NP-MRD: Showing NP-Card for (1r,2s,5s,6s,7r,8s,10s)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0²,⁶]undecan-7-yl (2e)-3-phenylprop-2-enoate (NP0330158)

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Record Information

Version

2.0

Created at

2022-09-12 15:14:25 UTC

Updated at

2022-09-12 15:14:25 UTC

NP-MRD ID

NP0330158

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,5s,6s,7r,8s,10s)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0²,⁶]undecan-7-yl (2e)-3-phenylprop-2-enoate

Description

Englerin B belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. (1r,2s,5s,6s,7r,8s,10s)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0²,⁶]undecan-7-yl (2e)-3-phenylprop-2-enoate is found in Phyllanthus engleri. (1r,2s,5s,6s,7r,8s,10s)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0²,⁶]undecan-7-yl (2e)-3-phenylprop-2-enoate was first documented in 2010 (PMID: 20496885). Based on a literature review a small amount of articles have been published on Englerin B (PMID: 29664306) (PMID: 35165752) (PMID: 30938023).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122217142D          

 28 31  0  0  1  0            999 V2000
    3.1344   -0.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5240    0.1246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3486    0.1507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0891    0.8256    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5320    1.5217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2640    2.3019    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8507    2.8819    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4869    2.5789    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3992    3.3992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0072    1.7775    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7859    2.1439    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0367    2.4894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4766    1.8837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8796    1.1638    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5341    0.4147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6888    1.3247    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2688    0.7380    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9918   -0.0392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1804   -0.1879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3785    0.0063    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9034   -0.9650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0919   -1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1850   -1.8909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3495   -2.5193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0726   -3.2964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7389   -3.4451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2734   -2.8167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9965   -2.0396    0.0000 C   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
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
  4 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 16 14  1  1  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
  4 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 23 28  1  0  0  0  0
M  END

     RDKit          3D

 60 63  0  0  0  0  0  0  0  0999 V2000
    0.4667   -0.4776    3.1343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1665    0.6818    2.4571 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9364    1.5564    1.8778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2053    0.3781    1.4414 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7180    1.6781    0.8858 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2143    1.4914    0.7505 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8972    2.2002    1.7386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3732    0.0236    1.0646 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6945   -0.3268    1.6559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3562   -0.1749    2.0001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0716   -0.8653   -0.0933 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9948   -0.7889   -1.2406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1559   -1.2381   -2.4166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7331   -1.4640   -1.8421 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5544   -2.8946   -1.5110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7461   -0.4869   -0.7322 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7364   -0.5695    0.3337 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5816   -0.3265   -0.0517 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5913   -1.2424    0.1137 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2848   -2.3361    0.6348 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9402   -0.8990   -0.3177 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2163    0.2524   -0.8558 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5564    0.6121   -1.2921 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6505   -0.2125   -1.1827 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8997    0.1952   -1.6184 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1014    1.4333   -2.1760 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0198    2.2783   -2.2966 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7933    1.8706   -1.8657 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0005   -1.4536    2.8940 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5466   -0.5422    2.9213 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3335   -0.3769    4.2517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6673    1.3426    3.2294 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6923    1.8255    0.8466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0684    2.5095    2.4344 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9263    1.0195    1.8838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5525    2.4759    1.6702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2184    2.0416   -0.0031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5823    1.7552   -0.2553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3817    3.0354    1.9251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4189   -0.7192    0.9022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5932   -1.1385    2.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1249    0.5434    2.1942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0004   -1.8993    0.2587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8431   -1.5064   -1.1069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4271    0.2196   -1.3931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5185   -2.1646   -2.8846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1339   -0.4082   -3.1513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0650   -1.1973   -2.6846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4904   -3.4933   -1.5410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9058   -3.3677   -2.2962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0564   -3.0412   -0.5564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8582    0.5240   -1.1879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7738   -1.5792    0.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6933   -1.6413   -0.1701 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4323    0.9916   -0.9955 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5112   -1.2017   -0.7419 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7469   -0.4647   -1.5249 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0967    1.7545   -2.5215 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1930    3.2657   -2.7441 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9502    2.5429   -1.9656 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  4  2  1  1
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  1
  8 10  1  0
  8 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
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 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 10  4  1  0
 16 11  1  0
 28 23  1  0
 17  4  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
  5 36  1  0
  5 37  1  0
  6 38  1  6
  7 39  1  0
  9 40  1  0
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  9 42  1  0
 11 43  1  1
 12 44  1  0
 12 45  1  0
 13 46  1  0
 13 47  1  0
 14 48  1  6
 15 49  1  0
 15 50  1  0
 15 51  1  0
 16 52  1  6
 17 53  1  1
 21 54  1  0
 22 55  1  0
 24 56  1  0
 25 57  1  0
 26 58  1  0
 27 59  1  0
 28 60  1  0
M  END


