NP-MRD: Showing NP-Card for K-252b (NP0021232)

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Record Information

Version

2.0

Created at

2021-01-06 06:30:32 UTC

Updated at

2021-07-15 17:35:48 UTC

NP-MRD ID

NP0021232

Secondary Accession Numbers

None

Natural Product Identification

Common Name

K-252b

Provided By

NPAtlas

Description

K-252b is found in Nocardiopsis and Nocardiopsis sp. K-290. Based on a literature review very few articles have been published on (15S,16R,18R)-3,16-dihydroxy-15-methyl-28-oxa-4,14,19-triazaoctacyclo[12.11.2.1¹⁵,¹⁸.0²,⁶.0⁷,²⁷.0⁸,¹³.0¹⁹,²⁶.0²⁰,²⁵]Octacosa-1,3,6,8,10,12,20,22,24,26-decaene-16-carboxylic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242120413D          

 53 60  0  0  0  0            999 V2000
   -3.0983   -1.1802   -1.6207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9207   -1.0939   -0.7185 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9090   -1.7307   -1.4890 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0715   -2.4133   -0.6314 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7852   -2.7250    0.6306 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0466   -1.8944    0.5444 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0120   -1.0021    1.6195 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2002   -2.7812    0.6025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3719   -3.6428   -0.2966 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1709   -2.7711    1.5923 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0793   -1.5358   -0.3557 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3483   -1.8944   -0.2224 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0768   -2.1509    0.1273 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5080   -0.8919    0.2027 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1520   -0.7775    0.0273 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2915    0.2944    0.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4423    1.6588    0.2355 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2893    2.4563    0.1802 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0398    1.9086   -0.0617 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5919    2.5021    0.5012 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7989    2.2155    0.6295 O   0  0  0  0  0  0  0  0  0  0  0  0
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  2  1  1  6  0  0  0
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M  END

     RDKit          3D

 53 60  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652306242120413D          

 53 60  0  0  0  0            999 V2000
   -3.0983   -1.1802   -1.6207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9207   -1.0939   -0.7185 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -0.1879   -2.5090    1.5316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0247   -3.8094    0.6427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3913   -1.3036    2.3402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0124   -2.1749    2.4042 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3246   -3.9944   -0.4841 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7346   -4.2670   -0.1809 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1491   -2.2401    0.2661 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1613   -0.0667    0.3955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9236    4.4968    0.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3784    5.0199   -0.0641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9720    3.1322   -0.5109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1764    0.8527   -0.7090 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2177    4.2995    1.3100 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4644    4.4189   -0.5116 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7282    4.6762    0.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  4 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 20 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
  6  2  1  0  0  0  0
 30 11  1  0  0  0  0
 28  2  1  0  0  0  0
 17 12  1  0  0  0  0
 30 18  1  0  0  0  0
 33 19  1  0  0  0  0
 29 21  1  0  0  0  0
 27 22  1  0  0  0  0
  1 35  1  0  0  0  0
  1 36  1  0  0  0  0
  1 37  1  0  0  0  0
  4 38  1  6  0  0  0
  5 39  1  0  0  0  0
  5 40  1  0  0  0  0
  7 41  1  0  0  0  0
 10 42  1  0  0  0  0
 13 43  1  0  0  0  0
 14 44  1  0  0  0  0
 15 45  1  0  0  0  0
 16 46  1  0  0  0  0
 23 47  1  0  0  0  0
 24 48  1  0  0  0  0
 25 49  1  0  0  0  0
 26 50  1  0  0  0  0
 31 51  1  0  0  0  0
 31 52  1  0  0  0  0
 32 53  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0021232

