NP-MRD: Showing NP-Card for SF2738E (NP0022517)

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Record Information

Version

1.0

Created at

2021-01-06 07:41:34 UTC

Updated at

2021-07-15 17:39:16 UTC

NP-MRD ID

NP0022517

Secondary Accession Numbers

None

Natural Product Identification

Common Name

SF2738E

Provided By

NPAtlas

Description

SF2738E is found in Streptomyces sp. It was first documented in 1994 (PMID: 7844033). Based on a literature review very few articles have been published on N-{[4-methoxy-5-(methylsulfanyl)-[2,2'-bipyridine]-6-yl]methyl}ethanimidic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242105363D          

 38 39  0  0  0  0            999 V2000
    2.5536    3.8031   -0.3256 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2082    3.4372   -0.3336 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7624    2.1314   -0.2653 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6732    1.1211   -0.1846 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2745   -0.2082   -0.1138 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3025   -1.2449   -0.0290 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9762   -2.5837    0.0439 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9445   -3.5431    0.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2730   -3.1629    0.1295 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5843   -1.8411    0.0573 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5997   -0.9329   -0.0189 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0360   -0.4901   -0.1261 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9869    0.4631   -0.2042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4345    0.2074   -0.2211 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7739   -1.1807   -0.1455 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1370   -1.5733   -0.1523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5379   -3.0113   -0.0750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0754   -0.7305   -0.2237 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5728    1.7943   -0.2748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7712    3.1068   -0.3801 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1798    3.6319    1.3078 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6213    4.8821   -0.0534 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9520    3.6268   -1.3578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1882    3.2496    0.3706 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7265    1.3381   -0.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9317   -2.8617    0.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7290   -4.5994    0.1812 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0759   -3.8783    0.1901 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6070   -1.4925    0.0592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8701    0.7039    0.6952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9454    0.7019   -1.0847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0502   -1.9166   -0.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6241   -3.6598   -0.0431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1884   -3.2705   -0.9364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1650   -3.1350    0.8315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9361    2.9454    1.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4489    4.6875    1.3299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2502    3.4849    1.9232 H   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
  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
  5 12  2  0  0  0  0
 12 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
 16 18  2  0  0  0  0
 13 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19  3  1  0  0  0  0
 11  6  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  4 25  1  0  0  0  0
  7 26  1  0  0  0  0
  8 27  1  0  0  0  0
  9 28  1  0  0  0  0
 10 29  1  0  0  0  0
 14 30  1  0  0  0  0
 14 31  1  0  0  0  0
 15 32  1  0  0  0  0
 17 33  1  0  0  0  0
 17 34  1  0  0  0  0
 17 35  1  0  0  0  0
 21 36  1  0  0  0  0
 21 37  1  0  0  0  0
 21 38  1  0  0  0  0
M  END

     RDKit          3D

 38 39  0  0  0  0  0  0  0  0999 V2000
    2.5536    3.8031   -0.3256 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2082    3.4372   -0.3336 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7624    2.1314   -0.2653 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6732    1.1211   -0.1846 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2745   -0.2082   -0.1138 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3025   -1.2449   -0.0290 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9762   -2.5837    0.0439 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9445   -3.5431    0.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2730   -3.1629    0.1295 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5843   -1.8411    0.0573 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5997   -0.9329   -0.0189 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0360   -0.4901   -0.1261 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9869    0.4631   -0.2042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4345    0.2074   -0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7739   -1.1807   -0.1455 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1370   -1.5733   -0.1523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5379   -3.0113   -0.0750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0754   -0.7305   -0.2237 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5728    1.7943   -0.2748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7712    3.1068   -0.3801 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1798    3.6319    1.3078 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6213    4.8821   -0.0534 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9520    3.6268   -1.3578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1882    3.2496    0.3706 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7265    1.3381   -0.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9317   -2.8617    0.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7290   -4.5994    0.1812 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0759   -3.8783    0.1901 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6070   -1.4925    0.0592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8701    0.7039    0.6952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9454    0.7019   -1.0847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0502   -1.9166   -0.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6241   -3.6598   -0.0431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1884   -3.2705   -0.9364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1650   -3.1350    0.8315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9361    2.9454    1.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4489    4.6875    1.3299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2502    3.4849    1.9232 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
  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  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 13 19  2  0
 19 20  1  0
 20 21  1  0
 19  3  1  0
 11  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  4 25  1  0
  7 26  1  0
  8 27  1  0
  9 28  1  0
 10 29  1  0
 14 30  1  0
 14 31  1  0
 15 32  1  0
 17 33  1  0
 17 34  1  0
 17 35  1  0
 21 36  1  0
 21 37  1  0
 21 38  1  0
M  END