  Mrv1652309122217142D          

 28 31  0  0  1  0            999 V2000
    3.1344   -0.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5240    0.1246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3486    0.1507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0891    0.8256    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5320    1.5217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2640    2.3019    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8507    2.8819    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4869    2.5789    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3992    3.3992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0072    1.7775    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7859    2.1439    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0367    2.4894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4766    1.8837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8796    1.1638    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5341    0.4147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6888    1.3247    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2688    0.7380    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9918   -0.0392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1804   -0.1879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3785    0.0063    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9034   -0.9650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0919   -1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1850   -1.8909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3495   -2.5193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0726   -3.2964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7389   -3.4451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2734   -2.8167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9965   -2.0396    0.0000 C   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
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
  4 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 16 14  1  1  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
  4 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 23 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0330158

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@]12C[C@H](O)[C@](C)(O1)[C@H]1CC[C@H](C)[C@@H]1[C@H]2OC(=O)\C=C\C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O4/c1-15(2)24-14-19(25)23(4,28-24)18-12-10-16(3)21(18)22(24)27-20(26)13-11-17-8-6-5-7-9-17/h5-9,11,13,15-16,18-19,21-22,25H,10,12,14H2,1-4H3/b13-11+/t16-,18-,19-,21-,22+,23+,24-/m0/s1

> <INCHI_KEY>
VWHNJBKOOIZSEF-AOIXHVRESA-N

> <FORMULA>
C24H32O4

> <MOLECULAR_WEIGHT>
384.516

> <EXACT_MASS>
384.23005951

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
43.34277280721068

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,5S,6S,7R,8S,10S)-10-hydroxy-1,5-dimethyl-8-(propan-2-yl)-11-oxatricyclo[6.2.1.0^{2,6}]undecan-7-yl (2E)-3-phenylprop-2-enoate

> <JCHEM_LOGP>
4.757992740666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.893434825915843

> <JCHEM_PKA_STRONGEST_BASIC>
-3.282811607144409

> <JCHEM_POLAR_SURFACE_AREA>
55.76

> <JCHEM_REFRACTIVITY>
108.8456

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,5S,6S,7R,8S,10S)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0^{2,6}]undecan-7-yl (2E)-3-phenylprop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       5.851  -1.125   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.578   0.233   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.117   0.281   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.766   1.541   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.593   2.840   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.093   4.297   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.188   5.380   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.642   4.814   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.479   6.345   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.613   3.318   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.334   4.002   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.935   4.647   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.890   3.516   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.642   2.172   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.997   0.774   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.152   2.473   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.235   1.378   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.718  -0.073   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.203  -0.351   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.707   0.012   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.686  -1.801   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.172  -2.079   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.345  -3.530   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.652  -4.703   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.135  -6.153   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.379  -6.431   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.377  -5.258   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.860  -3.807   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   10   17                                             
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8    4                                                       
CONECT   11    8   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   11   17                                                  
CONECT   17   16    4   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   23                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₂O₄

Average Mass

384.5160 Da

Monoisotopic Mass

384.23006 Da

IUPAC Name

(1R,2S,5S,6S,7R,8S,10S)-10-hydroxy-1,5-dimethyl-8-(propan-2-yl)-11-oxatricyclo[6.2.1.0^{2,6}]undecan-7-yl (2E)-3-phenylprop-2-enoate

Traditional Name

(1R,2S,5S,6S,7R,8S,10S)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0^{2,6}]undecan-7-yl (2E)-3-phenylprop-2-enoate

CAS Registry Number

Not Available

SMILES

CC(C)[C@]12C[C@H](O)[C@](C)(O1)[C@H]1CC[C@H](C)[C@@H]1[C@H]2OC(=O)\C=C\C1=CC=CC=C1

InChI Identifier

InChI=1S/C24H32O4/c1-15(2)24-14-19(25)23(4,28-24)18-12-10-16(3)21(18)22(24)27-20(26)13-11-17-8-6-5-7-9-17/h5-9,11,13,15-16,18-19,21-22,25H,10,12,14H2,1-4H3/b13-11+/t16-,18-,19-,21-,22+,23+,24-/m0/s1

