NP-MRD: Showing NP-Card for (4s,10s,13s,16s,19s,22r)-10-[(2s)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1r)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0⁴,⁸]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one (NP0145727)

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Record Information

Version

2.0

Created at

2022-09-02 00:58:49 UTC

Updated at

2022-09-02 00:58:49 UTC

NP-MRD ID

NP0145727

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4s,10s,13s,16s,19s,22r)-10-[(2s)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1r)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0⁴,⁸]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one

Description

Talaromin A belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds. (4s,10s,13s,16s,19s,22r)-10-[(2s)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1r)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0⁴,⁸]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one is found in Talaromyces wortmannii. Based on a literature review very few articles have been published on Talaromin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022202582D          

 55 58  0  0  1  0            999 V2000
    4.8462   -0.2882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6583   -0.4334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1901    0.1973    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9098    0.9732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0022    0.0521    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5341    0.6828    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.2538    1.4587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4416    1.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7856    2.0894    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.5977    1.9442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5053    2.8653    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.0371    3.4960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7568    4.2719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8492    3.3508    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.5689    4.1267    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.9973    4.7216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1007    4.7574    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3810    3.9815    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.1932    3.8363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7250    4.4670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4735    3.0604    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.2856    2.9152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8174    3.5459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5371    4.3218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0689    4.9525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8810    4.8073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4129    5.4380    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.1613    4.0314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6295    3.4007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9416    2.4297    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.2219    1.6537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0341    1.5085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6901    1.0230    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.5022    0.8778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7825    0.1019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3032    1.0755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9704    0.2471    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.4386   -0.3836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6265   -0.2384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   10.5310   -1.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8113   -2.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2795   -2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4674   -2.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1871   -1.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3750   -1.6450    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.8431   -2.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1234   -3.0516    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0310   -2.1305    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3797   -2.6369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6968   -2.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9262   -1.3814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7507   -1.3546    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.2825   -0.7239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0947   -0.8691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  4  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  4  0  0  0
 12 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 15 17  1  1  0  0  0
 14 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  4  0  0  0
 19 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 23 29  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  4  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 33 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  4  0  0  0
 38 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 40 45  1  0  0  0  0
 46 45  1  4  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 47 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
 52 53  1  0  0  0  0
 49 53  1  6  0  0  0
 53 54  1  0  0  0  0
  5 54  1  0  0  0  0
 54 55  2  0  0  0  0
M  END

     RDKit          3D

108111  0  0  0  0  0  0  0  0999 V2000
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 48101  1  0
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 36 95  1  0
 15 73  1  6
 16 74  1  0
 16 75  1  0
 16 76  1  0
 17 77  1  0
M  END


  Mrv1652309022202582D          

 55 58  0  0  1  0            999 V2000
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    6.4416    1.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   12.6295    3.4007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   10.2219    1.6537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0341    1.5085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6901    1.0230    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.5022    0.8778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7825    0.1019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3032    1.0755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9704    0.2471    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.4386   -0.3836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6265   -0.2384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7189   -1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5310   -1.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.4674   -2.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1871   -1.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.8431   -2.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.2825   -0.7239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0947   -0.8691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  4  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
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 15 17  1  1  0  0  0
 14 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  4  0  0  0
 19 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 23 29  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  4  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 33 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  4  0  0  0
 38 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 40 45  1  0  0  0  0
 46 45  1  4  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 47 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
 52 53  1  0  0  0  0
 49 53  1  6  0  0  0
 53 54  1  0  0  0  0
  5 54  1  0  0  0  0
 54 55  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0145727

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)[C@@H]1N=C(O)[C@H](C)N=C(O)[C@@H](N=C(O)[C@H](CC2=CC=C(O)C=C2)N=C(O)[C@H](N=C(O)C2=CC=CC=C2N=C(O)[C@@H]2CCCN2C1=O)C(C)C)[C@@H](C)O

