
 15 32  1  0
  5 24  1  0
  1 18  1  0
  1 19  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₃H₁₇NO₃

Average Mass

235.2830 Da

Monoisotopic Mass

235.12084 Da

IUPAC Name

(2S)-1-{4-[(2Z)-2-(hydroxyimino)ethyl]phenoxy}-3-methylbut-3-en-2-ol

Traditional Name

(2S)-1-{4-[(2Z)-2-(hydroxyimino)ethyl]phenoxy}-3-methylbut-3-en-2-ol

CAS Registry Number

Not Available

SMILES

[H]O\N=C(\[H])C([H])([H])C1=C([H])C([H])=C(OC([H])([H])[C@@]([H])(O[H])C(=C([H])[H])C([H])([H])[H])C([H])=C1[H]

InChI Identifier

InChI=1S/C13H17NO3/c1-10(2)13(15)9-17-12-5-3-11(4-6-12)7-8-14-16/h3-6,8,13,15-16H,1,7,9H2,2H3/b14-8-/t13-/m1/s1

InChI Key

RYDLTTLOGVZOMQ-HRYODUOUSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Stachylidium sp.	JEOL database	Almeida, C., et al, J. Nat. Prod. 74, 21 (2011)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenol ethers

Sub Class

Not Available

Direct Parent

Phenol ethers

Alternative Parents

Substituents

Phenoxy compound
Phenol ether
Alkyl aryl ether
Monocyclic benzene moiety
Aldoxime
Secondary alcohol
Ether
Oxime
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Alcohol
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	2.19	ALOGPS
logP	1.65	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	9.87	ChemAxon
pKa (Strongest Basic)	2.27	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	62.05 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	66.13 m³·mol⁻¹	ChemAxon
Polarizability	25.87 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

27026044

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139583943

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Almeida C, Part N, Bouhired S, Kehraus S, Konig GM: Stachylines A-D from the sponge-derived fungus Stachylidium sp. J Nat Prod. 2011 Jan 28;74(1):21-5. doi: 10.1021/np1005345. Epub 2010 Dec 16. [PubMed:21162532 ]
Almeida, C., et al. (2011). Almeida, C., et al, J. Nat. Prod. 74, 21 (2011). J. Nat. Prod..

Showing NP-Card for Z-stachyline A (NP0035743)

MOL for NP0035743 (Z-stachyline A)

3D MOL for NP0035743 (Z-stachyline A)

3D SDF for NP0035743 (Z-stachyline A)

3D-SDF for NP0035743 (Z-stachyline A)

PDB for NP0035743 (Z-stachyline A)

3D PDB for NP0035743 (Z-stachyline A)

SMILES for NP0035743 (Z-stachyline A)

INCHI for NP0035743 (Z-stachyline A)

Structure for NP0035743 (Z-stachyline A)

3D Structure for NP0035743 (Z-stachyline A)