NP-MRD: Showing NP-Card for (1s,2s,3'r,4'bs,8'as,9's,10's)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'h-spiro[cyclopropane-1,2'-phenanthren]-9'-yl acetate (NP0299766)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-10 11:46:54 UTC

Updated at

2022-09-10 11:46:54 UTC

NP-MRD ID

NP0299766

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,3'r,4'bs,8'as,9's,10's)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'h-spiro[cyclopropane-1,2'-phenanthren]-9'-yl acetate

Description

Plectrin belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (1s,2s,3'r,4'bs,8'as,9's,10's)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'h-spiro[cyclopropane-1,2'-phenanthren]-9'-yl acetate was first documented in 1997 (PMID: 9264040). Based on a literature review very few articles have been published on Plectrin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102213462D          

 29 32  0  0  1  0            999 V2000
    1.1270    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1414   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  2  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
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  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  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  6  0  0  0
 14 18  1  0  0  0  0
  8 18  1  0  0  0  0
 18 19  2  0  0  0  0
  9 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 27 28  1  0  0  0  0
 29 27  1  6  0  0  0
  5 29  1  0  0  0  0
 20 29  1  0  0  0  0
M  END

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
   -2.3440    4.0655   -1.5396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1367    3.2006   -0.3392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6827    3.5061    0.7476 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3553    2.0624   -0.3844 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1905    1.2772    0.7634 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2545    1.4475    1.2141 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3418    1.4226    2.6016 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1340    0.3979    0.6420 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7318   -0.5349   -0.2108 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8025   -1.3005   -0.8699 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5300   -1.9163   -1.9304 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1686   -1.3792   -0.3501 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1988   -2.3958    0.6304 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6351   -0.1143    0.3075 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6153    0.7811   -0.3481 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9972   -0.0760    0.8401 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0229   -1.1360    0.5277 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5356    0.4478    1.0912 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8083    0.9968    2.1974 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6952   -0.8140   -0.5028 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0950   -0.3580   -1.8790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9730   -2.3173   -0.4289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4623   -2.5440   -0.4855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8301   -3.6724   -0.8970 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4024   -1.5239   -0.0899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8577   -1.8030   -0.2787 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9631   -0.3801    0.4307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0383    0.5770    0.8134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5358   -0.1692    0.5875 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3457    4.2482   -1.9826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0516    3.6045   -2.2475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7586    5.0269   -1.2168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7867    1.6950    1.5909 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6186    2.4342    0.8694 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4926    0.4848    2.9170 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8687   -1.7165   -1.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7965   -1.9643    1.4490 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5663    1.8634   -0.1391 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9913    0.5153   -1.3538 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1279    0.4187    1.8286 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5483   -2.0838    0.2070 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7121   -0.7175   -0.2413 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6491   -1.3518    1.4177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6235    0.5998   -2.1722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1879   -0.3358   -1.9685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7196   -1.1235   -2.5994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6399   -2.7565    0.5156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5595   -2.7729   -1.3286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0064   -2.6451   -0.9670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3619   -0.8845   -0.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3449   -2.0519    0.6961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2513    1.2544   -0.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9675    0.0103    1.0894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7715    1.1846    1.6875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2090   -0.6837    1.5383 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 12  1  0
 12 13  1  0
 12 10  1  0
 10 11  2  0
 10  9  1  0
  9  8  2  0
  8  6  1  0
  6  7  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 29  1  0
 29 27  1  0
 27 28  1  0
 27 25  2  0
 25 26  1  0
 25 23  1  0
 23 24  2  0
 23 22  1  0
 22 20  1  0
 20 21  1  6
  8 18  1  0
 18 19  2  0
 14 16  1  0
 14 18  1  1
 20  9  1  0
 20 29  1  0
 17 41  1  0
 17 42  1  0
 17 43  1  0
 16 40  1  1
 15 38  1  0
 15 39  1  0
 12 36  1  6
 13 37  1  0
  6 34  1  6
  7 35  1  0
  5 33  1  1
  1 30  1  0
  1 31  1  0
  1 32  1  0
 29 55  1  1
 28 52  1  0
 28 53  1  0
 28 54  1  0
 26 49  1  0
 26 50  1  0
 26 51  1  0
 22 47  1  0
 22 48  1  0
 21 44  1  0
 21 45  1  0
 21 46  1  0
M  END


  Mrv1652309102213462D          

 29 32  0  0  1  0            999 V2000
    1.1270    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1414   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  2  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
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  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  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  6  0  0  0
 14 18  1  0  0  0  0
  8 18  1  0  0  0  0
 18 19  2  0  0  0  0
  9 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 27 28  1  0  0  0  0
 29 27  1  6  0  0  0
  5 29  1  0  0  0  0
 20 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0299766

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C[C@@]11[C@@H](O)C(=O)C2=C([C@H](O)[C@@H](OC(C)=O)[C@H]3C(C)=C(C)C(=O)C[C@]23C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H26O7/c1-8-6-22(8)19(27)13-15(17(26)20(22)28)21(5)7-12(24)9(2)10(3)14(21)18(16(13)25)29-11(4)23/h8,14,16,18,20,25,28H,6-7H2,1-5H3/t8-,14+,16-,18-,20-,21-,22+/m0/s1

