NP-MRD: Showing NP-Card for Aristolactam I N-beta-glucoside (NP0069110)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 14:26:25 UTC

Updated at

2022-04-28 14:26:25 UTC

NP-MRD ID

NP0069110

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Aristolactam I N-beta-glucoside

Description

N-Glucosylaristololactam belongs to the class of organic compounds known as aristolactams. These are phenanthrenic compounds containing a five-membered lactam ring and a 1,3-dioxolane ring fused to the phenanthrene ring system. Aristolactam I N-beta-glucoside is found in Annona cacans, Aristolochia clematitis , Aristolochia contorta , Aristolochia heterophylla Hemsl , Aristolochia indica, Aristolochia kaempferi, Aristolochia mollissima, Aristolochia pubescens, Aristolochia zollingeriana and Pachliopta aristolochiae. Based on a literature review very few articles have been published on N-Glucosylaristololactam.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282216262D          

 33 38  0  0  1  0            999 V2000
    0.4340   -2.2687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2515   -2.7277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1968   -3.5509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5435   -3.9150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2290   -3.4560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1742   -2.6328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1125   -2.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7609   -2.8430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6434   -3.6596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8774   -3.9661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5927   -4.7404    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7683   -4.7088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2582   -5.3572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0517   -5.4259    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8749   -5.3711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3339   -6.0566    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9698   -6.7969    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1466   -6.8517    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6876   -6.1662    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8644   -6.2210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7825   -7.5920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4288   -7.4824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1571   -6.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6161   -6.6873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5269   -2.5365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6445   -1.7200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9961   -1.2099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2301   -1.5163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1753   -3.0466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9413   -2.7402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8999   -2.2176    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6152   -1.4433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2092   -1.4749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  2  0  0  0  0
 14 11  1  6  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
 14 19  1  0  0  0  0
 19 20  1  1  0  0  0
 18 21  1  6  0  0  0
 17 22  1  1  0  0  0
 16 23  1  6  0  0  0
 23 24  1  0  0  0  0
  8 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
  7 28  2  0  0  0  0
 25 29  1  0  0  0  0
 29 30  1  0  0  0  0
  2 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
  1 33  1  0  0  0  0
M  END

     RDKit          3D

 54 59  0  0  0  0  0  0  0  0999 V2000
    2.4344    4.1068    2.1230 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0138    2.9325    1.4998 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8894    1.9372    1.0843 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2556    2.0118    1.2465 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0993    1.0089    0.8243 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5900   -0.1259    0.2127 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2362   -0.2121    0.0459 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3719    0.8051    0.4733 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0073    0.7165    0.3044 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4377   -0.3838   -0.2955 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3070   -1.3654   -0.7048 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6433   -2.4053   -1.2833 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4051   -3.4596   -1.7383 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7740   -3.4496   -1.6080 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4490   -2.3754   -1.0116 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6830   -1.3174   -0.5550 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7848   -2.6494   -1.0264 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9341   -4.0496   -1.1401 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7908   -4.3483   -1.9615 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7705   -2.0541   -1.2378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6949   -2.7639   -1.6758 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9112   -0.7839   -0.6182 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0773   -0.0061   -0.3377 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9979   -0.7081    0.4663 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8055    0.2105    1.0746 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0390   -0.5451    1.5892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8841    0.3668    2.2162 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1847    1.3872    0.2699 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5874    2.5530    0.8053 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9361    1.3115   -1.1900 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0965    1.0295   -1.9226 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8577    0.3450   -1.5945 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0161    0.8425   -2.5651 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3547    4.4586    1.5881 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6585    4.9064    2.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6468    3.9985    3.1970 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6557    2.8928    1.7217 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1707    1.1026    0.9690 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2984   -0.8693   -0.0926 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3674    1.5084    0.6401 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9257   -4.3002   -2.2007 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7700   -4.5652   -0.1622 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8724   -4.3453   -1.6153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8507    0.9567    0.1625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2765    0.5446    2.0148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5928   -1.0036    0.7475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7143   -1.3025    2.3396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9893    0.1551    3.1791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2925    1.5616    0.4137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3306    2.3641    1.7451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6030    2.3280   -1.5545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5116    0.1857   -1.6801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3541   -0.5741   -1.9852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4528    1.4354   -3.2163 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  8  2  0
  8  9  1  0
  9 10  2  0
 10 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 25 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 22 20  1  0
 20 21  2  0
 20 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 15 16  2  0
 16 11  1  0
 16  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
  7  8  1  0
 11 10  1  0
 32 23  1  0
 11 12  2  0
 19 14  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  9 40  1  0
 23 44  1  1
 25 45  1  1
 26 46  1  0
 26 47  1  0
 27 48  1  0
 28 49  1  6
 29 50  1  0
 30 51  1  6
 31 52  1  0
 32 53  1  6
 33 54  1  0
 13 41  1  0
 18 42  1  0
 18 43  1  0
  6 39  1  0
  5 38  1  0
  4 37  1  0
M  END


