NP-MRD: Showing NP-Card for (-)-Aglacin D (NP0080435)

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Record Information

Version

2.0

Created at

2022-04-29 01:27:33 UTC

Updated at

2022-04-29 01:27:33 UTC

NP-MRD ID

NP0080435

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Aglacin D

Description

Aglacin D belongs to the class of organic compounds known as aryltetralin lignans. These are lignans with a structure based on the 1-phenyltetralin skeleton. (-)-Aglacin D is found in Aglaia cordata and Aglaia tomentosa. Based on a literature review very few articles have been published on aglacin D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292203272D          

 32 35  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  1  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  2  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
    2.1434   -1.2375    0.0000 O   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
    3.5724    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    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  6  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
  9 10  2  0  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  7 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
  6 21  1  6  0  0  0
 21 22  2  0  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  2  0  0  0  0
 21 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  0  0  0  0
 23 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
    2.0499    2.5976    2.3040 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8587    1.5522    1.8604 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5376    0.6135    0.9162 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3051    0.6214    0.2797 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9689   -0.3168   -0.6721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2953   -0.2890   -1.3445 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3629   -0.1521   -0.3114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9895    1.0750   -0.1181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9841    1.1797    0.8305 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3880    0.1108    1.6020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3881    0.2035    2.5600 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0462    1.4360    2.7833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7785   -1.1096    1.4229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1689   -2.2037    2.1896 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2146   -3.0105    1.6659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7719   -1.2104    0.4616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2067   -2.4807    0.3453 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1142   -2.7958    1.1801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6297    2.2758   -0.9078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2122    3.3736   -0.7733 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5296    2.1547   -1.8962 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8348    2.8016   -3.2258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4122    1.9539   -4.2173 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0681    0.7613   -3.6450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5913    0.7053   -2.3644 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9594   -1.2694   -0.9433 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1683   -1.2967   -0.3350 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1069   -2.2650   -0.6464 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7832   -3.2333   -1.6167 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4651   -0.3443    0.6077 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7052   -0.3891    1.2177 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8489    0.2642    0.7491 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9628    2.3151    2.3911 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1350    3.4570    1.6116 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3322    2.9789    3.3061 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6420    1.4131    0.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4191   -1.3024   -1.8594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4540    2.1498    0.9585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3006    1.8379    1.7671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9590    1.3322    3.3684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3187    2.1133    3.2672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8129   -3.7510    0.9543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9644   -2.3716    1.1286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7609   -3.5289    2.4707 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3151   -1.9027    1.6621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4142   -3.5262    1.9816 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6463   -3.3567    0.5768 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4449    2.4620   -1.5412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9536    2.8988   -3.2793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4379    3.8240   -3.3079 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1519    0.7880   -3.7085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2638   -0.1038   -4.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6965    0.5839   -2.6157 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6975   -1.9881   -1.6744 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9704   -3.8725   -1.2158 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6473   -3.9074   -1.8134 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4028   -2.7621   -2.5465 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4170    0.7716    1.5644 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5469    1.0501    0.0411 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5369   -0.4569    0.2503 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5 26  2  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 27 30  2  0
 30 31  1  0
 31 32  1  0
  5  6  1  0
  6 25  1  0
 25 24  1  0
 24 23  1  0
 23 22  1  0
 22 21  1  0
 21 19  1  0
 19 20  2  0
 19  8  1  0
  8  7  2  0
  7 16  1  0
 16 17  1  0
 17 18  1  0
 16 13  2  0
 13 14  1  0
 14 15  1  0
 13 10  1  0
 10 11  1  0
 11 12  1  0
 10  9  2  0
 30  3  1  0
  7  6  1  0
 21 25  1  0
  9  8  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  4 36  1  0
 26 54  1  0
 29 55  1  0
 29 56  1  0
 29 57  1  0
 32 58  1  0
 32 59  1  0
 32 60  1  0
  6 37  1  6
 25 53  1  6
 24 51  1  0
 24 52  1  0
 22 49  1  0
 22 50  1  0
 21 48  1  1
 18 45  1  0
 18 46  1  0
 18 47  1  0
 15 42  1  0
 15 43  1  0
 15 44  1  0
 12 39  1  0
 12 40  1  0
 12 41  1  0
  9 38  1  0
M  END


  Mrv1652304292203272D          

 32 35  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  1  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  2  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
    2.1434   -1.2375    0.0000 O   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
    3.5724    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    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  6  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
  9 10  2  0  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  7 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
  6 21  1  6  0  0  0
 21 22  2  0  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  2  0  0  0  0
 21 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  0  0  0  0
 23 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0080435

