NP-MRD: Showing NP-Card for Nocardimicin S (NP0341983)

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Record Information

Version

2.0

Created at

2024-11-27 08:45:25 UTC

Updated at

2024-11-27 12:00:36 UTC

NP-MRD ID

NP0341983

Natural Product DOI

https://doi.org/10.57994/3474

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Nocardimicin S

Description

Based on a literature review very few articles have been published on Nocardimicin S.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 02242308552D          

 52 54  0  0  1  0            999 V2000
    1.2459  -10.6395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8712  -11.1776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6499  -10.9052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8033  -10.0945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2376   -9.4940    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6340   -8.7704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2816   -8.0245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7515   -7.3463    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3991   -6.6004    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5769   -6.5326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1070   -7.2107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2848   -7.1429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1850   -7.8210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0072   -7.7532    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4770   -8.4314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1247   -9.1773    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2992   -8.3636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3596   -7.0073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8689   -5.9222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5165   -5.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9864   -4.4981    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8086   -4.5659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1610   -5.3119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9832   -5.3797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3355   -6.1257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1577   -6.1935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5101   -6.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3323   -7.0073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6847   -7.7532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2149   -8.4314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6340   -3.7522    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8118   -3.6843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1038   -3.0740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7515   -2.3281    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2213   -1.6499    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8142   -0.9324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1213   -0.1667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9115    0.0706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5896   -0.3992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6451   -1.2224    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4108   -1.5295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0361   -1.7790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2734   -2.5691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9260   -3.1418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6911   -5.9900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4594   -7.9567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4446   -8.9238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5492   -9.7422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2752  -11.4433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1218  -12.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3431  -12.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7178  -11.9882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  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  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
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 11 12  1  0  0  0  0
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 14 18  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21 20  1  6  0  0  0
 21 22  1  0  0  0  0
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 23 24  1  0  0  0  0
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 29 30  1  0  0  0  0
 21 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 35 34  1  6  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 35 42  1  0  0  0  0
 42 43  2  0  0  0  0
 33 44  2  0  0  0  0
 19 45  2  0  0  0  0
  7 46  2  0  0  0  0
  6 47  2  0  0  0  0
 47 48  1  0  0  0  0
  4 48  1  0  0  0  0
  3 49  1  0  0  0  0
 49 50  2  0  0  0  0
 50 51  1  0  0  0  0
 51 52  2  0  0  0  0
  2 52  1  0  0  0  0
M  END


  Mrv2104 02242308552D          

 52 54  0  0  1  0            999 V2000
    1.2459  -10.6395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8712  -11.1776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6499  -10.9052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8033  -10.0945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2376   -9.4940    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6340   -8.7704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2816   -8.0245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7515   -7.3463    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3991   -6.6004    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5769   -6.5326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1070   -7.2107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2848   -7.1429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1850   -7.8210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0072   -7.7532    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4770   -8.4314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1247   -9.1773    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2992   -8.3636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3596   -7.0073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8689   -5.9222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5165   -5.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9864   -4.4981    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8086   -4.5659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1610   -5.3119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9832   -5.3797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3355   -6.1257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1577   -6.1935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5101   -6.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3323   -7.0073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6847   -7.7532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2149   -8.4314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6340   -3.7522    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8118   -3.6843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1038   -3.0740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7515   -2.3281    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2213   -1.6499    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8142   -0.9324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1213   -0.1667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9115    0.0706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5896   -0.3992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6451   -1.2224    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4108   -1.5295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0361   -1.7790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2734   -2.5691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9260   -3.1418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6911   -5.9900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4594   -7.9567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4446   -8.9238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5492   -9.7422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2752  -11.4433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1218  -12.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3431  -12.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7178  -11.9882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  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  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  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  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 14 18  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21 20  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
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 29 30  1  0  0  0  0
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 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 35 34  1  6  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 35 42  1  0  0  0  0
 42 43  2  0  0  0  0
 33 44  2  0  0  0  0
 19 45  2  0  0  0  0
  7 46  2  0  0  0  0
  6 47  2  0  0  0  0
 47 48  1  0  0  0  0
  4 48  1  0  0  0  0
  3 49  1  0  0  0  0
 49 50  2  0  0  0  0
 50 51  1  0  0  0  0
 51 52  2  0  0  0  0
  2 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0341983