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)[C@@]1(O[H])C([H])([H])[C@@]2([H])O[C@@]1(N1C3=C([H])C([H])=C([H])C([H])=C3C3=C4C(C(=O)N([H])C4([H])[H])=C4C5=C([H])C([H])=C([H])C([H])=C5N2C4=C13)C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C26H19N3O5/c1-25-26(33,24(31)32)10-17(34-25)28-15-8-4-2-6-12(15)19-20-14(11-27-23(20)30)18-13-7-3-5-9-16(13)29(25)22(18)21(19)28/h2-9,17,33H,10-11H2,1H3,(H,27,30)(H,31,32)/t17-,25+,26+/m1/s1

> <INCHI_KEY>
AMSOPBXQXSAAAC-PLZPTFKGSA-N

> <FORMULA>
C26H19N3O5

> <MOLECULAR_WEIGHT>
453.454

> <EXACT_MASS>
453.132470724

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
47.007208684495964

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(15S,16R,18R)-16-hydroxy-15-methyl-3-oxo-28-oxa-4,14,19-triazaoctacyclo[12.11.2.1^{15,18}.0^{2,6}.0^{7,27}.0^{8,13}.0^{19,26}.0^{20,25}]octacosa-1,6,8,10,12,20,22,24,26-nonaene-16-carboxylic acid

