NP-MRD: Showing NP-Card for 11-Carboxyl anatoxin A (NP0006911)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2020-12-09 03:49:42 UTC

Updated at

2021-07-15 16:56:08 UTC

NP-MRD ID

NP0006911

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11-Carboxyl anatoxin A

Provided By

NPAtlas

Description

11-Carboxyl anatoxin A is found in Aphanizomenon.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118363D          

 33 34  0  0  0  0            999 V2000
    3.3647    1.7138   -0.9210 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7887    0.6543   -0.3945 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9968    0.1473   -0.8259 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9779   -0.0181    0.6736 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8559   -0.7584    0.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1240   -1.9429   -0.3010 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4916   -0.2964   -0.0692 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2511    0.9509    0.3627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5310    2.1312    0.0260 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9917    1.8669   -0.2324 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5671    0.7527    0.5533 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4069   -0.6095    0.0320 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7768   -1.4722    1.1359 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7917   -2.3357    0.3519 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3449   -1.3534   -0.7086 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5815   -0.7765   -1.1157 N   0  0  2  0  0  0  0  0  0  0  0  0
    5.8105    0.0510   -0.2280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6864   -0.7443    1.1648 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7492    0.7183    1.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8400    1.1129    1.2534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1657    2.6600   -0.9056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4088    2.8974    0.8194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5209    2.8035    0.1036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2362    1.8152   -1.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1766    0.8626    1.6085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6741    0.9551    0.6722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3882   -1.1083   -0.1880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1787   -0.8424    1.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5240   -2.1034    1.6407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3408   -3.1621   -0.1625 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0342   -2.6835    0.9679 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1848   -1.8520   -1.5468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5502   -0.0340   -1.8035 H   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15  7  1  0  0  0  0
 16 12  1  0  0  0  0
  3 17  1  0  0  0  0
  4 18  1  0  0  0  0
  4 19  1  0  0  0  0
  8 20  1  0  0  0  0
  9 21  1  0  0  0  0
  9 22  1  0  0  0  0
 10 23  1  0  0  0  0
 10 24  1  0  0  0  0
 11 25  1  0  0  0  0
 11 26  1  0  0  0  0
 12 27  1  6  0  0  0
 13 28  1  0  0  0  0
 13 29  1  0  0  0  0
 14 30  1  0  0  0  0
 14 31  1  0  0  0  0
 15 32  1  6  0  0  0
 16 33  1  0  0  0  0
M  END

     RDKit          3D

 33 34  0  0  0  0  0  0  0  0999 V2000
    3.3647    1.7138   -0.9210 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7887    0.6543   -0.3945 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9968    0.1473   -0.8259 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9779   -0.0181    0.6736 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8559   -0.7584    0.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1240   -1.9429   -0.3010 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4916   -0.2964   -0.0692 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2511    0.9509    0.3627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5310    2.1312    0.0260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9917    1.8669   -0.2324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5671    0.7527    0.5533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4069   -0.6095    0.0320 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7768   -1.4722    1.1359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7917   -2.3357    0.3519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3449   -1.3534   -0.7086 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5815   -0.7765   -1.1157 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8105    0.0510   -0.2280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6864   -0.7443    1.1648 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7492    0.7183    1.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8400    1.1129    1.2534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1657    2.6600   -0.9056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4088    2.8974    0.8194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5209    2.8035    0.1036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2362    1.8152   -1.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1766    0.8626    1.6085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6741    0.9551    0.6722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3882   -1.1083   -0.1880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1787   -0.8424    1.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5240   -2.1034    1.6407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3408   -3.1621   -0.1625 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0342   -2.6835    0.9679 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1848   -1.8520   -1.5468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5502   -0.0340   -1.8035 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15  7  1  0
 16 12  1  0
  3 17  1  0
  4 18  1  0
  4 19  1  0
  8 20  1  0
  9 21  1  0
  9 22  1  0
 10 23  1  0
 10 24  1  0
 11 25  1  0
 11 26  1  0
 12 27  1  6
 13 28  1  0
 13 29  1  0
 14 30  1  0
 14 31  1  0
 15 32  1  6
 16 33  1  0
M  END


