NP-MRD: Showing NP-Card for (1r,3s,6s,7r,9s,10s,11s,13r,14r)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0¹,⁶.0⁷,¹³.0¹⁰,¹⁴]pentadecan-2-one (NP0211362)

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Record Information

Version

2.0

Created at

2022-09-05 09:36:59 UTC

Updated at

2022-09-05 09:36:59 UTC

NP-MRD ID

NP0211362

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3s,6s,7r,9s,10s,11s,13r,14r)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0¹,⁶.0⁷,¹³.0¹⁰,¹⁴]pentadecan-2-one

Description

Cinnzeylanone belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (1r,3s,6s,7r,9s,10s,11s,13r,14r)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0¹,⁶.0⁷,¹³.0¹⁰,¹⁴]pentadecan-2-one is found in Persea indica. (1r,3s,6s,7r,9s,10s,11s,13r,14r)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0¹,⁶.0⁷,¹³.0¹⁰,¹⁴]pentadecan-2-one was first documented in 2020 (PMID: 32450381). Based on a literature review a small amount of articles have been published on Cinnzeylanone (PMID: 35161399) (PMID: 34452277).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052211372D          

 27 31  0  0  1  0            999 V2000
   -0.3826   -2.5848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4777   -1.7653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2349   -1.4379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1845   -1.2732    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8620   -1.7441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0575   -0.5297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9818   -0.4483    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4197    0.1556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7251    0.3059    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2896    0.9075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2691    0.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7911    0.3656    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0233    0.2340    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6438   -0.1566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0434   -0.8893    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6871   -1.4752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4443   -2.2637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5268   -1.3559    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0438   -1.9988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8169   -0.5789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2695    0.0469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4251   -0.1389    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5685    0.6736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1925   -1.0338    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2226   -1.8582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4460   -0.3744    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3262   -0.0840    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  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  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  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  9 22  1  0  0  0  0
 15 22  1  0  0  0  0
 22 23  1  6  0  0  0
 15 24  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 12 26  1  0  0  0  0
  4 26  1  0  0  0  0
 26 27  1  1  0  0  0
M  END

     RDKit          3D

 57 61  0  0  0  0  0  0  0  0999 V2000
    4.5882   -0.4611   -0.4390 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5766    0.3426    0.3973 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7177   -0.0872    1.7984 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2761    0.2264   -0.2681 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4716    0.7789   -1.5715 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8088   -1.1847   -0.5482 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3650   -1.0024   -0.8776 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0124   -1.5254   -2.0927 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5514   -1.5314    0.2419 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7095   -3.0044    0.1837 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0878   -1.0569    1.5377 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4095    0.4055    1.4728 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8662    0.8727    2.6829 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8656    1.0197    1.3005 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1866    0.6681   -0.0144 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2183    1.5451   -0.5575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1018    2.3228   -1.4802 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5510    1.4249    0.1475 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5513    2.3541   -0.4275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0435   -0.0173    0.1233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9638   -0.9238    0.7371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7578   -0.7515   -0.0735 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0866   -0.9624   -1.4232 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0516    0.4980   -0.7862 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1874    1.1622   -1.9453 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1052    0.8867    0.2763 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1422    2.3904    0.2830 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7074   -1.4801    0.0223 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5438    0.0627   -0.5296 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1946   -0.6413   -1.4610 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9266    1.3991    0.3005 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1333   -0.9395    2.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6014    0.8238    2.4558 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7985   -0.3776    1.9681 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9753    1.6195   -1.4503 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0376   -1.8999    0.2347 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3085   -1.5750   -1.4827 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6166   -2.2618   -2.3471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7940   -3.3396   -0.8523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6794   -3.2707    0.6957 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0714   -3.5371    0.7625 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8809   -1.7065    1.8978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7402   -1.1507    2.3053 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7155    0.1881    3.3785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3657    1.6743    1.2117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1965    3.3996   -0.2446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5047    2.2288    0.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6145    2.1957   -1.5235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9741   -0.0584    0.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1706   -0.2954   -0.9220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3468   -1.9551    0.6016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8642   -0.7423    1.8115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7328   -1.6785   -1.5283 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0286    0.5650   -2.7279 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8001    2.8160    1.0562 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0973    2.7414    0.4175 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4920    2.8061   -0.6979 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  6
  4  6  1  0
  6  7  1  0
  7  8  1  6
  7  9  1  0
  9 10  1  1
  9 11  1  0
 11 12  1  0
 12 13  1  1
 12 14  1  0
 14 15  1  0
 15 16  1  6
 16 17  2  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  6
 15 24  1  0
 24 25  1  6
 24 26  1  0
 26 27  1  1
 26  4  1  0
 24  7  1  0
 22  9  1  0
 26 12  1  0
 22 15  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  3 34  1  0
  5 35  1  0
  6 36  1  0
  6 37  1  0
  8 38  1  0
 10 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 13 44  1  0
 18 45  1  1
 19 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  0
 21 52  1  0
 23 53  1  0
 25 54  1  0
 27 55  1  0
 27 56  1  0
 27 57  1  0
M  END


