NP-MRD: Showing NP-Card for 7-Hydroxy-aristolochic acid A (NP0069291)

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Record Information

Version

2.0

Created at

2022-04-28 14:39:02 UTC

Updated at

2022-04-28 14:39:02 UTC

NP-MRD ID

NP0069291

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-Hydroxy-aristolochic acid A

Description

9-Hydroxy-8-Methoxy-6-Nitro-Phenanthrol[3,4-D][1,3]Dioxole-5-Carboxylic Acid belongs to the class of organic compounds known as aristolochic acids and derivatives. These are organic heterocyclic compounds with a structure characterized by a nitrophenanthro[3,4-d][1,3]dioxole ring system substituted at position 5, 6, and 8 by a carboxyl group (or a derivative thereof), a nitro group, and a methoxy group, respectively. 7-Hydroxy-aristolochic acid A is found in Aristolochia cucurbitifolia, Aristolochia curcurbitifolia, Aristolochia foveolata, Aristolochia pubescens and Aristolochia tubiflora. 9-Hydroxy-8-Methoxy-6-Nitro-Phenanthrol[3,4-D][1,3]Dioxole-5-Carboxylic Acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

9AR
  Mrv0541 02231216202D          

 26 29  0  0  0  0            999 V2000
    1.2550   -1.0752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9500   -0.6306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9124    0.1936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1798    0.5731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4849    0.1285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5225   -0.6957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2476    0.5080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9425    0.0633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9049   -0.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1724   -1.1403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2852    1.3321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0178    1.7116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7127    1.2670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6751    0.4428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1301    1.5106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2927   -1.8993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1025    0.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3700   -0.0018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4997    0.7730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3144    1.3870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5977   -2.3440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0252   -2.2788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4452    1.6465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8297   -2.4091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2348   -2.7021    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -0.1348   -1.9645    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  6  1  0  0  0  0
  1 16  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3 19  1  0  0  0  0
  4  5  1  0  0  0  0
  4 20  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  6 10  1  0  0  0  0
  7  8  2  0  0  0  0
  7 11  1  0  0  0  0
  8  9  1  0  0  0  0
  8 14  1  0  0  0  0
  9 10  2  0  0  0  0
 10 26  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
 13 23  1  0  0  0  0
 14 18  1  0  0  0  0
 15 19  1  0  0  0  0
 15 20  1  0  0  0  0
 16 21  2  0  0  0  0
 16 22  1  0  0  0  0
 17 18  1  0  0  0  0
 24 26  2  0  0  0  0
 25 26  1  0  0  0  0
M  CHG  2  25  -1  26   1
M  END

     RDKit          3D

 37 40  0  0  0  0  0  0  0  0999 V2000
    4.1733   -1.9402   -0.0427 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4891   -1.2681   -1.0950 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7339   -0.1445   -0.7774 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2728    1.1211   -0.7706 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6101    1.2846   -1.0906 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5161    2.2117   -0.4559 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1618    2.0058   -0.1395 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5991    0.7483   -0.1402 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3853   -0.3552   -0.4614 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8582   -1.6039   -0.4619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4895   -1.7938   -0.1389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8203   -3.1492   -0.0461 N   0  0  0  0  0  4  0  0  0  0  0  0
   -0.3070   -3.9741   -0.8811 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6570   -3.6955    0.8532 O   0  0  0  0  0  1  0  0  0  0  0  0
   -1.2668   -0.7144    0.1613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5830   -0.8611    0.4217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3744   -2.0415    0.1220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2219   -2.6584   -0.9607 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3310   -2.5187    1.0212 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3786    0.2462    0.7192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8471    1.4992    0.7404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4911    1.7077    0.4611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7407    0.5914    0.1750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3503    3.0719    0.5780 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6016    3.7137    0.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4530    2.7470    1.0101 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7637   -1.1328    0.4862 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8604   -2.7176   -0.4289 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4602   -2.3209    0.7057 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0447    2.2064   -1.0888 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8593    3.2220   -0.4253 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5635    2.8544    0.1094 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5118   -2.4482   -0.7225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1077   -2.4289    2.0134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4279    0.1301    0.9369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6393    4.6998    0.8294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7753    3.7055   -0.7161 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
  4  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 15  1  0
 15 23  2  0
 23 22  1  0
 22 21  2  0
 21 26  1  0
 26 25  1  0
 25 24  1  0
 21 20  1  0
 20 16  2  0
 16 17  1  0
 17 19  1  0
 17 18  2  0
 11 12  1  0
 12 14  1  0
 12 13  2  0
  9  3  1  0
 16 15  1  0
 23  8  1  0
 24 22  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  5 30  1  0
  6 31  1  0
  7 32  1  0
 10 33  1  0
 25 36  1  0
 25 37  1  0
 20 35  1  0
 19 34  1  0
M  CHG  2  12   1  14  -1
M  END