  Mrv1652306242118363D          

 33 34  0  0  0  0            999 V2000
    3.3647    1.7138   -0.9210 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7887    0.6543   -0.3945 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9968    0.1473   -0.8259 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9779   -0.0181    0.6736 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8559   -0.7584    0.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1240   -1.9429   -0.3010 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4916   -0.2964   -0.0692 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2511    0.9509    0.3627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5310    2.1312    0.0260 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9917    1.8669   -0.2324 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5671    0.7527    0.5533 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4069   -0.6095    0.0320 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7768   -1.4722    1.1359 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7917   -2.3357    0.3519 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3449   -1.3534   -0.7086 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5815   -0.7765   -1.1157 N   0  0  2  0  0  0  0  0  0  0  0  0
    5.8105    0.0510   -0.2280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6864   -0.7443    1.1648 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7492    0.7183    1.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8400    1.1129    1.2534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1657    2.6600   -0.9056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4088    2.8974    0.8194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5209    2.8035    0.1036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2362    1.8152   -1.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1766    0.8626    1.6085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6741    0.9551    0.6722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3882   -1.1083   -0.1880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1787   -0.8424    1.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5240   -2.1034    1.6407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3408   -3.1621   -0.1625 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0342   -2.6835    0.9679 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1848   -1.8520   -1.5468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5502   -0.0340   -1.8035 H   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15  7  1  0  0  0  0
 16 12  1  0  0  0  0
  3 17  1  0  0  0  0
  4 18  1  0  0  0  0
  4 19  1  0  0  0  0
  8 20  1  0  0  0  0
  9 21  1  0  0  0  0
  9 22  1  0  0  0  0
 10 23  1  0  0  0  0
 10 24  1  0  0  0  0
 11 25  1  0  0  0  0
 11 26  1  0  0  0  0
 12 27  1  6  0  0  0
 13 28  1  0  0  0  0
 13 29  1  0  0  0  0
 14 30  1  0  0  0  0
 14 31  1  0  0  0  0
 15 32  1  6  0  0  0
 16 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0006911

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C([H])([H])C(=O)C1=C([H])/C([H])([H])C([H])([H])C([H])([H])[C@@]2([H])N([H])[C@]\1([H])C([H])([H])C2([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C12H17NO3/c14-11(7-12(15)16)9-4-2-1-3-8-5-6-10(9)13-8/h4,8,10,13H,1-3,5-7H2,(H,15,16)/b9-4+/t8-,10-/m1/s1

> <INCHI_KEY>
WYNQRSDHALABAA-CXQRGBQISA-N

> <FORMULA>
C12H17NO3

> <MOLECULAR_WEIGHT>
223.272

> <EXACT_MASS>
223.120843411

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
23.300165535995365

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[(1R,2E,7R)-10-azabicyclo[5.2.1]dec-2-en-2-yl]-3-oxopropanoic acid

> <ALOGPS_LOGP>
0.21

> <JCHEM_LOGP>
-0.9492512404577891

> <ALOGPS_LOGS>
-2.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.522081397303122

