NP-MRD: Showing NP-Card for (1r,8r,10r,11s)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-8-yl acetate (NP0329435)

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Record Information

Version

2.0

Created at

2022-09-12 13:48:23 UTC

Updated at

2022-09-12 13:48:23 UTC

NP-MRD ID

NP0329435

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,8r,10r,11s)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-8-yl acetate

Description

Sessein belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (1r,8r,10r,11s)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-8-yl acetate is found in Salvia regla and Salvia sessei. (1r,8r,10r,11s)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-8-yl acetate was first documented in 2018 (PMID: 29458147). Based on a literature review very few articles have been published on sessein.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122215482D          

 29 32  0  0  1  0            999 V2000
    2.5626   -2.7573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2355   -1.9999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4160   -1.9044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7279   -1.3380    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4008   -0.5806    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5263   -0.5879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2543    0.2723    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2497   -0.2022    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3886   -0.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9769   -0.5918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7666   -0.3531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1562    0.3741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7467    0.9343    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1903    1.5534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4006    1.3147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0110    0.5875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8100    0.6692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5662    0.8388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8933    0.0814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7127   -0.0141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0398   -0.7715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2051    0.6479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0246    0.5524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5170    1.2143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3516   -0.2050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8781    1.4053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3705    2.0672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0586    1.5007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7315    2.2581    0.0000 O   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  6  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  2  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 18 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
    1.5567    4.6464    0.7883 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8850    3.5694    0.0529 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5148    3.7289   -1.1402 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6109    2.3119    0.6085 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0389    1.2858   -0.1196 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3660    1.0812    0.5982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9959   -0.2380    0.3747 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4989   -0.0227    0.1931 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0165    0.7255    1.3727 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1991   -1.3714    0.1615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5644   -2.1769   -0.9206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0676   -2.3716   -0.7573 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3972   -1.0253   -0.7770 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7141   -0.4190   -2.1264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6724    0.6176   -2.0302 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6650    0.6551   -1.0924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7219    1.2747   -1.3392 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0541   -1.0812   -0.5185 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7184    0.0415   -0.2081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1611    0.0635    0.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7475    1.3065    0.3731 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9447   -0.9916    0.0308 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3992   -1.0091    0.2940 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1054    0.2907    0.2884 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7682   -1.8704    1.4929 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2676   -2.2757   -0.3088 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9872   -3.3023   -0.3479 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8429   -2.2936   -0.5751 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3174   -3.3947   -0.8558 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6189    4.7778    0.5374 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0442    5.6088    0.4973 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4471    4.5758    1.8831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2042    1.6863   -1.1412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0219    1.9126    0.2424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2294    1.2456    1.6868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8291   -0.8880    1.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0121    0.0255    2.2444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4830    1.6371    1.6356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1069    0.9478    1.1977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2402   -1.1808   -0.1180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1022   -1.9012    1.1265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8438   -1.7438   -1.8885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9974   -3.2171   -0.9198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7874   -2.9757   -1.6734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8926   -2.8861    0.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1349   -1.1847   -2.8462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8272   -0.0267   -2.6607 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1116    1.8910   -0.3863 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8351   -1.5963   -0.5901 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8573    1.0008    1.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0920    0.7297   -0.7465 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2128    0.0581    0.4845 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0124   -2.6502    1.6122 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7809   -1.2610    2.4236 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7372   -2.3407    1.2801 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 25  1  0
 23 22  1  0
 22 20  2  0
 20 21  1  0
 20 19  1  0
 19 18  2  0
 18 28  1  0
 28 29  2  0
 28 26  1  0
 26 27  2  0
 18 13  1  0
 13 12  1  6
 12 11  1  0
 11 10  1  0
 10  8  1  0
  8  9  1  1
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  8 16  1  0
 16 17  2  0
 16 15  1  0
 15 14  1  0
 26 22  1  0
  7 13  1  0
  5 19  1  0
 14 13  1  0
 24 50  1  0
 24 51  1  0
 24 52  1  0
 23 49  1  0
 25 53  1  0
 25 54  1  0
 25 55  1  0
 21 48  1  0
 12 44  1  0
 12 45  1  0
 11 42  1  0
 11 43  1  0
 10 40  1  0
 10 41  1  0
  9 37  1  0
  9 38  1  0
  9 39  1  0
  7 36  1  1
  6 34  1  0
  6 35  1  0
  5 33  1  6
  1 30  1  0
  1 31  1  0
  1 32  1  0
 14 46  1  0
 14 47  1  0
M  END


  Mrv1652309122215482D          

 29 32  0  0  1  0            999 V2000
    2.5626   -2.7573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2355   -1.9999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4160   -1.9044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7279   -1.3380    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4008   -0.5806    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5263   -0.5879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2543    0.2723    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2497   -0.2022    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3886   -0.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9769   -0.5918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7666   -0.3531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1562    0.3741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7467    0.9343    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1903    1.5534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4006    1.3147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0110    0.5875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8100    0.6692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5662    0.8388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8933    0.0814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7127   -0.0141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0398   -0.7715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2051    0.6479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0246    0.5524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5170    1.2143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3516   -0.2050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8781    1.4053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3705    2.0672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0586    1.5007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7315    2.2581    0.0000 O   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  6  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  2  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 18 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0329435

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=C(O)C2=C(C(=O)C1=O)[C@@]13CCC[C@@](C)([C@@H]1C[C@H]2OC(C)=O)C(=O)OC3

