NP-MRD: Showing NP-Card for 4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate (NP0280645)

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Record Information

Version

2.0

Created at

2022-09-09 06:33:29 UTC

Updated at

2022-09-09 06:33:29 UTC

NP-MRD ID

NP0280645

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate

Description

4A-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-7-yl acetate belongs to the class of organic compounds known as iridoids and derivatives. These are monoterpenes containing a skeleton structurally characterized by the presence of a cylopentane fused to a pyran ( forming a 4,7-dimethylcyclopenta[c]pyran), or a derivative where the pentane moiety is open. 4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate is found in Galeopsis pubescens. Based on a literature review very few articles have been published on 4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-7-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092208332D          

 27 29  0  0  0  0            999 V2000
   -1.0047   -1.7779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2902   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2902   -0.5404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4243   -1.7779    0.0000 O   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
    1.4743   -2.1191    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
    1.8371    0.5350    0.0000 O   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
    3.3523   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -3.9979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -5.2354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -5.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -6.0604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -5.2354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -3.5854    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
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  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  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 17 25  1  0  0  0  0
 25 26  1  0  0  0  0
 14 27  1  0  0  0  0
  9 27  1  0  0  0  0
  5 27  1  0  0  0  0
M  END

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
   -2.4947    3.6808   -0.3796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5268    2.3665    0.3312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4928    2.2969    1.5622 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5956    1.2150   -0.4027 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6196   -0.0885    0.0419 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7150   -0.4156    1.0061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0660   -0.8846   -1.2571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7025   -2.2951   -0.9547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5468   -2.2309   -0.0126 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4079   -2.7808   -0.5715 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8743   -2.9270    1.2407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7894   -2.3938    2.4411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3646   -1.0846    2.5769 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5860   -0.5710    1.5076 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0249    0.6456    1.7210 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3366    0.7044    1.8160 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0887    0.2652    0.5799 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4468    0.3636    0.8932 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2604   -0.0328   -0.1555 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5752    0.2713    0.2030 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9724    0.6319   -1.4625 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6460    1.8501   -1.5660 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4977    0.7824   -1.7668 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0102   -0.4643   -2.1535 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8260    1.2963   -0.5353 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5192    2.4609   -0.1499 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3147   -0.7294    0.2354 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5178    4.1081   -0.4121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1772    3.5342   -1.4330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7610    4.3758    0.0708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0297   -1.4711    0.8743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6101    0.1763    0.6627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5247   -0.1195    2.0450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1283   -0.7051   -1.4292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4405   -0.5173   -2.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3724   -2.8080   -1.9036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5737   -2.8551   -0.5621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5868   -3.0157   -1.5120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2148   -3.9777    1.1263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0613   -3.0134    3.2922 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2959   -1.3029    1.4487 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6209    1.7623    1.9999 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7157    0.0848    2.6775 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7787   -0.6990    0.1880 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2365   -1.1433   -0.3075 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6567    0.2366    1.1957 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4033   -0.0367   -2.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6193    1.6643   -1.6423 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4006    1.4689   -2.6206 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7443   -0.9901   -2.5999 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7680    1.5076   -0.6651 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3364    2.1979    0.3376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6360   -0.3948   -0.6047 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  5  4  1  6
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  6
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 14 27  1  0
 27  5  1  0
 27  9  1  0
 25 17  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  6 31  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  8 36  1  0
  8 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 14 41  1  6
 16 42  1  0
 16 43  1  0
 17 44  1  6
 19 45  1  6
 20 46  1  0
 21 47  1  6
 22 48  1  0
 23 49  1  6
 24 50  1  0
 25 51  1  6
 26 52  1  0
 27 53  1  6
M  END


  Mrv1652309092208332D          

 27 29  0  0  0  0            999 V2000
   -1.0047   -1.7779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2902   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2902   -0.5404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4243   -1.7779    0.0000 O   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
    1.4743   -2.1191    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
    1.8371    0.5350    0.0000 O   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
    3.3523   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -3.9979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -5.2354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -5.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -6.0604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -5.2354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -3.5854    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
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  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  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 17 25  1  0  0  0  0
 25 26  1  0  0  0  0
 14 27  1  0  0  0  0
  9 27  1  0  0  0  0
  5 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0280645