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.145890286287093

> <JCHEM_PKA_STRONGEST_BASIC>
10.299999705308979

> <JCHEM_POLAR_SURFACE_AREA>
66.39999999999999

> <JCHEM_REFRACTIVITY>
59.775800000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.10e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[(1R,2E,7R)-10-azabicyclo[5.2.1]dec-2-en-2-yl]-3-oxopropanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 33 34  0  0  0  0  0  0  0  0999 V2000
    3.3647    1.7138   -0.9210 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7887    0.6543   -0.3945 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9968    0.1473   -0.8259 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9779   -0.0181    0.6736 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8559   -0.7584    0.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1240   -1.9429   -0.3010 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4916   -0.2964   -0.0692 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2511    0.9509    0.3627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5310    2.1312    0.0260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9917    1.8669   -0.2324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5671    0.7527    0.5533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4069   -0.6095    0.0320 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7768   -1.4722    1.1359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7917   -2.3357    0.3519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3449   -1.3534   -0.7086 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5815   -0.7765   -1.1157 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8105    0.0510   -0.2280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6864   -0.7443    1.1648 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7492    0.7183    1.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8400    1.1129    1.2534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1657    2.6600   -0.9056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4088    2.8974    0.8194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5209    2.8035    0.1036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2362    1.8152   -1.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1766    0.8626    1.6085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6741    0.9551    0.6722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3882   -1.1083   -0.1880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1787   -0.8424    1.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5240   -2.1034    1.6407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3408   -3.1621   -0.1625 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0342   -2.6835    0.9679 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1848   -1.8520   -1.5468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5502   -0.0340   -1.8035 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15  7  1  0
 16 12  1  0
  3 17  1  0
  4 18  1  0
  4 19  1  0
  8 20  1  0
  9 21  1  0
  9 22  1  0
 10 23  1  0
 10 24  1  0
 11 25  1  0
 11 26  1  0
 12 27  1  6
 13 28  1  0
 13 29  1  0
 14 30  1  0
 14 31  1  0
 15 32  1  6
 16 33  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  O   UNK     0       3.365   1.714  -0.921  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.789   0.654  -0.395  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.997   0.147  -0.826  0.00  0.00           O+0
HETATM    4  C   UNK     0       2.978  -0.018   0.674  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.856  -0.758   0.097  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.124  -1.943  -0.301  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.492  -0.296  -0.069  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.251   0.951   0.363  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.531   2.131   0.026  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.992   1.867  -0.232  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.567   0.753   0.553  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.407  -0.610   0.032  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.777  -1.472   1.136  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.792  -2.336   0.352  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.345  -1.353  -0.709  0.00  0.00           C+0
HETATM   16  N   UNK     0      -1.581  -0.777  -1.116  0.00  0.00           N+0
HETATM   17  H   UNK     0       5.811   0.051  -0.228  0.00  0.00           H+0
HETATM   18  H   UNK     0       3.686  -0.744   1.165  0.00  0.00           H+0
HETATM   19  H   UNK     0       2.749   0.718   1.436  0.00  0.00           H+0
HETATM   20  H   UNK     0       0.840   1.113   1.253  0.00  0.00           H+0
HETATM   21  H   UNK     0      -0.166   2.660  -0.906  0.00  0.00           H+0
HETATM   22  H   UNK     0      -0.409   2.897   0.819  0.00  0.00           H+0
HETATM   23  H   UNK     0      -2.521   2.804   0.104  0.00  0.00           H+0
HETATM   24  H   UNK     0      -2.236   1.815  -1.324  0.00  0.00           H+0
HETATM   25  H   UNK     0      -2.177   0.863   1.609  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.674   0.955   0.672  0.00  0.00           H+0
HETATM   27  H   UNK     0      -3.388  -1.108  -0.188  0.00  0.00           H+0
HETATM   28  H   UNK     0      -1.179  -0.842   1.834  0.00  0.00           H+0
HETATM   29  H   UNK     0      -2.524  -2.103   1.641  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.341  -3.162  -0.163  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.034  -2.684   0.968  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.185  -1.852  -1.547  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.550  -0.034  -1.804  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2   17                                                       
CONECT    4    2    5   18   19                                             
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   15                                                  
CONECT    8    7    9   20                                                  
CONECT    9    8   10   21   22                                             
CONECT   10    9   11   23   24                                             
CONECT   11   10   12   25   26                                             
CONECT   12   11   13   16   27                                             
CONECT   13   12   14   28   29                                             
CONECT   14   13   15   30   31                                             
CONECT   15   14   16    7   32                                             
CONECT   16   15   12   33                                                  
CONECT   17    3                                                            
CONECT   18    4                                                            
CONECT   19    4                                                            
CONECT   20    8                                                            
CONECT   21    9                                                            
CONECT   22    9                                                            
CONECT   23   10                                                            
CONECT   24   10                                                            
CONECT   25   11                                                            
CONECT   26   11                                                            
CONECT   27   12                                                            
CONECT   28   13                                                            
CONECT   29   13                                                            
CONECT   30   14                                                            
CONECT   31   14                                                            
CONECT   32   15                                                            
CONECT   33   16                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   68    0
END

