NP-MRD: Showing NP-Card for Salternamide A (NP0014924)

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Record Information

Version

1.0

Created at

2021-01-05 23:57:50 UTC

Updated at

2021-07-15 17:18:33 UTC

NP-MRD ID

NP0014924

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Salternamide A

Provided By

NPAtlas

Description

Salternamide A is found in Streptomyces sp. It was first documented in 2015 (PMID: 26610526). Based on a literature review very few articles have been published on 5-[(1R)-3-chloro-1-hydroxy-5-{[(4S,6R)-1-hydroxy-4,6,8-trimethylnona-2,7-dien-1-ylidene]amino}-4-oxocyclohexa-2,5-dien-1-yl]pentanoic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117113D          

 62 62  0  0  0  0            999 V2000
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   -6.8297    0.2522    0.0467 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652306242117113D          

 62 62  0  0  0  0            999 V2000
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    5.0928   -3.4621   -1.9763 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3305   -3.1116   -1.9814 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7269   -4.5291   -1.2133 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6610    0.9575    0.3720 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2174    0.4800    1.4889 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2546    0.0442    2.8133 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.7224    0.2910    1.6498 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3343   -0.1732    2.7425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7730   -0.5666    0.3400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4444   -1.6168    0.9307 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.7045    1.5702   -1.6781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6243    2.2512   -0.2932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3767    0.9666   -1.2305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3269   -0.9045    0.8635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8145    1.4114   -1.0995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9107   -0.9430   -0.9325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4564   -1.1216   -1.8051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3133    0.1729   -2.2758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0828    1.8757    1.1537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7929    1.9392   -0.0476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9034   -0.2818    0.7106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4960   -1.5701    1.7212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1868   -0.2266    2.8140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5966   -0.9993    3.0967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3023    1.7446    2.9712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3320    2.2023    3.0109 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9809   -0.1512    0.0660 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7086    1.3220   -1.3738 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1201    3.1864   -0.4754 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3317    1.3250   -2.3162 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6933    1.2773   -2.9491 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9213   -1.0917   -1.4216 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9543   -0.9225   -3.1900 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6040   -1.3081   -1.2484 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2382   -0.7720   -2.8865 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6827   -2.5605   -3.8220 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2110   -3.2224   -2.9648 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2193   -4.7811   -0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7171    1.1141    0.2372 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
  2  4  2  3  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 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
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 17 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 15  1  0  0  0  0
  1 31  1  0  0  0  0
  1 32  1  0  0  0  0
  1 33  1  0  0  0  0
  3 34  1  0  0  0  0
  3 35  1  0  0  0  0
  3 36  1  0  0  0  0
  4 37  1  0  0  0  0
  5 38  1  6  0  0  0
  6 39  1  0  0  0  0
  6 40  1  0  0  0  0
  6 41  1  0  0  0  0
  7 42  1  0  0  0  0
  7 43  1  0  0  0  0
  8 44  1  6  0  0  0
  9 45  1  0  0  0  0
  9 46  1  0  0  0  0
  9 47  1  0  0  0  0
 10 48  1  0  0  0  0
 11 49  1  0  0  0  0
 14 50  1  0  0  0  0
 16 51  1  0  0  0  0
 18 52  1  0  0  0  0
 19 53  1  0  0  0  0
 19 54  1  0  0  0  0
 20 55  1  0  0  0  0
 20 56  1  0  0  0  0
 21 57  1  0  0  0  0
 21 58  1  0  0  0  0
 22 59  1  0  0  0  0
 22 60  1  0  0  0  0
 25 61  1  0  0  0  0
 26 62  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0014924

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C([H])([H])C([H])([H])C([H])([H])C([H])([H])[C@]1(O[H])C([H])=C(Cl)C(=O)C(N([H])C(=O)C(\[H])=C(\[H])[C@@]([H])(C([H])([H])[H])C([H])([H])[C@]([H])(C([H])=C(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C23H32ClNO5/c1-15(2)11-17(4)12-16(3)8-9-20(26)25-19-14-23(30,13-18(24)22(19)29)10-6-5-7-21(27)28/h8-9,11,13-14,16-17,30H,5-7,10,12H2,1-4H3,(H,25,26)(H,27,28)/b9-8-/t16-,17+,23+/m1/s1

