NP-MRD: Showing NP-Card for (1s,2s,3s,4r)-3-[(1e,3e)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate (NP0164627)

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Record Information

Version

2.0

Created at

2022-09-02 23:33:04 UTC

Updated at

2022-09-02 23:33:05 UTC

NP-MRD ID

NP0164627

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,3s,4r)-3-[(1e,3e)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate

Description

Ilicicolin F belongs to the class of organic compounds known as hydroxybenzaldehydes. These are organic aromatic compounds containing a benzene ring carrying an aldehyde group and a hydroxyl group. (1s,2s,3s,4r)-3-[(1e,3e)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate is found in Neonectria ditissima. Based on a literature review very few articles have been published on Ilicicolin F.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032201332D          

 32 33  0  0  1  0            999 V2000
    5.8138   -6.0442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0993   -5.6317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848   -6.0442    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0993   -4.8067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848   -4.3942    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6704   -4.8067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -4.3942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2414   -4.8067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -3.5692    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2414   -3.1567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6704   -3.1567    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1401   -2.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2007   -2.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0131   -2.6680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5434   -2.0360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2612   -1.2608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3559   -2.1793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8862   -1.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6986   -1.6906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2289   -1.0586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9468   -0.2833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0414   -1.2018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5717   -0.5698    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    9.3236   -1.9771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1360   -2.1203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7933   -2.6091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0754   -3.3843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5451   -4.0163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9808   -2.4658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4505   -3.0978    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848   -3.5692    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0993   -3.1567    0.0000 C   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
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  1  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 26 29  2  0  0  0  0
 19 29  1  0  0  0  0
 29 30  1  0  0  0  0
 11 31  1  0  0  0  0
  5 31  1  0  0  0  0
 31 32  1  6  0  0  0
M  END

     RDKit          3D

 63 64  0  0  0  0  0  0  0  0999 V2000
    5.9214   -0.6415    3.2332 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4376    0.4003    2.3002 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5779    1.6027    2.6159 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8537    0.0435    1.1267 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3789    1.0116    0.2087 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2452    0.9216   -1.0297 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8589   -0.2596   -1.8443 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4335   -0.6476   -2.8384 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6642   -1.0147   -1.3835 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2645   -2.0868   -2.3750 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5394   -0.0211   -1.1834 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3359    0.6746   -2.5053 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3244   -0.8435   -0.8258 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3676   -0.3697   -0.0715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8434   -1.0884    0.3268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1210   -2.4796   -0.0854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7485   -0.4925    1.1011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0025   -1.1438    1.5500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1940   -0.3634    1.1194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5043    0.7826    1.8025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7133    1.1815    2.8733 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5765    1.5330    1.4450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9509    2.9878    2.3284 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -6.3694    1.1328    0.3716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5252    1.9892    0.0233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0924   -0.0115   -0.3407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9231   -0.4116   -1.4496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9342    0.2615   -1.8162 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9970   -0.7568    0.0429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6620   -1.9142   -0.6260 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9199    0.8969   -0.0759 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3215    2.2801   -0.2116 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7144   -0.2595    4.2676 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2761   -1.5420    3.1318 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0008   -0.8624    3.1201 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5795    2.0325    0.6389 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2441    1.8671   -1.6113 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2881    0.7686   -0.6854 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9691   -1.4844   -0.4045 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3331   -1.8367   -2.9261 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0881   -2.3336   -3.0842 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0572   -3.0075   -1.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7395    0.1076   -3.3678 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7865    1.6798   -2.5557 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2444    0.7683   -2.6704 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2470   -1.8484   -1.2059 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5281    0.6684    0.2729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9822   -2.4366   -0.8177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3871   -3.0785    0.8228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2982   -2.9435   -0.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5459    0.5197    1.4119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0205   -1.2447    2.6617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1491   -2.1592    1.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8580    1.9952    3.4308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5696    2.8846    0.7046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4075    2.3749   -1.0293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4527    1.4037    0.1307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7021   -1.3002   -1.9974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1104   -2.3374   -1.4001 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4618    0.4694    0.8668 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5966    2.3569   -1.0454 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8891    2.6596    0.7357 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1528    2.9648   -0.4803 H   0  0  0  0  0  0  0  0  0  0  0  0
 32 31  1  0
 31  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 11 13  1  1
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  2  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 27 28  2  0
 26 29  2  0
 29 30  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
 11 31  1  0
 29 19  1  0
 32 61  1  0
 32 62  1  0
 32 63  1  0
 31 60  1  1
  5 36  1  1
  6 37  1  0
  6 38  1  0
  9 39  1  1
 10 40  1  0
 10 41  1  0
 10 42  1  0
 12 43  1  0
 12 44  1  0
 12 45  1  0
 13 46  1  0
 14 47  1  0
 16 48  1  0
 16 49  1  0
 16 50  1  0
 17 51  1  0
 18 52  1  0
 18 53  1  0
 21 54  1  0
 25 55  1  0
 25 56  1  0
 25 57  1  0
 27 58  1  0
 30 59  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
M  END


  Mrv1652309032201332D          

 32 33  0  0  1  0            999 V2000
    5.8138   -6.0442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0993   -5.6317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848   -6.0442    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0993   -4.8067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848   -4.3942    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6704   -4.8067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -4.3942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2414   -4.8067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -3.5692    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2414   -3.1567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6704   -3.1567    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1401   -2.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2007   -2.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0131   -2.6680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5434   -2.0360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2612   -1.2608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.2289   -1.0586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9468   -0.2833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0414   -1.2018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5717   -0.5698    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    9.3236   -1.9771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1360   -2.1203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7933   -2.6091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0754   -3.3843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5451   -4.0163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9808   -2.4658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4505   -3.0978    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848   -3.5692    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0993   -3.1567    0.0000 C   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
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
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 13 14  2  0  0  0  0
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 31 32  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0164627