> <INCHI_IDENTIFIER>
InChI=1S/C39H53N7O9/c1-7-21(4)31-39(55)46-18-10-13-29(46)36(52)41-27-12-9-8-11-26(27)34(50)43-30(20(2)3)37(53)42-28(19-24-14-16-25(48)17-15-24)35(51)45-32(23(6)47)38(54)40-22(5)33(49)44-31/h8-9,11-12,14-17,20-23,28-32,47-48H,7,10,13,18-19H2,1-6H3,(H,40,54)(H,41,52)(H,42,53)(H,43,50)(H,44,49)(H,45,51)/t21-,22-,23+,28-,29-,30+,31-,32-/m0/s1

> <INCHI_KEY>
XBWQUDIMYZXYAF-VBQPTGGPSA-N

> <FORMULA>
C39H53N7O9

> <MOLECULAR_WEIGHT>
763.893

> <EXACT_MASS>
763.390476315

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_ATOM_COUNT>
108

> <JCHEM_AVERAGE_POLARIZABILITY>
78.16791075445174

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4S,10S,13S,16S,19S,22R)-10-[(2S)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1R)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-13-methyl-22-(propan-2-yl)-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0^{4,8}]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one

> <ALOGPS_LOGP>
2.89

> <JCHEM_LOGP>
5.725803988567547

> <ALOGPS_LOGS>
-4.22

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
3.3795280951877915

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.8851526599525203

> <JCHEM_PKA_STRONGEST_BASIC>
1.5310658884506747

> <JCHEM_POLAR_SURFACE_AREA>
256.30999999999995

> <JCHEM_REFRACTIVITY>
205.52520000000013

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.56e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4S,10S,13S,16S,19S,22R)-10-[(2S)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1R)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0^{4,8}]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       9.046  -0.538   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.562  -0.809   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.555   0.368   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.032   1.817   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.071   0.097   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      14.064   1.274   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      13.540   2.723   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      12.024   2.994   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      14.533   3.900   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      16.049   3.629   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      14.010   5.349   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      15.003   6.526   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      14.479   7.974   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      16.519   6.255   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.995   7.703   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.928   8.814   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      16.988   8.881   0.000  0.00  0.00           O+0
HETATM   18  N   UNK     0      17.511   7.432   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0      19.027   7.161   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      20.020   8.338   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      19.550   5.713   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      21.066   5.442   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      22.059   6.619   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      21.536   8.067   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      22.529   9.245   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      24.045   8.974   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      25.037  10.151   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      24.568   7.525   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      23.575   6.348   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0      18.558   4.535   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0      19.081   3.087   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      20.597   2.816   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      18.088   1.910   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      19.604   1.639   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      20.127   0.190   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      21.099   2.008   0.000  0.00  0.00           C+0
HETATM   37  N   UNK     0      18.611   0.461   0.000  0.00  0.00           N+0
HETATM   38  C   UNK     0      17.619  -0.716   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      16.103  -0.445   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      18.142  -2.164   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      19.658  -2.436   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      20.181  -3.884   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      19.188  -5.061   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      17.672  -4.790   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      17.149  -3.342   0.000  0.00  0.00           C+0
HETATM   46  N   UNK     0      15.633  -3.071   0.000  0.00  0.00           N+0
HETATM   47  C   UNK     0      14.641  -4.248   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      15.164  -5.696   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      13.125  -3.977   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      11.909  -4.922   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      10.634  -4.058   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      11.062  -2.579   0.000  0.00  0.00           C+0
HETATM   53  N   UNK     0      12.601  -2.529   0.000  0.00  0.00           N+0
HETATM   54  C   UNK     0      13.594  -1.351   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0      15.110  -1.622   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   54                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   18                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   14   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   30                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   29                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   23                                                       
CONECT   30   21   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   37                                                  
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   33   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   45                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   40   46                                                  
CONECT   46   45   47                                                       
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   50   53                                                  
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   49   54                                                  
CONECT   54   53    5   55                                                  
CONECT   55   54                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  116    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₉H₅₃N₇O₉

Average Mass

763.8930 Da

Monoisotopic Mass

763.39048 Da

IUPAC Name

(4S,10S,13S,16S,19S,22R)-10-[(2S)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1R)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-13-methyl-22-(propan-2-yl)-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0^{4,8}]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one

