NP-MRD: Showing NP-Card for 5,16,22-trihydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,5,15,17,19,21-heptaen-4'-one (NP0200228)

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Record Information

Version

2.0

Created at

2022-09-04 19:01:30 UTC

Updated at

2022-09-04 19:01:30 UTC

NP-MRD ID

NP0200228

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,16,22-trihydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,5,15,17,19,21-heptaen-4'-one

Description

5,16,22-Trihydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]Tricosane-2,1'-cyclohexane]-1(22),3,5,15,17,19(23),20-heptaen-4'-one belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides. 5,16,22-Trihydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]Tricosane-2,1'-cyclohexane]-1(22),3,5,15,17,19(23),20-heptaen-4'-one is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004151519012D          

 32 34  0  0  0  0            999 V2000
    2.4552   -3.6828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2993   -2.8726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5198   -2.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3639   -1.7925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9875   -1.2524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8316   -0.4422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4552    0.0979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2993    0.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5198    1.1780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9230    1.4481    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7025    1.1780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8584    0.3679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6380    0.0979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7939   -0.7123    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5734   -0.9823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7294   -1.7925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5089   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6648   -2.8726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0412   -3.4127    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2616   -3.1427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6117   -2.3956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6380   -3.6828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8584   -3.4127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7025   -2.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5466   -1.7925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1702   -1.2524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9498   -1.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7718   -1.4520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1057   -2.3325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -2.8726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9230   -2.3325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7671   -1.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 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  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 22 20  1  4  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
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 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 24 30  1  0  0  0  0
 24 31  1  0  0  0  0
  2 31  1  0  0  0  0
 31 32  2  0  0  0  0
  5 32  1  0  0  0  0
M  END

     RDKit          3D

 65 67  0  0  0  0  0  0  0  0999 V2000
    3.1418   -2.1551    3.8548 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8717   -1.8052    2.7406 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5196   -2.3086    1.5025 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7162   -1.0639    0.5969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3550   -0.6194   -0.0060 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3213   -1.3118   -1.3268 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4395   -2.0874   -1.8695 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0106   -1.9904   -2.0869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4591   -2.0603   -3.3189 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0137   -1.8250   -1.1402 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3981   -2.7240   -0.0612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7276   -3.3832   -0.3423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7580   -2.9061    0.6299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2687   -1.5271    0.3304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9161   -0.5911    1.3968 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0142    0.7868    0.9746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6446    1.4242    0.9234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6253    2.7238    0.1838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0365    2.5520   -1.1216 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3868    3.5471   -1.8982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7314    3.5646   -3.1488 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4036    4.5158   -1.4337 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7725    4.2614   -0.8808 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6189    3.0759   -0.7585 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9719    3.4175   -1.0726 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0006    2.5382   -1.0453 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6798    1.2524   -0.6878 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7776    0.3853   -0.6832 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3659    0.8468   -0.3620 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3346    1.7702   -0.4025 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4056   -1.1069    1.0029 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8038   -0.7742    2.4320 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5702   -2.5853    1.7748 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0023   -3.1179    0.9905 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3752   -1.5033   -0.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1167   -0.3032    1.2428 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2849   -1.0485   -1.8562 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8636   -3.0469   -2.2755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6124   -0.9439   -1.1912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6079   -3.4607    0.1825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5261   -2.0945    0.8406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0039   -3.1061   -1.3991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6268   -4.4872   -0.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6315   -3.6167    0.5475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3734   -3.0262    1.6506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3952   -1.5098    0.2949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9353   -1.1358   -0.6386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4687   -0.7230    2.2510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6865    1.3241    1.6693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4862    0.8459   -0.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3868    1.6696    1.9960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8700    0.6987    0.6070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1084    3.5445    0.7277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6993    3.0645    0.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0948    1.5758   -1.5512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7461    5.5754   -1.6025 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1769    5.2397   -0.4331 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2498    4.4546   -1.3524 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0201    2.8250   -1.2908 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9665   -0.9653    3.1036 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2912    0.2035    2.5307 H   0  0  0  0  0  0  0  0  0  0  0  0
 28 27  1  0
 27 26  2  0
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  3  2  1  0
  2  1  2  0
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  7  8  1  0
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 12 13  1  0
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 15 16  1  0
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 17 18  1  0
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 20 21  2  0
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 22 23  2  0
 29 27  1  0
 31  5  1  0
 23 24  1  0
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 30 61  1  0
  4 35  1  0
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  3 33  1  0
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 32 64  1  0
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 31 62  1  0
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  6 37  1  0
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 11 40  1  0
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 16 50  1  0
 17 51  1  0
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 18 54  1  0
 19 55  1  0
 22 56  1  0
 23 57  1  0
M  END


  Mrv1533004151519012D          

 32 34  0  0  0  0            999 V2000
    2.4552   -3.6828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2993   -2.8726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5198   -2.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3639   -1.7925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9875   -1.2524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8316   -0.4422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4552    0.0979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2993    0.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5198    1.1780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9230    1.4481    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7025    1.1780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.6380    0.0979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.5089   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6648   -2.8726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0412   -3.4127    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2616   -3.1427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6117   -2.3956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6380   -3.6828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8584   -3.4127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7025   -2.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5466   -1.7925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9498   -1.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7718   -1.4520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1057   -2.3325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -2.8726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9230   -2.3325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7671   -1.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
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  2 31  1  0  0  0  0
 31 32  2  0  0  0  0
  5 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0200228

