NP-MRD: Showing NP-Card for n-[1-({[(8z,10z,16z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0²¹,²⁶]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid (NP0213969)

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Record Information

Version

2.0

Created at

2022-09-05 13:07:50 UTC

Updated at

2022-09-05 13:07:50 UTC

NP-MRD ID

NP0213969

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[1-({[(8z,10z,16z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0²¹,²⁶]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid

Description

N-[1-({[(8Z,10Z,16Z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0²¹,²⁶]Octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. N-acyl-alpha amino acids and derivatives are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom. Based on a literature review very few articles have been published on N-[1-({[(8Z,10Z,16Z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0²¹,²⁶]Octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052215072D          

 51 55  0  0  0  0            999 V2000
    9.1605    0.7906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8260    0.3031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7366   -0.5170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5343   -0.7277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2344   -1.1641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7748   -1.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1074   -2.5425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2027   -3.3619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0523   -4.1731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6694   -4.9039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0882   -5.4893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5805   -6.1514    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3999   -6.0560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7271   -5.2987    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8922   -6.7181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3257   -7.3178    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.5619   -8.1083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3646   -8.2990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9954   -8.7081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2316   -9.4985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6651  -10.0983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8625   -9.9076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6263   -9.1171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1928   -8.5174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6297   -6.3482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5812   -7.1718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3602   -5.8775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6354   -6.6552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5501   -6.0338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5839   -6.8581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7300   -5.9443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5193   -6.7420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9726   -5.6172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.9039   -4.3843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6875   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2234   -2.9609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0346   -3.1114    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9481   -2.1832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8764   -3.4377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4726   -1.3184    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.1346   -0.8261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7465   -0.0981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9123   -0.5509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  4  0  0  0
  4  5  2  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  1  0  0  0  0
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 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
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 17 19  1  0  0  0  0
 19 20  2  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  1  0  0  0  0
 19 24  1  0  0  0  0
 15 25  1  0  0  0  0
 25 26  1  0  0  0  0
 15 26  1  0  0  0  0
 11 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 36 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
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 45 47  2  0  0  0  0
 41 47  1  0  0  0  0
 48 39  1  4  0  0  0
 48 49  2  0  0  0  0
 49 50  1  0  0  0  0
 49 51  1  0  0  0  0
  3 51  1  0  0  0  0
M  END

     RDKit          3D

100104  0  0  0  0  0  0  0  0999 V2000
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  1  2  1  0
  2  3  1  0
  3 51  1  0
 51 49  1  0
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 29 83  1  1
 30 84  1  0
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 11 64  1  1
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 25 75  1  0
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 24 73  1  0
 24 74  1  0
 38 93  1  0
M  END


  Mrv1652309052215072D          

 51 55  0  0  0  0            999 V2000
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   10.5343   -0.7277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2344   -1.1641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7748   -1.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1074   -2.5425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2027   -3.3619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0523   -4.1731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6694   -4.9039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0882   -5.4893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5805   -6.1514    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3999   -6.0560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7271   -5.2987    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8922   -6.7181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3257   -7.3178    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.5619   -8.1083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3646   -8.2990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9954   -8.7081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2316   -9.4985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6651  -10.0983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8625   -9.9076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6263   -9.1171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1928   -8.5174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6297   -6.3482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5812   -7.1718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3602   -5.8775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6354   -6.6552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5501   -6.0338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5839   -6.8581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7300   -5.9443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5193   -6.7420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9726   -5.6172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3454   -5.0813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9039   -4.3843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6875   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2234   -2.9609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0346   -3.1114    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9481   -2.1832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1369   -2.0328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6011   -2.6600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8764   -3.4377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3405   -4.0650    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.5293   -3.9146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2540   -3.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4429   -2.9864    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7899   -2.5096    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4726   -1.3184    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.1346   -0.8261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7465   -0.0981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9123   -0.5509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  4  0  0  0
  4  5  2  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  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 16 15  1  4  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  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  1  0  0  0  0
 19 24  1  0  0  0  0
 15 25  1  0  0  0  0
 25 26  1  0  0  0  0
 15 26  1  0  0  0  0
 11 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 36 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  2  0  0  0  0
 41 47  1  0  0  0  0
 48 39  1  4  0  0  0
 48 49  2  0  0  0  0
 49 50  1  0  0  0  0
 49 51  1  0  0  0  0
  3 51  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0213969