  Mrv1652309052211372D          

 27 31  0  0  1  0            999 V2000
   -0.3826   -2.5848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4777   -1.7653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2349   -1.4379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1845   -1.2732    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8620   -1.7441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0575   -0.5297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9818   -0.4483    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4197    0.1556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7251    0.3059    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2896    0.9075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2691    0.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7911    0.3656    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0233    0.2340    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6438   -0.1566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0434   -0.8893    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6871   -1.4752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4443   -2.2637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5268   -1.3559    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0438   -1.9988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8169   -0.5789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2695    0.0469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4251   -0.1389    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5685    0.6736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1925   -1.0338    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2226   -1.8582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4460   -0.3744    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3262   -0.0840    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  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  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  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  9 22  1  0  0  0  0
 15 22  1  0  0  0  0
 22 23  1  6  0  0  0
 15 24  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 12 26  1  0  0  0  0
  4 26  1  0  0  0  0
 26 27  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0211362

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@]1(O)C[C@@]2(O)[C@@]3(C)C[C@]4(O)O[C@@]5(C(=O)[C@@H](C)CC[C@]35O)[C@@]2(O)[C@]14C

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O7/c1-10(2)15(22)9-17(24)13(4)8-18(25)14(15,5)20(17,26)19(27-18)12(21)11(3)6-7-16(13,19)23/h10-11,22-26H,6-9H2,1-5H3/t11-,13-,14+,15-,16-,17+,18-,19+,20+/m0/s1

> <INCHI_KEY>
MUEAKMKWVCXRCG-LBLGJGHOSA-N

> <FORMULA>
C20H30O7

> <MOLECULAR_WEIGHT>
382.453

> <EXACT_MASS>
382.199153306

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
39.32194674414825

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,3S,6S,7R,9S,10S,11S,13R,14R)-6,9,11,13,14-pentahydroxy-3,7,10-trimethyl-11-(propan-2-yl)-15-oxapentacyclo[7.5.1.0^{1,6}.0^{7,13}.0^{10,14}]pentadecan-2-one

> <JCHEM_LOGP>
0.03850286133333245

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.047083378062243

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.285377810684915

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3025981568858622

> <JCHEM_POLAR_SURFACE_AREA>
127.45000000000002

> <JCHEM_REFRACTIVITY>
92.7881

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3S,6S,7R,9S,10S,11S,13R,14R)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0^{1,6}.0^{7,13}.0^{10,14}]pentadecan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.714  -4.825   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.892  -3.295   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.305  -2.684   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.344  -2.377   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.609  -3.256   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -0.107  -0.989   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.833  -0.837   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.783   0.290   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.220   0.571   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.274   1.694   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.369   1.740   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.477   0.682   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.044   0.437   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       3.068  -0.292   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.814  -1.660   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.016  -2.754   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.563  -4.226   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.583  -2.531   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.548  -3.731   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.125  -1.081   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.103   0.088   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.527  -0.259   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.795   1.257   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.226  -1.930   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.282  -3.469   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       0.833  -0.699   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.609  -0.157   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6   26                                             
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8    9   24                                             
CONECT    8    7                                                            
CONECT    9    7   10   11   22                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   14   26                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   22   24                                             
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    9   15   23                                             
CONECT   23   22                                                            
CONECT   24   15    7   25   26                                             
CONECT   25   24                                                            
CONECT   26   24   12    4   27                                             
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₀O₇

Average Mass

382.4530 Da

Monoisotopic Mass

382.19915 Da

IUPAC Name

(1R,3S,6S,7R,9S,10S,11S,13R,14R)-6,9,11,13,14-pentahydroxy-3,7,10-trimethyl-11-(propan-2-yl)-15-oxapentacyclo[7.5.1.0^{1,6}.0^{7,13}.0^{10,14}]pentadecan-2-one

Traditional Name

(1R,3S,6S,7R,9S,10S,11S,13R,14R)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0^{1,6}.0^{7,13}.0^{10,14}]pentadecan-2-one