> <INCHI_KEY>
USCKUXUXQDJZGI-IIHXGUGSSA-N

> <FORMULA>
C22H26O7

> <MOLECULAR_WEIGHT>
402.443

> <EXACT_MASS>
402.167853177

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
41.45608323827783

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,3'R,4'bS,8'aS,9'S,10'S)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-3',4',4'b,5',6',8'a,9',10'-octahydro-1'H-spiro[cyclopropane-1,2'-phenanthrene]-9'-yl acetate

> <JCHEM_LOGP>
1.0605716263333322

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.416452700198487

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.64352298042622

> <JCHEM_PKA_STRONGEST_BASIC>
-3.540138006792165

> <JCHEM_POLAR_SURFACE_AREA>
117.97

> <JCHEM_REFRACTIVITY>
102.5303

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3'R,4'bS,8'aS,9'S,10'S)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'H-spiro[cyclopropane-1,2'-phenanthrene]-9'-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       2.104   7.438   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.874   6.105   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.414   6.105   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       2.104   4.771   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.184   4.771   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.414  -1.897   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       7.494  -1.897   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.827   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.827   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.597  -1.334   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.494   3.437   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.644  -0.564   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.206  -1.897   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.746   0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.206   3.437   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   29                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   18                                                  
CONECT    9    8   10   20                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   18                                             
CONECT   15   14   16                                                       
CONECT   16   15   14   17                                                  
CONECT   17   16                                                            
CONECT   18   14    8   19                                                  
CONECT   19   18                                                            
CONECT   20    9   21   22   29                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27    5   20                                                  
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

(1S,2S,3'R,4'bS,8'aS,9'S,10'S)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-3',4',4'b,5',6',8'a,9',10'-octahydro-1'H-spiro[cyclopropane-1,2'-phenanthrene]-9'-yl acetate

Traditional Name

(1S,2S,3'R,4'bS,8'aS,9'S,10'S)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'H-spiro[cyclopropane-1,2'-phenanthrene]-9'-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@H]1C[C@@]11[C@@H](O)C(=O)C2=C([C@H](O)[C@@H](OC(C)=O)[C@H]3C(C)=C(C)C(=O)C[C@]23C)C1=O

InChI Identifier

InChI=1S/C22H26O7/c1-8-6-22(8)19(27)13-15(17(26)20(22)28)21(5)7-12(24)9(2)10(3)14(21)18(16(13)25)29-11(4)23/h8,14,16,18,20,25,28H,6-7H2,1-5H3/t8-,14+,16-,18-,20-,21-,22+/m0/s1

InChI Key

USCKUXUXQDJZGI-IIHXGUGSSA-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 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

Abietane diterpenoid
Diterpenoid
Phenanthrene
Cyclohexenone
Carboxylic acid ester
Ketone
Secondary alcohol
Cyclic ketone
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxide
Organic oxygen compound
Alcohol
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	1.06	ChemAxon
pKa (Strongest Acidic)	12.64	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	117.97 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	102.53 m³·mol⁻¹	ChemAxon
Polarizability	41.46 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

101317816

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Chiarugi V: PI3K signal and DNA repair: a short commentary. Pharmacol Res. 1997 Apr;35(4):263-5. doi: 10.1006/phrs.1997.0151. [PubMed:9264040 ]
LOTUS database [Link]

Showing NP-Card for (1s,2s,3'r,4'bs,8'as,9's,10's)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'h-spiro[cyclopropane-1,2'-phenanthren]-9'-yl acetate (NP0299766)

MOL for NP0299766 ((1s,2s,3'r,4'bs,8'as,9's,10's)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'h-spiro[cyclopropane-1,2'-phenanthren]-9'-yl acetate)

3D MOL for NP0299766 ((1s,2s,3'r,4'bs,8'as,9's,10's)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'h-spiro[cyclopropane-1,2'-phenanthren]-9'-yl acetate)

3D SDF for NP0299766 ((1s,2s,3'r,4'bs,8'as,9's,10's)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'h-spiro[cyclopropane-1,2'-phenanthren]-9'-yl acetate)

3D-SDF for NP0299766 ((1s,2s,3'r,4'bs,8'as,9's,10's)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'h-spiro[cyclopropane-1,2'-phenanthren]-9'-yl acetate)

PDB for NP0299766 ((1s,2s,3'r,4'bs,8'as,9's,10's)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'h-spiro[cyclopropane-1,2'-phenanthren]-9'-yl acetate)

3D PDB for NP0299766 ((1s,2s,3'r,4'bs,8'as,9's,10's)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'h-spiro[cyclopropane-1,2'-phenanthren]-9'-yl acetate)

SMILES for NP0299766 ((1s,2s,3'r,4'bs,8'as,9's,10's)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'h-spiro[cyclopropane-1,2'-phenanthren]-9'-yl acetate)

INCHI for NP0299766 ((1s,2s,3'r,4'bs,8'as,9's,10's)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'h-spiro[cyclopropane-1,2'-phenanthren]-9'-yl acetate)

Structure for NP0299766 ((1s,2s,3'r,4'bs,8'as,9's,10's)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'h-spiro[cyclopropane-1,2'-phenanthren]-9'-yl acetate)

3D Structure for NP0299766 ((1s,2s,3'r,4'bs,8'as,9's,10's)-3',10'-dihydroxy-2,4'b,7',8'-tetramethyl-1',4',6'-trioxo-5',8'a,9',10'-tetrahydro-3'h-spiro[cyclopropane-1,2'-phenanthren]-9'-yl acetate)