RDKit          3D

33 34  0  0  0  0  0  0  0  0999 V2000
    3.3647    1.7138   -0.9210 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7887    0.6543   -0.3945 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9968    0.1473   -0.8259 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9779   -0.0181    0.6736 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8559   -0.7584    0.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1240   -1.9429   -0.3010 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4916   -0.2964   -0.0692 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2511    0.9509    0.3627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5310    2.1312    0.0260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9917    1.8669   -0.2324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5671    0.7527    0.5533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4069   -0.6095    0.0320 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7768   -1.4722    1.1359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7917   -2.3357    0.3519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3449   -1.3534   -0.7086 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5815   -0.7765   -1.1157 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8105    0.0510   -0.2280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6864   -0.7443    1.1648 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7492    0.7183    1.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8400    1.1129    1.2534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1657    2.6600   -0.9056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4088    2.8974    0.8194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5209    2.8035    0.1036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2362    1.8152   -1.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1766    0.8626    1.6085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6741    0.9551    0.6722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3882   -1.1083   -0.1880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1787   -0.8424    1.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5240   -2.1034    1.6407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3408   -3.1621   -0.1625 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0342   -2.6835    0.9679 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1848   -1.8520   -1.5468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5502   -0.0340   -1.8035 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15  7  1  0
 16 12  1  0
  3 17  1  0
  4 18  1  0
  4 19  1  0
  8 20  1  0
  9 21  1  0
  9 22  1  0
 10 23  1  0
 10 24  1  0
 11 25  1  0
 11 26  1  0
 12 27  1  6
 13 28  1  0
 13 29  1  0
 14 30  1  0
 14 31  1  0
 15 32  1  6
 16 33  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₂H₁₇NO₃

Average Mass

223.2720 Da

Monoisotopic Mass

223.12084 Da

IUPAC Name

3-[(1R,2E,7R)-10-azabicyclo[5.2.1]dec-2-en-2-yl]-3-oxopropanoic acid

Traditional Name

3-[(1R,2E,7R)-10-azabicyclo[5.2.1]dec-2-en-2-yl]-3-oxopropanoic acid

CAS Registry Number

Not Available

SMILES

OC(=O)CC(=O)C1=C/CCC[C@@H]2CC[C@H]\1N2

InChI Identifier

InChI=1S/C12H17NO3/c14-11(7-12(15)16)9-4-2-1-3-8-5-6-10(9)13-8/h4,8,10,13H,1-3,5-7H2,(H,15,16)/b9-4+/t8-,10-/m1/s1

InChI Key

WYNQRSDHALABAA-CXQRGBQISA-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
Aphanizomenon	NPAtlas	17310714

Chemical Taxonomy

Classification

Not classified

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	0.21	ALOGPS
logP	-0.95	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	4.15	ChemAxon
pKa (Strongest Basic)	10.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.4 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	59.78 m³·mol⁻¹	ChemAxon
Polarizability	23.3 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Showing NP-Card for 11-Carboxyl anatoxin A (NP0006911)

MOL for NP0006911 (11-Carboxyl anatoxin A)

3D MOL for NP0006911 (11-Carboxyl anatoxin A)

3D SDF for NP0006911 (11-Carboxyl anatoxin A)

3D-SDF for NP0006911 (11-Carboxyl anatoxin A)

PDB for NP0006911 (11-Carboxyl anatoxin A)

3D PDB for NP0006911 (11-Carboxyl anatoxin A)

SMILES for NP0006911 (11-Carboxyl anatoxin A)

INCHI for NP0006911 (11-Carboxyl anatoxin A)

Structure for NP0006911 (11-Carboxyl anatoxin A)

3D Structure for NP0006911 (11-Carboxyl anatoxin A)