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC(OC)=C1OC)[C@@H]1[C@@H]2COC[C@H]2C(=O)C2=C1C(OC)=C(OC)C(OC)=C2

> <INCHI_IDENTIFIER>
InChI=1S/C24H28O8/c1-26-16-7-12(8-17(27-2)22(16)29-4)19-14-10-32-11-15(14)21(25)13-9-18(28-3)23(30-5)24(31-6)20(13)19/h7-9,14-15,19H,10-11H2,1-6H3/t14-,15-,19-/m1/s1

> <INCHI_KEY>
UDMGAFIGOTWFTR-SPYBWZPUSA-N

> <FORMULA>
C24H28O8

> <MOLECULAR_WEIGHT>
444.48

> <EXACT_MASS>
444.178417862

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
46.239954150059305

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aS,9S,9aS)-6,7,8-trimethoxy-9-(3,4,5-trimethoxyphenyl)-1H,3H,3aH,4H,9H,9aH-naphtho[2,3-c]furan-4-one

> <ALOGPS_LOGP>
3.03

> <JCHEM_LOGP>
2.108133047000001

> <ALOGPS_LOGS>
-4.51

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.589159424459769

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8397787628219366

> <JCHEM_POLAR_SURFACE_AREA>
81.68000000000002

> <JCHEM_REFRACTIVITY>
116.9889

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.39e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3aS,9S,9aS)-6,7,8-trimethoxy-9-(3,4,5-trimethoxyphenyl)-1H,3H,3aH,9H,9aH-naphtho[2,3-c]furan-4-one

> <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  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.000   4.620   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.001   6.930   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.668   6.930   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.001   8.470   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       2.667   9.240   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       1.334   6.930   0.000  0.00  0.00           O+0
HETATM   32  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   21                                                  
CONECT    7    6    8   14                                                  
CONECT    8    7    9   11                                                  
CONECT    9    8    3   10                                                  
CONECT   10    9                                                            
CONECT   11    8   12                                                       
CONECT   12   11   13   19                                                  
CONECT   13   12   14   17                                                  
CONECT   14   13    7   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   13   18                                                       
CONECT   18   17                                                            
CONECT   19   12   20                                                       
CONECT   20   19                                                            
CONECT   21    6   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   31                                                  
CONECT   24   23   25   29                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25   21                                                       
CONECT   27   25   28                                                       
CONECT   28   27                                                            
CONECT   29   24   30                                                       
CONECT   30   29                                                            
CONECT   31   23   32                                                       
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₈O₈

Average Mass

444.4800 Da

Monoisotopic Mass

444.17842 Da

IUPAC Name

(3aS,9S,9aS)-6,7,8-trimethoxy-9-(3,4,5-trimethoxyphenyl)-1H,3H,3aH,4H,9H,9aH-naphtho[2,3-c]furan-4-one

Traditional Name

(3aS,9S,9aS)-6,7,8-trimethoxy-9-(3,4,5-trimethoxyphenyl)-1H,3H,3aH,9H,9aH-naphtho[2,3-c]furan-4-one

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC(OC)=C1OC)[C@@H]1[C@@H]2COC[C@H]2C(=O)C2=C1C(OC)=C(OC)C(OC)=C2

InChI Identifier

InChI=1S/C24H28O8/c1-26-16-7-12(8-17(27-2)22(16)29-4)19-14-10-32-11-15(14)21(25)13-9-18(28-3)23(30-5)24(31-6)20(13)19/h7-9,14-15,19H,10-11H2,1-6H3/t14-,15-,19-/m1/s1

InChI Key

UDMGAFIGOTWFTR-SPYBWZPUSA-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
Aglaia tomentosa	LOTUS Database	35616633

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
Tetralin
Phenoxy compound
Anisole
Methoxybenzene
Aryl alkyl ketone
Aryl ketone
Phenol ether
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Oxolane
Ketone
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
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	3.03	ALOGPS
logP	2.11	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	13.59	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	81.68 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	116.99 m³·mol⁻¹	ChemAxon
Polarizability	46.24 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

C00045619

Chemspider ID

8518873

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10343414

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (-)-Aglacin D (NP0080435)

MOL for NP0080435 ((-)-Aglacin D)

3D MOL for NP0080435 ((-)-Aglacin D)

3D SDF for NP0080435 ((-)-Aglacin D)

3D-SDF for NP0080435 ((-)-Aglacin D)

PDB for NP0080435 ((-)-Aglacin D)

3D PDB for NP0080435 ((-)-Aglacin D)

SMILES for NP0080435 ((-)-Aglacin D)

INCHI for NP0080435 ((-)-Aglacin D)

Structure for NP0080435 ((-)-Aglacin D)

3D Structure for NP0080435 ((-)-Aglacin D)