CAS Registry Number

Not Available

SMILES

CC(C)[C@@]1(O)C[C@@]2(O)[C@@]3(C)C[C@]4(O)O[C@@]5(C(=O)[C@@H](C)CC[C@]35O)[C@@]2(O)[C@]14C

InChI Identifier

InChI=1S/C20H30O7/c1-10(2)15(22)9-17(24)13(4)8-18(25)14(15,5)20(17,26)19(27-18)12(21)11(3)6-7-16(13,19)23/h10-11,22-26H,6-9H2,1-5H3/t11-,13-,14+,15-,16-,17+,18-,19+,20+/m0/s1

InChI Key

MUEAKMKWVCXRCG-LBLGJGHOSA-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
Persea indica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Ryanodane diterpenoid
Oxepane
Monosaccharide
Oxane
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Ketone
Hemiacetal
Polyol
Organoheterocyclic compound
Oxacycle
Hydrocarbon derivative
Organooxygen compound
Alcohol
Organic oxide
Organic oxygen compound
Carbonyl group
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	0.039	ChemAxon
pKa (Strongest Acidic)	11.29	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	127.45 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	92.79 m³·mol⁻¹	ChemAxon
Polarizability	39.32 Å³	ChemAxon
Number of Rings	5	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

C00036450

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

101693755

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Gonzalez-Coloma A, Andres MF, Contreras R, Zuniga GE, Diaz CE: Sustainable Production of Insecticidal Compounds from Persea indica. Plants (Basel). 2022 Feb 3;11(3):418. doi: 10.3390/plants11030418. [PubMed:35161399 ]
Choi SM, Pham VC, Lee S, Kim JA: Metabolism of Diterpenoids Derived from the Bark of Cinnamomum cassia in Human Liver Microsomes. Pharmaceutics. 2021 Aug 23;13(8):1316. doi: 10.3390/pharmaceutics13081316. [PubMed:34452277 ]
Fraga BM, Diaz CE, Bolanos P, Bailen M, Andres MF, Gonzalez-Coloma A: Alkane-, alkene-, alkyne-gamma-lactones and ryanodane diterpenes from aeroponically grown Persea indica roots. Phytochemistry. 2020 Aug;176:112398. doi: 10.1016/j.phytochem.2020.112398. Epub 2020 May 23. [PubMed:32450381 ]
LOTUS database [Link]

Showing NP-Card for (1r,3s,6s,7r,9s,10s,11s,13r,14r)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0¹,⁶.0⁷,¹³.0¹⁰,¹⁴]pentadecan-2-one (NP0211362)

MOL for NP0211362 ((1r,3s,6s,7r,9s,10s,11s,13r,14r)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0¹,⁶.0⁷,¹³.0¹⁰,¹⁴]pentadecan-2-one)

3D MOL for NP0211362 ((1r,3s,6s,7r,9s,10s,11s,13r,14r)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0¹,⁶.0⁷,¹³.0¹⁰,¹⁴]pentadecan-2-one)

3D SDF for NP0211362 ((1r,3s,6s,7r,9s,10s,11s,13r,14r)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0¹,⁶.0⁷,¹³.0¹⁰,¹⁴]pentadecan-2-one)

3D-SDF for NP0211362 ((1r,3s,6s,7r,9s,10s,11s,13r,14r)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0¹,⁶.0⁷,¹³.0¹⁰,¹⁴]pentadecan-2-one)

PDB for NP0211362 ((1r,3s,6s,7r,9s,10s,11s,13r,14r)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0¹,⁶.0⁷,¹³.0¹⁰,¹⁴]pentadecan-2-one)

3D PDB for NP0211362 ((1r,3s,6s,7r,9s,10s,11s,13r,14r)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0¹,⁶.0⁷,¹³.0¹⁰,¹⁴]pentadecan-2-one)

SMILES for NP0211362 ((1r,3s,6s,7r,9s,10s,11s,13r,14r)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0¹,⁶.0⁷,¹³.0¹⁰,¹⁴]pentadecan-2-one)

INCHI for NP0211362 ((1r,3s,6s,7r,9s,10s,11s,13r,14r)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0¹,⁶.0⁷,¹³.0¹⁰,¹⁴]pentadecan-2-one)

Structure for NP0211362 ((1r,3s,6s,7r,9s,10s,11s,13r,14r)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0¹,⁶.0⁷,¹³.0¹⁰,¹⁴]pentadecan-2-one)

3D Structure for NP0211362 ((1r,3s,6s,7r,9s,10s,11s,13r,14r)-6,9,11,13,14-pentahydroxy-11-isopropyl-3,7,10-trimethyl-15-oxapentacyclo[7.5.1.0¹,⁶.0⁷,¹³.0¹⁰,¹⁴]pentadecan-2-one)