  Mrv1652306242105363D          

 38 39  0  0  0  0            999 V2000
    2.5536    3.8031   -0.3256 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2082    3.4372   -0.3336 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7624    2.1314   -0.2653 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6732    1.1211   -0.1846 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2745   -0.2082   -0.1138 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3025   -1.2449   -0.0290 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9762   -2.5837    0.0439 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9445   -3.5431    0.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2730   -3.1629    0.1295 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5843   -1.8411    0.0573 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5997   -0.9329   -0.0189 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0360   -0.4901   -0.1261 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9869    0.4631   -0.2042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4345    0.2074   -0.2211 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7739   -1.1807   -0.1455 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1370   -1.5733   -0.1523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5379   -3.0113   -0.0750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0754   -0.7305   -0.2237 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5728    1.7943   -0.2748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7712    3.1068   -0.3801 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1798    3.6319    1.3078 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6213    4.8821   -0.0534 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9520    3.6268   -1.3578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1882    3.2496    0.3706 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7265    1.3381   -0.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9317   -2.8617    0.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7290   -4.5994    0.1812 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0759   -3.8783    0.1901 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6070   -1.4925    0.0592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8701    0.7039    0.6952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9454    0.7019   -1.0847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0502   -1.9166   -0.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6241   -3.6598   -0.0431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1884   -3.2705   -0.9364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1650   -3.1350    0.8315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9361    2.9454    1.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4489    4.6875    1.3299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2502    3.4849    1.9232 H   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
  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
  5 12  2  0  0  0  0
 12 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
 16 18  2  0  0  0  0
 13 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19  3  1  0  0  0  0
 11  6  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  4 25  1  0  0  0  0
  7 26  1  0  0  0  0
  8 27  1  0  0  0  0
  9 28  1  0  0  0  0
 10 29  1  0  0  0  0
 14 30  1  0  0  0  0
 14 31  1  0  0  0  0
 15 32  1  0  0  0  0
 17 33  1  0  0  0  0
 17 34  1  0  0  0  0
 17 35  1  0  0  0  0
 21 36  1  0  0  0  0
 21 37  1  0  0  0  0
 21 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0022517

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]N(C(=O)C([H])([H])[H])C([H])([H])C1=C(SC([H])([H])[H])C(OC([H])([H])[H])=C([H])C(=N1)C1=C([H])C([H])=C([H])C([H])=N1

> <INCHI_IDENTIFIER>
InChI=1S/C15H17N3O2S/c1-10(19)17-9-13-15(21-3)14(20-2)8-12(18-13)11-6-4-5-7-16-11/h4-8H,9H2,1-3H3,(H,17,19)

> <INCHI_KEY>
BQJMSLCILFVYMK-UHFFFAOYSA-N

> <FORMULA>
C15H17N3O2S

> <MOLECULAR_WEIGHT>
303.38

> <EXACT_MASS>
303.104147973

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
33.15830458206043

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-{[4-methoxy-5-(methylsulfanyl)-[2,2'-bipyridine]-6-yl]methyl}acetamide

> <ALOGPS_LOGP>
2.13

> <JCHEM_LOGP>
1.4534597773333338

> <ALOGPS_LOGS>
-4.34

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.688666485370323

> <JCHEM_PKA_STRONGEST_BASIC>
3.2820181546492337

> <JCHEM_POLAR_SURFACE_AREA>
64.11000000000001

> <JCHEM_REFRACTIVITY>
82.75349999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.40e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-{[4-methoxy-5-(methylsulfanyl)-[2,2'-bipyridine]-6-yl]methyl}acetamide

