NP-MRD: Showing NP-Card for Cyanogripeptide A (NP0331695)

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Record Information

Version

2.0

Created at

2023-06-27 16:03:41 UTC

Updated at

2025-02-11 15:45:27 UTC

NP-MRD ID

NP0331695

Natural Product DOI

https://doi.org/10.57994/0703

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Cyanogripeptide A

Description

Cyanogripeptide A belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating. Cyanogripeptide A was first documented in 2023 (PMID: 37317791). Based on a literature review very few articles have been published on Cyanogripeptide A.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652306272318032D          

 55 55  0  0  1  0            999 V2000
   -1.0575    0.1190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4302   -0.6170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2489   -0.5150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8127   -1.1173    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5729   -1.9067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6162   -0.9302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1799   -1.5325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8559   -0.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4048    0.2952    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8101   -1.2732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.1173    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5401   -1.7409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2700   -0.3377    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8101   -0.9613    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6203   -0.8054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1604   -1.4291    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8903   -2.2086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0802   -2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8101   -3.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2700   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2700   -4.7032    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0802   -4.2355    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9705   -1.2732    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5106   -1.8968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3207   -1.7409    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8608   -2.3645    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6709   -2.2086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2110   -2.8323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0212   -2.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5612   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3714   -3.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2912   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9410   -1.4291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5908   -0.9613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0507   -0.3377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2405   -0.4936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3207    0.4418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2405   -2.6764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8903   -0.0259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0802   -0.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3502    0.5978    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8101    1.2214    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0802    2.0010    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5401    2.6246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8903    2.1569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1604    2.9364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4304    1.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    1.0655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    1.6891    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3502    1.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6825    0.6938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9251    0.3668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2700    0.2859    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8837   -0.3689    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  1  6  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  3  9  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  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  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 16 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 28 34  2  0  0  0  0
 26 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 25 39  2  0  0  0  0
 15 40  2  0  0  0  0
 13 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  6  0  0  0
 44 45  1  6  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 43 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
  9 52  1  0  0  0  0
 52 53  2  0  0  0  0
 49 54  2  0  0  0  0
 41 55  2  0  0  0  0
M  END


  Mrv1652306272318032D          

 55 55  0  0  1  0            999 V2000
   -1.0575    0.1190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4302   -0.6170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2489   -0.5150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8127   -1.1173    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5729   -1.9067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6162   -0.9302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1799   -1.5325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8559   -0.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4048    0.2952    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8101   -1.2732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.1173    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5401   -1.7409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2700   -0.3377    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8101   -0.9613    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6203   -0.8054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1604   -1.4291    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8903   -2.2086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0802   -2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8101   -3.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2700   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2700   -4.7032    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0802   -4.2355    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9705   -1.2732    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5106   -1.8968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3207   -1.7409    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8608   -2.3645    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6709   -2.2086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2110   -2.8323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0212   -2.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5612   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3714   -3.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2912   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9410   -1.4291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5908   -0.9613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0507   -0.3377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2405   -0.4936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3207    0.4418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2405   -2.6764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8903   -0.0259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0802   -0.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3502    0.5978    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8101    1.2214    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0802    2.0010    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5401    2.6246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8903    2.1569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1604    2.9364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4304    1.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    1.0655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    1.6891    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3502    1.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6825    0.6938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9251    0.3668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2700    0.2859    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8837   -0.3689    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  1  6  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  3  9  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  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  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 16 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 28 34  2  0  0  0  0
 26 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 25 39  2  0  0  0  0
 15 40  2  0  0  0  0
 13 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  6  0  0  0
 44 45  1  6  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 43 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
  9 52  1  0  0  0  0
 52 53  2  0  0  0  0
 49 54  2  0  0  0  0
 41 55  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0331695

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CCC(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CCCNC(N)=N)C(=O)N[C@H]1[C@@H](C)OC(=O)[C@@H](NC(=O)CNC(=O)[C@@H](NC1=O)[C@H](C)C(C)C)[C@H](C)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C38H69N9O8/c1-19(2)14-15-28(48)43-27(17-20(3)4)34(51)44-26(13-12-16-41-38(39)40)33(50)47-32-25(11)55-37(54)31(24(10)22(7)8)45-29(49)18-42-35(52)30(46-36(32)53)23(9)21(5)6/h19-27,30-32H,12-18H2,1-11H3,(H,42,52)(H,43,48)(H,44,51)(H,45,49)(H,46,53)(H,47,50)(H4,39,40,41)/t23-,24-,25-,26-,27+,30+,31+,32+/m1/s1

