NP-MRD: Showing NP-Card for (1r,2r,4s,7e,9r,10r)-9-(acetyloxy)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2z)-2-methylbut-2-enoate (NP0279485)

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Record Information

Version

2.0

Created at

2022-09-09 04:53:44 UTC

Updated at

2022-09-09 04:53:44 UTC

NP-MRD ID

NP0279485

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,4s,7e,9r,10r)-9-(acetyloxy)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2z)-2-methylbut-2-enoate

Description

Karwinsinolide A belongs to the class of organic compounds known as germacranolides and derivatives. These are sesquiterpene lactones with a structure based on the germacranolide skeleton, characterized by a gamma lactone fused to a 1,7-dimethylcyclodec-1-ene moiety. Based on a literature review very few articles have been published on Karwinsinolide A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092206532D          

 29 31  0  0  1  0            999 V2000
    5.0951   -1.6841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3518   -1.3260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2047   -0.5142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7749    0.0820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3871   -0.4034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0291   -1.1466    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6253   -1.7168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7725   -2.5286    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5900   -2.6395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9027   -3.4029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3979   -4.0554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7202   -3.5138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2250   -2.8612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0330   -4.2772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5282   -4.9297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4144   -3.2718    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8052   -3.9984    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3714   -4.7001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5468   -4.6753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7622   -5.4267    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5969   -3.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4497   -2.3492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8703   -3.5518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2741   -2.9816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1269   -2.1698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4850   -1.4266    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6835   -1.2308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5098   -0.6019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2115   -1.0357    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 29 28  1  6  0  0  0
  6 29  1  0  0  0  0
 26 29  1  0  0  0  0
M  END

     RDKit          3D

 57 59  0  0  0  0  0  0  0  0999 V2000
    0.8873   -1.2357   -3.0277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1879   -0.5863   -2.7154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4344   -0.5364   -3.5164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6195   -1.0794   -4.6528 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3558    0.2119   -2.7935 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9826   -0.0373   -1.4084 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4987    0.2448   -1.5579 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3253    0.1274   -0.3585 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5439    0.8403   -0.5008 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7801    0.2721   -0.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8038   -0.9340    0.0253 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9637    1.0879   -0.4775 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8451    2.5111   -0.8662 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1676    0.5837   -0.2965 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3511   -0.8208    0.0895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4133    0.6275    0.8790 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4092    1.5149    1.6250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0266    2.8030    1.8339 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7847    3.8043    2.6130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1369    3.1451    1.3561 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7891   -0.5133    1.7578 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3732   -1.3347    2.2665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0294   -0.8065    2.0772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2578   -0.1238    1.6774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0283   -0.7297    0.5550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3628   -1.7791   -0.2417 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2458   -2.9926   -0.5809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0638   -2.1287    0.0057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3360   -1.4527   -1.1557 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9025   -1.8053   -3.9619 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7979   -1.2886   -2.4668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5329    0.7292   -0.8760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4764    1.3133   -1.9360 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6102   -0.9173   -0.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8330    2.9401   -1.1251 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1666    2.6579   -1.7334 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4753    3.0964    0.0171 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0541    1.2116   -0.4330 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9419   -1.4709   -0.7071 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4439   -1.0622    0.1710 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8737   -1.0842    1.0684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3028    1.1514    0.5821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1318    4.6315    2.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1891    3.3295    3.5365 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5954    4.2073    1.9724 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1981   -0.6223    2.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1166   -1.8027    3.2397 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7152   -2.0626    1.5186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1601   -1.6873    2.7341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8854   -0.0500    2.6249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1181    0.9713    1.4277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4169    0.0546   -0.1648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9900   -1.1304    1.0013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7874   -3.5727   -1.3954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2778   -2.6483   -0.8661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3772   -3.6409    0.3079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1866   -2.1313   -2.0511 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 12  2  0
 12 13  1  0
 12 10  1  0
 10 11  2  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
  6 29  1  0
 29 28  1  0
 28 26  1  0
 26 27  1  6
 26 25  1  0
 25 24  1  0
 24 23  1  0
 23 21  2  0
 21 22  1  0
 21 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 16  8  1  0
  2  7  1  0
 26 29  1  0
 15 39  1  0
 15 40  1  0
 15 41  1  0
 14 38  1  0
 13 35  1  0
 13 36  1  0
 13 37  1  0
  8 34  1  1
  7 33  1  6
  6 32  1  1
  1 30  1  0
  1 31  1  0
 29 57  1  6
 27 54  1  0
 27 55  1  0
 27 56  1  0
 25 52  1  0
 25 53  1  0
 24 50  1  0
 24 51  1  0
 23 49  1  0
 22 46  1  0
 22 47  1  0
 22 48  1  0
 16 42  1  6
 19 43  1  0
 19 44  1  0
 19 45  1  0
M  END


  Mrv1652309092206532D          

 29 31  0  0  1  0            999 V2000
    5.0951   -1.6841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3518   -1.3260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2047   -0.5142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7749    0.0820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3871   -0.4034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0291   -1.1466    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6253   -1.7168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7725   -2.5286    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5900   -2.6395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9027   -3.4029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3979   -4.0554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7202   -3.5138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2250   -2.8612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0330   -4.2772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5282   -4.9297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4144   -3.2718    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8052   -3.9984    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3714   -4.7001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5468   -4.6753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7622   -5.4267    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5969   -3.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4497   -2.3492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8703   -3.5518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2741   -2.9816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1269   -2.1698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4850   -1.4266    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6835   -1.2308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5098   -0.6019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2115   -1.0357    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 29 28  1  6  0  0  0
  6 29  1  0  0  0  0
 26 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0279485