> <INCHI_KEY>
TXGICURJQBELHX-DGGJZMOXSA-N

> <FORMULA>
C23H32ClNO5

> <MOLECULAR_WEIGHT>
437.96

> <EXACT_MASS>
437.1969008

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
47.8677713822014

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-[(1R)-3-chloro-1-hydroxy-4-oxo-5-[(2E,4S,6R)-4,6,8-trimethylnona-2,7-dienamido]cyclohexa-2,5-dien-1-yl]pentanoic acid

> <ALOGPS_LOGP>
3.63

> <JCHEM_LOGP>
4.098710392

> <ALOGPS_LOGS>
-5.34

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.901697065593293

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.200426138539593

> <JCHEM_PKA_STRONGEST_BASIC>
-3.139353806394038

> <JCHEM_POLAR_SURFACE_AREA>
103.70000000000002

> <JCHEM_REFRACTIVITY>
122.10809999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.99e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-[(1R)-3-chloro-1-hydroxy-4-oxo-5-[(2E,4S,6R)-4,6,8-trimethylnona-2,7-dienamido]cyclohexa-2,5-dien-1-yl]pentanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 62 62  0  0  0  0  0  0  0  0999 V2000
   -7.8047   -0.5872    0.8512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8297    0.2522    0.0467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3659    1.2910   -0.8320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5455   -0.0777    0.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4193    0.6026   -0.4702 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7288   -0.3765   -1.4209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4423    1.1835    0.4984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6467    0.3180    1.3698 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3205   -0.6135    2.3030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7395    1.2361    2.2280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4655    1.2289    1.9596 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8136    1.2376    1.7081 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7498    1.9635    2.3479 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4823    0.4702    0.6809 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8996    0.6515    0.5369 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4006    1.1139   -0.5604 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8136    1.3547   -0.8064 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9516    2.7920   -0.8451 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3270    0.8410   -2.0698 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3565   -0.6095   -2.3229 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0061   -1.2698   -2.2909 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1800   -2.6976   -2.7868 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0928   -3.4621   -1.9763 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3305   -3.1116   -1.9814 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7269   -4.5291   -1.2133 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6610    0.9575    0.3720 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2174    0.4800    1.4889 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2546    0.0442    2.8133 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.7224    0.2910    1.6498 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3343   -0.1732    2.7425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7730   -0.5666    0.3400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4444   -1.6168    0.9307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9571   -0.1211    1.8565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7045    1.5702   -1.6781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6243    2.2512   -0.2932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3767    0.9666   -1.2305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3269   -0.9045    0.8635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8145    1.4114   -1.0995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9107   -0.9430   -0.9325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4564   -1.1216   -1.8051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3133    0.1729   -2.2758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0828    1.8757    1.1537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7929    1.9392   -0.0476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9034   -0.2818    0.7106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4960   -1.5701    1.7212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1868   -0.2266    2.8140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5966   -0.9993    3.0967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3023    1.7446    2.9712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3320    2.2023    3.0109 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9809   -0.1512    0.0660 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7086    1.3220   -1.3738 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1201    3.1864   -0.4754 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3317    1.3250   -2.3162 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6933    1.2773   -2.9491 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9213   -1.0917   -1.4216 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9543   -0.9225   -3.1900 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6040   -1.3081   -1.2484 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2382   -0.7720   -2.8865 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6827   -2.5605   -3.8220 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2110   -3.2224   -2.9648 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2193   -4.7811   -0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7171    1.1141    0.2372 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  6