> <INCHI_KEY>
BFEKVXPJQSHMSY-YJZKUPLCSA-N

> <FORMULA>
C38H69N9O8

> <MOLECULAR_WEIGHT>
780.025

> <EXACT_MASS>
779.526910218

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
124

> <JCHEM_AVERAGE_POLARIZABILITY>
85.74518735993702

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-N-[(1R)-4-carbamimidamido-1-{[(3S,9S,12S,13R)-13-methyl-3,9-bis[(2R)-3-methylbutan-2-yl]-2,5,8,11-tetraoxo-1-oxa-4,7,10-triazacyclotridecan-12-yl]carbamoyl}butyl]-4-methyl-2-(4-methylpentanamido)pentanamide

> <JCHEM_LOGP>
0.9269420168471241

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
11.209968047788635

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.7102887114891

> <JCHEM_PKA_STRONGEST_BASIC>
11.698334861792663

> <JCHEM_POLAR_SURFACE_AREA>
262.79999999999995

> <JCHEM_REFRACTIVITY>
216.17180000000022

> <JCHEM_ROTATABLE_BOND_COUNT>
18

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-N-[(1R)-4-carbamimidamido-1-{[(3S,9S,12S,13R)-13-methyl-3,9-bis[(2R)-3-methylbutan-2-yl]-2,5,8,11-tetraoxo-1-oxa-4,7,10-triazacyclotridecan-12-yl]carbamoyl}butyl]-4-methyl-2-(4-methylpentanamido)pentanamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 27-JUN-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-JUN-23         0                                  
HETATM    1  O   UNK     0      -1.974   0.222   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -2.670  -1.152   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.198  -0.961   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.250  -2.086   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.803  -3.559   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.750  -1.736   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -7.803  -2.861   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -7.198  -0.263   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -4.489   0.551   0.000  0.00  0.00           N+0
HETATM   10  O   UNK     0      -1.512  -2.377   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.000  -2.086   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.008  -3.250   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.504  -0.630   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       1.512  -1.795   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       3.024  -1.503   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.033  -2.668   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.529  -4.123   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.016  -4.414   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.512  -5.869   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0      -0.000  -6.160   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0      -0.504  -7.615   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       0.504  -8.779   0.000  0.00  0.00           N+0
HETATM   23  N   UNK     0      -2.016  -7.906   0.000  0.00  0.00           N+0
HETATM   24  N   UNK     0       5.545  -2.377   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0       6.553  -3.541   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.065  -3.250   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0       9.073  -4.414   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0      10.586  -4.123   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.594  -5.287   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      13.106  -4.996   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      14.114  -6.160   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      15.627  -5.869   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      13.610  -7.615   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      11.090  -2.668   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       8.569  -1.795   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.561  -0.630   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.049  -0.921   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.065   0.825   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       6.049  -4.996   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       3.529  -0.048   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       2.016  -0.339   0.000  0.00  0.00           C+0
HETATM   42  N   UNK     0       2.520   1.116   0.000  0.00  0.00           N+0
HETATM   43  C   UNK     0       1.512   2.280   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       2.016   3.735   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       1.008   4.899   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       3.529   4.026   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       4.033   5.481   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       4.537   2.862   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -0.000   1.989   0.000  0.00  0.00           C+0
HETATM   50  N   UNK     0      -1.008   3.153   0.000  0.00  0.00           N+0
HETATM   51  C   UNK     0      -2.520   2.862   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      -3.141   1.295   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      -1.727   0.685   0.000  0.00  0.00           O+0
HETATM   54  O   UNK     0      -0.504   0.534   0.000  0.00  0.00           O+0
HETATM   55  O   UNK     0       3.516  -0.689   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   10                                                  
CONECT    3    2    4    9                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    3   52                                                       
CONECT   10    2   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   41                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   40                                                  
CONECT   16   15   17   24                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   16   25                                                       
CONECT   25   24   26   39                                                  
CONECT   26   25   27   35                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   34                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   28                                                            
CONECT   35   26   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36                                                            
CONECT   39   25                                                            
CONECT   40   15                                                            
CONECT   41   13   42   55                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44   49                                                  
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46                                                            
CONECT   49   43   50   54                                                  
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51    9   53                                                  
CONECT   53   52                                                            
CONECT   54   49                                                            
CONECT   55   41                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  110    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₈H₆₉N₉O₈