InChI Key

VWHNJBKOOIZSEF-AOIXHVRESA-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
Phyllanthus engleri	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Cinnamic acid or derivatives
Cinnamic acid ester
Styrene
Fatty acid ester
Monocyclic benzene moiety
Oxane
Fatty acyl
Benzenoid
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Tetrahydrofuran
Enoate ester
Secondary alcohol
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Alcohol
Organic oxide
Organic oxygen compound
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	4.76	ChemAxon
pKa (Strongest Acidic)	13.89	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	108.85 m³·mol⁻¹	ChemAxon
Polarizability	43.34 Å³	ChemAxon
Number of Rings	4	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

25194883

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Nicolaou KC, Kang Q, Ng SY, Chen DY: Total synthesis of englerin A. J Am Chem Soc. 2010 Jun 16;132(23):8219-22. doi: 10.1021/ja102927n. [PubMed:20496885 ]
Liu P, Cui Y, Chen K, Zhou X, Pan W, Ren J, Wang Z: Total Syntheses of (-)-Englerins A/B, (+)-Orientalols E/F, and (-)-Oxyphyllol. Org Lett. 2018 May 4;20(9):2517-2521. doi: 10.1021/acs.orglett.8b00552. Epub 2018 Apr 17. [PubMed:29664306 ]
Schremmer C, Steinritz D, Gudermann T, Beech DJ, Dietrich A: An ex vivo perfused ventilated murine lung model suggests lack of acute pulmonary toxicity of the potential novel anticancer agent (-)-englerin A. Arch Toxicol. 2022 Apr;96(4):1055-1063. doi: 10.1007/s00204-022-03235-z. Epub 2022 Feb 14. [PubMed:35165752 ]
Guo L, Plietker B: beta-Ketoesters as Mono- or Bisnucleophiles: A Concise Enantioselective Total Synthesis of (-)-Englerin A and B. Angew Chem Int Ed Engl. 2019 Jun 17;58(25):8346-8350. doi: 10.1002/anie.201900401. Epub 2019 May 10. [PubMed:30938023 ]
LOTUS database [Link]

Showing NP-Card for (1r,2s,5s,6s,7r,8s,10s)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0²,⁶]undecan-7-yl (2e)-3-phenylprop-2-enoate (NP0330158)

MOL for NP0330158 ((1r,2s,5s,6s,7r,8s,10s)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0²,⁶]undecan-7-yl (2e)-3-phenylprop-2-enoate)

3D MOL for NP0330158 ((1r,2s,5s,6s,7r,8s,10s)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0²,⁶]undecan-7-yl (2e)-3-phenylprop-2-enoate)

3D SDF for NP0330158 ((1r,2s,5s,6s,7r,8s,10s)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0²,⁶]undecan-7-yl (2e)-3-phenylprop-2-enoate)

3D-SDF for NP0330158 ((1r,2s,5s,6s,7r,8s,10s)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0²,⁶]undecan-7-yl (2e)-3-phenylprop-2-enoate)

PDB for NP0330158 ((1r,2s,5s,6s,7r,8s,10s)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0²,⁶]undecan-7-yl (2e)-3-phenylprop-2-enoate)

3D PDB for NP0330158 ((1r,2s,5s,6s,7r,8s,10s)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0²,⁶]undecan-7-yl (2e)-3-phenylprop-2-enoate)

SMILES for NP0330158 ((1r,2s,5s,6s,7r,8s,10s)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0²,⁶]undecan-7-yl (2e)-3-phenylprop-2-enoate)

INCHI for NP0330158 ((1r,2s,5s,6s,7r,8s,10s)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0²,⁶]undecan-7-yl (2e)-3-phenylprop-2-enoate)

Structure for NP0330158 ((1r,2s,5s,6s,7r,8s,10s)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0²,⁶]undecan-7-yl (2e)-3-phenylprop-2-enoate)

3D Structure for NP0330158 ((1r,2s,5s,6s,7r,8s,10s)-10-hydroxy-8-isopropyl-1,5-dimethyl-11-oxatricyclo[6.2.1.0²,⁶]undecan-7-yl (2e)-3-phenylprop-2-enoate)