NP-MRD: Showing NP-Card for 5-chloroacremine A (NP0011964)

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Record Information

Version

2.0

Created at

2021-01-05 21:29:16 UTC

Updated at

2021-07-15 17:10:27 UTC

NP-MRD ID

NP0011964

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-chloroacremine A

Provided By

NPAtlas

Description

5-Chloroacremine A belongs to the class of organic compounds known as cyclohexenones. Cyclohexenones are compounds containing a cylohexenone moiety, which is a six-membered aliphatic ring that carries a ketone and has one endocyclic double bond. 5-chloroacremine A is found in Acremonium persicinum. 5-chloroacremine A was first documented in 2013 (PMID: 23883432). Based on a literature review very few articles have been published on 5-chloroacremine A.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117003D          

 34 34  0  0  0  0            999 V2000
    3.9555   -1.2484   -0.5255 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3261    0.1157   -0.3215 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0687    0.8625    0.7446 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3794    0.8549   -1.4941 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8998   -0.1092    0.0789 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9297    0.2729   -0.7255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4789    0.1083   -0.4459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3663    0.5327   -1.3309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8023    0.3940   -1.1040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6903    0.6537   -1.9454 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2101   -0.0941    0.2354 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6410   -0.5760    0.2641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1079    0.9710    1.1269 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2513   -1.1968    0.6186 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0308   -2.3180   -0.7653 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.8831   -0.5348    0.8292 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0317    0.4111    1.8202 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5405   -1.9238    0.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0608   -1.1846   -0.4763 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6593   -1.6857   -1.5021 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414    0.5425    0.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0248    1.9536    0.4978 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6306    0.6232    1.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1405    0.2345   -2.2479 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6531   -0.5802    1.0192 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2222    0.7394   -1.6533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0708    1.0049   -2.2692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7851   -1.0642    1.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2987    0.3134    0.2554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8982   -1.2362   -0.5788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3377    1.8245    0.6450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5619   -1.7544    1.5101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2152   -1.3724    1.1227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9711   -0.0575    2.6918 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
  2  4  1  6  0  0  0
  2  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  1  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16  7  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
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
  3 23  1  0  0  0  0
  4 24  1  0  0  0  0
  5 25  1  0  0  0  0
  6 26  1  0  0  0  0
  8 27  1  0  0  0  0
 12 28  1  0  0  0  0
 12 29  1  0  0  0  0
 12 30  1  0  0  0  0
 13 31  1  0  0  0  0
 14 32  1  1  0  0  0
 16 33  1  1  0  0  0
 17 34  1  0  0  0  0
M  END

     RDKit          3D

 34 34  0  0  0  0  0  0  0  0999 V2000
    3.9555   -1.2484   -0.5255 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3261    0.1157   -0.3215 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0687    0.8625    0.7446 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3794    0.8549   -1.4941 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8998   -0.1092    0.0789 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9297    0.2729   -0.7255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4789    0.1083   -0.4459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3663    0.5327   -1.3309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8023    0.3940   -1.1040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6903    0.6537   -1.9454 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2101   -0.0941    0.2354 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6410   -0.5760    0.2641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1079    0.9710    1.1269 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2513   -1.1968    0.6186 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0308   -2.3180   -0.7653 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.8831   -0.5348    0.8292 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0317    0.4111    1.8202 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5405   -1.9238    0.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0608   -1.1846   -0.4763 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6593   -1.6857   -1.5021 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414    0.5425    0.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0248    1.9536    0.4978 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6306    0.6232    1.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1405    0.2345   -2.2479 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6531   -0.5802    1.0192 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2222    0.7394   -1.6533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0708    1.0049   -2.2692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7851   -1.0642    1.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2987    0.3134    0.2554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8982   -1.2362   -0.5788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3377    1.8245    0.6450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5619   -1.7544    1.5101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2152   -1.3724    1.1227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9711   -0.0575    2.6918 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  6
  2  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 11 13  1  1
 11 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16  7  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  5 25  1  0
  6 26  1  0
  8 27  1  0
 12 28  1  0
 12 29  1  0
 12 30  1  0
 13 31  1  0
 14 32  1  1
 16 33  1  1
 17 34  1  0
M  END