Average Mass

780.0250 Da

Monoisotopic Mass

779.52691 Da

IUPAC Name

(2S)-N-[(1R)-4-carbamimidamido-1-{[(3S,9S,12S,13R)-13-methyl-3,9-bis[(2R)-3-methylbutan-2-yl]-2,5,8,11-tetraoxo-1-oxa-4,7,10-triazacyclotridecan-12-yl]carbamoyl}butyl]-4-methyl-2-(4-methylpentanamido)pentanamide

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(C)CCC(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CCCNC(N)=N)C(=O)N[C@H]1[C@@H](C)OC(=O)[C@@H](NC(=O)CNC(=O)[C@@H](NC1=O)[C@H](C)C(C)C)[C@H](C)C(C)C

InChI Identifier

InChI=1S/C38H69N9O8/c1-19(2)14-15-28(48)43-27(17-20(3)4)34(51)44-26(13-12-16-41-38(39)40)33(50)47-32-25(11)55-37(54)31(24(10)22(7)8)45-29(49)18-42-35(52)30(46-36(32)53)23(9)21(5)6/h19-27,30-32H,12-18H2,1-11H3,(H,42,52)(H,43,48)(H,44,51)(H,45,49)(H,46,53)(H,47,50)(H4,39,40,41)/t23-,24-,25-,26-,27+,30+,31+,32+/m1/s1

InChI Key

BFEKVXPJQSHMSY-YJZKUPLCSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D_DEPT NMR	¹³C NMR Spectrum (1D, 151 MHz, C2D6OS, experimental)	shuaishuaizhang66@163.com	Not Available	Not Available	2024-05-11	View Spectrum
TOCSY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, C2D6OS, experimental)	shuaishuaizhang66@163.com	Not Available	Not Available	2023-06-27	View Spectrum
ROESY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, C2D6OS, experimental)	shuaishuaizhang66@163.com	Not Available	Not Available	2023-06-27	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, C2D6OS, experimental)	shuaishuaizhang66@163.com	Not Available	Not Available	2023-06-27	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, C2D6OS, experimental)	shuaishuaizhang66@163.com	Not Available	Not Available	2023-06-27	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, C2D6OS, experimental)	shuaishuaizhang66@163.com	Not Available	Not Available	2023-06-27	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, C2D6OS, experimental)	shuaishuaizhang66@163.com	Not Available	Not Available	2023-06-27	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, C2D6OS, experimental)	shuaishuaizhang66@163.com	Not Available	Not Available	2023-06-27	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 600.133705802, C2D6OS, simulated)	Not Available	Not Available	Not Available	2024-05-11	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
Actinoalloteichus cyanogriseus		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Peptidomimetics

Sub Class

Depsipeptides

Direct Parent

Cyclic depsipeptides

Alternative Parents

Substituents

Cyclic depsipeptide
Arginine or derivatives
Leucine or derivatives
N-acyl-alpha amino acid or derivatives
Macrolactam
Alpha-amino acid ester
Alpha-amino acid amide
Alpha-amino acid or derivatives
N-substituted-alpha-amino acid
Fatty acid ester
Fatty acyl
N-acyl-amine
Fatty amide
Lactone
Lactam
Guanidine
Carboxylic acid ester
Carboxamide group
Oxacycle
Azacycle
Organoheterocyclic compound
Carboximidamide
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Imine
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic 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	0.93	ChemAxon
pKa (Strongest Acidic)	10.71	ChemAxon
pKa (Strongest Basic)	11.7	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	262.8 Å²	ChemAxon
Rotatable Bond Count	18	ChemAxon
Refractivity	216.17 m³·mol⁻¹	ChemAxon
Polarizability	85.75 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

DOI: 10.1021/acs.jnatprod.3c00127

Showing NP-Card for Cyanogripeptide A (NP0331695)

MOL for NP0331695 (Cyanogripeptide A)

3D MOL for NP0331695 (Cyanogripeptide A)

3D SDF for NP0331695 (Cyanogripeptide A)

3D-SDF for NP0331695 (Cyanogripeptide A)

PDB for NP0331695 (Cyanogripeptide A)

3D PDB for NP0331695 (Cyanogripeptide A)

SMILES for NP0331695 (Cyanogripeptide A)

INCHI for NP0331695 (Cyanogripeptide A)

Structure for NP0331695 (Cyanogripeptide A)

3D Structure for NP0331695 (Cyanogripeptide A)