NP-MRD: Showing NP-Card for (2r,3r,4s,5s,6r)-2-{[(12s)-12-hydroxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0296061)

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Record Information

Version

2.0

Created at

2022-09-10 05:25:14 UTC

Updated at

2022-09-10 05:25:15 UTC

NP-MRD ID

NP0296061

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,4s,5s,6r)-2-{[(12s)-12-hydroxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Description

Aceroside I belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones. (2r,3r,4s,5s,6r)-2-{[(12s)-12-hydroxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol is found in Acer nikoense. Based on a literature review very few articles have been published on Aceroside I.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102207252D          

 33 36  0  0  1  0            999 V2000
    1.1583   -0.0154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8837    0.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5868   -0.0541    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3122    0.3388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0152   -0.0929    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7406    0.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7629    1.1248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5048    1.5065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5384    2.3376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8436    2.8034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1098    2.3953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0354    1.5505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2563    1.1609    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3926    1.2764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6560    2.0639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1641    2.7230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3343    2.6276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0206    1.8432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5480    1.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463    3.4785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4667    4.2965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0799    4.8777    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6828    5.6008    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9049    5.0846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7388    4.9120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4200    4.4033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8120    3.6504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9928   -0.9176    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6958   -1.3493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2674   -1.3105    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2451   -2.1352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5644   -0.8788    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8390   -1.2718    0.0000 O   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  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 10 27  1  0  0  0  0
  5 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
  3 32  1  0  0  0  0
 32 33  1  6  0  0  0
M  END

     RDKit          3D

 65 68  0  0  0  0  0  0  0  0999 V2000
   -3.6380   -3.7816    0.8018 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0084   -2.5816    1.0733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0304   -1.4922    1.4306 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3630   -0.3466    1.6899 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.3501    1.5390    1.0538 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.3038    3.1439   -0.1040 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8168    2.0762   -0.8130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3811    1.5484   -0.4071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9350    0.3251   -1.0752 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1548   -0.7038   -1.0423 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0032   -0.7238   -2.0977 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1243   -1.6080   -2.1199 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3556   -2.4628   -1.0536 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4608   -2.4409   -0.0033 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3482   -1.5360   -0.0230 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7114   -3.1781   -0.9513 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7727   -2.0683   -0.6327 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1725   -0.9384    0.1004 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3673   -1.2118    1.4780 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7418    0.4459   -0.1395 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6489    1.4644   -0.4044 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7967    2.8005    0.2099 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6575    3.7731   -0.1448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5018    1.0508    0.1070 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6985    2.3059    0.6629 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5989    0.0765    0.4379 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.6315    0.2750   -0.4817 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9918   -1.3013    0.2872 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9701   -2.2932    0.2542 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3462   -3.9207    1.4835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4752   -2.2142    0.1479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2835   -2.6570    1.8999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6306   -1.8630    2.3107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8141   -0.1275   -0.1996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2468    3.5334    2.1851 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9286    4.5193    1.5338 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3280    1.7647   -1.8036 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9794   -0.1626   -3.0716 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6155   -1.4309   -3.1056 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3719   -3.0261    0.9415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2721   -1.6956    0.9148 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0007   -3.7733   -1.8225 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8638   -3.8879   -0.1576 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0834   -1.6869   -1.6507 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6187   -2.5778   -0.1685 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0902   -0.8215   -0.0067 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3426   -1.2819    1.6314 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2801    0.7604    0.7696 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4626    0.4972   -0.9642 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7034    0.9752   -0.0482 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5841    1.5443   -1.4992 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8821    2.7181    1.3326 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7232    3.2942   -0.1105 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9567    4.3243   -1.0389 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7853    4.5612    0.6502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4509    1.1607   -0.9869 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.3792    0.8044   -0.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3805   -1.3286   -0.6583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6743   -2.0777    0.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
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  5  6  1  0
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 17 16  2  0
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 19 18  2  0
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 32  3  1  0
 12  7  1  0
 11 10  1  0
 18 17  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  1
  5 38  1  6
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 27 58  1  0
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 26 56  1  0
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 21 48  1  0
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 16 43  1  0
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 19 45  1  0
 18 44  1  0
 28 60  1  6
 29 61  1  0
 30 62  1  1
 31 63  1  0
 32 64  1  6
 33 65  1  0
M  END


  Mrv1652309102207252D          

 33 36  0  0  1  0            999 V2000
    1.1583   -0.0154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8837    0.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5868   -0.0541    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3122    0.3388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0152   -0.0929    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7406    0.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7629    1.1248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5048    1.5065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5384    2.3376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1098    2.3953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0354    1.5505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2563    1.1609    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1641    2.7230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3343    2.6276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0206    1.8432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.2463    3.4785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0799    4.8777    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6828    5.6008    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9049    5.0846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7388    4.9120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4200    4.4033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8120    3.6504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9928   -0.9176    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6958   -1.3493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2674   -1.3105    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2451   -2.1352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5644   -0.8788    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8390   -1.2718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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 30 32  1  0  0  0  0
  3 32  1  0  0  0  0
 32 33  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0296061