  Mrv1652306242117003D          

 34 34  0  0  0  0            999 V2000
    3.9555   -1.2484   -0.5255 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3261    0.1157   -0.3215 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0687    0.8625    0.7446 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3794    0.8549   -1.4941 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8998   -0.1092    0.0789 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9297    0.2729   -0.7255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4789    0.1083   -0.4459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3663    0.5327   -1.3309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8023    0.3940   -1.1040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6903    0.6537   -1.9454 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2101   -0.0941    0.2354 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6410   -0.5760    0.2641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1079    0.9710    1.1269 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2513   -1.1968    0.6186 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0308   -2.3180   -0.7653 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.8831   -0.5348    0.8292 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0317    0.4111    1.8202 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5405   -1.9238    0.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0608   -1.1846   -0.4763 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6593   -1.6857   -1.5021 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414    0.5425    0.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0248    1.9536    0.4978 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6306    0.6232    1.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1405    0.2345   -2.2479 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6531   -0.5802    1.0192 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2222    0.7394   -1.6533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0708    1.0049   -2.2692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7851   -1.0642    1.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2987    0.3134    0.2554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8982   -1.2362   -0.5788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3377    1.8245    0.6450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5619   -1.7544    1.5101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2152   -1.3724    1.1227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9711   -0.0575    2.6918 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
  2  4  1  6  0  0  0
  2  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  1  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16  7  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
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
  3 23  1  0  0  0  0
  4 24  1  0  0  0  0
  5 25  1  0  0  0  0
  6 26  1  0  0  0  0
  8 27  1  0  0  0  0
 12 28  1  0  0  0  0
 12 29  1  0  0  0  0
 12 30  1  0  0  0  0
 13 31  1  0  0  0  0
 14 32  1  1  0  0  0
 16 33  1  1  0  0  0
 17 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0011964

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C12H17ClO4/c1-11(2,16)5-4-7-6-8(14)12(3,17)10(13)9(7)15/h4-6,9-10,15-17H,1-3H3/b5-4+/t9-,10+,12+/m1/s1

> <INCHI_KEY>
BEHCJZAKUQKRSB-QTIKQWDBSA-N

> <FORMULA>
C12H17ClO4

> <MOLECULAR_WEIGHT>
260.71

> <EXACT_MASS>
260.0815367

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
26.300978494277516

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R,5S,6S)-5-chloro-4,6-dihydroxy-3-[(1E)-3-hydroxy-3-methylbut-1-en-1-yl]-6-methylcyclohex-2-en-1-one

> <ALOGPS_LOGP>
0.75

> <JCHEM_LOGP>
0.5953673030000008

> <ALOGPS_LOGS>
-2.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.496911954182675