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C(=O)N(O)CCCC[C@H](NC(=O)C1=COC(=N1)C1=C(O)C=CC=C1)C(=O)O[C@@H](CCCCCCCCC)[C@@H](C)C(=O)N[C@@H]1CCCCN(O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C36H53N5O10/c1-3-4-5-6-7-8-9-20-31(25(2)32(44)37-27-17-13-15-22-41(49)35(27)46)51-36(47)28(18-12-14-21-40(48)24-42)38-33(45)29-23-50-34(39-29)26-16-10-11-19-30(26)43/h10-11,16,19,23-25,27-28,31,43,48-49H,3-9,12-15,17-18,20-22H2,1-2H3,(H,37,44)(H,38,45)/t25-,27-,28+,31+/m1/s1

> <INCHI_KEY>
CBKMOSAUYXXTRP-DFKYUQDGSA-N

> <FORMULA>
C36H53N5O10

> <MOLECULAR_WEIGHT>
715.845

> <EXACT_MASS>
715.379242927

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
76.9013574314247

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S)-1-{[(3R)-1-hydroxy-2-oxoazepan-3-yl]carbamoyl}-1-methylundecan-2-yl (2S)-6-(N-hydroxyformamido)-2-{[2-(2-hydroxyphenyl)-1,3-oxazol-4-yl]formamido}hexanoate

> <JCHEM_LOGP>
4.603867201999998

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.421525156524865

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.9287641637837005

> <JCHEM_PKA_STRONGEST_BASIC>
-1.388217501035845

> <JCHEM_POLAR_SURFACE_AREA>
211.83999999999997

> <JCHEM_REFRACTIVITY>
196.5133

> <JCHEM_ROTATABLE_BOND_COUNT>
22

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S)-1-{[(3R)-1-hydroxy-2-oxoazepan-3-yl]carbamoyl}-1-methylundecan-2-yl (2S)-6-(N-hydroxyformamido)-2-{[2-(2-hydroxyphenyl)-1,3-oxazol-4-yl]formamido}hexanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-23         0                                  
HETATM    1  O   UNK     0       2.326 -19.860   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.493 -20.865   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.946 -20.356   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.233 -18.843   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       4.177 -17.722   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       4.917 -16.371   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.259 -14.979   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       5.136 -13.713   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       4.478 -12.321   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.944 -12.194   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.066 -13.460   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.532 -13.333   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.345 -14.599   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      -1.880 -14.473   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      -2.757 -15.739   0.000  0.00  0.00           C+0
HETATM   16  H   UNK     0      -2.099 -17.131   0.000  0.00  0.00           H+0
HETATM   17  O   UNK     0      -4.292 -15.612   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -2.538 -13.080   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.355 -11.055   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.698  -9.662   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.575  -8.396   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.109  -8.523   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.767  -9.916   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.302 -10.042   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.960 -11.435   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.494 -11.561   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.152 -12.954   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.687 -13.080   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      14.345 -14.473   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      13.468 -15.739   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.917  -7.004   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.382  -6.877   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.794  -5.738   0.000  0.00  0.00           C+0
HETATM   34  N   UNK     0       5.136  -4.346   0.000  0.00  0.00           N+0
HETATM   35  C   UNK     0       6.013  -3.080   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.253  -1.740   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.826  -0.311   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.301   0.132   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       8.567  -0.745   0.000  0.00  0.00           C+0
HETATM   40  N   UNK     0       8.671  -2.282   0.000  0.00  0.00           N+0
HETATM   41  O   UNK     0      10.100  -2.855   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       7.534  -3.321   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       7.977  -4.796   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0       7.329  -5.865   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0       6.890 -11.181   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0       2.724 -14.852   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       6.430 -16.658   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       6.625 -18.185   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       6.114 -21.361   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       5.827 -22.874   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       4.374 -23.383   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       3.207 -22.378   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   52                                                  
CONECT    3    2    4   49                                                  
CONECT    4    3    5   48                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   47                                                  
CONECT    7    6    8   46                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   19                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   18                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   14                                                            
CONECT   19    9   20   45                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   31                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31   21   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   44                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   42                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   35   43                                                  
CONECT   43   42                                                            
CONECT   44   33                                                            
CONECT   45   19                                                            
CONECT   46    7                                                            
CONECT   47    6   48                                                       
CONECT   48   47    4                                                       
CONECT   49    3   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51    2                                                       
MASTER        0    0    0    0    0    0    0    0   52    0  108    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₅₃N₅O₁₀

