NP-MRD: Showing NP-Card for Psammaplin I (NP0077020)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 22:11:39 UTC

Updated at

2022-04-28 22:11:40 UTC

NP-MRD ID

NP0077020

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Psammaplin I

Description

Psammaplin I is found in Pseudoceratina purpurea.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 37  0  0  0  0  0  0  0  0999 V2000
    5.3901    2.1112    0.0206 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1565    0.3766    0.2063 S   0  0  0  0  0  6  0  0  0  0  0  0
    6.5099   -0.2494    0.1012 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5097    0.1909    1.5362 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9576    0.2023   -1.4602 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.4121   -1.3689   -1.7033 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4524   -2.0005   -0.7086 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2065   -1.2711   -0.5911 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2361   -1.7725    0.3052 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4337   -2.8181    0.9883 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0216   -1.0773    0.4518 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2902    0.1624   -0.3370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6338    0.6697   -0.0187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8775    1.5576    0.9969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1491    2.0301    1.2890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2128    1.5961    0.5354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4810    2.0439    0.7985 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9794    0.7021   -0.4899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4496    0.0799   -1.5588 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -3.7144    0.2328   -0.7796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9121   -1.5234    1.2616 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7054   -2.6737    2.0172 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9875    2.3154   -0.9090 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0539    2.4149    0.8584 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4808    2.7059    0.0969 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8929   -1.5078   -2.7021 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2530   -2.1260   -1.7792 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9122   -1.9867    0.3235 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2842   -3.0726   -0.9297 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0193   -0.4228   -1.1294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1935   -0.0733   -1.4110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5592    0.9774   -0.0686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0198    1.8945    1.5890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2898    2.7339    2.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6433    2.6954    1.5476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5211   -0.4661   -1.5789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4947   -3.2828    2.1699 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  2  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  2  0
 11 21  2  0
 21 22  1  0
 20 13  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  6 26  1  0
  6 27  1  0
  7 28  1  0
  7 29  1  0
  8 30  1  0
 12 31  1  0
 12 32  1  0
 14 33  1  0
 15 34  1  0
 17 35  1  0
 20 36  1  0
 22 37  1  0
M  END


  Mrv1652304292200112D          

 22 22  0  0  0  0            999 V2000
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    5.7750    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    6.1875    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559    5.4730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7309    6.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   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
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  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
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 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
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  2  0  0  0  0
 17 20  1  0  0  0  0
  3 21  1  0  0  0  0
  2 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0077020

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CS(=O)(=O)SCCNC(=O)C(\CC1=CC=C(O)C(Br)=C1)=N/O

> <INCHI_IDENTIFIER>
InChI=1S/C12H15BrN2O5S2/c1-22(19,20)21-5-4-14-12(17)10(15-18)7-8-2-3-11(16)9(13)6-8/h2-3,6,16,18H,4-5,7H2,1H3,(H,14,17)/b15-10-

> <INCHI_KEY>
FIEIPKPRYNAIPC-GDNBJRDFSA-N

> <FORMULA>
C12H15BrN2O5S2

> <MOLECULAR_WEIGHT>
411.29

> <EXACT_MASS>
409.960577

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
35.49694320971355

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2Z)-3-(3-bromo-4-hydroxyphenyl)-2-(N-hydroxyimino)-N-[2-(methanesulfonylsulfanyl)ethyl]propanamide

> <ALOGPS_LOGP>
1.03

> <JCHEM_LOGP>
1.3039191416666673

> <ALOGPS_LOGS>
-3.64

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.132962871371594

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.344498095229882

> <JCHEM_PKA_STRONGEST_BASIC>
-1.8355052950028732

> <JCHEM_POLAR_SURFACE_AREA>
116.06000000000002

> <JCHEM_REFRACTIVITY>
88.50999999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.53e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2Z)-3-(3-bromo-4-hydroxyphenyl)-2-(N-hydroxyimino)-N-[2-(methanesulfonylsulfanyl)ethyl]propanamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -1.334   3.850   0.000  0.00  0.00           N+0
HETATM   10  O   UNK     0      -2.667   4.620   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.334   6.930   0.000  0.00  0.00           O+0
HETATM   13  N   UNK     0      -1.334   6.930   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      -1.334   8.470   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.667   9.240   0.000  0.00  0.00           C+0
HETATM   16  S   UNK     0      -2.667  10.780   0.000  0.00  0.00           S+0
HETATM   17  S   UNK     0      -4.001  11.550   0.000  0.00  0.00           S+0
HETATM   18  O   UNK     0      -5.335  12.320   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -4.771  10.216   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -3.231  12.884   0.000  0.00  0.00           C+0
HETATM   21 Br   UNK     0      -1.334  -0.770   0.000  0.00  0.00          Br+0
HETATM   22  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   22                                                  
CONECT    3    2    4   21                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17                                                            
CONECT   21    3                                                            
CONECT   22    2                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₂H₁₅BrN₂O₅S₂

Average Mass

411.2900 Da

Monoisotopic Mass

409.96058 Da

IUPAC Name

(2Z)-3-(3-bromo-4-hydroxyphenyl)-2-(N-hydroxyimino)-N-[2-(methanesulfonylsulfanyl)ethyl]propanamide

Traditional Name

(2Z)-3-(3-bromo-4-hydroxyphenyl)-2-(N-hydroxyimino)-N-[2-(methanesulfonylsulfanyl)ethyl]propanamide

CAS Registry Number

Not Available

SMILES

CS(=O)(=O)SCCNC(=O)C(\CC1=CC=C(O)C(Br)=C1)=N/O

InChI Identifier

InChI=1S/C12H15BrN2O5S2/c1-22(19,20)21-5-4-14-12(17)10(15-18)7-8-2-3-11(16)9(13)6-8/h2-3,6,16,18H,4-5,7H2,1H3,(H,14,17)/b15-10-

InChI Key

FIEIPKPRYNAIPC-GDNBJRDFSA-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
Pseudoceratina purpurea	-	KNApSAcK

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	1.03	ALOGPS
logP	1.3	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	6.34	ChemAxon
pKa (Strongest Basic)	-1.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	116.06 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	88.51 m³·mol⁻¹	ChemAxon
Polarizability	35.5 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Not Available

Showing NP-Card for Psammaplin I (NP0077020)

MOL for NP0077020 (Psammaplin I)

3D MOL for NP0077020 (Psammaplin I)

3D SDF for NP0077020 (Psammaplin I)

3D-SDF for NP0077020 (Psammaplin I)

PDB for NP0077020 (Psammaplin I)

3D PDB for NP0077020 (Psammaplin I)

SMILES for NP0077020 (Psammaplin I)

INCHI for NP0077020 (Psammaplin I)

Structure for NP0077020 (Psammaplin I)

3D Structure for NP0077020 (Psammaplin I)