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1CC(O)=NC2=CC3=C(SCC(O)=N3)C(CC\C=C(C)/C(O)C(C)C(C\C=C/C=C\C=C1)OC(=O)C1(CC1)N=C(O)C1=CCCCC1)=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C39H49N3O8S/c1-24-13-12-17-28-35(46)29(22-30-36(28)51-23-33(44)41-30)40-32(43)21-27(49-3)16-10-5-4-6-11-18-31(25(2)34(24)45)50-38(48)39(19-20-39)42-37(47)26-14-8-7-9-15-26/h4-6,10-11,13-14,16,22,25,27,31,34,45-46H,7-9,12,15,17-21,23H2,1-3H3,(H,40,43)(H,41,44)(H,42,47)/b5-4-,11-6-,16-10?,24-13-

> <INCHI_KEY>
YIMYDHUFVYSTEY-VCNTWYPCSA-N

> <FORMULA>
C39H49N3O8S

> <MOLECULAR_WEIGHT>
719.89

> <EXACT_MASS>
719.324036724

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
78.32395044378441

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-[1-({[(8Z,10Z,16Z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0^{21,26}]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid

> <JCHEM_LOGP>
7.7637962190000005

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.905447146807708

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.9723882865857716

> <JCHEM_PKA_STRONGEST_BASIC>
1.6054414540275779

> <JCHEM_POLAR_SURFACE_AREA>
173.76

> <JCHEM_REFRACTIVITY>
207.52610000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-[1-({[(8Z,10Z,16Z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0^{21,26}]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      17.100   1.476   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      18.342   0.566   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      18.175  -0.965   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      19.664  -1.358   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      20.971  -2.173   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      21.980  -3.337   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      22.601  -4.746   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      22.778  -6.276   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      22.498  -7.790   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      21.783  -9.154   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      20.698 -10.247   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      21.617 -11.483   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      23.147 -11.305   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      23.757  -9.891   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      24.065 -12.540   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      23.008 -13.660   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      23.449 -15.135   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      24.947 -15.491   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      22.391 -16.255   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      22.832 -17.731   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      21.775 -18.850   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      20.277 -18.494   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      19.836 -17.019   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      20.893 -15.899   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      25.442 -11.850   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      25.352 -13.387   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      19.339 -10.971   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      19.853 -12.423   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      17.827 -11.263   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      17.890 -12.802   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      16.296 -11.096   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      15.903 -12.585   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      14.882 -10.485   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      13.711  -9.485   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.887  -8.184   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      12.483  -6.698   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      13.484  -5.527   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      14.998  -5.808   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      12.970  -4.075   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      11.456  -3.795   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      10.455  -4.965   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      10.969  -6.417   0.000  0.00  0.00           C+0
HETATM   43  S   UNK     0       9.969  -7.588   0.000  0.00  0.00           S+0
HETATM   44  C   UNK     0       8.455  -7.307   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       7.941  -5.855   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       6.427  -5.575   0.000  0.00  0.00           O+0
HETATM   47  N   UNK     0       8.941  -4.685   0.000  0.00  0.00           N+0
HETATM   48  N   UNK     0      13.949  -2.461   0.000  0.00  0.00           N+0
HETATM   49  C   UNK     0      15.185  -1.542   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      14.460  -0.183   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      16.636  -1.028   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   51                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   27                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   25   26                                             
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19                                                       
CONECT   25   15   26                                                       
CONECT   26   25   15                                                       
CONECT   27   11   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   42                                                  
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   48                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   47                                                  
CONECT   42   41   36   43                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   41                                                       
CONECT   48   39   49                                                       
CONECT   49   48   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49    3                                                       
MASTER        0    0    0    0    0    0    0    0   51    0  110    0
END