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 17 26  1  0
 26 27  2  0
 27 28  1  0
 27 29  1  0
 29 30  2  0
 29 15  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  5 38  1  6
  6 39  1  0
  6 40  1  0
  6 41  1  0
  7 42  1  0
  7 43  1  0
  8 44  1  6
  9 45  1  0
  9 46  1  0
  9 47  1  0
 10 48  1  0
 11 49  1  0
 14 50  1  0
 16 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 20 55  1  0
 20 56  1  0
 21 57  1  0
 21 58  1  0
 22 59  1  0
 22 60  1  0
 25 61  1  0
 26 62  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      -7.805  -0.587   0.851  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.830   0.252   0.047  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.366   1.291  -0.832  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.545  -0.078   0.207  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.419   0.603  -0.470  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.729  -0.377  -1.421  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.442   1.184   0.498  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.647   0.318   1.370  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.321  -0.614   2.303  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.740   1.236   2.228  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.466   1.229   1.960  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.814   1.238   1.708  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.750   1.964   2.348  0.00  0.00           O+0
HETATM   14  N   UNK     0       1.482   0.470   0.681  0.00  0.00           N+0
HETATM   15  C   UNK     0       2.900   0.652   0.537  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.401   1.114  -0.560  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.814   1.355  -0.806  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.952   2.792  -0.845  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.327   0.841  -2.070  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.356  -0.610  -2.323  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.006  -1.270  -2.291  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.180  -2.698  -2.787  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.093  -3.462  -1.976  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.330  -3.112  -1.981  0.00  0.00           O+0
HETATM   25  O   UNK     0       4.727  -4.529  -1.213  0.00  0.00           O+0
HETATM   26  C   UNK     0       5.661   0.958   0.372  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.217   0.480   1.489  0.00  0.00           C+0
HETATM   28 Cl   UNK     0       6.255   0.044   2.813  0.00  0.00          Cl+0
HETATM   29  C   UNK     0       3.722   0.291   1.650  0.00  0.00           C+0
HETATM   30  O   UNK     0       3.334  -0.173   2.743  0.00  0.00           O+0
HETATM   31  H   UNK     0      -8.773  -0.567   0.340  0.00  0.00           H+0
HETATM   32  H   UNK     0      -7.444  -1.617   0.931  0.00  0.00           H+0
HETATM   33  H   UNK     0      -7.957  -0.121   1.857  0.00  0.00           H+0
HETATM   34  H   UNK     0      -6.705   1.570  -1.678  0.00  0.00           H+0
HETATM   35  H   UNK     0      -7.624   2.251  -0.293  0.00  0.00           H+0
HETATM   36  H   UNK     0      -8.377   0.967  -1.230  0.00  0.00           H+0
HETATM   37  H   UNK     0      -5.327  -0.905   0.864  0.00  0.00           H+0
HETATM   38  H   UNK     0      -4.814   1.411  -1.099  0.00  0.00           H+0
HETATM   39  H   UNK     0      -2.911  -0.943  -0.933  0.00  0.00           H+0
HETATM   40  H   UNK     0      -4.456  -1.122  -1.805  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.313   0.173  -2.276  0.00  0.00           H+0
HETATM   42  H   UNK     0      -4.083   1.876   1.154  0.00  0.00           H+0
HETATM   43  H   UNK     0      -2.793   1.939  -0.048  0.00  0.00           H+0
HETATM   44  H   UNK     0      -1.903  -0.282   0.711  0.00  0.00           H+0
HETATM   45  H   UNK     0      -3.496  -1.570   1.721  0.00  0.00           H+0
HETATM   46  H   UNK     0      -4.187  -0.227   2.814  0.00  0.00           H+0
HETATM   47  H   UNK     0      -2.597  -0.999   3.097  0.00  0.00           H+0
HETATM   48  H   UNK     0      -2.302   1.745   2.971  0.00  0.00           H+0
HETATM   49  H   UNK     0      -0.332   2.202   3.011  0.00  0.00           H+0
HETATM   50  H   UNK     0       0.981  -0.151   0.066  0.00  0.00           H+0
HETATM   51  H   UNK     0       2.709   1.322  -1.374  0.00  0.00           H+0
HETATM   52  H   UNK     0       4.120   3.186  -0.475  0.00  0.00           H+0
