NP-MRD: Showing NP-Card for [3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate (NP0146212)

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Record Information

Version

2.0

Created at

2022-09-02 01:34:06 UTC

Updated at

2022-09-02 01:34:07 UTC

NP-MRD ID

NP0146212

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate

Description

[3,4,5-Trihydroxy-6-({7-methyl-1-oxo-octahydrocyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. [3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate is found in Catalpa ovata. [3,4,5-Trihydroxy-6-({7-methyl-1-oxo-octahydrocyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241517202D          

 32 35  0  0  0  0            999 V2000
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    0.0165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0587    1.4455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8837    1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2962    0.7310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2962    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1212    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5337    2.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1212    3.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5337    4.3034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2962    3.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8837    2.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    2.1599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    2.1599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    0.7310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  2 11  1  0  0  0  0
  5 11  1  0  0  0  0
  3 12  1  0  0  0  0
 12 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
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 20 26  1  0  0  0  0
 15 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 13 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END

     RDKit          3D

 60 63  0  0  0  0  0  0  0  0999 V2000
   -4.2023   -1.0939    2.0820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0150   -0.2073    1.7206 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5381   -0.4461    0.3246 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2299   -0.7105    0.1680 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8413   -1.8339   -0.5014 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2950   -1.6729   -1.7432 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0962   -1.3802   -1.7417 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3106    0.0217   -1.3828 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5404    0.6006   -1.3231 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6081    0.5499   -0.4964 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5458   -0.1707    0.5182 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8474    1.3089   -0.7381 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9110    1.2333    0.1184 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0775    1.9639   -0.1333 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1500    2.7645   -1.2544 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3070    3.5021   -1.5228 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0882    2.8374   -2.1054 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9259    2.1044   -1.8474 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7856   -2.4938   -1.0803 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1542   -2.4902   -1.1182 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3062   -2.7564    0.3264 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8979   -3.9092    0.7982 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2327   -2.9142    0.3004 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6121   -2.9765    1.6171 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8498    0.8413   -0.4253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7559    1.6456    0.4618 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1952    1.4702    0.0629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1709    1.9687    1.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6610    2.1392    2.3565 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5642    1.4124    2.7910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4570    0.9098    3.9393 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4504    1.2138    1.8503 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1374   -0.4934    2.1947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0561   -1.5880    3.0653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3278   -1.9139    1.3462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2433   -0.3971    2.4918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2262   -1.2168   -0.1327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8804   -2.2909   -0.7657 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3093   -1.4249   -2.8886 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6561    0.7076   -2.0402 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7535    0.1841   -0.3723 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9022    0.6225    1.0065 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9268    1.9157    0.5323 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3637    4.0827   -2.3317 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1281    3.4686   -3.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1291    2.2135   -2.5658 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4231   -3.4370   -1.6457 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5153   -3.3176   -1.4741 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5773   -1.9026    0.9570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4862   -4.7209    0.3844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4049   -3.9222   -0.1453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5714   -3.2365    1.6392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3319    0.6842   -1.3868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9288    1.4392   -0.6033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5258    2.7306    0.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3437    2.0478   -0.8798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3782    0.3969   -0.2279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6946    2.9105    0.7340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0106    1.2160    1.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5910    1.8103    2.2265 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  2  0
 30 32  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
  7 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 32  2  1  0
 23  5  1  0
 32 26  1  0
 18 12  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  1
  3 37  1  6
 25 53  1  0
 25 54  1  0
 26 55  1  1
 27 56  1  0
 27 57  1  0
 28 58  1  0
 28 59  1  0
 32 60  1  1
  5 38  1  6
  7 39  1  6
  8 40  1  0
  8 41  1  0
 13 42  1  0
 14 43  1  0
 16 44  1  0
 17 45  1  0
 18 46  1  0
 19 47  1  6
 20 48  1  0
 21 49  1  1
 22 50  1  0
 23 51  1  6
 24 52  1  0
M  END


  Mrv1533004241517202D          

 32 35  0  0  0  0            999 V2000
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    0.0165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0587    1.4455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8837    1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2962    0.7310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2962    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1212    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5337    2.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1212    3.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5337    4.3034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2962    3.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8837    2.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    2.1599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    2.1599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    0.7310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  2 11  1  0  0  0  0
  5 11  1  0  0  0  0
  3 12  1  0  0  0  0
 12 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
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 20 26  1  0  0  0  0
 15 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 13 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0146212

