NP-MRD: Showing NP-Card for Acremine O (NP0011966)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2021-01-05 21:29:20 UTC

Updated at

2021-07-15 17:10:28 UTC

NP-MRD ID

NP0011966

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Acremine O

Provided By

NPAtlas

Description

(3R,5R)-7-chloro-3-hydroxy-2,2,8-trimethyl-1-oxaspiro[4.5]Dec-7-ene-6,9-dione 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. Acremine O is found in Acremonium persicinum. Based on a literature review very few articles have been published on (3R,5R)-7-chloro-3-hydroxy-2,2,8-trimethyl-1-oxaspiro[4.5]Dec-7-ene-6,9-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117003D          

 32 33  0  0  0  0            999 V2000
    4.5521    0.2116    0.0646 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0843   -0.0501    0.2090 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4678    0.0401    1.3712 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3945    0.4796    2.7885 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.0445   -0.2304    1.4289 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5591   -0.6231    2.5168 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1295   -0.0697    0.2763 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8646    0.0094   -1.0221 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2834   -0.4171   -0.9490 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8309   -1.1026   -1.8782 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6847    1.1831    0.5565 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0825    0.6261    0.7353 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0635    1.4912    0.2880 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0029   -0.6085   -0.1596 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1082   -0.1301   -1.5764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1131   -1.5688    0.1107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7766   -1.1226    0.1798 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9624   -0.5266   -0.6628 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0517    0.1975    1.0360 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6709    1.2140   -0.4224 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8403    1.0330   -1.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3935   -0.6429   -1.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6417    1.8993   -0.2808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3915    1.6990    1.4709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2602    0.3009    1.7889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1377    2.2432    0.8968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5325    0.7875   -1.7876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9345   -0.9436   -2.3110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1886    0.1626   -1.7280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7013   -2.6056   -0.0646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9147   -1.4667   -0.6763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5954   -1.4698    1.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
  9  2  1  0  0  0  0
  7 17  1  6  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  8 21  1  0  0  0  0
  8 22  1  0  0  0  0
 11 23  1  0  0  0  0
 11 24  1  0  0  0  0
 12 25  1  1  0  0  0
 13 26  1  0  0  0  0
 15 27  1  0  0  0  0
 15 28  1  0  0  0  0
 15 29  1  0  0  0  0
 16 30  1  0  0  0  0
 16 31  1  0  0  0  0
 16 32  1  0  0  0  0
M  END

     RDKit          3D

 32 33  0  0  0  0  0  0  0  0999 V2000
    4.5521    0.2116    0.0646 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0843   -0.0501    0.2090 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4678    0.0401    1.3712 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3945    0.4796    2.7885 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.0445   -0.2304    1.4289 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5591   -0.6231    2.5168 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1295   -0.0697    0.2763 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8646    0.0094   -1.0221 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2834   -0.4171   -0.9490 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8309   -1.1026   -1.8782 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6847    1.1831    0.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0825    0.6261    0.7353 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0635    1.4912    0.2880 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0029   -0.6085   -0.1596 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1082   -0.1301   -1.5764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1131   -1.5688    0.1107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7766   -1.1226    0.1798 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9624   -0.5266   -0.6628 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0517    0.1975    1.0360 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6709    1.2140   -0.4224 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8403    1.0330   -1.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3935   -0.6429   -1.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6417    1.8993   -0.2808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3915    1.6990    1.4709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2602    0.3009    1.7889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1377    2.2432    0.8968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5325    0.7875   -1.7876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9345   -0.9436   -2.3110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1886    0.1626   -1.7280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7013   -2.6056   -0.0646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9147   -1.4667   -0.6763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5954   -1.4698    1.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  7 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  6
 14 16  1  0
 14 17  1  0
  9  2  1  0
  7 17  1  6
  1 18  1  0
  1 19  1  0
  1 20  1  0
  8 21  1  0
  8 22  1  0
 11 23  1  0
 11 24  1  0
 12 25  1  1
 13 26  1  0
 15 27  1  0
 15 28  1  0
 15 29  1  0
 16 30  1  0
 16 31  1  0
 16 32  1  0
M  END