> <ALOGPS_LOGP>
2.11

> <JCHEM_LOGP>
3.337313462999999

> <ALOGPS_LOGS>
-3.74

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.197810370296056

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.8674484859666043

> <JCHEM_PKA_STRONGEST_BASIC>
-1.4854378245477888

> <JCHEM_POLAR_SURFACE_AREA>
105.72

> <JCHEM_REFRACTIVITY>
121.35069999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.23e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(15S,16R,18R)-16-hydroxy-15-methyl-3-oxo-28-oxa-4,14,19-triazaoctacyclo[12.11.2.1^{15,18}.0^{2,6}.0^{7,27}.0^{8,13}.0^{19,26}.0^{20,25}]octacosa-1,6,8,10,12,20,22,24,26-nonaene-16-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 53 60  0  0  0  0  0  0  0  0999 V2000
   -3.0983   -1.1802   -1.6207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9207   -1.0939   -0.7185 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9090   -1.7307   -1.4890 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0715   -2.4133   -0.6314 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7852   -2.7250    0.6306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0466   -1.8944    0.5444 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0120   -1.0021    1.6195 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2002   -2.7812    0.6025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3719   -3.6428   -0.2966 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1709   -2.7711    1.5923 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0793   -1.5358   -0.3557 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3483   -1.8944   -0.2224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9546   -3.1416   -0.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3144   -3.2750   -0.1176 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0768   -2.1509    0.1273 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5080   -0.8919    0.2027 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1520   -0.7775    0.0273 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2915    0.2944    0.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4423    1.6588    0.2355 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2893    2.4563    0.1802 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0398    1.9086   -0.0617 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2201    2.4385   -0.1525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6657    3.7381   -0.0305 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0152    3.9924   -0.1589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9010    2.9615   -0.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4761    1.6514   -0.5306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1333    1.3982   -0.4038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4204    0.2473   -0.4658 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1108    0.5843   -0.2538 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0109   -0.2068   -0.2016 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6773    3.8442    0.4123 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0975    3.8489    0.6066 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5919    2.5021    0.5012 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7989    2.2155    0.6295 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0735   -1.3726   -1.1447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9844   -2.1122   -2.2827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0918   -0.3645   -2.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2926   -3.3137   -1.1608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1879   -2.5090    1.5316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0247   -3.8094    0.6427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3913   -1.3036    2.3402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0124   -2.1749    2.4042 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3246   -3.9944   -0.4841 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7346   -4.2670   -0.1809 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1491   -2.2401    0.2661 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1613   -0.0667    0.3955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9236    4.4968    0.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3784    5.0199   -0.0641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9720    3.1322   -0.5109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1764    0.8527   -0.7090 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2177    4.2995    1.3100 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4644    4.4189   -0.5116 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7282    4.6762    0.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  2  0
  8 10  1  0
  4 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  1  0
 29 30  2  0
 20 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  2  0
  6  2  1  0
 30 11  1  0
 28  2  1  0
 17 12  1  0
 30 18  1  0
 33 19  1  0
 29 21  1  0
 27 22  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  4 38  1  6
  5 39  1  0
  5 40  1  0
  7 41  1  0
 10 42  1  0
 13 43  1  0
 14 44  1  0
 15 45  1  0
 16 46  1  0
 23 47  1  0
 24 48  1  0
 25 49  1  0
 26 50  1  0
 31 51  1  0
 31 52  1  0
 32 53  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      -3.098  -1.180  -1.621  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.921  -1.094  -0.719  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.909  -1.731  -1.489  0.00  0.00           O+0
HETATM    4  C   UNK     0      -0.072  -2.413  -0.631  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.785  -2.725   0.631  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.047  -1.894   0.544  0.00  0.00           C+0
HETATM    7  O   UNK     0      -2.012  -1.002   1.619  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.200  -2.781   0.603  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.372  -3.643  -0.297  0.00  0.00           O+0
HETATM   10  O   UNK     0      -4.171  -2.771   1.592  0.00  0.00           O+0
HETATM   11  N   UNK     0       1.079  -1.536  -0.356  0.00  0.00           N+0
HETATM   12  C   UNK     0       2.348  -1.894  -0.222  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.955  -3.142  -0.291  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.314  -3.275  -0.118  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.077  -2.151   0.127  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.508  -0.892   0.203  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.152  -0.778   0.027  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.292   0.294   0.039  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.442   1.659   0.236  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.289   2.456   0.180  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.040   1.909  -0.062  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.220   2.438  -0.153  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.666   3.738  -0.031  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.015   3.992  -0.159  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.901   2.962  -0.405  0.00  0.00           C+0
HETATM   26  C   UNK     0      -3.476   1.651  -0.531  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.133   1.398  -0.404  0.00  0.00           C+0
HETATM   28  N   UNK     0      -1.420   0.247  -0.466  0.00  0.00           N+0
HETATM   29  C   UNK     0      -0.111   0.584  -0.254  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.011  -0.207  -0.202  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.677   3.844   0.412  0.00  0.00           C+0
HETATM   32  N   UNK     0       3.098   3.849   0.607  0.00  0.00           N+0
HETATM   33  C   UNK     0       3.592   2.502   0.501  0.00  0.00           C+0
HETATM   34  O   UNK     0       4.799   2.216   0.630  0.00  0.00           O+0
HETATM   35  H   UNK     0      -4.074  -1.373  -1.145  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.984  -2.112  -2.283  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.092  -0.365  -2.346  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.293  -3.314  -1.161  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.188  -2.509   1.532  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.025  -3.809   0.643  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.391  -1.304   2.340  0.00  0.00           H+0
HETATM   42  H   UNK     0      -4.012  -2.175   2.404  0.00  0.00           H+0
HETATM   43  H   UNK     0       2.325  -3.994  -0.484  0.00  0.00           H+0
HETATM   44  H   UNK     0       4.735  -4.267  -0.181  0.00  0.00           H+0
HETATM   45  H   UNK     0       6.149  -2.240   0.266  0.00  0.00           H+0
HETATM   46  H   UNK     0       5.161  -0.067   0.396  0.00  0.00           H+0
HETATM   47  H   UNK     0      -0.924   4.497   0.162  0.00  0.00           H+0
HETATM   48  H   UNK     0      -3.378   5.020  -0.064  0.00  0.00           H+0
HETATM   49  H   UNK     0      -4.972   3.132  -0.511  0.00  0.00           H+0
HETATM   50  H   UNK     0      -4.176   0.853  -0.709  0.00  0.00           H+0
HETATM   51  H   UNK     0       1.218   4.300   1.310  0.00  0.00           H+0
HETATM   52  H   UNK     0       1.464   4.419  -0.512  0.00  0.00           H+0
HETATM   53  H   UNK     0       3.728   4.676   0.799  0.00  0.00           H+0
CONECT    1    2   35   36   37                                             
CONECT    2    1    3    6   28                                             
CONECT    3    2    4                                                       
CONECT    4    3    5   11   38                                             
CONECT    5    4    6   39   40                                             
CONECT    6    5    7    8    2                                             
CONECT    7    6   41                                                       
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   42                                                       
CONECT   11    4   12   30                                                  
CONECT   12   11   13   17                                                  
CONECT   13   12   14   43                                                  
CONECT   14   13   15   44                                                  
CONECT   15   14   16   45                                                  
CONECT   16   15   17   46                                                  
CONECT   17   16   18   12                                                  
CONECT   18   17   19   30                                                  
CONECT   19   18   20   33                                                  
CONECT   20   19   21   31                                                  
CONECT   21   20   22   29                                                  
CONECT   22   21   23   27                                                  
CONECT   23   22   24   47                                                  
CONECT   24   23   25   48                                                  
CONECT   25   24   26   49                                                  
CONECT   26   25   27   50                                                  
CONECT   27   26   28   22                                                  
CONECT   28   27   29    2                                                  
CONECT   29   28   30   21                                                  
CONECT   30   29   11   18                                                  
CONECT   31   20   32   51   52                                             
CONECT   32   31   33   53                                                  
CONECT   33   32   34   19                                                  
CONECT   34   33                                                            
CONECT   35    1                                                            
CONECT   36    1                                                            
CONECT   37    1                                                            
CONECT   38    4                                                            
CONECT   39    5                                                            
CONECT   40    5                                                            
CONECT   41    7                                                            
CONECT   42   10                                                            
CONECT   43   13                                                            
CONECT   44   14                                                            
CONECT   45   15                                                            
CONECT   46   16                                                            
CONECT   47   23                                                            
CONECT   48   24                                                            
CONECT   49   25                                                            
CONECT   50   26                                                            
CONECT   51   31                                                            
CONECT   52   31                                                            
CONECT   53   32                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  120    0
END