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C(CC2CCOC(=O)C12)OC1OC(COC(=O)C2=CC=C(O)C=C2)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C22H28O10/c1-10-14(8-12-6-7-29-21(28)16(10)12)31-22-19(26)18(25)17(24)15(32-22)9-30-20(27)11-2-4-13(23)5-3-11/h2-5,10,12,14-19,22-26H,6-9H2,1H3

> <INCHI_KEY>
DEDRXCYIYLIKTC-UHFFFAOYSA-N

> <FORMULA>
C22H28O10

> <MOLECULAR_WEIGHT>
452.456

> <EXACT_MASS>
452.168247102

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
45.34859282541363

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[3,4,5-trihydroxy-6-({7-methyl-1-oxo-octahydrocyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate

> <ALOGPS_LOGP>
0.47

> <JCHEM_LOGP>
0.8041212883333324

> <ALOGPS_LOGS>
-2.31

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.212240437641633

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.49769487453218

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6490926697041095

> <JCHEM_POLAR_SURFACE_AREA>
151.98

> <JCHEM_REFRACTIVITY>
107.18830000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.19e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3H-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.126  -0.057   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.258  -2.073   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.924  -4.383   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.320  -1.303   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -1.090   0.031   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -2.630   0.031   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -3.400   1.365   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.940   1.365   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -5.710   2.698   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -7.250   2.698   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -8.020   1.365   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -8.020   4.032   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -9.560   4.032   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -10.330   5.366   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -9.560   6.699   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0     -10.330   8.033   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -8.020   6.699   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -7.250   5.366   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.630   2.698   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -3.400   4.032   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -1.090   2.698   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -0.320   4.032   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -0.320   1.365   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       1.220   1.365   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4   12                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9    2    5                                                  
CONECT   12    3   13                                                       
CONECT   13   12   14   31                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   27                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   26                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   20                                                       
CONECT   27   15   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   13   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Value	Source
[3,4,5-Trihydroxy-6-({7-methyl-1-oxo-octahydrocyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoic acid	Generator

Chemical Formula

C₂₂H₂₈O₁₀

Average Mass

452.4560 Da

Monoisotopic Mass

452.16825 Da

IUPAC Name

[3,4,5-trihydroxy-6-({7-methyl-1-oxo-octahydrocyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate

Traditional Name

[3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3H-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate

CAS Registry Number

Not Available

SMILES

CC1C(CC2CCOC(=O)C12)OC1OC(COC(=O)C2=CC=C(O)C=C2)C(O)C(O)C1O

InChI Identifier

InChI=1S/C22H28O10/c1-10-14(8-12-6-7-29-21(28)16(10)12)31-22-19(26)18(25)17(24)15(32-22)9-30-20(27)11-2-4-13(23)5-3-11/h2-5,10,12,14-19,22-26H,6-9H2,1H3

InChI Key

DEDRXCYIYLIKTC-UHFFFAOYSA-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
Catalpa ovata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
P-hydroxybenzoic acid alkyl ester
P-hydroxybenzoic acid ester
Glycosyl compound
Iridoid-skeleton
O-glycosyl compound
Aromatic monoterpenoid
Benzoate ester
Bicyclic monoterpenoid
Monoterpenoid
Benzoic acid or derivatives
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Delta valerolactone
Phenol
Delta_valerolactone
Monocyclic benzene moiety
Benzenoid
Dicarboxylic acid or derivatives
Oxane
Monosaccharide
Secondary alcohol
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Polyol
Acetal
Alcohol
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
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	0.47	ALOGPS
logP	0.8	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	8.5	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	151.98 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	107.19 m³·mol⁻¹	ChemAxon
Polarizability	45.35 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	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate (NP0146212)

MOL for NP0146212 ([3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate)

3D MOL for NP0146212 ([3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate)

3D SDF for NP0146212 ([3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate)

3D-SDF for NP0146212 ([3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate)

PDB for NP0146212 ([3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate)

3D PDB for NP0146212 ([3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate)

SMILES for NP0146212 ([3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate)

INCHI for NP0146212 ([3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate)

Structure for NP0146212 ([3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate)

3D Structure for NP0146212 ([3,4,5-trihydroxy-6-({7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl}oxy)oxan-2-yl]methyl 4-hydroxybenzoate)