NP-MRD: Showing NP-Card for 3-{4b,7,7,10a-tetramethyl-5h,6h,6ah,8h,9h,10h,10bh,11h,12h-naphtho[2,1-f]isoquinolin-3-yl}propanoic acid (NP0314607)

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Record Information

Version

2.0

Created at

2022-09-11 12:47:24 UTC

Updated at

2022-09-11 12:47:24 UTC

NP-MRD ID

NP0314607

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-{4b,7,7,10a-tetramethyl-5h,6h,6ah,8h,9h,10h,10bh,11h,12h-naphtho[2,1-f]isoquinolin-3-yl}propanoic acid

Description

3-{1,11,15,15-Tetramethyl-5-azatetracyclo[8.8.0.0²,⁷.0¹¹,¹⁶]Octadeca-2,4,6-trien-4-yl}propanoic acid belongs to the class of organic compounds known as pyridines and derivatives. Pyridines and derivatives are compounds containing a pyridine ring, which is a six-member aromatic heterocycle which consists of one nitrogen atom and five carbon atoms. 3-{4b,7,7,10a-tetramethyl-5h,6h,6ah,8h,9h,10h,10bh,11h,12h-naphtho[2,1-f]isoquinolin-3-yl}propanoic acid is found in Petrosaspongia nigra. Based on a literature review very few articles have been published on 3-{1,11,15,15-tetramethyl-5-azatetracyclo[8.8.0.0²,⁷.0¹¹,¹⁶]Octadeca-2,4,6-trien-4-yl}propanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112214472D          

 27 30  0  0  0  0            999 V2000
    0.4509   -2.0969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1589   -2.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4531   -1.7497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6188   -3.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8889   -3.9236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6990   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2391   -3.4559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5091   -4.2355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9690   -2.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5091   -2.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -2.2086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5893   -2.9882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1294   -2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3994   -3.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9395   -2.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7497   -2.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2897   -2.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0197   -1.2732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5598   -0.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2897    0.1300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3699   -0.8054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0197   -3.4559    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4796   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6695   -3.9236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1294   -4.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -4.3914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0492   -3.6118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  2  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
 12 14  1  0  0  0  0
 14 15  2  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
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 16 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 14 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
 12 27  1  0  0  0  0
  7 27  1  0  0  0  0
M  END

     RDKit          3D

 62 65  0  0  0  0  0  0  0  0999 V2000
    3.8470    1.3946    1.5515 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1379    1.6436    0.2617 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7719    3.1345    0.2366 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1317    1.4437   -0.8555 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3733    0.0122   -1.1942 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0939   -0.7402   -1.4924 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0840   -0.5583   -0.3980 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5681   -1.4420    0.7254 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8986    0.8704    0.0262 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9293    0.9292    1.1603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3651    0.2551    0.9485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3609   -0.9974    0.1158 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3107   -2.2490    0.9723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6747   -1.0445   -0.5621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8510   -1.0936    0.2108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1041   -1.1481   -0.3475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3818   -1.2386    0.3810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0797    0.0740    0.5361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3706    1.0982    1.2665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2648    0.9558    1.7823 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9863    2.3543    1.4009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2103   -1.1560   -1.7043 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1412   -1.1112   -2.4826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8907   -1.0555   -1.9101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7308   -0.9783   -2.8493 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2661   -0.1173   -2.0375 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7205   -1.0000   -0.9353 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5717    0.5392    1.5076 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2201    1.3397    2.4414 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5188    2.2905    1.7179 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3365    3.6950   -0.5363 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6995    3.2805   -0.0049 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0095    3.6310    1.2021 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8446    2.0001   -1.7584 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0978    1.8732   -0.4998 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0279   -0.5181   -0.4739 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9570    0.0069   -2.1624 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3961   -1.8311   -1.5014 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7943   -0.5178   -2.4996 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7009   -1.5364    0.6901 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2403   -2.4821    0.5261 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3796   -1.0643    1.7262 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3772    1.3785   -0.8422 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7158    2.0336    1.3117 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3429    0.6237    2.1414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1205    0.9943    0.5494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7948   -0.0377    1.9482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0438   -3.0822    0.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2835   -2.1741    1.8742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3399   -2.4926    1.3000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7539   -1.1032    1.2714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1161   -1.9062   -0.1636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2260   -1.7547    1.3573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2536    0.4947   -0.5137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1155   -0.0676    0.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6568    2.6964    0.7224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2615   -1.1188   -3.5731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2843   -1.9645   -3.0431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0569   -0.4404   -3.7453 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9833    0.2975   -2.7183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3619    0.7520   -1.6778 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7885   -2.0703   -1.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  1
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  1
 12 27  1  0
 27 26  1  0
 26 25  1  0
 25 24  1  0
 24 23  2  0
 23 22  1  0
 22 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 21  1  0
 19 20  2  0
 16 15  1  0
 15 14  2  0
  9  2  1  0
 14 12  1  0
 27  7  1  0
 14 24  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  5 37  1  0
  6 38  1  0
  6 39  1  0
  8 40  1  0
  8 41  1  0
  8 42  1  0
  9 43  1  6
 10 44  1  0
 10 45  1  0
 11 46  1  0
 11 47  1  0
 13 48  1  0
 13 49  1  0
 13 50  1  0
 27 62  1  6
 26 60  1  0
 26 61  1  0
 25 58  1  0
 25 59  1  0
 23 57  1  0
 17 52  1  0
 17 53  1  0
 18 54  1  0
 18 55  1  0
 21 56  1  0
 15 51  1  0
M  END


