NP-MRD: Showing NP-Card for (3Z)-phytochromobilin (NP0339656)

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Record Information

Version

2.0

Created at

2024-09-11 22:54:52 UTC

Updated at

2024-09-11 22:54:53 UTC

NP-MRD ID

NP0339656

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3Z)-phytochromobilin

Description

Based on a literature review very few articles have been published on (3Z)-phytochromobilin.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 05272301272D          

 43 46  0  0  0  0            999 V2000
    2.6693   -3.9730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3837   -4.3855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3837   -5.2105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7163   -5.6954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9317   -5.4405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3186   -5.9925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5116   -5.8210    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0991   -6.5354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7214   -6.6217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2063   -5.9542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9514   -5.1696    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6188   -4.6847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6188   -3.8597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3333   -3.4472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0870   -3.7828    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6390   -3.1697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4595   -3.2559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2265   -2.4552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5620   -1.7015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3825   -1.6153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4195   -2.6267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8064   -2.0747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2862   -5.1696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0709   -4.9147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0313   -5.9542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5162   -6.6217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3367   -6.5354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8216   -7.2029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4861   -7.9566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6421   -7.1166    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    0.6511   -7.1485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4796   -7.9555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0927   -8.5075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9212   -9.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5343   -9.8665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1365   -9.5694    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    1.4048   -6.8130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1193   -7.2255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9712   -6.4800    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7962   -6.4800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2811   -7.1475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0512   -5.6954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8358   -5.4405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  4  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 13 12  1  4  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 18 21  2  0  0  0  0
 21 22  1  0  0  0  0
 14 21  1  0  0  0  0
 12 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 10 25  1  0  0  0  0
  8 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 31 37  1  0  0  0  0
 37 38  1  0  0  0  0
  6 37  2  0  0  0  0
  4 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
  3 42  1  0  0  0  0
M  CHG  2  30  -1  36  -1
M  END


  Mrv2104 05272301272D          

 43 46  0  0  0  0            999 V2000
    2.6693   -3.9730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3837   -4.3855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3837   -5.2105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7163   -5.6954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9317   -5.4405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3186   -5.9925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5116   -5.8210    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0991   -6.5354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7214   -6.6217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2063   -5.9542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9514   -5.1696    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6188   -4.6847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6188   -3.8597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3333   -3.4472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0870   -3.7828    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6390   -3.1697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4595   -3.2559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2265   -2.4552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5620   -1.7015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3825   -1.6153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4195   -2.6267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8064   -2.0747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2862   -5.1696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0709   -4.9147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0313   -5.9542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5162   -6.6217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3367   -6.5354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8216   -7.2029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4861   -7.9566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6421   -7.1166    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    0.6511   -7.1485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4796   -7.9555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0927   -8.5075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9212   -9.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5343   -9.8665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1365   -9.5694    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    1.4048   -6.8130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1193   -7.2255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9712   -6.4800    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7962   -6.4800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2811   -7.1475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0512   -5.6954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8358   -5.4405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  4  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 13 12  1  4  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 18 21  2  0  0  0  0
 21 22  1  0  0  0  0
 14 21  1  0  0  0  0
 12 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 10 25  1  0  0  0  0
  8 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 31 37  1  0  0  0  0
 37 38  1  0  0  0  0
  6 37  2  0  0  0  0
  4 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
  3 42  1  0  0  0  0
M  CHG  2  30  -1  36  -1
M  END
> <DATABASE_ID>
NP0339656

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C1C(C)C(=O)NC1=CC1=C(C)C(CCC([O-])=O)=C(N1)C=C1N=C(C=C2NC(=O)C(C=C)=C2C)C(C)=C1CCC([O-])=O

> <INCHI_IDENTIFIER>
InChI=1/C33H36N4O6/c1-7-20-19(6)32(42)37-27(20)14-25-18(5)23(10-12-31(40)41)29(35-25)15-28-22(9-11-30(38)39)17(4)24(34-28)13-26-16(3)21(8-2)33(43)36-26/h7-8,13-15,19,35H,2,9-12H2,1,3-6H3,(H,36,43)(H,37,42)(H,38,39)(H,40,41)/p-2

> <INCHI_KEY>
DKMLMZVDTGOEGU-UHFFFAOYNA-L

> <FORMULA>
C33H34N4O6

> <MOLECULAR_WEIGHT>
582.658

> <EXACT_MASS>
582.248931991

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
64.75640903797655

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
-2

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-(2-{[3-(2-carboxylatoethyl)-5-[(4-ethenyl-3-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-ylidene)methyl]-4-methyl-2H-pyrrol-2-ylidene]methyl}-5-[(3-ethylidene-4-methyl-5-oxopyrrolidin-2-ylidene)methyl]-4-methyl-1H-pyrrol-3-yl)propanoate