9AR
  Mrv0541 02231216202D          

 26 29  0  0  0  0            999 V2000
    1.2550   -1.0752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9500   -0.6306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9124    0.1936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1798    0.5731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4849    0.1285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5225   -0.6957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2476    0.5080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9425    0.0633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9049   -0.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1724   -1.1403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2852    1.3321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0178    1.7116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7127    1.2670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6751    0.4428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1301    1.5106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2927   -1.8993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1025    0.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3700   -0.0018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4997    0.7730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3144    1.3870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5977   -2.3440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0252   -2.2788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4452    1.6465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8297   -2.4091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2348   -2.7021    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -0.1348   -1.9645    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  6  1  0  0  0  0
  1 16  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3 19  1  0  0  0  0
  4  5  1  0  0  0  0
  4 20  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  6 10  1  0  0  0  0
  7  8  2  0  0  0  0
  7 11  1  0  0  0  0
  8  9  1  0  0  0  0
  8 14  1  0  0  0  0
  9 10  2  0  0  0  0
 10 26  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
 13 23  1  0  0  0  0
 14 18  1  0  0  0  0
 15 19  1  0  0  0  0
 15 20  1  0  0  0  0
 16 21  2  0  0  0  0
 16 22  1  0  0  0  0
 17 18  1  0  0  0  0
 24 26  2  0  0  0  0
 25 26  1  0  0  0  0
M  CHG  2  25  -1  26   1
M  END
> <DATABASE_ID>
NP0069291

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C=CC2=C1C=C(C1=C2C2=C(OCO2)C=C1C(O)=O)[N+]([O-])=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H11NO8/c1-24-15-8-4-10(18(22)23)13-9(17(20)21)5-12-16(26-6-25-12)14(13)7(8)2-3-11(15)19/h2-5,19H,6H2,1H3,(H,20,21)

> <INCHI_KEY>
UCLGCTLOEZZSLA-UHFFFAOYSA-N

> <FORMULA>
C17H11NO8

> <MOLECULAR_WEIGHT>
357.2711

> <EXACT_MASS>
357.048466333

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_AVERAGE_POLARIZABILITY>
33.240571558757054

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-hydroxy-6-methoxy-9-nitro-14,16-dioxatetracyclo[8.7.0.0²,⁷.0¹³,¹⁷]heptadeca-1(10),2(7),3,5,8,11,13(17)-heptaene-11-carboxylic acid

> <ALOGPS_LOGP>
2.53

> <JCHEM_LOGP>
2.711763307000001

> <ALOGPS_LOGS>
-3.68

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.734056892277941

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.3241536635251046

> <JCHEM_PKA_STRONGEST_BASIC>
-4.537806430486822

> <JCHEM_POLAR_SURFACE_AREA>
131.04000000000002

> <JCHEM_REFRACTIVITY>
87.75029999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.47e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-6-methoxy-9-nitro-14,16-dioxatetracyclo[8.7.0.0²,⁷.0¹³,¹⁷]heptadeca-1(10),2(7),3,5,8,11,13(17)-heptaene-11-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: 9AR                                               
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  C   UNK     0       2.343  -2.007   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.640  -1.177   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.570   0.361   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.202   1.070   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.905   0.240   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.975  -1.299   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.462   0.948   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.759   0.118   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.689  -1.420   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.322  -2.129   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.532   2.487   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.900   3.195   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.197   2.365   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.127   0.827   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.976   2.820   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.413  -3.545   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -5.791   0.705   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -4.424  -0.003   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       4.666   1.443   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       2.454   2.589   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       1.116  -4.375   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       3.780  -4.254   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -4.564   3.073   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -1.549  -4.497   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       0.438  -5.044   0.000  0.00  0.00           O-1
HETATM   26  N   UNK     0      -0.252  -3.667   0.000  0.00  0.00           N+1
CONECT    1    2    6   16                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5   20                                                  
CONECT    5    4    6    7                                                  
CONECT    6    1    5   10                                                  
CONECT    7    5    8   11                                                  
CONECT    8    7    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    6    9   26                                                  
CONECT   11    7   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   23                                                  
CONECT   14    8   13   18                                                  
CONECT   15   19   20                                                       
CONECT   16    1   21   22                                                  
CONECT   17   18                                                            
CONECT   18   14   17                                                       
CONECT   19    3   15                                                       
CONECT   20    4   15                                                       
CONECT   21   16                                                            
CONECT   22   16                                                            
CONECT   23   13                                                            
CONECT   24   26                                                            
CONECT   25   26                                                            
CONECT   26   10   24   25                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Value	Source
9-Hydroxy-8-methoxy-6-nitro-phenanthrol[3,4-D][1,3]dioxole-5-carboxylate	Generator
5-Hydroxy-6-methoxy-9-nitro-14,16-dioxatetracyclo[8.7.0.0²,⁷.0¹³,¹⁷]heptadeca-1,3,5,7,9,11,13(17)-heptaene-11-carboxylate	Generator
9-Hydroxy aristolochate	Generator