  Mrv1652306242117003D          

 32 33  0  0  0  0            999 V2000
    4.5521    0.2116    0.0646 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0843   -0.0501    0.2090 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4678    0.0401    1.3712 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3945    0.4796    2.7885 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.0445   -0.2304    1.4289 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5591   -0.6231    2.5168 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1295   -0.0697    0.2763 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8646    0.0094   -1.0221 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2834   -0.4171   -0.9490 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8309   -1.1026   -1.8782 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6847    1.1831    0.5565 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0825    0.6261    0.7353 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0635    1.4912    0.2880 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0029   -0.6085   -0.1596 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1082   -0.1301   -1.5764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1131   -1.5688    0.1107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7766   -1.1226    0.1798 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9624   -0.5266   -0.6628 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0517    0.1975    1.0360 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6709    1.2140   -0.4224 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8403    1.0330   -1.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3935   -0.6429   -1.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6417    1.8993   -0.2808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3915    1.6990    1.4709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2602    0.3009    1.7889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1377    2.2432    0.8968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5325    0.7875   -1.7876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9345   -0.9436   -2.3110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1886    0.1626   -1.7280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7013   -2.6056   -0.0646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9147   -1.4667   -0.6763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5954   -1.4698    1.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
  9  2  1  0  0  0  0
  7 17  1  6  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  8 21  1  0  0  0  0
  8 22  1  0  0  0  0
 11 23  1  0  0  0  0
 11 24  1  0  0  0  0
 12 25  1  1  0  0  0
 13 26  1  0  0  0  0
 15 27  1  0  0  0  0
 15 28  1  0  0  0  0
 15 29  1  0  0  0  0
 16 30  1  0  0  0  0
 16 31  1  0  0  0  0
 16 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0011966

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]1([H])C([H])([H])[C@]2(OC1(C([H])([H])[H])C([H])([H])[H])C(=O)C(Cl)=C(C(=O)C2([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C12H15ClO4/c1-6-7(14)4-12(10(16)9(6)13)5-8(15)11(2,3)17-12/h8,15H,4-5H2,1-3H3/t8-,12+/m1/s1

> <INCHI_KEY>
VJXALBGDINDGFL-PELKAZGASA-N

> <FORMULA>
C12H15ClO4

> <MOLECULAR_WEIGHT>
258.7

> <EXACT_MASS>
258.0658867

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
25.16962920825833

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,5R)-7-chloro-3-hydroxy-2,2,8-trimethyl-1-oxaspiro[4.5]dec-7-ene-6,9-dione