> <JCHEM_LOGP>
0.6624802570759725

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.4484509073479455

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.8555038914379582

> <JCHEM_PKA_STRONGEST_BASIC>
5.850349378642474

> <JCHEM_POLAR_SURFACE_AREA>
166.60999999999999

> <JCHEM_REFRACTIVITY>
191.2259000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
3-(2-{[3-(2-carboxylatoethyl)-5-[(4-ethenyl-3-methyl-5-oxo-1H-pyrrol-2-ylidene)methyl]-4-methylpyrrol-2-ylidene]methyl}-5-[(3-ethylidene-4-methyl-5-oxopyrrolidin-2-ylidene)methyl]-4-methyl-1H-pyrrol-3-yl)propanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 27-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-MAY-23         0                                  
HETATM    1  C   UNK     0       4.983  -7.416   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.316  -8.186   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.316  -9.726   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.070 -10.631   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.606 -10.156   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.461 -11.186   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       0.955 -10.866   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       0.185 -12.199   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.347 -12.360   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.252 -11.115   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      -1.776  -9.650   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -3.022  -8.745   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.022  -7.205   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.355  -6.435   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0      -5.762  -7.061   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0      -6.793  -5.917   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -8.324  -6.078   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -6.023  -4.583   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -6.649  -3.176   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -8.181  -3.015   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.516  -4.903   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.372  -3.873   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.268  -9.650   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.732  -9.174   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.792 -11.115   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.697 -12.360   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -6.229 -12.199   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -7.134 -13.445   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -6.507 -14.852   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -8.665 -13.284   0.000  0.00  0.00           O-1
HETATM   31  C   UNK     0       1.215 -13.344   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.895 -14.850   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.040 -15.881   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.720 -17.387   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       2.864 -18.418   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       0.255 -17.863   0.000  0.00  0.00           O-1
HETATM   37  C   UNK     0       2.622 -12.718   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.956 -13.488   0.000  0.00  0.00           C+0
HETATM   39  N   UNK     0       5.546 -12.096   0.000  0.00  0.00           N+0
HETATM   40  C   UNK     0       7.086 -12.096   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       7.991 -13.342   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       7.562 -10.631   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       9.027 -10.156   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   42                                                  
CONECT    4    3    5   39                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   37                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   31                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   25                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   23                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22   14                                                  
CONECT   22   21                                                            
CONECT   23   12   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   10                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31    8   32   37                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   31   38    6                                                  
CONECT   38   37                                                            
CONECT   39    4   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43    3                                                  
CONECT   43   42                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₃₄N₄O₆

Average Mass

582.6580 Da

Monoisotopic Mass

582.24893 Da

IUPAC Name

3-(2-{[3-(2-carboxylatoethyl)-5-[(4-ethenyl-3-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-ylidene)methyl]-4-methyl-2H-pyrrol-2-ylidene]methyl}-5-[(3-ethylidene-4-methyl-5-oxopyrrolidin-2-ylidene)methyl]-4-methyl-1H-pyrrol-3-yl)propanoate

Traditional Name

3-(2-{[3-(2-carboxylatoethyl)-5-[(4-ethenyl-3-methyl-5-oxo-1H-pyrrol-2-ylidene)methyl]-4-methylpyrrol-2-ylidene]methyl}-5-[(3-ethylidene-4-methyl-5-oxopyrrolidin-2-ylidene)methyl]-4-methyl-1H-pyrrol-3-yl)propanoate

CAS Registry Number

Not Available

SMILES

CC=C1C(C)C(=O)NC1=CC1=C(C)C(CCC([O-])=O)=C(N1)C=C1N=C(C=C2NC(=O)C(C=C)=C2C)C(C)=C1CCC([O-])=O

InChI Identifier

InChI=1/C33H36N4O6/c1-7-20-19(6)32(42)37-27(20)14-25-18(5)23(10-12-31(40)41)29(35-25)15-28-22(9-11-30(38)39)17(4)24(34-28)13-26-16(3)21(8-2)33(43)36-26/h7-8,13-15,19,35H,2,9-12H2,1,3-6H3,(H,36,43)(H,37,42)(H,38,39)(H,40,41)/p-2

InChI Key

DKMLMZVDTGOEGU-UHFFFAOYNA-L

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

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	0.66	ChemAxon
pKa (Strongest Acidic)	3.86	ChemAxon
pKa (Strongest Basic)	5.85	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	166.61 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	191.23 m³·mol⁻¹	ChemAxon
Polarizability	64.76 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (3Z)-phytochromobilin (NP0339656)

MOL for NP0339656 ((3Z)-phytochromobilin)

3D MOL for NP0339656 ((3Z)-phytochromobilin)

3D SDF for NP0339656 ((3Z)-phytochromobilin)

3D-SDF for NP0339656 ((3Z)-phytochromobilin)

PDB for NP0339656 ((3Z)-phytochromobilin)

3D PDB for NP0339656 ((3Z)-phytochromobilin)

SMILES for NP0339656 ((3Z)-phytochromobilin)

INCHI for NP0339656 ((3Z)-phytochromobilin)

Structure for NP0339656 ((3Z)-phytochromobilin)

3D Structure for NP0339656 ((3Z)-phytochromobilin)