HETATM   53  H   UNK     0       6.332   1.325  -2.316  0.00  0.00           H+0
HETATM   54  H   UNK     0       4.693   1.277  -2.949  0.00  0.00           H+0
HETATM   55  H   UNK     0       5.921  -1.092  -1.422  0.00  0.00           H+0
HETATM   56  H   UNK     0       5.954  -0.923  -3.190  0.00  0.00           H+0
HETATM   57  H   UNK     0       3.604  -1.308  -1.248  0.00  0.00           H+0
HETATM   58  H   UNK     0       3.238  -0.772  -2.886  0.00  0.00           H+0
HETATM   59  H   UNK     0       4.683  -2.561  -3.822  0.00  0.00           H+0
HETATM   60  H   UNK     0       3.211  -3.222  -2.965  0.00  0.00           H+0
HETATM   61  H   UNK     0       5.219  -4.781  -0.339  0.00  0.00           H+0
HETATM   62  H   UNK     0       6.717   1.114   0.237  0.00  0.00           H+0
CONECT    1    2   31   32   33                                             
CONECT    2    1    3    4                                                  
CONECT    3    2   34   35   36                                             
CONECT    4    2    5   37                                                  
CONECT    5    4    6    7   38                                             
CONECT    6    5   39   40   41                                             
CONECT    7    5    8   42   43                                             
CONECT    8    7    9   10   44                                             
CONECT    9    8   45   46   47                                             
CONECT   10    8   11   48                                                  
CONECT   11   10   12   49                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   50                                                  
CONECT   15   14   16   29                                                  
CONECT   16   15   17   51                                                  
CONECT   17   16   18   19   26                                             
CONECT   18   17   52                                                       
CONECT   19   17   20   53   54                                             
CONECT   20   19   21   55   56                                             
CONECT   21   20   22   57   58                                             
CONECT   22   21   23   59   60                                             
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   61                                                       
CONECT   26   17   27   62                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   15                                                  
CONECT   30   29                                                            
CONECT   31    1                                                            
CONECT   32    1                                                            
CONECT   33    1                                                            
CONECT   34    3                                                            
CONECT   35    3                                                            
CONECT   36    3                                                            
CONECT   37    4                                                            
CONECT   38    5                                                            
CONECT   39    6                                                            
CONECT   40    6                                                            
CONECT   41    6                                                            
CONECT   42    7                                                            
CONECT   43    7                                                            
CONECT   44    8                                                            
CONECT   45    9                                                            
CONECT   46    9                                                            
CONECT   47    9                                                            
CONECT   48   10                                                            
CONECT   49   11                                                            
CONECT   50   14                                                            
CONECT   51   16                                                            
CONECT   52   18                                                            
CONECT   53   19                                                            
CONECT   54   19                                                            
CONECT   55   20                                                            
CONECT   56   20                                                            
CONECT   57   21                                                            
CONECT   58   21                                                            
CONECT   59   22                                                            
CONECT   60   22                                                            
CONECT   61   25                                                            
CONECT   62   26                                                            
MASTER        0    0    0    0    0    0    0    0   62    0  124    0
END