Traditional Name

(4S,10S,13S,16S,19S,22R)-10-[(2S)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1R)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0^{4,8}]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one

CAS Registry Number

Not Available

SMILES

CC[C@H](C)[C@@H]1N=C(O)[C@H](C)N=C(O)[C@@H](N=C(O)[C@H](CC2=CC=C(O)C=C2)N=C(O)[C@H](N=C(O)C2=CC=CC=C2N=C(O)[C@@H]2CCCN2C1=O)C(C)C)[C@@H](C)O

InChI Identifier

InChI=1S/C39H53N7O9/c1-7-21(4)31-39(55)46-18-10-13-29(46)36(52)41-27-12-9-8-11-26(27)34(50)43-30(20(2)3)37(53)42-28(19-24-14-16-25(48)17-15-24)35(51)45-32(23(6)47)38(54)40-22(5)33(49)44-31/h8-9,11-12,14-17,20-23,28-32,47-48H,7,10,13,18-19H2,1-6H3,(H,40,54)(H,41,52)(H,42,53)(H,43,50)(H,44,49)(H,45,51)/t21-,22-,23+,28-,29-,30+,31-,32-/m0/s1

InChI Key

XBWQUDIMYZXYAF-VBQPTGGPSA-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

Species Name	Source	Reference
Talaromyces wortmannii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Cyclic alpha peptide
Macrolactam
Alpha-amino acid or derivatives
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Pyrrolidine
Tertiary carboxylic acid amide
Vinylogous amide
Carboxamide group
Lactam
Secondary alcohol
Secondary carboxylic acid amide
Azacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic nitrogen compound
Organopnictogen compound
Alcohol
Carbonyl group
Organic oxygen compound
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	2.89	ALOGPS
logP	5.73	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	2.89	ChemAxon
pKa (Strongest Basic)	1.53	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	256.31 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	205.53 m³·mol⁻¹	ChemAxon
Polarizability	78.17 Å³	ChemAxon
Number of Rings	4	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

78437735

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71600231

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4s,10s,13s,16s,19s,22r)-10-[(2s)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1r)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0⁴,⁸]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one (NP0145727)

MOL for NP0145727 ((4s,10s,13s,16s,19s,22r)-10-[(2s)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1r)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0⁴,⁸]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one)

3D MOL for NP0145727 ((4s,10s,13s,16s,19s,22r)-10-[(2s)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1r)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0⁴,⁸]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one)

3D SDF for NP0145727 ((4s,10s,13s,16s,19s,22r)-10-[(2s)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1r)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0⁴,⁸]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one)

3D-SDF for NP0145727 ((4s,10s,13s,16s,19s,22r)-10-[(2s)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1r)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0⁴,⁸]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one)

PDB for NP0145727 ((4s,10s,13s,16s,19s,22r)-10-[(2s)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1r)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0⁴,⁸]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one)

3D PDB for NP0145727 ((4s,10s,13s,16s,19s,22r)-10-[(2s)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1r)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0⁴,⁸]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one)

SMILES for NP0145727 ((4s,10s,13s,16s,19s,22r)-10-[(2s)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1r)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0⁴,⁸]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one)

INCHI for NP0145727 ((4s,10s,13s,16s,19s,22r)-10-[(2s)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1r)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0⁴,⁸]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one)

Structure for NP0145727 ((4s,10s,13s,16s,19s,22r)-10-[(2s)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1r)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0⁴,⁸]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one)

3D Structure for NP0145727 ((4s,10s,13s,16s,19s,22r)-10-[(2s)-butan-2-yl]-3,12,15,18,21,24-hexahydroxy-16-[(1r)-1-hydroxyethyl]-19-[(4-hydroxyphenyl)methyl]-22-isopropyl-13-methyl-2,8,11,14,17,20,23-heptaazatricyclo[23.4.0.0⁴,⁸]nonacosa-1(29),2,11,14,17,20,23,25,27-nonaen-9-one)