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC[C@H]1O[C@H](OC2=CC=C3CCCC[C@H](O)CCC4=CC=C(OC2=C3)C=C4)[C@H](O)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C25H32O8/c26-14-21-22(28)23(29)24(30)25(33-21)32-19-12-8-16-3-1-2-4-17(27)9-5-15-6-10-18(11-7-15)31-20(19)13-16/h6-8,10-13,17,21-30H,1-5,9,14H2/t17-,21+,22+,23-,24+,25-/m0/s1

> <INCHI_KEY>
LYWCEZCFIUWAGY-CHTWLVHHSA-N

> <FORMULA>
C25H32O8

> <MOLECULAR_WEIGHT>
460.523

> <EXACT_MASS>
460.20971799

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
47.56839848536718

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3R,4S,5S,6R)-2-{[(12S)-12-hydroxy-2-oxatricyclo[13.2.2.1^{3,7}]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_LOGP>
2.3011412580000004

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.19261743127199

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.199628284432627

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6891359822486187

> <JCHEM_POLAR_SURFACE_AREA>
128.84

> <JCHEM_REFRACTIVITY>
119.37880000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4S,5S,6R)-2-{[(12S)-12-hydroxy-2-oxatricyclo[13.2.2.1^{3,7}]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  O   UNK     0       2.162  -0.029   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.516   0.705   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.829  -0.101   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       6.183   0.633   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.495  -0.173   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       8.849   0.560   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.891   2.100   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.276   2.812   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.338   4.363   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.041   5.233   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.672   4.471   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.533   2.894   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.078   2.167   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.466   2.383   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.958   3.853   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.040   5.083   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.491   4.905   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.905   3.441   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.890   2.210   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.326   6.493   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.738   8.020   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.882   9.105   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       3.141  10.455   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.422   9.491   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.979   9.169   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.251   8.219   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.982   6.814   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.453  -1.713   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       8.766  -2.519   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.099  -2.446   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       6.057  -3.986   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.787  -1.640   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       3.433  -2.374   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   32                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   28                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   27                                                  
CONECT   11   10   12                                                       
CONECT   12   11    7   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18   14                                                       
CONECT   20   17   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   10                                                       
CONECT   28    5   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30    3   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₂O₈

Average Mass

460.5230 Da

Monoisotopic Mass

460.20972 Da

IUPAC Name

(2R,3R,4S,5S,6R)-2-{[(12S)-12-hydroxy-2-oxatricyclo[13.2.2.1^{3,7}]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

(2R,3R,4S,5S,6R)-2-{[(12S)-12-hydroxy-2-oxatricyclo[13.2.2.1^{3,7}]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

OC[C@H]1O[C@H](OC2=CC=C3CCCC[C@H](O)CCC4=CC=C(OC2=C3)C=C4)[C@H](O)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C25H32O8/c26-14-21-22(28)23(29)24(30)25(33-21)32-19-12-8-16-3-1-2-4-17(27)9-5-15-6-10-18(11-7-15)31-20(19)13-16/h6-8,10-13,17,21-30H,1-5,9,14H2/t17-,21+,22+,23-,24+,25-/m0/s1

InChI Key

LYWCEZCFIUWAGY-CHTWLVHHSA-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
Acer nikoense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Lignan glycosides

Sub Class

Not Available

Direct Parent

Lignan glycosides

Alternative Parents

Substituents

Lignan glycoside
Meta,para-diphenylether diarylheptanoid
Phenolic glycoside
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Hexose monosaccharide
Diaryl ether
Glycosyl compound
O-glycosyl compound
Fatty acyl
Benzenoid
Monosaccharide
Oxane
Secondary alcohol
Organoheterocyclic compound
Acetal
Oxacycle
Ether
Polyol
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Primary alcohol
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	2.3	ChemAxon
pKa (Strongest Acidic)	12.2	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	128.84 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	119.38 m³·mol⁻¹	ChemAxon
Polarizability	47.57 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	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00029628

Chemspider ID

24649569

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24896756

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r,4s,5s,6r)-2-{[(12s)-12-hydroxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0296061)

MOL for NP0296061 ((2r,3r,4s,5s,6r)-2-{[(12s)-12-hydroxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for NP0296061 ((2r,3r,4s,5s,6r)-2-{[(12s)-12-hydroxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for NP0296061 ((2r,3r,4s,5s,6r)-2-{[(12s)-12-hydroxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for NP0296061 ((2r,3r,4s,5s,6r)-2-{[(12s)-12-hydroxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for NP0296061 ((2r,3r,4s,5s,6r)-2-{[(12s)-12-hydroxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for NP0296061 ((2r,3r,4s,5s,6r)-2-{[(12s)-12-hydroxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for NP0296061 ((2r,3r,4s,5s,6r)-2-{[(12s)-12-hydroxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for NP0296061 ((2r,3r,4s,5s,6r)-2-{[(12s)-12-hydroxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for NP0296061 ((2r,3r,4s,5s,6r)-2-{[(12s)-12-hydroxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for NP0296061 ((2r,3r,4s,5s,6r)-2-{[(12s)-12-hydroxy-2-oxatricyclo[13.2.2.1³,⁷]icosa-1(17),3(20),4,6,15,18-hexaen-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)