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C2C=C1C1(CCC(=O)CC1)C=CC(=O)NCCCCNCCCNC(=O)C=C2

> <INCHI_IDENTIFIER>
InChI=1S/C25H33N3O4/c29-20-8-11-25(12-9-20)13-10-24(32)27-16-2-1-14-26-15-3-17-28-23(31)7-5-19-4-6-22(30)21(25)18-19/h4-7,10,13,18,26,30H,1-3,8-9,11-12,14-17H2,(H,27,32)(H,28,31)

> <INCHI_KEY>
RXFSZEHSQXSBSX-UHFFFAOYSA-N

> <FORMULA>
C25H33N3O4

> <MOLECULAR_WEIGHT>
439.556

> <EXACT_MASS>
439.247106555

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
47.985856427928624

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
22-hydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,17,19,21-pentaene-4',5,16-trione

> <ALOGPS_LOGP>
1.95

> <JCHEM_LOGP>
0.5207437212807154

> <ALOGPS_LOGS>
-4.62

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
15.799796819358438

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.121551211584402

> <JCHEM_PKA_STRONGEST_BASIC>
10.220904974030372

> <JCHEM_POLAR_SURFACE_AREA>
107.53

> <JCHEM_REFRACTIVITY>
126.87819999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.05e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
22-hydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,17,19,21-pentaene-4',5,16-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-15         0                                  
HETATM    1  O   UNK     0       4.583  -6.874   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       4.292  -5.362   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.837  -4.858   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.546  -3.346   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.710  -2.338   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.419  -0.826   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.583   0.183   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.292   1.695   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.837   2.199   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0       5.456   2.703   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       6.911   2.199   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.202   0.687   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.658   0.183   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       8.949  -1.330   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      10.404  -1.834   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.695  -3.346   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.150  -3.850   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.441  -5.362   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0      11.277  -6.370   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       9.822  -5.866   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      10.475  -4.472   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.658  -6.874   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.202  -6.370   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.911  -4.858   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.620  -3.346   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.784  -2.338   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.240  -2.842   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      10.774  -2.710   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       9.531  -4.354   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.367  -5.362   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.456  -4.354   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.165  -2.842   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   31                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   32                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   30   31                                             
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   24                                                       
CONECT   31   24    2   32                                                  
CONECT   32   31    5                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₃N₃O₄

Average Mass

439.5560 Da

Monoisotopic Mass

439.24711 Da

IUPAC Name

22-hydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,17,19,21-pentaene-4',5,16-trione

Traditional Name

22-hydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,17,19,21-pentaene-4',5,16-trione

CAS Registry Number

Not Available

SMILES

OC1=CC=C2C=C1C1(CCC(=O)CC1)C=CC(=O)NCCCCNCCCNC(=O)C=C2

InChI Identifier

InChI=1S/C25H33N3O4/c29-20-8-11-25(12-9-20)13-10-24(32)27-16-2-1-14-26-15-3-17-28-23(31)7-5-19-4-6-22(30)21(25)18-19/h4-7,10,13,18,26,30H,1-3,8-9,11-12,14-17H2,(H,27,32)(H,28,31)

InChI Key

RXFSZEHSQXSBSX-UHFFFAOYSA-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 macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolactams

Sub Class

Not Available

Direct Parent

Macrolactams

Alternative Parents

Substituents

Macrolactam
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Amino acid or derivatives
Carboxamide group
Ketone
Lactam
Secondary carboxylic acid amide
Cyclic ketone
Carboxylic acid derivative
Secondary aliphatic amine
Secondary amine
Azacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Amine
Organonitrogen compound
Organooxygen compound
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	1.95	ALOGPS
logP	0.52	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	9.12	ChemAxon
pKa (Strongest Basic)	10.22	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.53 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	126.88 m³·mol⁻¹	ChemAxon
Polarizability	47.99 Å³	ChemAxon
Number of Rings	3	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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5,16,22-trihydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,5,15,17,19,21-heptaen-4'-one (NP0200228)

MOL for NP0200228 (5,16,22-trihydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,5,15,17,19,21-heptaen-4'-one)

3D MOL for NP0200228 (5,16,22-trihydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,5,15,17,19,21-heptaen-4'-one)

3D SDF for NP0200228 (5,16,22-trihydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,5,15,17,19,21-heptaen-4'-one)

3D-SDF for NP0200228 (5,16,22-trihydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,5,15,17,19,21-heptaen-4'-one)

PDB for NP0200228 (5,16,22-trihydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,5,15,17,19,21-heptaen-4'-one)

3D PDB for NP0200228 (5,16,22-trihydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,5,15,17,19,21-heptaen-4'-one)

SMILES for NP0200228 (5,16,22-trihydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,5,15,17,19,21-heptaen-4'-one)

INCHI for NP0200228 (5,16,22-trihydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,5,15,17,19,21-heptaen-4'-one)

Structure for NP0200228 (5,16,22-trihydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,5,15,17,19,21-heptaen-4'-one)

3D Structure for NP0200228 (5,16,22-trihydroxy-6,11,15-triazaspiro[bicyclo[17.3.1]tricosane-2,1'-cyclohexane]-1(23),3,5,15,17,19,21-heptaen-4'-one)