  Mrv1652309112214472D          

 27 30  0  0  0  0            999 V2000
    0.4509   -2.0969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1589   -2.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4531   -1.7497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6188   -3.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8889   -3.9236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6990   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2391   -3.4559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5091   -4.2355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9690   -2.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5091   -2.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -2.2086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5893   -2.9882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1294   -2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3994   -3.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9395   -2.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7497   -2.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2897   -2.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0197   -1.2732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5598   -0.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2897    0.1300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3699   -0.8054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0197   -3.4559    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4796   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6695   -3.9236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1294   -4.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -4.3914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0492   -3.6118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  2  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
 12 14  1  0  0  0  0
 14 15  2  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
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 16 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 14 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
 12 27  1  0  0  0  0
  7 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0314607

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CCCC2(C)C1CCC1(C)C2CCC2=CN=C(CCC(O)=O)C=C12

> <INCHI_IDENTIFIER>
InChI=1S/C24H35NO2/c1-22(2)11-5-12-24(4)19(22)10-13-23(3)18-14-17(7-9-21(26)27)25-15-16(18)6-8-20(23)24/h14-15,19-20H,5-13H2,1-4H3,(H,26,27)

> <INCHI_KEY>
QBCQXEYQSRWFAF-UHFFFAOYSA-N

> <FORMULA>
C24H35NO2

> <MOLECULAR_WEIGHT>
369.549

> <EXACT_MASS>
369.266779371

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
44.16310763279251

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-{1,11,15,15-tetramethyl-5-azatetracyclo[8.8.0.0^{2,7}.0^{11,16}]octadeca-2,4,6-trien-4-yl}propanoic acid

> <JCHEM_LOGP>
4.082471640659915

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.121703377704102

> <JCHEM_PKA_STRONGEST_BASIC>
5.409501114912959

> <JCHEM_POLAR_SURFACE_AREA>
50.19

> <JCHEM_REFRACTIVITY>
107.83599999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-{1,11,15,15-tetramethyl-5-azatetracyclo[8.8.0.0^{2,7}.0^{11,16}]octadeca-2,4,6-trien-4-yl}propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       0.842  -3.914   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.163  -4.705   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.712  -3.266   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.155  -5.869   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.659  -7.324   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.171  -7.615   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.180  -6.451   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.684  -7.906   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.676  -4.996   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.684  -3.832   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.196  -4.123   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.700  -5.578   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.708  -4.414   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.212  -5.869   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.220  -4.705   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.733  -4.996   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.741  -3.832   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.237  -2.377   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.245  -1.212   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      11.741   0.243   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      13.757  -1.503   0.000  0.00  0.00           O+0
HETATM   22  N   UNK     0      11.237  -6.451   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0      10.229  -7.615   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.716  -7.324   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.708  -8.488   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.196  -8.197   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.692  -6.742   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4    9                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   27                                             
CONECT    8    7                                                            
CONECT    9    7    2   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   27                                             
CONECT   13   12                                                            
CONECT   14   12   15   24                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   16   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   14   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   12    7                                                  
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Value	Source
3-{1,11,15,15-tetramethyl-5-azatetracyclo[8.8.0.0,.0,]octadeca-2,4,6-trien-4-yl}propanoate	Generator

