NP-MRD: Showing NP-Card for Harderoporphyrin (NP0086632)

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Record Information

Version

2.0

Created at

2022-05-11 16:26:37 UTC

Updated at

2022-05-11 16:26:37 UTC

NP-MRD ID

NP0086632

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Harderoporphyrin

Description

Harderoporphyrin belongs to the class of organic compounds known as porphyrins. Porphyrins are compounds containing a fundamental skeleton of four pyrrole nuclei united through the alpha-positions by four methine groups to form a macrocyclic structure. Harderoporphyrin was first documented in 1983 (PMID: 6886003). Harderoporphyrin is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

Harderoporphyrin.mol
  Mrv1652305231919192D          

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M  END

     RDKit          3D

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M  END

Harderoporphyrin.mol
  Mrv1652305231919192D          

 45 49  0  0  0  0            999 V2000
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   -2.2520   -1.1474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5382   -0.4392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8114   -2.6053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0000   -2.5303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2004   -3.3445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0057   -3.5783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5987   -2.9853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2060   -4.3925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4614   -3.2512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0657    3.3663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8760    3.5828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0937    4.3925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4689    2.9897    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5355   -1.9061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3177    0.5374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7369   -0.1886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5756   -0.1886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9948    0.5374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9948   -0.9150    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2130    1.9137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8008    2.2859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5884   -3.6051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9948   -1.2056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1770    1.1858    0.0000 C   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
  1  5  1  0  0  0  0
  5 11  2  0  0  0  0
  3 23  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 10  2  0  0  0  0
 10 17  1  0  0  0  0
  8 11  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 12 16  1  0  0  0  0
 16 24  1  0  0  0  0
 14 17  2  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 18 22  1  0  0  0  0
 22 23  2  0  0  0  0
 20 24  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 19 30  1  0  0  0  0
 18 35  1  0  0  0  0
  7 41  1  0  0  0  0
  6 36  1  0  0  0  0
 25 13  1  0  0  0  0
  1 42  1  0  0  0  0
 12 43  1  0  0  0  0
 42 31  1  0  0  0  0
 35 44  2  0  0  0  0
  2 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0086632

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C2NC(\C=C3/N=C(/C=C4\N\C(=C/C5=N/C(=C\2)/C(CCC(O)=O)=C5C)C(C=C)=C4C)C(C)=C3CCC(O)=O)=C1CCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C35H36N4O6/c1-6-21-17(2)25-13-26-18(3)23(8-11-34(42)43)31(37-26)16-32-24(9-12-35(44)45)20(5)28(39-32)15-30-22(7-10-33(40)41)19(4)27(38-30)14-29(21)36-25/h6,13-16,36,39H,1,7-12H2,2-5H3,(H,40,41)(H,42,43)(H,44,45)/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16-

> <INCHI_KEY>
KECOXFKVIHSIBO-UJJXFSCMSA-N

> <FORMULA>
C35H36N4O6

> <MOLECULAR_WEIGHT>
608.6835

> <EXACT_MASS>
608.263484904

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
69.90952968238936

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[15,19-bis(2-carboxyethyl)-9-ethenyl-5,10,14,20-tetramethyl-21,22,23,24-tetraazapentacyclo[16.2.1.1^{3,6}.1^{8,11}.1^{13,16}]tetracosa-1(20),2,4,6(24),7,9,11,13(22),14,16,18-undecaen-4-yl]propanoic acid

> <ALOGPS_LOGP>
3.56

> <JCHEM_LOGP>
5.801804282995526

> <ALOGPS_LOGS>
-4.37

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
4.041865583669789

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6247141246692554

> <JCHEM_PKA_STRONGEST_BASIC>
5.109589177230174

> <JCHEM_POLAR_SURFACE_AREA>
169.26

> <JCHEM_REFRACTIVITY>
170.03350000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.59e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[15,19-bis(2-carboxyethyl)-9-ethenyl-5,10,14,20-tetramethyl-21,22,23,24-tetraazapentacyclo[16.2.1.1^{3,6}.1^{8,11}.1^{13,16}]tetracosa-1(20),2,4,6(24),7,9,11,13(22),14,16,18-undecaen-4-yl]propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-MAY-19   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: Harderoporphyrin.mol                              
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-MAY-19         0                                  
HETATM    1  C   UNK     0      -3.362   2.703   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.440   1.827   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.865   0.396   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0      -2.492   0.448   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0      -2.069   1.875   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.763   0.913   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.843   2.065   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.527   1.583   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       0.626   0.149   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       1.994  -0.318   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.747   2.410   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.098  -5.164   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.230  -4.287   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.708  -2.861   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       0.224  -2.959   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0      -0.135  -4.283   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.523  -1.692   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.037  -3.469   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.162  -4.565   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.684  -4.048   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0      -2.831  -2.562   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0      -4.204  -2.142   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.738  -0.820   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.515  -4.863   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.733  -4.723   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.107  -6.243   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.611  -6.679   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.717  -5.573   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       5.985  -8.199   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -4.595  -6.069   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -3.856   6.284   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -5.369   6.688   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -5.775   8.199   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -6.475   5.581   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -6.600  -3.558   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.326   1.003   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.109  -0.352   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.674  -0.352   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       7.457   1.003   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       7.457  -1.708   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       2.264   3.572   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -3.362   4.267   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       1.098  -6.729   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -7.457  -2.250   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -5.930   2.213   0.000  0.00  0.00           C+0
CONECT    1    2    5   42                                                  
CONECT    2    1    3   45                                                  
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    1   11                                                  
CONECT    6    7   10   36                                                  
CONECT    7    6    8   41                                                  
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9    6   17                                                  
CONECT   11    5    8                                                       
CONECT   12   13   16   43                                                  
CONECT   13   12   14   25                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15   12   24                                                  
CONECT   17   10   14                                                       
CONECT   18   19   22   35                                                  
CONECT   19   18   20   30                                                  
CONECT   20   19   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   18   23                                                  
CONECT   23    3   22                                                       
CONECT   24   16   20                                                       
CONECT   25   26   13                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   19                                                            
CONECT   31   32   42                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   18   44                                                       
CONECT   36   37    6                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41    7                                                            
CONECT   42    1   31                                                       
CONECT   43   12                                                            
CONECT   44   35                                                            
CONECT   45    2                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   98    0
END

