NP-MRD: Showing NP-Card for (+)-Aglacin C (NP0080434)

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Record Information

Version

2.0

Created at

2022-04-29 01:27:30 UTC

Updated at

2022-04-29 01:27:30 UTC

NP-MRD ID

NP0080434

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Aglacin C

Description

(3AR,4R,9aS)-4-(3,4-dimethoxyphenyl)-5,6,7-trimethoxy-1H,3H,3aH,4H,9H,9aH-naphtho[2,3-c]furan belongs to the class of organic compounds known as aryltetralin lignans. These are lignans with a structure based on the 1-phenyltetralin skeleton. (+)-Aglacin C is found in Aglaia cordata. Based on a literature review very few articles have been published on (3aR,4R,9aS)-4-(3,4-dimethoxyphenyl)-5,6,7-trimethoxy-1H,3H,3aH,4H,9H,9aH-naphtho[2,3-c]furan.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292203272D          

 29 32  0  0  1  0            999 V2000
    4.1274    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  1  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  3  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
  6 20  1  1  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
 24 25  2  0  0  0  0
 20 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END

     RDKit          3D

 57 60  0  0  0  0  0  0  0  0999 V2000
    4.9894    0.0011   -2.8078 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7118   -0.6546   -1.5932 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5385   -0.3385   -0.9336 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6288    0.5876   -1.4090 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4747    0.8469   -0.6854 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1667    0.2225    0.5128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0595    0.4876    1.2918 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3248    0.1580    0.6094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0472    1.1859    0.0508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2603    0.9073   -0.5894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7808   -0.3561   -0.6937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0042   -0.5910   -1.3461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6698    0.5312   -1.8870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0602   -1.3817   -0.1362 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4903   -2.6912   -0.1827 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1953   -3.6096   -1.1870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8543   -1.1106    0.5008 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1534   -2.1767    1.0523 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2239   -2.9669    0.3757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5852    2.5727    0.1156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6658    2.9284    1.2160 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5142    3.7623    0.7639 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6681    3.0556    1.0767 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3602    2.2603    2.1767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0744    1.8204    1.9792 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1348   -0.7026    0.9310 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2730   -0.9805    0.2494 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1521   -1.9260    0.7819 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8823   -2.5891    1.9997 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8752    1.0942   -2.6139 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0046   -0.2568   -3.1692 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1876   -0.2740   -3.5259 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8511    1.0844   -2.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8134    1.5644   -1.0981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0162   -0.2542    2.1576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8345    1.7304   -1.0346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5825    0.2781   -2.4236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8317    1.2786   -1.0689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9356    1.0118   -2.5943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7592   -4.5650   -0.8116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5885   -3.2050   -2.0155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1763   -3.9071   -1.6570 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2443   -2.4706   -0.5004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6116   -3.9705    0.0854 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6165   -3.1687    1.0980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1209    2.9205   -0.8564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5214    3.2178    0.1561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2247    3.5886    1.9464 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4897    3.8961   -0.3400 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5765    4.7434    1.2598 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0729    1.4124    2.1785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5078    2.7926    3.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5085    1.7505    3.0188 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9376   -1.2222    1.8718 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0308   -1.8499    2.8165 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5974   -3.4336    2.0744 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8609   -3.0384    2.0182 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 11  1  0
 11 10  2  0
 10  9  1  0
  9  8  2  0
  8  7  1  0
  7 25  1  0
 25 24  1  0
 24 23  1  0
 23 22  1  0
 22 21  1  0
 21 20  1  0
  7  6  1  0
  6 26  2  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 27  3  2  0
  3  2  1  0
  2  1  1  0
  3  4  1  0
  4  5  2  0
  8 17  1  0
 17 18  1  0
 18 19  1  0
 17 14  2  0
 14 15  1  0
 15 16  1  0
 14 11  1  0
 20  9  1  0
  5  6  1  0
 21 25  1  0
 13 37  1  0
 13 38  1  0
 13 39  1  0
 10 36  1  0
  7 35  1  1
 25 53  1  1
 24 51  1  0
 24 52  1  0
 22 49  1  0
 22 50  1  0
 21 48  1  1
 20 46  1  0
 20 47  1  0
 26 54  1  0
 29 55  1  0
 29 56  1  0
 29 57  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
  5 34  1  0
 19 43  1  0
 19 44  1  0
 19 45  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
M  END


  Mrv1652304292203272D          

 29 32  0  0  1  0            999 V2000
    4.1274    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  1  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  3  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
  6 20  1  1  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
 24 25  2  0  0  0  0
 20 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0080434