Average Mass

715.8450 Da

Monoisotopic Mass

715.37924 Da

IUPAC Name

(1R,2S)-1-{[(3R)-1-hydroxy-2-oxoazepan-3-yl]carbamoyl}-1-methylundecan-2-yl (2S)-6-(N-hydroxyformamido)-2-{[2-(2-hydroxyphenyl)-1,3-oxazol-4-yl]formamido}hexanoate

Traditional Name

(1R,2S)-1-{[(3R)-1-hydroxy-2-oxoazepan-3-yl]carbamoyl}-1-methylundecan-2-yl (2S)-6-(N-hydroxyformamido)-2-{[2-(2-hydroxyphenyl)-1,3-oxazol-4-yl]formamido}hexanoate

CAS Registry Number

Not Available

SMILES

[H]C(=O)N(O)CCCC[C@H](NC(=O)C1=COC(=N1)C1=C(O)C=CC=C1)C(=O)O[C@@H](CCCCCCCCC)[C@@H](C)C(=O)N[C@@H]1CCCCN(O)C1=O

InChI Identifier

InChI=1S/C36H53N5O10/c1-3-4-5-6-7-8-9-20-31(25(2)32(44)37-27-17-13-15-22-41(49)35(27)46)51-36(47)28(18-12-14-21-40(48)24-42)38-33(45)29-23-50-34(39-29)26-16-10-11-19-30(26)43/h10-11,16,19,23-25,27-28,31,43,48-49H,3-9,12-15,17-18,20-22H2,1-2H3,(H,37,44)(H,38,45)/t25-,27-,28+,31+/m1/s1

InChI Key

CBKMOSAUYXXTRP-DFKYUQDGSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, C2D6OS, experimental)	1584281463@qq.com	Ocean University of China	Suling Xu	2024-11-27	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, C2D6OS, experimental)	1584281463@qq.com	Ocean University of China	Suling Xu	2024-11-27	View Spectrum
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, C2D6OS, experimental)	1584281463@qq.com	Ocean University of China	Suling Xu	2024-11-27	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, C2D6OS, experimental)	1584281463@qq.com	Ocean University of China	Suling Xu	2024-11-27	View Spectrum
HETLOC NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, C2D6OS, experimental)	1584281463@qq.com	Ocean University of China	Suling Xu	2024-11-27	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, C2D6OS, experimental)	1584281463@qq.com	Ocean University of China	Suling Xu	2024-11-27	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, C2D6OS, experimental)	1584281463@qq.com	Ocean University of China	Suling Xu	2024-11-27	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Moorena sp.		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	4.6	ChemAxon
pKa (Strongest Acidic)	7.93	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	211.84 Å²	ChemAxon
Rotatable Bond Count	22	ChemAxon
Refractivity	196.51 m³·mol⁻¹	ChemAxon
Polarizability	76.9 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	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 Nocardimicin S (NP0341983)

MOL for NP0341983 (Nocardimicin S)

3D MOL for NP0341983 (Nocardimicin S)

3D SDF for NP0341983 (Nocardimicin S)

3D-SDF for NP0341983 (Nocardimicin S)

PDB for NP0341983 (Nocardimicin S)

3D PDB for NP0341983 (Nocardimicin S)

SMILES for NP0341983 (Nocardimicin S)

INCHI for NP0341983 (Nocardimicin S)

Structure for NP0341983 (Nocardimicin S)

3D Structure for NP0341983 (Nocardimicin S)