NP-MRD: Showing NP-Card for methyl (1r,2r,4s,6r,8r,9s,14s)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0¹,⁹.0⁴,⁸]hexadec-12-ene-13-carboxylate (NP0146403)

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Record Information

Version

2.0

Created at

2022-09-02 01:47:47 UTC

Updated at

2022-09-02 01:47:47 UTC

NP-MRD ID

NP0146403

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1r,2r,4s,6r,8r,9s,14s)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0¹,⁹.0⁴,⁸]hexadec-12-ene-13-carboxylate

Description

CHEMBL3263394 belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations. Based on a literature review very few articles have been published on CHEMBL3263394.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022203472D          

 31 35  0  0  1  0            999 V2000
    0.7878   -0.2271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1141    0.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8308    0.7854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2679    1.4005    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0857    1.5090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5886    0.8550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2736    0.0925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4064    0.9635    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7625    2.1078    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5232    1.7884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1801    2.2875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9408    1.9682    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0763    3.1060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7332    3.6051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6270    0.9700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9701    0.4709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2094    0.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1056    1.6087    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5589    1.2173    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0323    0.6051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7968    0.9257    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5019    0.4973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5697   -0.3249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3726   -0.5145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8010    0.1906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2629    0.8159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7291    1.7521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0746    1.9464    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3996    2.7477    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2496    2.8066    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5966    3.5551    0.0000 O   0  0  0  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  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 10 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 17  1  1  0  0  0
  9 18  1  0  0  0  0
 18 19  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 22 26  2  0  0  0  0
 21 27  1  0  0  0  0
 28 27  1  1  0  0  0
 19 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  9 30  1  0  0  0  0
 30 31  1  1  0  0  0
M  END

     RDKit          3D

 57 61  0  0  0  0  0  0  0  0999 V2000
    0.9789    0.6824   -2.9761 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7887    0.0271   -1.8763 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2549   -1.3437   -1.8389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9807   -1.4362   -0.9150 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0965   -0.9137   -1.5522 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1322   -1.6235   -2.0295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3310   -0.9984   -2.7078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1527   -2.8577   -1.9330 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6528   -0.7802    0.4200 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8068   -0.8393    1.3312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5999   -2.0839    1.4986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3673   -3.1593    0.9280 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6848   -2.0664    2.3499 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5136   -3.1978    2.5858 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1801    0.2078    2.0414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5592    1.5458    2.0579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1690    1.4569    1.4110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2272    0.6316    0.1929 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0790    0.6354   -0.5365 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7773    1.9447   -0.6050 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7543    1.8725    0.5437 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0445    2.4245    0.0902 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9539    1.7702   -0.7105 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0227    2.6245   -0.9019 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7474    3.7267   -0.2421 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5908    3.6541    0.3584 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8202    0.5880    0.9881 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1416   -0.2386    0.0828 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7151   -1.3995    0.5909 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4755   -1.5700    1.0323 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3824   -1.5297    2.4515 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7320    0.1375   -3.9209 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3299    1.6722   -3.1480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0778   -1.7146   -2.8354 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0332   -2.0342   -1.4946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0965   -2.4994   -0.7692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5064   -1.4165   -3.6982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0731    0.0728   -2.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1852   -1.0613   -2.0110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5800   -2.9453    2.3495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4705   -3.5256    3.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2140   -4.0564    1.9532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0506    0.0967    2.7057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4632    1.9323    3.0902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1997    2.2448    1.4974 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5233    1.1824    2.1963 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0433    2.5155    1.1178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9578    1.1500   -0.5121 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1066    2.8058   -0.5794 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3704    2.0580   -1.5604 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3840    2.5112    1.3582 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9285    0.7840   -1.1520 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9382    2.5070   -1.4581 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0696    4.3823    0.9803 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8834   -0.4485   -0.7198 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1945   -2.6520    0.8166 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2644   -1.4533    2.8587 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 11  1  0
 11 12  2  0
 11 10  1  0
 10 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30  9  1  0
  9  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  2  0
 21 22  1  0
 22 26  2  0
 26 25  1  0
 25 24  1  0
 24 23  2  0
  9 10  1  1
 23 22  1  0
  9 18  1  0
 28 19  1  0
 19  2  1  6
 14 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 16 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  6
 20 49  1  0
 20 50  1  0
 21 51  1  1
 28 55  1  6
 30 56  1  6
 31 57  1  0
  4 36  1  1
  3 34  1  0
  3 35  1  0
  1 32  1  0
  1 33  1  0
  7 37  1  0
  7 38  1  0
  7 39  1  0
 26 54  1  0
 24 53  1  0
 23 52  1  0
M  END