> <ALOGPS_LOGP>
1.06

> <JCHEM_LOGP>
1.4102255023333334

> <ALOGPS_LOGS>
-1.99

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.843751922481736

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.76281880137282

> <JCHEM_PKA_STRONGEST_BASIC>
-3.281388549865805

> <JCHEM_POLAR_SURFACE_AREA>
63.6

> <JCHEM_REFRACTIVITY>
63.077200000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.64e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R,5R)-7-chloro-3-hydroxy-2,2,8-trimethyl-1-oxaspiro[4.5]dec-7-ene-6,9-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 32 33  0  0  0  0  0  0  0  0999 V2000
    4.5521    0.2116    0.0646 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0843   -0.0501    0.2090 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4678    0.0401    1.3712 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3945    0.4796    2.7885 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.0445   -0.2304    1.4289 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5591   -0.6231    2.5168 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1295   -0.0697    0.2763 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8646    0.0094   -1.0221 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2834   -0.4171   -0.9490 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8309   -1.1026   -1.8782 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6847    1.1831    0.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0825    0.6261    0.7353 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0635    1.4912    0.2880 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0029   -0.6085   -0.1596 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1082   -0.1301   -1.5764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1131   -1.5688    0.1107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7766   -1.1226    0.1798 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9624   -0.5266   -0.6628 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0517    0.1975    1.0360 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6709    1.2140   -0.4224 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8403    1.0330   -1.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3935   -0.6429   -1.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6417    1.8993   -0.2808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3915    1.6990    1.4709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2602    0.3009    1.7889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1377    2.2432    0.8968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5325    0.7875   -1.7876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9345   -0.9436   -2.3110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1886    0.1626   -1.7280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7013   -2.6056   -0.0646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9147   -1.4667   -0.6763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5954   -1.4698    1.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  7 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  6
 14 16  1  0
 14 17  1  0
  9  2  1  0
  7 17  1  6
  1 18  1  0
  1 19  1  0
  1 20  1  0
  8 21  1  0
  8 22  1  0
 11 23  1  0
 11 24  1  0
 12 25  1  1
 13 26  1  0
 15 27  1  0
 15 28  1  0
 15 29  1  0
 16 30  1  0
 16 31  1  0
 16 32  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       4.552   0.212   0.065  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.084  -0.050   0.209  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.468   0.040   1.371  0.00  0.00           C+0
HETATM    4 Cl   UNK     0       3.394   0.480   2.789  0.00  0.00          Cl+0
HETATM    5  C   UNK     0       1.044  -0.230   1.429  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.559  -0.623   2.517  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.130  -0.070   0.276  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.865   0.009  -1.022  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.283  -0.417  -0.949  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.831  -1.103  -1.878  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.685   1.183   0.557  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.083   0.626   0.735  0.00  0.00           C+0
HETATM   13  O   UNK     0      -3.063   1.491   0.288  0.00  0.00           O+0
HETATM   14  C   UNK     0      -2.003  -0.609  -0.160  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.108  -0.130  -1.576  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.113  -1.569   0.111  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.777  -1.123   0.180  0.00  0.00           O+0
HETATM   18  H   UNK     0       4.962  -0.527  -0.663  0.00  0.00           H+0
HETATM   19  H   UNK     0       5.052   0.198   1.036  0.00  0.00           H+0
HETATM   20  H   UNK     0       4.671   1.214  -0.422  0.00  0.00           H+0
HETATM   21  H   UNK     0       0.840   1.033  -1.466  0.00  0.00           H+0
HETATM   22  H   UNK     0       0.394  -0.643  -1.815  0.00  0.00           H+0
HETATM   23  H   UNK     0      -0.642   1.899  -0.281  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.392   1.699   1.471  0.00  0.00           H+0
HETATM   25  H   UNK     0      -2.260   0.301   1.789  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.138   2.243   0.897  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.533   0.788  -1.788  0.00  0.00           H+0
HETATM   28  H   UNK     0      -1.935  -0.944  -2.311  0.00  0.00           H+0
HETATM   29  H   UNK     0      -3.189   0.163  -1.728  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.701  -2.606  -0.065  0.00  0.00           H+0
HETATM   31  H   UNK     0      -3.915  -1.467  -0.676  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.595  -1.470   1.082  0.00  0.00           H+0
CONECT    1    2   18   19   20                                             
CONECT    2    1    3    9                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   11   17                                             
CONECT    8    7    9   21   22                                             
CONECT    9    8   10    2                                                  
CONECT   10    9                                                            
CONECT   11    7   12   23   24                                             
CONECT   12   11   13   14   25                                             
CONECT   13   12   26                                                       
CONECT   14   12   15   16   17                                             
CONECT   15   14   27   28   29                                             
CONECT   16   14   30   31   32                                             
CONECT   17   14    7                                                       
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    8                                                            
CONECT   22    8                                                            
CONECT   23   11                                                            
CONECT   24   11                                                            
CONECT   25   12                                                            
CONECT   26   13                                                            
CONECT   27   15                                                            
CONECT   28   15                                                            
CONECT   29   15                                                            
CONECT   30   16                                                            
CONECT   31   16                                                            
CONECT   32   16                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   66    0
END