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(\C)C(=O)O[C@@H]1C2[C@@H](OC(=O)C2=C)[C@H]2O[C@@]2(C)CC\C=C(C)\[C@H]1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H28O7/c1-7-11(2)20(24)27-17-15-13(4)21(25)28-18(15)19-22(6,29-19)10-8-9-12(3)16(17)26-14(5)23/h7,9,15-19H,4,8,10H2,1-3,5-6H3/b11-7-,12-9+/t15?,16-,17-,18-,19-,22+/m1/s1

> <INCHI_KEY>
LVSYJPJJICOXAF-FLUKRXJJSA-N

> <FORMULA>
C22H28O7

> <MOLECULAR_WEIGHT>
404.459

> <EXACT_MASS>
404.183503242

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
41.698676639359135

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,4S,7E,9R,10R)-9-(acetyloxy)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0^{2,4}]tetradec-7-en-10-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_LOGP>
3.4611972963333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.241022251728612

> <JCHEM_POLAR_SURFACE_AREA>
91.43

> <JCHEM_REFRACTIVITY>
104.3124

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,4S,7E,9R,10R)-9-(acetyloxy)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0^{2,4}]tetradec-7-en-10-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       9.511  -3.144   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.123  -2.475   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.849  -0.960   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       8.913   0.153   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       6.323  -0.753   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       5.654  -2.140   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.767  -3.205   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.042  -4.720   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.568  -4.927   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       9.152  -6.352   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.209  -7.570   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      10.678  -6.559   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.620  -5.341   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.262  -7.984   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.319  -9.202   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.374  -6.107   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.103  -7.464   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.293  -8.774   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.754  -8.727   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.023 -10.130   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.847  -5.900   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.573  -4.385   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.491  -6.630   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.378  -5.566   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.104  -4.050   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.772  -2.663   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.276  -2.298   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.818  -1.124   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.128  -1.933   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   29                                                  
CONECT    7    6    2    8                                                  
CONECT    8    7    9   16                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14                                                            
CONECT   16    8   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   16   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28    6   26                                                  
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₈O₇

Average Mass

404.4590 Da

Monoisotopic Mass

404.18350 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C\C=C(\C)C(=O)O[C@@H]1C2[C@@H](OC(=O)C2=C)[C@H]2O[C@@]2(C)CC\C=C(C)\[C@H]1OC(C)=O

InChI Identifier

InChI=1S/C22H28O7/c1-7-11(2)20(24)27-17-15-13(4)21(25)28-18(15)19-22(6,29-19)10-8-9-12(3)16(17)26-14(5)23/h7,9,15-19H,4,8,10H2,1-3,5-6H3/b11-7-,12-9+/t15?,16-,17-,18-,19-,22+/m1/s1

InChI Key

LVSYJPJJICOXAF-FLUKRXJJSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as germacranolides and derivatives. These are sesquiterpene lactones with a structure based on the germacranolide skeleton, characterized by a gamma lactone fused to a 1,7-dimethylcyclodec-1-ene moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Germacranolides and derivatives

Alternative Parents

Substituents

Germacranolide
Sesquiterpenoid
Germacrane sesquiterpenoid
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Gamma butyrolactone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen 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

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

101921625

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,4s,7e,9r,10r)-9-(acetyloxy)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2z)-2-methylbut-2-enoate (NP0279485)

MOL for NP0279485 ((1r,2r,4s,7e,9r,10r)-9-(acetyloxy)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2z)-2-methylbut-2-enoate)

3D MOL for NP0279485 ((1r,2r,4s,7e,9r,10r)-9-(acetyloxy)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2z)-2-methylbut-2-enoate)

3D SDF for NP0279485 ((1r,2r,4s,7e,9r,10r)-9-(acetyloxy)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2z)-2-methylbut-2-enoate)

3D-SDF for NP0279485 ((1r,2r,4s,7e,9r,10r)-9-(acetyloxy)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2z)-2-methylbut-2-enoate)

PDB for NP0279485 ((1r,2r,4s,7e,9r,10r)-9-(acetyloxy)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2z)-2-methylbut-2-enoate)

3D PDB for NP0279485 ((1r,2r,4s,7e,9r,10r)-9-(acetyloxy)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2z)-2-methylbut-2-enoate)

SMILES for NP0279485 ((1r,2r,4s,7e,9r,10r)-9-(acetyloxy)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2z)-2-methylbut-2-enoate)

INCHI for NP0279485 ((1r,2r,4s,7e,9r,10r)-9-(acetyloxy)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2z)-2-methylbut-2-enoate)

Structure for NP0279485 ((1r,2r,4s,7e,9r,10r)-9-(acetyloxy)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2z)-2-methylbut-2-enoate)

3D Structure for NP0279485 ((1r,2r,4s,7e,9r,10r)-9-(acetyloxy)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2z)-2-methylbut-2-enoate)