  Mrv1652309022203472D          

 31 35  0  0  1  0            999 V2000
    0.7878   -0.2271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1141    0.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8308    0.7854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2679    1.4005    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0857    1.5090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5886    0.8550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2736    0.0925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4064    0.9635    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7625    2.1078    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5232    1.7884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1801    2.2875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9408    1.9682    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0763    3.1060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7332    3.6051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6270    0.9700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9701    0.4709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2094    0.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1056    1.6087    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5589    1.2173    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0323    0.6051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7968    0.9257    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5019    0.4973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5697   -0.3249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3726   -0.5145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8010    0.1906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2629    0.8159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7291    1.7521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0746    1.9464    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3996    2.7477    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2496    2.8066    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5966    3.5551    0.0000 O   0  0  0  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  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 10 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 17  1  1  0  0  0
  9 18  1  0  0  0  0
 18 19  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 22 26  2  0  0  0  0
 21 27  1  0  0  0  0
 28 27  1  1  0  0  0
 19 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  9 30  1  0  0  0  0
 30 31  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0146403

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CCC[C@H]2[C@@]34C[C@@H](O[C@H]3O[C@@H](O)[C@@]12[C@H](CC4=C)OC(C)=O)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H26O8/c1-12-9-18(29-13(2)24)23-15(19(25)27-3)5-4-6-17(23)22(12)10-16(14-7-8-28-11-14)30-21(22)31-20(23)26/h5,7-8,11,16-18,20-21,26H,1,4,6,9-10H2,2-3H3/t16-,17+,18+,20-,21+,22+,23+/m1/s1

> <INCHI_KEY>
HTVMZRDDOHBSER-CDSWCQBOSA-N

> <FORMULA>
C23H26O8

> <MOLECULAR_WEIGHT>
430.453

> <EXACT_MASS>
430.162767797

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
43.14779663490701

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1R,2R,4S,6R,8R,9S,14S)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0^{1,9}.0^{4,8}]hexadec-12-ene-13-carboxylate

> <ALOGPS_LOGP>
2.89

> <JCHEM_LOGP>
2.121814882333334

> <ALOGPS_LOGS>
-3.61

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.724537813833287

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8649125497978716

> <JCHEM_POLAR_SURFACE_AREA>
104.43000000000002

> <JCHEM_REFRACTIVITY>
106.39469999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.06e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,2R,4S,6R,8R,9S,14S)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0^{1,9}.0^{4,8}]hexadec-12-ene-13-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       1.471  -0.424   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.080   0.990   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.417   1.466   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.233   2.614   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       5.760   2.817   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       6.699   1.596   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.111   0.173   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.225   1.799   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.290   3.934   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.710   3.338   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.936   4.270   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.356   3.674   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       5.742   5.798   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.969   6.729   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.904   1.811   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.677   0.879   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.257   1.475   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.064   3.003   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.043   2.272   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.060   1.130   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.487   1.728   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.803   0.928   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.930  -0.607   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.429  -0.960   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -5.229   0.356   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -4.224   1.523   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -1.361   3.270   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       0.139   3.633   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       0.746   5.129   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       2.333   5.239   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       2.980   6.636   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    4   10   18   30                                             
CONECT   10    9   11   15                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13                                                            
CONECT   15   10   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17    9   19                                                  
CONECT   19   18    2   20   28                                             
CONECT   20   19   21                                                       
CONECT   21   20   22   27                                                  
CONECT   22   21   23   26                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   22                                                       
CONECT   27   21   28                                                       
CONECT   28   27   19   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29    9   31                                                  
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₆O₈