RDKit          3D

32 33  0  0  0  0  0  0  0  0999 V2000
    4.5521    0.2116    0.0646 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0843   -0.0501    0.2090 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4678    0.0401    1.3712 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3945    0.4796    2.7885 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.0445   -0.2304    1.4289 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5591   -0.6231    2.5168 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1295   -0.0697    0.2763 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8646    0.0094   -1.0221 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2834   -0.4171   -0.9490 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8309   -1.1026   -1.8782 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6847    1.1831    0.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0825    0.6261    0.7353 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0635    1.4912    0.2880 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0029   -0.6085   -0.1596 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1082   -0.1301   -1.5764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1131   -1.5688    0.1107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7766   -1.1226    0.1798 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9624   -0.5266   -0.6628 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0517    0.1975    1.0360 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6709    1.2140   -0.4224 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8403    1.0330   -1.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3935   -0.6429   -1.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6417    1.8993   -0.2808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3915    1.6990    1.4709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2602    0.3009    1.7889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1377    2.2432    0.8968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5325    0.7875   -1.7876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9345   -0.9436   -2.3110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1886    0.1626   -1.7280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7013   -2.6056   -0.0646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9147   -1.4667   -0.6763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5954   -1.4698    1.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  7 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  6
 14 16  1  0
 14 17  1  0
  9  2  1  0
  7 17  1  6
  1 18  1  0
  1 19  1  0
  1 20  1  0
  8 21  1  0
  8 22  1  0
 11 23  1  0
 11 24  1  0
 12 25  1  1
 13 26  1  0
 15 27  1  0
 15 28  1  0
 15 29  1  0
 16 30  1  0
 16 31  1  0
 16 32  1  0
M  END

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

Synonyms

Not Available

Chemical Formula

C₁₂H₁₅ClO₄

Average Mass

258.7000 Da

Monoisotopic Mass

258.06589 Da

IUPAC Name

(3R,5R)-7-chloro-3-hydroxy-2,2,8-trimethyl-1-oxaspiro[4.5]dec-7-ene-6,9-dione

Traditional Name

(3R,5R)-7-chloro-3-hydroxy-2,2,8-trimethyl-1-oxaspiro[4.5]dec-7-ene-6,9-dione

CAS Registry Number

Not Available

SMILES

CC1=C(Cl)C(=O)[C@@]2(C[C@@H](O)C(C)(C)O2)CC1=O

InChI Identifier

InChI=1S/C12H15ClO4/c1-6-7(14)4-12(10(16)9(6)13)5-8(15)11(2,3)17-12/h8,15H,4-5H2,1-3H3/t8-,12+/m1/s1

InChI Key

VJXALBGDINDGFL-PELKAZGASA-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
Monosaccharide
Alpha-haloketone
Alpha-chloroketone
Oxolane
Vinylogous halide
Secondary alcohol
Dialkyl ether
Ether
Oxacycle
Vinyl chloride
Vinyl halide
Chloroalkene
Haloalkene
Organoheterocyclic compound
Alcohol
Organic oxide
Organohalogen compound
Organochloride
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.06	ALOGPS
logP	1.41	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	13.76	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	63.08 m³·mol⁻¹	ChemAxon
Polarizability	25.17 Å³	ChemAxon
Number of Rings	2	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

NPA007641

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

30771259

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

72191328

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Acremine O (NP0011966)

MOL for NP0011966 (Acremine O)

3D MOL for NP0011966 (Acremine O)

3D SDF for NP0011966 (Acremine O)

3D-SDF for NP0011966 (Acremine O)

PDB for NP0011966 (Acremine O)

3D PDB for NP0011966 (Acremine O)

SMILES for NP0011966 (Acremine O)

INCHI for NP0011966 (Acremine O)

Structure for NP0011966 (Acremine O)

3D Structure for NP0011966 (Acremine O)