RDKit          3D

62 62  0  0  0  0  0  0  0  0999 V2000
   -7.8047   -0.5872    0.8512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8297    0.2522    0.0467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3659    1.2910   -0.8320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5455   -0.0777    0.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4193    0.6026   -0.4702 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7288   -0.3765   -1.4209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4423    1.1835    0.4984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6467    0.3180    1.3698 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3205   -0.6135    2.3030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7395    1.2361    2.2280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4655    1.2289    1.9596 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8136    1.2376    1.7081 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7498    1.9635    2.3479 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4823    0.4702    0.6809 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8996    0.6515    0.5369 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4006    1.1139   -0.5604 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8136    1.3547   -0.8064 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9516    2.7920   -0.8451 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3270    0.8410   -2.0698 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3565   -0.6095   -2.3229 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0061   -1.2698   -2.2909 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1800   -2.6976   -2.7868 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0928   -3.4621   -1.9763 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3305   -3.1116   -1.9814 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7269   -4.5291   -1.2133 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6610    0.9575    0.3720 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2174    0.4800    1.4889 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2546    0.0442    2.8133 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.7224    0.2910    1.6498 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3343   -0.1732    2.7425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7730   -0.5666    0.3400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4444   -1.6168    0.9307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9571   -0.1211    1.8565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7045    1.5702   -1.6781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6243    2.2512   -0.2932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3767    0.9666   -1.2305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3269   -0.9045    0.8635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8145    1.4114   -1.0995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9107   -0.9430   -0.9325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4564   -1.1216   -1.8051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3133    0.1729   -2.2758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0828    1.8757    1.1537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7929    1.9392   -0.0476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9034   -0.2818    0.7106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4960   -1.5701    1.7212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1868   -0.2266    2.8140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5966   -0.9993    3.0967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3023    1.7446    2.9712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3320    2.2023    3.0109 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9809   -0.1512    0.0660 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7086    1.3220   -1.3738 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1201    3.1864   -0.4754 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3317    1.3250   -2.3162 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6933    1.2773   -2.9491 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9213   -1.0917   -1.4216 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9543   -0.9225   -3.1900 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6040   -1.3081   -1.2484 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2382   -0.7720   -2.8865 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6827   -2.5605   -3.8220 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2110   -3.2224   -2.9648 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2193   -4.7811   -0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7171    1.1141    0.2372 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  6
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 17 26  1  0
 26 27  2  0
 27 28  1  0
 27 29  1  0
 29 30  2  0
 29 15  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  5 38  1  6
  6 39  1  0
  6 40  1  0
  6 41  1  0
  7 42  1  0
  7 43  1  0
  8 44  1  6
  9 45  1  0
  9 46  1  0
  9 47  1  0
 10 48  1  0
 11 49  1  0
 14 50  1  0
 16 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 20 55  1  0
 20 56  1  0
 21 57  1  0
 21 58  1  0
 22 59  1  0
 22 60  1  0
 25 61  1  0
 26 62  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
5-[(1R)-3-Chloro-1-hydroxy-5-{[(4S,6R)-1-hydroxy-4,6,8-trimethylnona-2,7-dien-1-ylidene]amino}-4-oxocyclohexa-2,5-dien-1-yl]pentanoate	Generator

Chemical Formula

C₂₃H₃₂ClNO₅

Average Mass

437.9600 Da

Monoisotopic Mass

437.19690 Da

IUPAC Name

5-[(1R)-3-chloro-1-hydroxy-4-oxo-5-[(2E,4S,6R)-4,6,8-trimethylnona-2,7-dienamido]cyclohexa-2,5-dien-1-yl]pentanoic acid

Traditional Name

5-[(1R)-3-chloro-1-hydroxy-4-oxo-5-[(2E,4S,6R)-4,6,8-trimethylnona-2,7-dienamido]cyclohexa-2,5-dien-1-yl]pentanoic acid

CAS Registry Number

Not Available

SMILES

C[C@@H](C[C@@H](C)C=C(C)C)C=CC(=O)NC1=C[C@](O)(CCCCC(O)=O)C=C(Cl)C1=O

InChI Identifier

InChI=1S/C23H32ClNO5/c1-15(2)11-17(4)12-16(3)8-9-20(26)25-19-14-23(30,13-18(24)22(19)29)10-6-5-7-21(27)28/h8-9,11,13-14,16-17,30H,5-7,10,12H2,1-4H3,(H,25,26)(H,27,28)/t16-,17+,23+/m1/s1

InChI Key

TXGICURJQBELHX-DGGJZMOXSA-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	26610526

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	3.63	ALOGPS
logP	4.1	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	4.2	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	103.7 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	122.11 m³·mol⁻¹	ChemAxon
Polarizability	47.87 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA010978

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78439737

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139586147

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Bach DH, Kim SH, Hong JY, Park HJ, Oh DC, Lee SK: Salternamide A Suppresses Hypoxia-Induced Accumulation of HIF-1alpha and Induces Apoptosis in Human Colorectal Cancer Cells. Mar Drugs. 2015 Nov 19;13(11):6962-76. doi: 10.3390/md13116962. [PubMed:26610526 ]

Showing NP-Card for Salternamide A (NP0014924)

MOL for NP0014924 (Salternamide A)

3D MOL for NP0014924 (Salternamide A)

3D SDF for NP0014924 (Salternamide A)

3D-SDF for NP0014924 (Salternamide A)

PDB for NP0014924 (Salternamide A)

3D PDB for NP0014924 (Salternamide A)

SMILES for NP0014924 (Salternamide A)

INCHI for NP0014924 (Salternamide A)

Structure for NP0014924 (Salternamide A)

3D Structure for NP0014924 (Salternamide A)