RDKit          3D

53 60  0  0  0  0  0  0  0  0999 V2000
   -3.0983   -1.1802   -1.6207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9207   -1.0939   -0.7185 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9090   -1.7307   -1.4890 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0715   -2.4133   -0.6314 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7852   -2.7250    0.6306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0466   -1.8944    0.5444 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0120   -1.0021    1.6195 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2002   -2.7812    0.6025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3719   -3.6428   -0.2966 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1709   -2.7711    1.5923 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0793   -1.5358   -0.3557 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3483   -1.8944   -0.2224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9546   -3.1416   -0.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3144   -3.2750   -0.1176 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0768   -2.1509    0.1273 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5080   -0.8919    0.2027 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1520   -0.7775    0.0273 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2915    0.2944    0.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4423    1.6588    0.2355 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2893    2.4563    0.1802 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0398    1.9086   -0.0617 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2201    2.4385   -0.1525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6657    3.7381   -0.0305 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0152    3.9924   -0.1589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9010    2.9615   -0.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4761    1.6514   -0.5306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1333    1.3982   -0.4038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4204    0.2473   -0.4658 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1108    0.5843   -0.2538 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0109   -0.2068   -0.2016 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6773    3.8442    0.4123 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0975    3.8489    0.6066 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5919    2.5021    0.5012 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7989    2.2155    0.6295 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0735   -1.3726   -1.1447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9844   -2.1122   -2.2827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0918   -0.3645   -2.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2926   -3.3137   -1.1608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1879   -2.5090    1.5316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0247   -3.8094    0.6427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3913   -1.3036    2.3402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0124   -2.1749    2.4042 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3246   -3.9944   -0.4841 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7346   -4.2670   -0.1809 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1491   -2.2401    0.2661 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1613   -0.0667    0.3955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9236    4.4968    0.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3784    5.0199   -0.0641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9720    3.1322   -0.5109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1764    0.8527   -0.7090 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2177    4.2995    1.3100 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4644    4.4189   -0.5116 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7282    4.6762    0.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  2  0
  8 10  1  0
  4 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  1  0
 29 30  2  0
 20 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  2  0
  6  2  1  0
 30 11  1  0
 28  2  1  0
 17 12  1  0
 30 18  1  0
 33 19  1  0
 29 21  1  0
 27 22  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  4 38  1  6
  5 39  1  0
  5 40  1  0
  7 41  1  0
 10 42  1  0
 13 43  1  0
 14 44  1  0
 15 45  1  0
 16 46  1  0
 23 47  1  0
 24 48  1  0
 25 49  1  0
 26 50  1  0
 31 51  1  0
 31 52  1  0
 32 53  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(15S,16R,18R)-3,16-Dihydroxy-15-methyl-28-oxa-4,14,19-triazaoctacyclo[12.11.2.1,.0,.0,.0,.0,.0,]octacosa-1,3,6,8,10,12,20,22,24,26-decaene-16-carboxylate	Generator
3'-(S)-Epi-K-252a	MeSH
Staurosporine aglycone	MeSH
Staurosporinone	MeSH