View in JSmol

Synonyms

Value	Source
N-[1-({[(8Z,10Z,16Z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0,]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidate	Generator

Chemical Formula

C₃₉H₄₉N₃O₈S

Average Mass

719.8900 Da

Monoisotopic Mass

719.32404 Da

IUPAC Name

N-[1-({[(8Z,10Z,16Z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0^{21,26}]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1CC(O)=NC2=CC3=C(SCC(O)=N3)C(CC\C=C(C)/C(O)C(C)C(C\C=C/C=C\C=C1)OC(=O)C1(CC1)N=C(O)C1=CCCCC1)=C2O

InChI Identifier

InChI=1S/C39H49N3O8S/c1-24-13-12-17-28-35(46)29(22-30-36(28)51-23-33(44)41-30)40-32(43)21-27(49-3)16-10-5-4-6-11-18-31(25(2)34(24)45)50-38(48)39(19-20-39)42-37(47)26-14-8-7-9-15-26/h4-6,10-11,13-14,16,22,25,27,31,34,45-46H,7-9,12,15,17-21,23H2,1-3H3,(H,40,43)(H,41,44)(H,42,47)/b5-4-,11-6-,16-10?,24-13-

InChI Key

YIMYDHUFVYSTEY-VCNTWYPCSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. N-acyl-alpha amino acids and derivatives are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

N-acyl-alpha amino acids and derivatives

Alternative Parents

Substituents

N-acyl-alpha amino acid or derivatives
Benzothiazine
Aryl thioether
Alkylarylthioether
Benzenoid
Cyclopropanecarboxylic acid or derivatives
Para-thiazine
Cyclic carboximidic acid
Secondary alcohol
Carboxylic acid ester
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Thioether
Polyol
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboximidic acid derivative
Carboximidic acid
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	7.76	ChemAxon
pKa (Strongest Acidic)	3.97	ChemAxon
pKa (Strongest Basic)	1.61	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	173.76 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	207.53 m³·mol⁻¹	ChemAxon
Polarizability	78.32 Å³	ChemAxon
Number of Rings	5	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

139585991

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-[1-({[(8z,10z,16z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0²¹,²⁶]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid (NP0213969)

MOL for NP0213969 (n-[1-({[(8z,10z,16z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0²¹,²⁶]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid)

3D MOL for NP0213969 (n-[1-({[(8z,10z,16z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0²¹,²⁶]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid)

3D SDF for NP0213969 (n-[1-({[(8z,10z,16z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0²¹,²⁶]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid)

3D-SDF for NP0213969 (n-[1-({[(8z,10z,16z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0²¹,²⁶]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid)

PDB for NP0213969 (n-[1-({[(8z,10z,16z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0²¹,²⁶]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid)

3D PDB for NP0213969 (n-[1-({[(8z,10z,16z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0²¹,²⁶]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid)

SMILES for NP0213969 (n-[1-({[(8z,10z,16z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0²¹,²⁶]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid)

INCHI for NP0213969 (n-[1-({[(8z,10z,16z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0²¹,²⁶]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid)

Structure for NP0213969 (n-[1-({[(8z,10z,16z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0²¹,²⁶]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid)

3D Structure for NP0213969 (n-[1-({[(8z,10z,16z)-3,15,24,28-tetrahydroxy-5-methoxy-14,16-dimethyl-22-thia-2,25-diazatricyclo[18.7.1.0²¹,²⁶]octacosa-1(27),2,6,8,10,16,20(28),21(26),24-nonaen-13-yl]oxy}carbonyl)cyclopropyl]cyclohex-1-ene-1-carboximidic acid)