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 38 39  0  0  0  0  0  0  0  0999 V2000
    2.5536    3.8031   -0.3256 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2082    3.4372   -0.3336 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7624    2.1314   -0.2653 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6732    1.1211   -0.1846 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2745   -0.2082   -0.1138 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3025   -1.2449   -0.0290 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9762   -2.5837    0.0439 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9445   -3.5431    0.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2730   -3.1629    0.1295 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5843   -1.8411    0.0573 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5997   -0.9329   -0.0189 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0360   -0.4901   -0.1261 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9869    0.4631   -0.2042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4345    0.2074   -0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7739   -1.1807   -0.1455 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1370   -1.5733   -0.1523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5379   -3.0113   -0.0750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0754   -0.7305   -0.2237 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5728    1.7943   -0.2748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7712    3.1068   -0.3801 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1798    3.6319    1.3078 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6213    4.8821   -0.0534 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9520    3.6268   -1.3578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1882    3.2496    0.3706 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7265    1.3381   -0.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9317   -2.8617    0.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7290   -4.5994    0.1812 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0759   -3.8783    0.1901 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6070   -1.4925    0.0592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8701    0.7039    0.6952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9454    0.7019   -1.0847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0502   -1.9166   -0.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6241   -3.6598   -0.0431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1884   -3.2705   -0.9364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1650   -3.1350    0.8315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9361    2.9454    1.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4489    4.6875    1.3299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2502    3.4849    1.9232 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
  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  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 13 19  2  0
 19 20  1  0
 20 21  1  0
 19  3  1  0
 11  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  4 25  1  0
  7 26  1  0
  8 27  1  0
  9 28  1  0
 10 29  1  0
 14 30  1  0
 14 31  1  0
 15 32  1  0
 17 33  1  0
 17 34  1  0
 17 35  1  0
 21 36  1  0
 21 37  1  0
 21 38  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       2.554   3.803  -0.326  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.208   3.437  -0.334  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.762   2.131  -0.265  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.673   1.121  -0.185  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.274  -0.208  -0.114  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.303  -1.245  -0.029  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.976  -2.584   0.044  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.945  -3.543   0.123  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.273  -3.163   0.130  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.584  -1.841   0.057  0.00  0.00           C+0
HETATM   11  N   UNK     0       3.600  -0.933  -0.019  0.00  0.00           N+0
HETATM   12  N   UNK     0      -0.036  -0.490  -0.126  0.00  0.00           N+0
HETATM   13  C   UNK     0      -0.987   0.463  -0.204  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.434   0.207  -0.221  0.00  0.00           C+0
HETATM   15  N   UNK     0      -2.774  -1.181  -0.146  0.00  0.00           N+0
HETATM   16  C   UNK     0      -4.137  -1.573  -0.152  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.538  -3.011  -0.075  0.00  0.00           C+0
HETATM   18  O   UNK     0      -5.075  -0.731  -0.224  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.573   1.794  -0.275  0.00  0.00           C+0
HETATM   20  S   UNK     0      -1.771   3.107  -0.380  0.00  0.00           S+0
HETATM   21  C   UNK     0      -2.180   3.632   1.308  0.00  0.00           C+0
HETATM   22  H   UNK     0       2.621   4.882  -0.053  0.00  0.00           H+0
HETATM   23  H   UNK     0       2.952   3.627  -1.358  0.00  0.00           H+0
HETATM   24  H   UNK     0       3.188   3.250   0.371  0.00  0.00           H+0
HETATM   25  H   UNK     0       2.727   1.338  -0.174  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.932  -2.862   0.037  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.729  -4.599   0.181  0.00  0.00           H+0
HETATM   28  H   UNK     0       5.076  -3.878   0.190  0.00  0.00           H+0
HETATM   29  H   UNK     0       5.607  -1.492   0.059  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.870   0.704   0.695  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.945   0.702  -1.085  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.050  -1.917  -0.085  0.00  0.00           H+0
HETATM   33  H   UNK     0      -3.624  -3.660  -0.043  0.00  0.00           H+0
HETATM   34  H   UNK     0      -5.188  -3.271  -0.936  0.00  0.00           H+0
HETATM   35  H   UNK     0      -5.165  -3.135   0.832  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.936   2.945   1.696  0.00  0.00           H+0
HETATM   37  H   UNK     0      -2.449   4.688   1.330  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.250   3.485   1.923  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5   25                                                  
CONECT    5    4    6   12                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8   26                                                  
CONECT    8    7    9   27                                                  
CONECT    9    8   10   28                                                  
CONECT   10    9   11   29                                                  
CONECT   11   10    6                                                       
CONECT   12    5   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15   30   31                                             
CONECT   15   14   16   32                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16   33   34   35                                             
CONECT   18   16                                                            
CONECT   19   13   20    3                                                  
CONECT   20   19   21                                                       
CONECT   21   20   36   37   38                                             
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    4                                                            
CONECT   26    7                                                            
CONECT   27    8                                                            
CONECT   28    9                                                            
CONECT   29   10                                                            
CONECT   30   14                                                            
CONECT   31   14                                                            
CONECT   32   15                                                            
CONECT   33   17                                                            
CONECT   34   17                                                            
CONECT   35   17                                                            
CONECT   36   21                                                            
CONECT   37   21                                                            
CONECT   38   21                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   78    0
END