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.191558534498071

> <JCHEM_PKA_STRONGEST_BASIC>
-1.5752715818133423

> <JCHEM_POLAR_SURFACE_AREA>
77.76

> <JCHEM_REFRACTIVITY>
66.59849999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.17e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4R,5S,6S)-5-chloro-4,6-dihydroxy-3-[(1E)-3-hydroxy-3-methylbut-1-en-1-yl]-6-methylcyclohex-2-en-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 34 34  0  0  0  0  0  0  0  0999 V2000
    3.9555   -1.2484   -0.5255 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3261    0.1157   -0.3215 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0687    0.8625    0.7446 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3794    0.8549   -1.4941 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8998   -0.1092    0.0789 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9297    0.2729   -0.7255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4789    0.1083   -0.4459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3663    0.5327   -1.3309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8023    0.3940   -1.1040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6903    0.6537   -1.9454 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2101   -0.0941    0.2354 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6410   -0.5760    0.2641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1079    0.9710    1.1269 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2513   -1.1968    0.6186 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0308   -2.3180   -0.7653 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.8831   -0.5348    0.8292 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0317    0.4111    1.8202 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5405   -1.9238    0.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0608   -1.1846   -0.4763 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6593   -1.6857   -1.5021 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414    0.5425    0.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0248    1.9536    0.4978 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6306    0.6232    1.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1405    0.2345   -2.2479 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6531   -0.5802    1.0192 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2222    0.7394   -1.6533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0708    1.0049   -2.2692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7851   -1.0642    1.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2987    0.3134    0.2554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8982   -1.2362   -0.5788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3377    1.8245    0.6450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5619   -1.7544    1.5101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2152   -1.3724    1.1227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9711   -0.0575    2.6918 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  6
  2  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 11 13  1  1
 11 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16  7  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  5 25  1  0
  6 26  1  0
  8 27  1  0
 12 28  1  0
 12 29  1  0
 12 30  1  0
 13 31  1  0
 14 32  1  1
 16 33  1  1
 17 34  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       3.955  -1.248  -0.526  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.326   0.116  -0.322  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.069   0.863   0.745  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.379   0.855  -1.494  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.900  -0.109   0.079  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.930   0.273  -0.726  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.479   0.108  -0.446  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.366   0.533  -1.331  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.802   0.394  -1.104  0.00  0.00           C+0
HETATM   10  O   UNK     0      -3.690   0.654  -1.945  0.00  0.00           O+0
HETATM   11  C   UNK     0      -3.210  -0.094   0.235  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.641  -0.576   0.264  0.00  0.00           C+0
HETATM   13  O   UNK     0      -3.108   0.971   1.127  0.00  0.00           O+0
HETATM   14  C   UNK     0      -2.251  -1.197   0.619  0.00  0.00           C+0
HETATM   15 Cl   UNK     0      -2.031  -2.318  -0.765  0.00  0.00          Cl+0
HETATM   16  C   UNK     0      -0.883  -0.535   0.829  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.032   0.411   1.820  0.00  0.00           O+0
HETATM   18  H   UNK     0       3.541  -1.924   0.258  0.00  0.00           H+0
HETATM   19  H   UNK     0       5.061  -1.185  -0.476  0.00  0.00           H+0
HETATM   20  H   UNK     0       3.659  -1.686  -1.502  0.00  0.00           H+0
HETATM   21  H   UNK     0       5.141   0.543   0.697  0.00  0.00           H+0
HETATM   22  H   UNK     0       4.025   1.954   0.498  0.00  0.00           H+0
HETATM   23  H   UNK     0       3.631   0.623   1.713  0.00  0.00           H+0
HETATM   24  H   UNK     0       3.140   0.235  -2.248  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.653  -0.580   1.019  0.00  0.00           H+0
HETATM   26  H   UNK     0       1.222   0.739  -1.653  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.071   1.005  -2.269  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.785  -1.064   1.258  0.00  0.00           H+0
HETATM   29  H   UNK     0      -5.299   0.313   0.255  0.00  0.00           H+0
HETATM   30  H   UNK     0      -4.898  -1.236  -0.579  0.00  0.00           H+0
HETATM   31  H   UNK     0      -3.338   1.825   0.645  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.562  -1.754   1.510  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.215  -1.372   1.123  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.971  -0.058   2.692  0.00  0.00           H+0
CONECT    1    2   18   19   20                                             
CONECT    2    1    3    4    5                                             
CONECT    3    2   21   22   23                                             
CONECT    4    2   24                                                       
CONECT    5    2    6   25                                                  
CONECT    6    5    7   26                                                  
CONECT    7    6    8   16                                                  
CONECT    8    7    9   27                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13   14                                             
CONECT   12   11   28   29   30                                             
CONECT   13   11   31                                                       
CONECT   14   11   15   16   32                                             
CONECT   15   14                                                            
CONECT   16   14   17    7   33                                             
CONECT   17   16   34                                                       
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    3                                                            
CONECT   22    3                                                            
CONECT   23    3                                                            
CONECT   24    4                                                            
CONECT   25    5                                                            
CONECT   26    6                                                            
CONECT   27    8                                                            
CONECT   28   12                                                            
CONECT   29   12                                                            
CONECT   30   12                                                            
CONECT   31   13                                                            
CONECT   32   14                                                            
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
    3.9555   -1.2484   -0.5255 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3261    0.1157   -0.3215 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0687    0.8625    0.7446 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3794    0.8549   -1.4941 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8998   -0.1092    0.0789 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9297    0.2729   -0.7255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4789    0.1083   -0.4459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3663    0.5327   -1.3309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8023    0.3940   -1.1040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6903    0.6537   -1.9454 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2101   -0.0941    0.2354 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6410   -0.5760    0.2641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1079    0.9710    1.1269 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2513   -1.1968    0.6186 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0308   -2.3180   -0.7653 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.8831   -0.5348    0.8292 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0317    0.4111    1.8202 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5405   -1.9238    0.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0608   -1.1846   -0.4763 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6593   -1.6857   -1.5021 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414    0.5425    0.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0248    1.9536    0.4978 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6306    0.6232    1.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1405    0.2345   -2.2479 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6531   -0.5802    1.0192 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2222    0.7394   -1.6533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0708    1.0049   -2.2692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7851   -1.0642    1.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2987    0.3134    0.2554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8982   -1.2362   -0.5788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3377    1.8245    0.6450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5619   -1.7544    1.5101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2152   -1.3724    1.1227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9711   -0.0575    2.6918 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  6
  2  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 11 13  1  1
 11 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16  7  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  5 25  1  0
  6 26  1  0
  8 27  1  0
 12 28  1  0
 12 29  1  0
 12 30  1  0
 13 31  1  0
 14 32  1  1
 16 33  1  1
 17 34  1  0
M  END