  Mrv1652304282216262D          

 33 38  0  0  1  0            999 V2000
    0.4340   -2.2687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2515   -2.7277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1968   -3.5509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5435   -3.9150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2290   -3.4560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1742   -2.6328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1125   -2.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7609   -2.8430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6434   -3.6596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8774   -3.9661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5927   -4.7404    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7683   -4.7088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2582   -5.3572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0517   -5.4259    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8749   -5.3711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3339   -6.0566    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9698   -6.7969    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1466   -6.8517    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6876   -6.1662    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8644   -6.2210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7825   -7.5920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4288   -7.4824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1571   -6.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6161   -6.6873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5269   -2.5365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6445   -1.7200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9961   -1.2099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2301   -1.5163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1753   -3.0466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9413   -2.7402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8999   -2.2176    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6152   -1.4433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2092   -1.4749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  2  0  0  0  0
 14 11  1  6  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
 14 19  1  0  0  0  0
 19 20  1  1  0  0  0
 18 21  1  6  0  0  0
 17 22  1  1  0  0  0
 16 23  1  6  0  0  0
 23 24  1  0  0  0  0
  8 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
  7 28  2  0  0  0  0
 25 29  1  0  0  0  0
 29 30  1  0  0  0  0
  2 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
  1 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0069110

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2C=C3N([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(=O)C4=CC5=C(OCO5)C(=C34)C2=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H21NO9/c1-30-13-4-2-3-9-10(13)5-12-16-11(6-14-21(17(9)16)32-8-31-14)22(29)24(12)23-20(28)19(27)18(26)15(7-25)33-23/h2-6,15,18-20,23,25-28H,7-8H2,1H3/t15-,18-,19+,20-,23-/m1/s1

> <INCHI_KEY>
GIDCUQKCIZAUKW-BSTKLLGTSA-N

> <FORMULA>
C23H21NO9

> <MOLECULAR_WEIGHT>
455.419

> <EXACT_MASS>
455.12163126

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
45.83371356391861

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
14-methoxy-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,5-dioxa-10-azapentacyclo[9.7.1.0^{2,6}.0^{8,19}.0^{13,18}]nonadeca-1(19),2(6),7,11,13,15,17-heptaen-9-one

> <ALOGPS_LOGP>
0.47

> <JCHEM_LOGP>
-0.013495559666666684

> <ALOGPS_LOGS>
-2.35

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.326587243768902

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.436548895200698

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9802659217001874

> <JCHEM_POLAR_SURFACE_AREA>
138.15

> <JCHEM_REFRACTIVITY>
111.44200000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.01e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-methoxy-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,5-dioxa-10-azapentacyclo[9.7.1.0^{2,6}.0^{8,19}.0^{13,18}]nonadeca-1(19),2(6),7,11,13,15,17-heptaen-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       0.810  -4.235   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.470  -5.092   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.367  -6.628   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.015  -7.308   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.294  -6.451   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.192  -4.915   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.943  -4.355   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.154  -5.307   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.934  -6.831   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.505  -7.403   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       2.973  -8.849   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       1.434  -8.790   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.482 -10.000   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.830 -10.128   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.366 -10.026   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.223 -11.306   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.544 -12.688   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.007 -12.790   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.150 -11.510   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.614 -11.612   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       3.327 -14.172   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       6.400 -13.967   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       7.760 -11.203   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.617 -12.483   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.584  -4.735   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.803  -3.211   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.593  -2.258   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.163  -2.831   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       7.794  -5.687   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       9.224  -5.115   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -1.680  -4.140   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -1.148  -2.694   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       0.391  -2.753   0.000  0.00  0.00           O+0
CONECT    1    2    6   33                                                  
CONECT    2    1    3   31                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   12                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8   28                                                  
CONECT    8    7    9   25                                                  
CONECT    9    8   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10   12   14                                                  
CONECT   12   11    4   13                                                  
CONECT   13   12                                                            
CONECT   14   11   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19   21                                                  
CONECT   19   18   14   20                                                  
CONECT   20   19                                                            
CONECT   21   18                                                            
CONECT   22   17                                                            
CONECT   23   16   24                                                       
CONECT   24   23                                                            
CONECT   25    8   26   29                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27    7                                                       
CONECT   29   25   30                                                       
CONECT   30   29                                                            
CONECT   31    2   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32    1                                                       
MASTER        0    0    0    0    0    0    0    0   33    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₁NO₉