View in JSmol

Synonyms

Value	Source
3,8,13,17-Tetramethyl-12-vinyl-2,7,18-porphinetripropionate	HMDB
3,8,13,17-Tetramethyl-12-vinyl-2,7,18-porphinetripropionic acid	HMDB
4,6,7-Tris(2-carboxyethyl)-1,3,5,8-tetramethyl-2-vinylporphyrin	HMDB
3-[15,20-Bis(2-carboxyethyl)-10-ethenyl-5,9,14,19-tetramethyl-21,22,23,24-tetraazapentacyclo[16.2.1.1³,⁶.1⁸,¹¹.1¹³,¹⁶]tetracosa-1(20),2,4,6(24),7,9,11,13(22),14,16,18-undecaen-4-yl]propanoate	HMDB

Chemical Formula

C₃₅H₃₆N₄O₆

Average Mass

608.6835 Da

Monoisotopic Mass

608.26348 Da

IUPAC Name

3-[15,19-bis(2-carboxyethyl)-9-ethenyl-5,10,14,20-tetramethyl-21,22,23,24-tetraazapentacyclo[16.2.1.1^{3,6}.1^{8,11}.1^{13,16}]tetracosa-1(20),2,4,6(24),7,9,11,13(22),14,16,18-undecaen-4-yl]propanoic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

CC1=C2NC(\C=C3/N=C(/C=C4\N\C(=C/C5=N/C(=C\2)/C(CCC(O)=O)=C5C)C(C=C)=C4C)C(C)=C3CCC(O)=O)=C1CCC(O)=O

InChI Identifier

InChI=1S/C35H36N4O6/c1-6-21-17(2)25-13-26-18(3)23(8-11-34(42)43)31(37-26)16-32-24(9-12-35(44)45)20(5)28(39-32)15-30-22(7-10-33(40)41)19(4)27(38-30)14-29(21)36-25/h6,13-16,36,39H,1,7-12H2,2-5H3,(H,40,41)(H,42,43)(H,44,45)/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16-

InChI Key

KECOXFKVIHSIBO-UJJXFSCMSA-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
Anas platyrhynchos	FooDB	FooDB
Anatidae	FooDB	FooDB
Anser anser	FooDB	FooDB
Bison bison	FooDB	FooDB
Bos taurus	FooDB	FooDB
Bos taurus X Bison bison	FooDB	FooDB
Bubalus bubalis	FooDB	FooDB
Capra aegagrus hircus	FooDB	FooDB
Cervidae	FooDB	FooDB
Cervus canadensis	FooDB	FooDB
Columba	FooDB	FooDB
Columbidae	FooDB	FooDB
Dromaius novaehollandiae	FooDB	FooDB
Equus caballus	FooDB	FooDB
Gallus gallus	FooDB	FooDB
Lagopus muta	FooDB	FooDB
Leporidae	FooDB	FooDB
Lepus timidus	FooDB	FooDB
Melanitta fusca	FooDB	FooDB
Meleagris gallopavo	FooDB	FooDB
Numida meleagris	FooDB	FooDB
Odocoileus	FooDB	FooDB
Oryctolagus	FooDB	FooDB
Ovis aries	FooDB	FooDB
Phasianidae	FooDB	FooDB
Phasianus colchicus	FooDB	FooDB
Struthio camelus	FooDB	FooDB
Sus scrofa	FooDB	FooDB
Sus scrofa domestica	FooDB	FooDB

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as porphyrins. Porphyrins are compounds containing a fundamental skeleton of four pyrrole nuclei united through the alpha-positions by four methine groups to form a macrocyclic structure.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Tetrapyrroles and derivatives

Sub Class

Porphyrins

Direct Parent

Porphyrins

Alternative Parents

Not Available

Substituents

Not Available

Molecular Framework

Not Available

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	3.56	ALOGPS
logP	5.8	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	3.62	ChemAxon
pKa (Strongest Basic)	5.11	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	169.26 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	170.03 m³·mol⁻¹	ChemAxon
Polarizability	69.91 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

HMDB0000683

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB022180

KNApSAcK ID

Not Available

Chemspider ID

2339065

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

5652

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Nordmann Y, Grandchamp B, de Verneuil H, Phung L, Cartigny B, Fontaine G: Harderoporphyria: a variant hereditary coproporphyria. J Clin Invest. 1983 Sep;72(3):1139-49. doi: 10.1172/JCI111039. [PubMed:6886003 ]

Showing NP-Card for Harderoporphyrin (NP0086632)

MOL for NP0086632 (Harderoporphyrin)

3D MOL for NP0086632 (Harderoporphyrin)

3D SDF for NP0086632 (Harderoporphyrin)

3D-SDF for NP0086632 (Harderoporphyrin)

PDB for NP0086632 (Harderoporphyrin)

3D PDB for NP0086632 (Harderoporphyrin)

SMILES for NP0086632 (Harderoporphyrin)

INCHI for NP0086632 (Harderoporphyrin)

Structure for NP0086632 (Harderoporphyrin)

3D Structure for NP0086632 (Harderoporphyrin)