NP-MRD: Showing NP-Card for 2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid (NP0158135)

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Record Information

Version

2.0

Created at

2022-09-02 15:40:17 UTC

Updated at

2022-09-02 15:40:17 UTC

NP-MRD ID

NP0158135

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid

Description

H-Cys(Trt)-OH belongs to the class of organic compounds known as triphenyl compounds. These are aromatic compounds containing a triphenyl moiety. 2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid is found in Allium sativum. Based on a literature review very few articles have been published on H-Cys(Trt)-OH.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022217402D          

 26 28  0  0  0  0            999 V2000
   -0.9355    2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    1.2375    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7605    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9980   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9980    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4934    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4934    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    2.4750    0.0000 O   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
  2 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
M  END

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
    4.7553    1.1492    0.8279 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8366    0.2287    0.2265 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3816    0.6052    0.5439 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3393   -0.5898   -0.2432 S   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4216   -0.3683   -0.0171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8922   -0.5567    1.3516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3197   -1.4688    2.2119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8019   -1.5976    3.4918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8621   -0.8375    3.9749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4353    0.0726    3.1217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9421    0.2002    1.8221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7553    1.0094   -0.4795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3432    2.0617    0.3046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6287    3.3462   -0.0936 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3212    3.5473   -1.2681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7420    2.5077   -2.0662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4461    1.2228   -1.6507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1313   -1.3205   -0.9325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4130   -2.0285   -1.8711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0923   -2.8973   -2.6902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4523   -3.0910   -2.6155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1286   -2.3628   -1.6633 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4756   -1.4851   -0.8282 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0059    0.1294   -1.2439 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2693   -0.6422   -1.9045 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9547    0.8555   -1.9604 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6844    1.0648    1.8474 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7194    0.8677    0.5508 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9892   -0.7877    0.6484 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2881    0.7096    1.6218 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2796    1.6369    0.0950 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5240   -2.1042    1.9023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3647   -2.2995    4.1602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2462   -0.9263    4.9648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2598    0.6680    3.4881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4683    0.9593    1.2291 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2009    1.9262    1.2342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3149    4.2191    0.5083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5425    4.5662   -1.5741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2943    2.6694   -3.0021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7652    0.3642   -2.2644 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6811   -1.8961   -1.9567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5303   -3.4474   -3.4215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0128   -3.7654   -3.2452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2091   -2.4684   -1.5495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0594   -0.9236   -0.0768 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7626    1.2776   -1.5090 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
  5 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
  5 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
  2 24  1  0
 24 26  1  0
 24 25  2  0
 11  6  1  0
 17 12  1  0
 23 18  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  1
  3 30  1  0
  3 31  1  0
  7 32  1  0
  8 33  1  0
  9 34  1  0
 10 35  1  0
 11 36  1  0
 13 37  1  0
 14 38  1  0
 15 39  1  0
 16 40  1  0
 17 41  1  0
 19 42  1  0
 20 43  1  0
 21 44  1  0
 22 45  1  0
 23 46  1  0
 26 47  1  0
M  END


  Mrv1652309022217402D          

 26 28  0  0  0  0            999 V2000
   -0.9355    2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    1.2375    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7605    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9980   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9980    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4934    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4934    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    2.4750    0.0000 O   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
  2 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0158135

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NC(CSC(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H21NO2S/c23-20(21(24)25)16-26-22(17-10-4-1-5-11-17,18-12-6-2-7-13-18)19-14-8-3-9-15-19/h1-15,20H,16,23H2,(H,24,25)

> <INCHI_KEY>
DLMYFMLKORXJPO-UHFFFAOYSA-N

> <FORMULA>
C22H21NO2S

> <MOLECULAR_WEIGHT>
363.48

> <EXACT_MASS>
363.129300094

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
39.67423509781541

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid

> <ALOGPS_LOGP>
1.78

> <JCHEM_LOGP>
2.440735992278879

> <ALOGPS_LOGS>
-6.10

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.371311075158299

> <JCHEM_PKA_STRONGEST_BASIC>
9.116664904342848

> <JCHEM_POLAR_SURFACE_AREA>
63.32000000000001

> <JCHEM_REFRACTIVITY>
108.07240000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.89e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  N   UNK     0      -1.746   5.390   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0      -0.413   4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.413   3.080   0.000  0.00  0.00           C+0
HETATM    4  S   UNK     0      -1.746   2.310   0.000  0.00  0.00           S+0
HETATM    5  C   UNK     0      -1.746   0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.746  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.413  -1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.413  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.746  -3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.080  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.080  -1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.286   0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.056  -0.564   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.596  -0.564   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -6.366   0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.596   2.104   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.056   2.104   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.921   5.390   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       0.921   6.930   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       2.255   4.620   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   24                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   12   18                                             
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    6                                                       
CONECT   12    5   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18    5   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   18                                                       
CONECT   24    2   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Value	Source
3-Tritylthio-L-alanine	MeSH
3-Tritylthio-L-alanine, (D)-isomer	MeSH
S-Trityl-L-cysteine	MeSH

Chemical Formula

C₂₂H₂₁NO₂S

Average Mass

363.4800 Da

Monoisotopic Mass

363.12930 Da

IUPAC Name

2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid

Traditional Name

2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid

CAS Registry Number

Not Available

SMILES

NC(CSC(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1)C(O)=O

InChI Identifier

InChI=1S/C22H21NO2S/c23-20(21(24)25)16-26-22(17-10-4-1-5-11-17,18-12-6-2-7-13-18)19-14-8-3-9-15-19/h1-15,20H,16,23H2,(H,24,25)

InChI Key

DLMYFMLKORXJPO-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
Allium sativum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triphenyl compounds. These are aromatic compounds containing a triphenyl moiety.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Triphenyl compounds

Sub Class

Not Available

Direct Parent

Triphenyl compounds

Alternative Parents

Substituents

Triphenyl compound
Cysteine or derivatives
Alpha-amino acid
Alpha-amino acid or derivatives
Monocyclic benzene moiety
Amino acid or derivatives
Amino acid
Carboxylic acid derivative
Dialkylthioether
Sulfenyl compound
Thioether
Carboxylic acid
Monocarboxylic acid or derivatives
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organosulfur compound
Primary aliphatic amine
Primary amine
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organopnictogen compound
Amine
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.78	ALOGPS
logP	2.44	ChemAxon
logS	-6.1	ALOGPS
pKa (Strongest Acidic)	2.37	ChemAxon
pKa (Strongest Basic)	9.12	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	63.32 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	108.07 m³·mol⁻¹	ChemAxon
Polarizability	39.67 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

224876

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

256411

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid (NP0158135)

MOL for NP0158135 (2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid)

3D MOL for NP0158135 (2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid)

3D SDF for NP0158135 (2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid)

3D-SDF for NP0158135 (2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid)

PDB for NP0158135 (2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid)

3D PDB for NP0158135 (2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid)

SMILES for NP0158135 (2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid)

INCHI for NP0158135 (2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid)

Structure for NP0158135 (2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid)

3D Structure for NP0158135 (2-amino-3-[(triphenylmethyl)sulfanyl]propanoic acid)