Average Mass

430.4530 Da

Monoisotopic Mass

430.16277 Da

IUPAC Name

methyl (1R,2R,4S,6R,8R,9S,14S)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0^{1,9}.0^{4,8}]hexadec-12-ene-13-carboxylate

Traditional Name

methyl (1R,2R,4S,6R,8R,9S,14S)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0^{1,9}.0^{4,8}]hexadec-12-ene-13-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CCC[C@H]2[C@@]34C[C@@H](O[C@H]3O[C@@H](O)[C@@]12[C@H](CC4=C)OC(C)=O)C1=COC=C1

InChI Identifier

InChI=1S/C23H26O8/c1-12-9-18(29-13(2)24)23-15(19(25)27-3)5-4-6-17(23)22(12)10-16(14-7-8-28-11-14)30-21(22)31-20(23)26/h5,7-8,11,16-18,20-21,26H,1,4,6,9-10H2,2-3H3/t16-,17+,18+,20-,21+,22+,23+/m1/s1

InChI Key

HTVMZRDDOHBSER-CDSWCQBOSA-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 colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Colensane and clerodane diterpenoids

Alternative Parents

Substituents

Clerodane diterpenoid
Furopyran
Dicarboxylic acid or derivatives
Oxane
Pyran
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Furan
Methyl ester
Tetrahydrofuran
Carboxylic acid ester
Hemiacetal
Organoheterocyclic compound
Acetal
Carboxylic acid derivative
Oxacycle
Organooxygen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	2.89	ALOGPS
logP	2.12	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	11.72	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	104.43 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	106.39 m³·mol⁻¹	ChemAxon
Polarizability	43.15 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

Not Available

Chemspider ID

34251586

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

90676778

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1r,2r,4s,6r,8r,9s,14s)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0¹,⁹.0⁴,⁸]hexadec-12-ene-13-carboxylate (NP0146403)

MOL for NP0146403 (methyl (1r,2r,4s,6r,8r,9s,14s)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0¹,⁹.0⁴,⁸]hexadec-12-ene-13-carboxylate)

3D MOL for NP0146403 (methyl (1r,2r,4s,6r,8r,9s,14s)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0¹,⁹.0⁴,⁸]hexadec-12-ene-13-carboxylate)

3D SDF for NP0146403 (methyl (1r,2r,4s,6r,8r,9s,14s)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0¹,⁹.0⁴,⁸]hexadec-12-ene-13-carboxylate)

3D-SDF for NP0146403 (methyl (1r,2r,4s,6r,8r,9s,14s)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0¹,⁹.0⁴,⁸]hexadec-12-ene-13-carboxylate)

PDB for NP0146403 (methyl (1r,2r,4s,6r,8r,9s,14s)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0¹,⁹.0⁴,⁸]hexadec-12-ene-13-carboxylate)

3D PDB for NP0146403 (methyl (1r,2r,4s,6r,8r,9s,14s)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0¹,⁹.0⁴,⁸]hexadec-12-ene-13-carboxylate)

SMILES for NP0146403 (methyl (1r,2r,4s,6r,8r,9s,14s)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0¹,⁹.0⁴,⁸]hexadec-12-ene-13-carboxylate)

INCHI for NP0146403 (methyl (1r,2r,4s,6r,8r,9s,14s)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0¹,⁹.0⁴,⁸]hexadec-12-ene-13-carboxylate)

Structure for NP0146403 (methyl (1r,2r,4s,6r,8r,9s,14s)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0¹,⁹.0⁴,⁸]hexadec-12-ene-13-carboxylate)

3D Structure for NP0146403 (methyl (1r,2r,4s,6r,8r,9s,14s)-14-(acetyloxy)-6-(furan-3-yl)-2-hydroxy-16-methylidene-3,5-dioxatetracyclo[6.5.3.0¹,⁹.0⁴,⁸]hexadec-12-ene-13-carboxylate)