> <INCHI_IDENTIFIER>
InChI=1S/C22H26O7/c1-10(2)14-17(24)15-12(29-11(3)23)8-13-21(4)6-5-7-22(13,9-28-20(21)27)16(15)19(26)18(14)25/h10,12-13,24H,5-9H2,1-4H3/t12-,13+,21+,22-/m1/s1

> <INCHI_KEY>
BPQUGAYODDFVMA-NJEWNWGJSA-N

> <FORMULA>
C22H26O7

> <MOLECULAR_WEIGHT>
402.443

> <EXACT_MASS>
402.167853177

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
41.42863736776446

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,8R,10R,11S)-6-hydroxy-11-methyl-3,4,12-trioxo-5-(propan-2-yl)-13-oxatetracyclo[9.3.3.0^{1,10}.0^{2,7}]heptadeca-2(7),5-dien-8-yl acetate

> <JCHEM_LOGP>
2.5213766533333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.497540626702686

> <JCHEM_PKA_STRONGEST_BASIC>
-6.760053498703543

> <JCHEM_POLAR_SURFACE_AREA>
106.97

> <JCHEM_REFRACTIVITY>
103.27939999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,8R,10R,11S)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0^{1,10}.0^{2,7}]heptadeca-2(7),5-dien-8-yl acetate

> <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       4.783  -5.147   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.173  -3.733   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.643  -3.555   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       5.092  -2.498   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.482  -1.084   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.849  -1.097   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.341   0.508   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.466  -0.377   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.725  -1.353   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.824  -1.105   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.298  -0.659   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.025   0.698   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.261   1.744   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.222   2.900   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.748   2.454   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.020   1.097   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.512   1.249   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.790   1.566   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.401   0.152   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.930  -0.026   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.541  -1.440   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.850   1.209   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.379   1.031   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.298   2.267   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.990  -0.383   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.239   2.623   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.158   3.859   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.709   2.801   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       5.099   4.215   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   19                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   13                                                  
CONECT    8    7    9   10   16                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    7   14   18                                             
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    8   17                                                  
CONECT   17   16                                                            
CONECT   18   13   19   28                                                  
CONECT   19   18    5   20                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   26                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   22   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   18   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₆O₇

Average Mass

402.4430 Da

Monoisotopic Mass

402.16785 Da

IUPAC Name

(1R,8R,10R,11S)-6-hydroxy-11-methyl-3,4,12-trioxo-5-(propan-2-yl)-13-oxatetracyclo[9.3.3.0^{1,10}.0^{2,7}]heptadeca-2(7),5-dien-8-yl acetate

Traditional Name

(1R,8R,10R,11S)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0^{1,10}.0^{2,7}]heptadeca-2(7),5-dien-8-yl acetate

CAS Registry Number

Not Available

SMILES

CC(C)C1=C(O)C2=C(C(=O)C1=O)[C@@]13CCC[C@@](C)([C@@H]1C[C@H]2OC(C)=O)C(=O)OC3

InChI Identifier

InChI=1S/C22H26O7/c1-10(2)14-17(24)15-12(29-11(3)23)8-13-21(4)6-5-7-22(13,9-28-20(21)27)16(15)19(26)18(14)25/h10,12-13,24H,5-9H2,1-4H3/t12-,13+,21+,22-/m1/s1

InChI Key

BPQUGAYODDFVMA-NJEWNWGJSA-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
Salvia regla	LOTUS Database	35616633
Salvia sessei	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Naphthopyran
Naphthalene
Delta valerolactone
Delta_valerolactone
Dicarboxylic acid or derivatives
Oxane
Pyran
Vinylogous acid
Lactone
Ketone
Carboxylic acid ester
Cyclic ketone
Enol
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
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	2.52	ChemAxon
pKa (Strongest Acidic)	4.5	ChemAxon
pKa (Strongest Basic)	-6.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	106.97 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	103.28 m³·mol⁻¹	ChemAxon
Polarizability	41.43 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

13967167

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Gomez-Rivera A, Gonzalez-Cortazar M, Herrera-Ruiz M, Zamilpa A, Rodriguez-Lopez V: Sessein and isosessein with anti-inflammatory, antibacterial and antioxidant activity isolated from Salvia sessei Benth. J Ethnopharmacol. 2018 May 10;217:212-219. doi: 10.1016/j.jep.2018.02.012. Epub 2018 Feb 16. [PubMed:29458147 ]
LOTUS database [Link]

Showing NP-Card for (1r,8r,10r,11s)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-8-yl acetate (NP0329435)

MOL for NP0329435 ((1r,8r,10r,11s)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-8-yl acetate)

3D MOL for NP0329435 ((1r,8r,10r,11s)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-8-yl acetate)

3D SDF for NP0329435 ((1r,8r,10r,11s)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-8-yl acetate)

3D-SDF for NP0329435 ((1r,8r,10r,11s)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-8-yl acetate)

PDB for NP0329435 ((1r,8r,10r,11s)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-8-yl acetate)

3D PDB for NP0329435 ((1r,8r,10r,11s)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-8-yl acetate)

SMILES for NP0329435 ((1r,8r,10r,11s)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-8-yl acetate)

INCHI for NP0329435 ((1r,8r,10r,11s)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-8-yl acetate)

Structure for NP0329435 ((1r,8r,10r,11s)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-8-yl acetate)

3D Structure for NP0329435 ((1r,8r,10r,11s)-6-hydroxy-5-isopropyl-11-methyl-3,4,12-trioxo-13-oxatetracyclo[9.3.3.0¹,¹⁰.0²,⁷]heptadeca-2(7),5-dien-8-yl acetate)