Chemical Formula

C₂₆H₁₉N₃O₅

Average Mass

453.4540 Da

Monoisotopic Mass

453.13247 Da

IUPAC Name

(15S,16R,18R)-16-hydroxy-15-methyl-3-oxo-28-oxa-4,14,19-triazaoctacyclo[12.11.2.1^{15,18}.0^{2,6}.0^{7,27}.0^{8,13}.0^{19,26}.0^{20,25}]octacosa-1,6,8,10,12,20,22,24,26-nonaene-16-carboxylic acid

Traditional Name

(15S,16R,18R)-16-hydroxy-15-methyl-3-oxo-28-oxa-4,14,19-triazaoctacyclo[12.11.2.1^{15,18}.0^{2,6}.0^{7,27}.0^{8,13}.0^{19,26}.0^{20,25}]octacosa-1,6,8,10,12,20,22,24,26-nonaene-16-carboxylic acid

CAS Registry Number

Not Available

SMILES

C[C@]12O[C@H](C[C@]1(O)C(O)=O)N1C3=CC=CC=C3C3=C4C(=O)NCC4=C4C5=CC=CC=C5N2C4=C13

InChI Identifier

InChI=1S/C26H19N3O5/c1-25-26(33,24(31)32)10-17(34-25)28-15-8-4-2-6-12(15)19-20-14(11-27-23(20)30)18-13-7-3-5-9-16(13)29(25)22(18)21(19)28/h2-9,17,33H,10-11H2,1H3,(H,27,30)(H,31,32)/t17-,25+,26+/m1/s1

InChI Key

AMSOPBXQXSAAAC-PLZPTFKGSA-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
Nocardiopsis	NPAtlas	3759659
Nocardiopsis sp. K-290	-	KNApSAcK

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	2.11	ALOGPS
logP	3.34	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	3.87	ChemAxon
pKa (Strongest Basic)	-1.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	105.72 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	121.35 m³·mol⁻¹	ChemAxon
Polarizability	47.01 Å³	ChemAxon
Number of Rings	8	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

NPA018253

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

8156936

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9981344

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for K-252b (NP0021232)

MOL for NP0021232 (K-252b)

3D MOL for NP0021232 (K-252b)

3D SDF for NP0021232 (K-252b)

3D-SDF for NP0021232 (K-252b)

PDB for NP0021232 (K-252b)

3D PDB for NP0021232 (K-252b)

SMILES for NP0021232 (K-252b)

INCHI for NP0021232 (K-252b)

Structure for NP0021232 (K-252b)

3D Structure for NP0021232 (K-252b)