RDKit          3D

38 39  0  0  0  0  0  0  0  0999 V2000
    2.5536    3.8031   -0.3256 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2082    3.4372   -0.3336 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7624    2.1314   -0.2653 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6732    1.1211   -0.1846 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2745   -0.2082   -0.1138 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3025   -1.2449   -0.0290 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9762   -2.5837    0.0439 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9445   -3.5431    0.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2730   -3.1629    0.1295 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5843   -1.8411    0.0573 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5997   -0.9329   -0.0189 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0360   -0.4901   -0.1261 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9869    0.4631   -0.2042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4345    0.2074   -0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7739   -1.1807   -0.1455 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1370   -1.5733   -0.1523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5379   -3.0113   -0.0750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0754   -0.7305   -0.2237 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5728    1.7943   -0.2748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7712    3.1068   -0.3801 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1798    3.6319    1.3078 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6213    4.8821   -0.0534 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9520    3.6268   -1.3578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1882    3.2496    0.3706 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7265    1.3381   -0.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9317   -2.8617    0.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7290   -4.5994    0.1812 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0759   -3.8783    0.1901 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6070   -1.4925    0.0592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8701    0.7039    0.6952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9454    0.7019   -1.0847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0502   -1.9166   -0.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6241   -3.6598   -0.0431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1884   -3.2705   -0.9364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1650   -3.1350    0.8315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9361    2.9454    1.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4489    4.6875    1.3299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2502    3.4849    1.9232 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
  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  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 13 19  2  0
 19 20  1  0
 20 21  1  0
 19  3  1  0
 11  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  4 25  1  0
  7 26  1  0
  8 27  1  0
  9 28  1  0
 10 29  1  0
 14 30  1  0
 14 31  1  0
 15 32  1  0
 17 33  1  0
 17 34  1  0
 17 35  1  0
 21 36  1  0
 21 37  1  0
 21 38  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
N-{[4-methoxy-5-(methylsulfanyl)-[2,2'-bipyridine]-6-yl]methyl}ethanimidate	Generator
N-{[4-methoxy-5-(methylsulphanyl)-[2,2'-bipyridine]-6-yl]methyl}ethanimidate	Generator
N-{[4-methoxy-5-(methylsulphanyl)-[2,2'-bipyridine]-6-yl]methyl}ethanimidic acid	Generator

Chemical Formula

C₁₅H₁₇N₃O₂S

Average Mass

303.3800 Da

Monoisotopic Mass

303.10415 Da

IUPAC Name

N-{[4-methoxy-5-(methylsulfanyl)-[2,2'-bipyridine]-6-yl]methyl}acetamide

Traditional Name

N-{[4-methoxy-5-(methylsulfanyl)-[2,2'-bipyridine]-6-yl]methyl}acetamide

CAS Registry Number

Not Available

SMILES

COC1=CC(=NC(CNC(C)=O)=C1SC)C1=CC=CC=N1

InChI Identifier

InChI=1S/C15H17N3O2S/c1-10(19)17-9-13-15(21-3)14(20-2)8-12(18-13)11-6-4-5-7-16-11/h4-8H,9H2,1-3H3,(H,17,19)

InChI Key

BQJMSLCILFVYMK-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, 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
Streptomyces sp.	NPAtlas	7844033

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as bipyridines and oligopyridines. These are organic compounds containing two pyridine rings linked to each other.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyridines and derivatives

Sub Class

Bipyridines and oligopyridines

Direct Parent

Bipyridines and oligopyridines

Alternative Parents

Substituents

Bipyridine
Aryl thioether
Alkyl aryl ether
Alkylarylthioether
Heteroaromatic compound
Acetamide
Carboxamide group
Secondary carboxylic acid amide
Carboxylic acid derivative
Ether
Thioether
Sulfenyl compound
Azacycle
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Organosulfur compound
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organic oxide
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	2.13	ALOGPS
logP	1.45	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	13.69	ChemAxon
pKa (Strongest Basic)	3.28	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	64.11 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	82.75 m³·mol⁻¹	ChemAxon
Polarizability	33.16 Å³	ChemAxon
Number of Rings	2	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

NPAtlas ID

NPA017793

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

8193434

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10017861

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Gomi S, Amano S, Sato E, Miyadoh S, Kodama Y: Novel antibiotics SF2738A, B and C, and their analogs produced by Streptomyces sp. J Antibiot (Tokyo). 1994 Dec;47(12):1385-94. doi: 10.7164/antibiotics.47.1385. [PubMed:7844033 ]

Showing NP-Card for SF2738E (NP0022517)

MOL for NP0022517 (SF2738E)

3D MOL for NP0022517 (SF2738E)

3D SDF for NP0022517 (SF2738E)

3D-SDF for NP0022517 (SF2738E)

PDB for NP0022517 (SF2738E)

3D PDB for NP0022517 (SF2738E)

SMILES for NP0022517 (SF2738E)

INCHI for NP0022517 (SF2738E)

Structure for NP0022517 (SF2738E)

3D Structure for NP0022517 (SF2738E)