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C([C@H]([C@H]3COC[C@H]3C2)C2=CC(OC)=C(OC)C=C2)C(OC)=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C23H28O6/c1-24-17-7-6-13(9-18(17)25-2)20-16-12-29-11-15(16)8-14-10-19(26-3)22(27-4)23(28-5)21(14)20/h6-7,9-10,15-16,20H,8,11-12H2,1-5H3/t15-,16+,20+/m1/s1

> <INCHI_KEY>
RKVVUMUMIOPICX-GUXCAODWSA-N

> <FORMULA>
C23H28O6

> <MOLECULAR_WEIGHT>
400.471

> <EXACT_MASS>
400.188588622

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
43.23560734647437

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aR,4R,9aS)-4-(3,4-dimethoxyphenyl)-5,6,7-trimethoxy-1H,3H,3aH,4H,9H,9aH-naphtho[2,3-c]furan

> <ALOGPS_LOGP>
3.39

> <JCHEM_LOGP>
3.0762587543333333

> <ALOGPS_LOGS>
-4.95

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.865326272628702

> <JCHEM_POLAR_SURFACE_AREA>
55.38000000000001

> <JCHEM_REFRACTIVITY>
109.7903

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.52e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3aR,4R,9aS)-4-(3,4-dimethoxyphenyl)-5,6,7-trimethoxy-1H,3H,3aH,4H,9H,9aH-naphtho[2,3-c]furan

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  O   UNK     0       7.705   0.770   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       6.799  -0.476   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.799   2.016   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -0.000   4.620   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.001   6.930   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.001   8.470   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.667   9.240   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.334   6.930   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.334   8.470   0.000  0.00  0.00           C+0
CONECT    1    2    5                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4    1                                                       
CONECT    6    4    7   20                                                  
CONECT    7    6    8   13                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8    3                                                       
CONECT   10    8   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13   16                                                  
CONECT   13   12    7   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   12   17                                                       
CONECT   17   16                                                            
CONECT   18   11   19                                                       
CONECT   19   18                                                            
CONECT   20    6   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   28                                                  
CONECT   23   22   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24   20                                                       
CONECT   26   23   27                                                       
CONECT   27   26                                                            
CONECT   28   22   29                                                       
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₈O₆

Average Mass

400.4710 Da

Monoisotopic Mass

400.18859 Da

IUPAC Name

(3aR,4R,9aS)-4-(3,4-dimethoxyphenyl)-5,6,7-trimethoxy-1H,3H,3aH,4H,9H,9aH-naphtho[2,3-c]furan

Traditional Name

(3aR,4R,9aS)-4-(3,4-dimethoxyphenyl)-5,6,7-trimethoxy-1H,3H,3aH,4H,9H,9aH-naphtho[2,3-c]furan

CAS Registry Number

Not Available

SMILES

COC1=CC2=C([C@H]([C@H]3COC[C@H]3C2)C2=CC(OC)=C(OC)C=C2)C(OC)=C1OC

InChI Identifier

InChI=1S/C23H28O6/c1-24-17-7-6-13(9-18(17)25-2)20-16-12-29-11-15(16)8-14-10-19(26-3)22(27-4)23(28-5)21(14)20/h6-7,9-10,15-16,20H,8,11-12H2,1-5H3/t15-,16+,20+/m1/s1

InChI Key

RKVVUMUMIOPICX-GUXCAODWSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Aglaia cordata	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aryltetralin lignans. These are lignans with a structure based on the 1-phenyltetralin skeleton.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Aryltetralin lignans

Sub Class

Not Available

Direct Parent

Aryltetralin lignans

Alternative Parents

Substituents

1-aryltetralin lignan
Naphthofuran
O-dimethoxybenzene
Dimethoxybenzene
Tetralin
Phenoxy compound
Methoxybenzene
Phenol ether
Anisole
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Tetrahydrofuran
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
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	3.39	ALOGPS
logP	3.08	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	55.38 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	109.79 m³·mol⁻¹	ChemAxon
Polarizability	43.24 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

163012302

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Aglacin C (NP0080434)

MOL for NP0080434 ((+)-Aglacin C)

3D MOL for NP0080434 ((+)-Aglacin C)

3D SDF for NP0080434 ((+)-Aglacin C)

3D-SDF for NP0080434 ((+)-Aglacin C)

PDB for NP0080434 ((+)-Aglacin C)

3D PDB for NP0080434 ((+)-Aglacin C)

SMILES for NP0080434 ((+)-Aglacin C)

INCHI for NP0080434 ((+)-Aglacin C)

Structure for NP0080434 ((+)-Aglacin C)

3D Structure for NP0080434 ((+)-Aglacin C)