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1(C)CCC2(O)C=COC(OCC3OC(O)C(O)C(O)C3O)C12

> <INCHI_IDENTIFIER>
InChI=1S/C17H26O10/c1-8(18)27-16(2)3-4-17(23)5-6-24-15(13(16)17)25-7-9-10(19)11(20)12(21)14(22)26-9/h5-6,9-15,19-23H,3-4,7H2,1-2H3

> <INCHI_KEY>
IZBSPNKFNIQBCC-UHFFFAOYSA-N

> <FORMULA>
C17H26O10

> <MOLECULAR_WEIGHT>
390.385

> <EXACT_MASS>
390.152597037

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
37.787306097474826

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-7-yl acetate

> <JCHEM_LOGP>
-2.6833429690000012

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.662508794370009

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.297003391909746

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3153455211545735

> <JCHEM_POLAR_SURFACE_AREA>
155.14000000000001

> <JCHEM_REFRACTIVITY>
87.03750000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1H,5H,6H,7aH-cyclopenta[c]pyran-7-yl acetate

> <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      -1.875  -3.319   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.542  -2.549   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.542  -1.009   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       0.792  -3.319   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.752  -3.956   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.126  -0.057   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.429   0.999   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.258  -2.073   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.924  -4.383   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.258  -5.153   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.258  -6.693   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.591  -7.463   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.591  -9.003   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.925  -9.773   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.258  -9.773   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.258 -11.313   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.924  -9.003   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.590  -9.773   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       4.924  -7.463   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.590  -6.693   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.590  -2.073   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    7   27                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11   27                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   27                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   17   26                                                  
CONECT   26   25                                                            
CONECT   27   14    9    5                                                  
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Value	Source
4a-Hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1H,4ah,5H,6H,7H,7ah-cyclopenta[c]pyran-7-yl acetic acid	Generator

Chemical Formula

C₁₇H₂₆O₁₀

Average Mass

390.3850 Da

Monoisotopic Mass

390.15260 Da

IUPAC Name

4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-7-yl acetate

Traditional Name

4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1H,5H,6H,7aH-cyclopenta[c]pyran-7-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1(C)CCC2(O)C=COC(OCC3OC(O)C(O)C(O)C3O)C12

InChI Identifier

InChI=1S/C17H26O10/c1-8(18)27-16(2)3-4-17(23)5-6-24-15(13(16)17)25-7-9-10(19)11(20)12(21)14(22)26-9/h5-6,9-15,19-23H,3-4,7H2,1-2H3

InChI Key

IZBSPNKFNIQBCC-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
Galeopsis pubescens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as iridoids and derivatives. These are monoterpenes containing a skeleton structurally characterized by the presence of a cylopentane fused to a pyran ( forming a 4,7-dimethylcyclopenta[c]pyran), or a derivative where the pentane moiety is open.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Iridoids and derivatives

Alternative Parents

Substituents

Iridoid-skeleton
Bicyclic monoterpenoid
Monosaccharide
Oxane
Cyclic alcohol
Tertiary alcohol
Secondary alcohol
Hemiacetal
Carboxylic acid ester
Polyol
Oxacycle
Monocarboxylic acid or derivatives
Acetal
Carboxylic acid derivative
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	-2.7	ChemAxon
pKa (Strongest Acidic)	11.3	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	155.14 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	87.04 m³·mol⁻¹	ChemAxon
Polarizability	37.79 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

162981707

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate (NP0280645)

MOL for NP0280645 (4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate)

3D MOL for NP0280645 (4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate)

3D SDF for NP0280645 (4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate)

3D-SDF for NP0280645 (4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate)

PDB for NP0280645 (4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate)

3D PDB for NP0280645 (4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate)

SMILES for NP0280645 (4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate)

INCHI for NP0280645 (4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate)

Structure for NP0280645 (4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate)

3D Structure for NP0280645 (4a-hydroxy-7-methyl-1-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]-1h,5h,6h,7ah-cyclopenta[c]pyran-7-yl acetate)