Average Mass

455.4190 Da

Monoisotopic Mass

455.12163 Da

IUPAC Name

14-methoxy-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,5-dioxa-10-azapentacyclo[9.7.1.0^{2,6}.0^{8,19}.0^{13,18}]nonadeca-1(19),2(6),7,11,13,15,17-heptaen-9-one

Traditional Name

14-methoxy-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,5-dioxa-10-azapentacyclo[9.7.1.0^{2,6}.0^{8,19}.0^{13,18}]nonadeca-1(19),2(6),7,11,13,15,17-heptaen-9-one

CAS Registry Number

Not Available

SMILES

COC1=C2C=C3N([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(=O)C4=CC5=C(OCO5)C(=C34)C2=CC=C1

InChI Identifier

InChI=1S/C23H21NO9/c1-30-13-4-2-3-9-10(13)5-12-16-11(6-14-21(17(9)16)32-8-31-14)22(29)24(12)23-20(28)19(27)18(26)15(7-25)33-23/h2-6,15,18-20,23,25-28H,7-8H2,1H3/t15-,18-,19+,20-,23-/m1/s1

InChI Key

GIDCUQKCIZAUKW-BSTKLLGTSA-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
Annona cacans	Plant	KNApSAcK
Aristolochia clematitis	Plant	KNApSAcK
Aristolochia contorta	Plant	KNApSAcK
Aristolochia heterophylla Hemsl	Plant	KNApSAcK
Aristolochia indica	LOTUS Database	35616633
Aristolochia kaempferi	LOTUS Database	35616633
Aristolochia mollissima	Plant	KNApSAcK
Aristolochia pubescens	Plant	KNApSAcK
Aristolochia zollingeriana	LOTUS Database	35616633
Pachliopta aristolochiae	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aristolactams. These are phenanthrenic compounds containing a five-membered lactam ring and a 1,3-dioxolane ring fused to the phenanthrene ring system.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Aristolactams

Sub Class

Not Available

Direct Parent

Aristolactams

Alternative Parents

Substituents

Aristolactam
Phenanthrene
Hexose monosaccharide
Glycosyl compound
N-glycosyl compound
Isoindolone
Naphthalene
Benzodioxole
Indole or derivatives
Isoindole or derivatives
Anisole
Alkyl aryl ether
Benzenoid
Monosaccharide
Oxane
Tertiary carboxylic acid amide
Carboxamide group
Secondary alcohol
Lactam
Polyol
Carboxylic acid derivative
Acetal
Organoheterocyclic compound
Azacycle
Oxacycle
Ether
Organooxygen compound
Hydrocarbon derivative
Alcohol
Organonitrogen compound
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Primary alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	0.47	ALOGPS
logP	-0.013	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	12.44	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	138.15 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	111.44 m³·mol⁻¹	ChemAxon
Polarizability	45.83 Å³	ChemAxon
Number of Rings	6	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

Not Available

Chemspider ID

8587126

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10411690

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Aristolactam I N-beta-glucoside (NP0069110)

MOL for NP0069110 (Aristolactam I N-beta-glucoside)

3D MOL for NP0069110 (Aristolactam I N-beta-glucoside)

3D SDF for NP0069110 (Aristolactam I N-beta-glucoside)

3D-SDF for NP0069110 (Aristolactam I N-beta-glucoside)

PDB for NP0069110 (Aristolactam I N-beta-glucoside)

3D PDB for NP0069110 (Aristolactam I N-beta-glucoside)

SMILES for NP0069110 (Aristolactam I N-beta-glucoside)

INCHI for NP0069110 (Aristolactam I N-beta-glucoside)

Structure for NP0069110 (Aristolactam I N-beta-glucoside)

3D Structure for NP0069110 (Aristolactam I N-beta-glucoside)