View in JSmol View NMR Assignments View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₂H₁₇ClO₄

Average Mass

260.7100 Da

Monoisotopic Mass

260.08154 Da

IUPAC Name

(4R,5S,6S)-5-chloro-4,6-dihydroxy-3-[(1E)-3-hydroxy-3-methylbut-1-en-1-yl]-6-methylcyclohex-2-en-1-one

Traditional Name

(4R,5S,6S)-5-chloro-4,6-dihydroxy-3-[(1E)-3-hydroxy-3-methylbut-1-en-1-yl]-6-methylcyclohex-2-en-1-one

CAS Registry Number

Not Available

SMILES

CC(C)(O)\C=C\C1=CC(=O)[C@](C)(O)[C@@H](Cl)[C@@H]1O

InChI Identifier

InChI=1S/C12H17ClO4/c1-11(2,16)5-4-7-6-8(14)12(3,17)10(13)9(7)15/h4-6,9-10,15-17H,1-3H3/b5-4+/t9-,10+,12+/m1/s1

InChI Key

BEHCJZAKUQKRSB-QTIKQWDBSA-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
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Acremonium persicinum	NPAtlas	23883432

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclohexenones. Cyclohexenones 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
Acyloin
Tertiary alcohol
Secondary alcohol
Halohydrin
Chlorohydrin
Organic oxide
Hydrocarbon derivative
Organochloride
Organohalogen compound
Alkyl halide
Alkyl chloride
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic 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	0.75	ALOGPS
logP	0.6	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	12.19	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	77.76 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	66.6 m³·mol⁻¹	ChemAxon
Polarizability	26.3 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

NPAtlas ID

NPA010081

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

30771257

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

72191326

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Suciati, Fraser JA, Lambert LK, Pierens GK, Bernhardt PV, Garson MJ: Secondary metabolites of the sponge-derived fungus Acremonium persicinum. J Nat Prod. 2013 Aug 23;76(8):1432-40. doi: 10.1021/np4002114. Epub 2013 Jul 24. [PubMed:23883432 ]

Showing NP-Card for 5-chloroacremine A (NP0011964)

MOL for NP0011964 (5-chloroacremine A)

3D MOL for NP0011964 (5-chloroacremine A)

3D SDF for NP0011964 (5-chloroacremine A)

3D-SDF for NP0011964 (5-chloroacremine A)

PDB for NP0011964 (5-chloroacremine A)

3D PDB for NP0011964 (5-chloroacremine A)

SMILES for NP0011964 (5-chloroacremine A)

INCHI for NP0011964 (5-chloroacremine A)

Structure for NP0011964 (5-chloroacremine A)

3D Structure for NP0011964 (5-chloroacremine A)