Chemical Formula

C₂₄H₃₅NO₂

Average Mass

369.5490 Da

Monoisotopic Mass

369.26678 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1(C)CCCC2(C)C1CCC1(C)C2CCC2=CN=C(CCC(O)=O)C=C12

InChI Identifier

InChI=1S/C24H35NO2/c1-22(2)11-5-12-24(4)19(22)10-13-23(3)18-14-17(7-9-21(26)27)25-15-16(18)6-8-20(23)24/h14-15,19-20H,5-13H2,1-4H3,(H,26,27)

InChI Key

QBCQXEYQSRWFAF-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, 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
Petrosaspongia nigra	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyridines and derivatives. Pyridines and derivatives are compounds containing a pyridine ring, which is a six-member aromatic heterocycle which consists of one nitrogen atom and five carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyridines and derivatives

Sub Class

Not Available

Direct Parent

Pyridines and derivatives

Alternative Parents

Substituents

Pyridine
Heteroaromatic compound
Azacycle
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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

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

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

73807717

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-{4b,7,7,10a-tetramethyl-5h,6h,6ah,8h,9h,10h,10bh,11h,12h-naphtho[2,1-f]isoquinolin-3-yl}propanoic acid (NP0314607)

MOL for NP0314607 (3-{4b,7,7,10a-tetramethyl-5h,6h,6ah,8h,9h,10h,10bh,11h,12h-naphtho[2,1-f]isoquinolin-3-yl}propanoic acid)

3D MOL for NP0314607 (3-{4b,7,7,10a-tetramethyl-5h,6h,6ah,8h,9h,10h,10bh,11h,12h-naphtho[2,1-f]isoquinolin-3-yl}propanoic acid)

3D SDF for NP0314607 (3-{4b,7,7,10a-tetramethyl-5h,6h,6ah,8h,9h,10h,10bh,11h,12h-naphtho[2,1-f]isoquinolin-3-yl}propanoic acid)

3D-SDF for NP0314607 (3-{4b,7,7,10a-tetramethyl-5h,6h,6ah,8h,9h,10h,10bh,11h,12h-naphtho[2,1-f]isoquinolin-3-yl}propanoic acid)

PDB for NP0314607 (3-{4b,7,7,10a-tetramethyl-5h,6h,6ah,8h,9h,10h,10bh,11h,12h-naphtho[2,1-f]isoquinolin-3-yl}propanoic acid)

3D PDB for NP0314607 (3-{4b,7,7,10a-tetramethyl-5h,6h,6ah,8h,9h,10h,10bh,11h,12h-naphtho[2,1-f]isoquinolin-3-yl}propanoic acid)

SMILES for NP0314607 (3-{4b,7,7,10a-tetramethyl-5h,6h,6ah,8h,9h,10h,10bh,11h,12h-naphtho[2,1-f]isoquinolin-3-yl}propanoic acid)

INCHI for NP0314607 (3-{4b,7,7,10a-tetramethyl-5h,6h,6ah,8h,9h,10h,10bh,11h,12h-naphtho[2,1-f]isoquinolin-3-yl}propanoic acid)

Structure for NP0314607 (3-{4b,7,7,10a-tetramethyl-5h,6h,6ah,8h,9h,10h,10bh,11h,12h-naphtho[2,1-f]isoquinolin-3-yl}propanoic acid)

3D Structure for NP0314607 (3-{4b,7,7,10a-tetramethyl-5h,6h,6ah,8h,9h,10h,10bh,11h,12h-naphtho[2,1-f]isoquinolin-3-yl}propanoic acid)