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@H](CC(=O)[C@H](C)[C@@]1(C)\C=C\C(\C)=C\CC1=C(O)C(Cl)=C(C)C(C=O)=C1O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H31ClO6/c1-13(7-8-18-23(30)19(12-27)14(2)22(26)24(18)31)9-10-25(6)15(3)20(29)11-21(16(25)4)32-17(5)28/h7,9-10,12,15-16,21,30-31H,8,11H2,1-6H3/b10-9+,13-7+/t15-,16+,21-,25+/m0/s1

> <INCHI_KEY>
ACSLMZYXJATICN-IRMIYARYSA-N

> <FORMULA>
C25H31ClO6

> <MOLECULAR_WEIGHT>
462.97

> <EXACT_MASS>
462.1809164

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
49.12428353852326

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,3S,4R)-3-[(1E,3E)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate

> <ALOGPS_LOGP>
4.90

> <JCHEM_LOGP>
5.942536952000001

> <ALOGPS_LOGS>
-5.25

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.527442619852563

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.841100529614715

> <JCHEM_PKA_STRONGEST_BASIC>
-6.043439126273062

> <JCHEM_POLAR_SURFACE_AREA>
100.90000000000002

> <JCHEM_REFRACTIVITY>
126.99119999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.62e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3S,4R)-3-[(1E,3E)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      10.852 -11.283   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.519 -10.513   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       8.185 -11.283   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       9.519  -8.973   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.185  -8.203   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.851  -8.973   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.518  -8.203   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.184  -8.973   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.518  -6.663   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.184  -5.893   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.851  -5.893   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.861  -4.713   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.841  -4.713   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.358  -4.980   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.348  -3.801   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.821  -2.353   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.864  -4.068   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.854  -2.888   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.371  -3.156   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      15.361  -1.976   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      14.834  -0.529   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      16.877  -2.243   0.000  0.00  0.00           C+0
HETATM   23 Cl   UNK     0      17.867  -1.064   0.000  0.00  0.00          Cl+0
HETATM   24  C   UNK     0      17.404  -3.691   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      18.921  -3.958   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      16.414  -4.870   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      16.941  -6.317   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      15.951  -7.497   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      14.898  -4.603   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      13.908  -5.783   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       8.185  -6.663   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.519  -5.893   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   31                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13   31                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   29                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   19   30                                                  
CONECT   30   29                                                            
CONECT   31   11    5   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₁ClO₆

Average Mass

462.9700 Da

Monoisotopic Mass

462.18092 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@H](CC(=O)[C@H](C)[C@@]1(C)\C=C\C(\C)=C\CC1=C(O)C(Cl)=C(C)C(C=O)=C1O)OC(C)=O

InChI Identifier

InChI=1S/C25H31ClO6/c1-13(7-8-18-23(30)19(12-27)14(2)22(26)24(18)31)9-10-25(6)15(3)20(29)11-21(16(25)4)32-17(5)28/h7,9-10,12,15-16,21,30-31H,8,11H2,1-6H3/b10-9+,13-7+/t15-,16+,21-,25+/m0/s1

InChI Key

ACSLMZYXJATICN-IRMIYARYSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Neonectria ditissima	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxybenzaldehydes. These are organic aromatic compounds containing a benzene ring carrying an aldehyde group and a hydroxyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Hydroxybenzaldehydes

Alternative Parents

Substituents

Hydroxybenzaldehyde
2-halophenol
4-halophenol
M-cresol
2-chlorophenol
Benzoyl
4-chlorophenol
Resorcinol
Halobenzene
Chlorobenzene
Toluene
Phenol
Benzenoid
Aryl halide
Monocyclic benzene moiety
Aryl chloride
Vinylogous acid
Cyclic ketone
Carboxylic acid ester
Ketone
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organic oxide
Organochloride
Organohalogen 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	4.9	ALOGPS
logS	-5.2	ALOGPS

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

28296297

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

51136289

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,3s,4r)-3-[(1e,3e)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate (NP0164627)

MOL for NP0164627 ((1s,2s,3s,4r)-3-[(1e,3e)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate)

3D MOL for NP0164627 ((1s,2s,3s,4r)-3-[(1e,3e)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate)

3D SDF for NP0164627 ((1s,2s,3s,4r)-3-[(1e,3e)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate)

3D-SDF for NP0164627 ((1s,2s,3s,4r)-3-[(1e,3e)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate)

PDB for NP0164627 ((1s,2s,3s,4r)-3-[(1e,3e)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate)

3D PDB for NP0164627 ((1s,2s,3s,4r)-3-[(1e,3e)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate)

SMILES for NP0164627 ((1s,2s,3s,4r)-3-[(1e,3e)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate)

INCHI for NP0164627 ((1s,2s,3s,4r)-3-[(1e,3e)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate)

Structure for NP0164627 ((1s,2s,3s,4r)-3-[(1e,3e)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate)

3D Structure for NP0164627 ((1s,2s,3s,4r)-3-[(1e,3e)-5-(3-chloro-5-formyl-2,6-dihydroxy-4-methylphenyl)-3-methylpenta-1,3-dien-1-yl]-2,3,4-trimethyl-5-oxocyclohexyl acetate)