Chemical Formula

C₁₇H₁₁NO₈

Average Mass

357.2711 Da

Monoisotopic Mass

357.04847 Da

IUPAC Name

5-hydroxy-6-methoxy-9-nitro-14,16-dioxatetracyclo[8.7.0.0²,⁷.0¹³,¹⁷]heptadeca-1(10),2(7),3,5,8,11,13(17)-heptaene-11-carboxylic acid

Traditional Name

5-hydroxy-6-methoxy-9-nitro-14,16-dioxatetracyclo[8.7.0.0²,⁷.0¹³,¹⁷]heptadeca-1(10),2(7),3,5,8,11,13(17)-heptaene-11-carboxylic acid

CAS Registry Number

Not Available

SMILES

COC1=C(O)C=CC2=C1C=C(C1=C2C2=C(OCO2)C=C1C(O)=O)[N+]([O-])=O

InChI Identifier

InChI=1S/C17H11NO8/c1-24-15-8-4-10(18(22)23)13-9(17(20)21)5-12-16(26-6-25-12)14(13)7(8)2-3-11(15)19/h2-5,19H,6H2,1H3,(H,20,21)

InChI Key

UCLGCTLOEZZSLA-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, 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
Aristolochia cucurbitifolia	LOTUS Database	35616633
Aristolochia curcurbitifolia	Plant	KNApSAcK
Aristolochia foveolata	Plant	KNApSAcK
Aristolochia pubescens	Plant	KNApSAcK
Aristolochia tubiflora	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aristolochic acids and derivatives. These are organic heterocyclic compounds with a structure characterized by a nitrophenanthro[3,4-d][1,3]dioxole ring system substituted at position 5, 6, and 8 by a carboxyl group (or a derivative thereof), a nitro group, and a methoxy group, respectively.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Aristolochic acids and derivatives

Direct Parent

Aristolochic acids and derivatives

Alternative Parents

Substituents

Aristolochic acid or derivatives
Phenanthrol
1-naphthalenecarboxylic acid
1-naphthalenecarboxylic acid or derivatives
1-nitronaphthalene
2-nitronaphthalene
2-naphthol
Naphthalene
Benzodioxole
Nitroaromatic compound
Anisole
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Organic nitro compound
C-nitro compound
Acetal
Carboxylic acid derivative
Carboxylic acid
Ether
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Organic oxoazanium
Allyl-type 1,3-dipolar organic compound
Propargyl-type 1,3-dipolar organic compound
Organic oxide
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organooxygen compound
Hydrocarbon derivative
Organonitrogen 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	2.53	ALOGPS
logP	2.71	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	3.32	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	131.04 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	87.75 m³·mol⁻¹	ChemAxon
Polarizability	33.24 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	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

DB02636

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

1941

PDB ID

9AR

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 7-Hydroxy-aristolochic acid A (NP0069291)

MOL for NP0069291 (7-Hydroxy-aristolochic acid A)

3D MOL for NP0069291 (7-Hydroxy-aristolochic acid A)

3D SDF for NP0069291 (7-Hydroxy-aristolochic acid A)

3D-SDF for NP0069291 (7-Hydroxy-aristolochic acid A)

PDB for NP0069291 (7-Hydroxy-aristolochic acid A)

3D PDB for NP0069291 (7-Hydroxy-aristolochic acid A)

SMILES for NP0069291 (7-Hydroxy-aristolochic acid A)

INCHI for NP0069291 (7-Hydroxy-aristolochic acid A)

Structure for NP0069291 (7-Hydroxy-aristolochic acid A)

3D Structure for NP0069291 (7-Hydroxy-aristolochic acid A)