NP-MRD: Showing NP-Card for n-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid (NP0306393)

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Record Information

Version

2.0

Created at

2022-09-10 22:50:06 UTC

Updated at

2022-09-10 22:50:06 UTC

NP-MRD ID

NP0306393

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid

Description

N-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid belongs to the class of organic compounds known as methylcarbamates. These are methyl esters of carbamic acid. n-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid is found in Pseudoceratina purpurea. N-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid is a very weakly acidic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 32 31  0  0  0  0  0  0  0  0999 V2000
   -6.1338   -0.8084    1.1022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2722    0.1691    0.4898 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3887   -0.2439   -0.4874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3730   -1.4670   -0.8068 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4780    0.6166   -1.1761 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6041    0.0712   -2.1648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6534   -0.9734   -1.6642 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5308   -0.4045   -0.4081 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.9345    0.9677   -1.1044 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.4073    0.0478   -1.6775 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0027   -0.6971   -0.5064 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4583    0.0136    0.5648 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9040    0.7088    1.6126 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2987    1.5162    2.3988 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2937    0.6126    2.0250 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7475    1.3527    3.1373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1659   -0.6524    0.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0151   -0.7960    2.1943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8047   -1.8329    0.7557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4778    1.6557   -0.9334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1871   -0.2488   -3.0543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9956    0.9445   -2.5619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1872   -1.8584   -1.2839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0205   -1.3027   -2.5471 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1407    0.8032   -2.0215 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2144   -0.6346   -2.4924 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8879   -1.2661   -0.9642 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2928   -1.5159   -0.2187 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2213    0.6052    0.7166 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0888    1.0438    3.9842 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7816    1.1229    3.4061 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6136    2.4502    2.9874 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  5 20  1  0
  6 21  1  0
  6 22  1  0
  7 23  1  0
  7 24  1  0
 10 25  1  0
 10 26  1  0
 11 27  1  0
 11 28  1  0
 12 29  1  0
 16 30  1  0
 16 31  1  0
 16 32  1  0
M  END


  Mrv1533004251509012D          

 16 15  0  0  0  0            999 V2000
    4.7586    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4730    3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9020    3.9849    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.6164    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3309    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0454    3.5724    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    9.7599    3.9849    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   10.4743    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1888    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9033    3.5724    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.6177    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6177    4.8099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3322    3.5724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0467    3.9849    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
  3  4  2  0  0  0  0
  3  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
  8  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
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0306393

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)NCCSSCCNC(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C8H16N2O4S2/c1-13-7(11)9-3-5-15-16-6-4-10-8(12)14-2/h3-6H2,1-2H3,(H,9,11)(H,10,12)

> <INCHI_KEY>
QIZMTUIOULZKTJ-UHFFFAOYSA-N

> <FORMULA>
C8H16N2O4S2

> <MOLECULAR_WEIGHT>
268.35

> <EXACT_MASS>
268.055149351

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
27.483395447231047

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl N-[2-({2-[(methoxycarbonyl)amino]ethyl}disulfanyl)ethyl]carbamate

> <ALOGPS_LOGP>
0.45

> <JCHEM_LOGP>
0.12351212533333351

> <ALOGPS_LOGS>
-2.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.909439008636419

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.430043196518177

> <JCHEM_POLAR_SURFACE_AREA>
76.66000000000001

> <JCHEM_REFRACTIVITY>
65.3468

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.65e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl N-[2-({2-[(methoxycarbonyl)amino]ethyl}disulfanyl)ethyl]carbamate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       8.883   6.668   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      10.216   7.438   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      11.550   6.668   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      11.550   5.128   0.000  0.00  0.00           O+0
HETATM    5  N   UNK     0      12.884   7.438   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      14.217   6.668   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      15.551   7.438   0.000  0.00  0.00           C+0
HETATM    8  S   UNK     0      16.885   6.668   0.000  0.00  0.00           S+0
HETATM    9  S   UNK     0      18.218   7.438   0.000  0.00  0.00           S+0
HETATM   10  C   UNK     0      19.552   6.668   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      20.886   7.438   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      22.219   6.668   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      23.553   7.438   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      23.553   8.978   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      24.887   6.668   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      26.220   7.438   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   30    0
END

View in JSmol

Synonyms

Value	Source
N-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidate	Generator
N-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulphanyl]ethyl}methoxycarboximidate	Generator
N-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulphanyl]ethyl}methoxycarboximidic acid	Generator

Chemical Formula

C₈H₁₆N₂O₄S₂

Average Mass

268.3500 Da

Monoisotopic Mass

268.05515 Da

IUPAC Name

methyl N-[2-({2-[(methoxycarbonyl)amino]ethyl}disulfanyl)ethyl]carbamate

Traditional Name

methyl N-[2-({2-[(methoxycarbonyl)amino]ethyl}disulfanyl)ethyl]carbamate

CAS Registry Number

Not Available

SMILES

COC(=O)NCCSSCCNC(=O)OC

InChI Identifier

InChI=1S/C8H16N2O4S2/c1-13-7(11)9-3-5-15-16-6-4-10-8(12)14-2/h3-6H2,1-2H3,(H,9,11)(H,10,12)

InChI Key

QIZMTUIOULZKTJ-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
Pseudoceratina purpurea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as methylcarbamates. These are methyl esters of carbamic acid.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Methylcarbamates

Alternative Parents

Substituents

Methylcarbamate
Dialkyldisulfide
Organic disulfide
Sulfenyl compound
Organic nitrogen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	0.45	ALOGPS
logP	0.12	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	14.43	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	76.66 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	65.35 m³·mol⁻¹	ChemAxon
Polarizability	27.48 Å³	ChemAxon
Number of Rings	0	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

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

15730445

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid (NP0306393)

MOL for NP0306393 (n-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid)

3D MOL for NP0306393 (n-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid)

3D SDF for NP0306393 (n-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid)

3D-SDF for NP0306393 (n-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid)

PDB for NP0306393 (n-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid)

3D PDB for NP0306393 (n-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid)

SMILES for NP0306393 (n-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid)

INCHI for NP0306393 (n-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid)

Structure for NP0306393 (n-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid)

3D Structure for NP0306393 (n-{2-[(2-{[hydroxy(methoxy)methylidene]amino}ethyl)disulfanyl]ethyl}methoxycarboximidic acid)