NP-MRD: Showing NP-Card for 20-hydroxy-11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14,19-tetraen-3-one (NP0277332)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-09 01:55:43 UTC

Updated at

2022-09-09 01:55:43 UTC

NP-MRD ID

NP0277332

Secondary Accession Numbers

None

Natural Product Identification

Common Name

20-hydroxy-11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14,19-tetraen-3-one

Description

20-Hydroxy-11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]Icosa-4,11,14,19-tetraen-3-one belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. 20-Hydroxy-11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]Icosa-4,11,14,19-tetraen-3-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191513442D          

 29 32  0  0  0  0            999 V2000
    0.9317    1.6364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3203    0.9087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1448    0.8813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8844    0.2082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2730   -0.5195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0901   -0.6329    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0306   -1.3323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9770   -1.8054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5071   -1.8337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2997   -1.6049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4979   -0.8040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9034   -0.2320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2905   -0.5752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8850   -1.1472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6868   -1.9481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4795   -1.7193    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2813   -2.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0832   -3.3210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2905   -3.5498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6961   -2.9778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9034   -3.2066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3089   -2.6345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5163   -2.8633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0782   -2.2913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8708   -2.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1200   -1.4905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4745   -0.9184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9126   -1.2617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8942   -2.1769    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 13 11  1  4  0  0  0
 13 14  2  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
 15 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
 21 22  1  4  0  0  0
  9 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
  5 28  1  0  0  0  0
  9 28  1  0  0  0  0
 20 29  1  0  0  0  0
M  END

     RDKit          3D

 62 65  0  0  0  0  0  0  0  0999 V2000
    0.7544   -3.8892   -1.6851 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5825   -2.7693   -0.7175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5397   -2.7365   -0.0219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7883   -1.6292    0.9816 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1210   -1.6199    1.5176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2384   -1.0477    1.0977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5583   -1.1686    1.8254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3015   -0.2267   -0.1400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6782    0.2763   -0.4773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5045    1.6563   -1.0822 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4967    1.9253   -2.3910 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2624    1.5245   -1.9393 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2061    2.4964   -1.6190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9344    2.2214   -1.5132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2421    0.9564   -1.6690 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5782    0.9039   -2.6787 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3130   -0.1754   -0.9336 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1290   -0.4278    0.4301 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0977    0.7679    1.2954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8398    1.1467    2.2215 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0692    1.4904    0.8226 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0760    0.5439    0.4318 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3276    0.6009    1.2402 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0675    1.8940    1.2225 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4962    2.3197   -0.1679 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4194    3.0193    1.9317 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3825   -0.7829    0.5219 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6795   -1.7412   -0.5779 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9456   -2.5577   -0.2855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2479   -4.1108   -2.1500 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9925   -4.8308   -1.1084 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5167   -3.6964   -2.4416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3256   -3.4608   -0.1119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1048   -1.9778    1.8329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3133   -2.1862    2.4643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3646   -1.4656    1.1288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8174   -0.2614    2.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4406   -2.0219    2.5211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7043    0.6552    0.1088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9659   -0.8629   -0.9509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1866   -0.3669   -1.1984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3009    0.4484    0.4470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4573    2.5270   -0.3862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9276    0.5853   -2.3660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5382    3.5222   -1.4560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2843    3.0885   -1.2776 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1560    2.5276    0.7685 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3905    0.6782   -0.6296 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0100   -0.2259    0.9456 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0606    0.3996    2.3098 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0474    1.7011    1.7590 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7991    1.3901   -0.7042 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3208    3.0310   -0.0721 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6147    2.7165   -0.7202 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0321    3.8364    1.2865 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1905    3.5421    2.5819 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6152    2.6627    2.6143 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5629   -1.2986    1.4879 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8061   -1.2918   -1.5719 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0659   -2.7415    0.7836 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8853   -3.5165   -0.8713 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7858   -1.9674   -0.7302 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 24  1  0
 24 26  1  0
 24 23  1  0
 23 22  1  0
 22 21  1  0
 21 19  1  0
 19 20  2  0
 19 18  1  0
 18 17  1  6
 17 15  1  0
 15 16  2  0
 15 14  1  0
 14 13  2  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  6  1  0
  6  7  1  0
  6  5  2  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 28  1  0
 28 29  1  0
 28 27  1  0
 27 22  1  0
  4 18  1  0
 27 18  1  0
 10 12  1  0
 25 52  1  0
 25 53  1  0
 25 54  1  0
 24 51  1  0
 26 55  1  0
 26 56  1  0
 26 57  1  0
 23 49  1  0
 23 50  1  0
 22 48  1  6
 21 47  1  0
 14 46  1  0
 13 45  1  0
 12 44  1  6
 10 43  1  1
  9 41  1  0
  9 42  1  0
  8 39  1  0
  8 40  1  0
  7 36  1  0
  7 37  1  0
  7 38  1  0
  5 35  1  0
  4 34  1  1
  3 33  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 28 59  1  6
 29 60  1  0
 29 61  1  0
 29 62  1  0
 27 58  1  1
M  END


  Mrv1533004191513442D          

 29 32  0  0  0  0            999 V2000
    0.9317    1.6364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3203    0.9087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1448    0.8813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8844    0.2082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2730   -0.5195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0901   -0.6329    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0306   -1.3323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9770   -1.8054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5071   -1.8337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2997   -1.6049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4979   -0.8040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9034   -0.2320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2905   -0.5752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8850   -1.1472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6868   -1.9481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4795   -1.7193    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2813   -2.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0832   -3.3210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2905   -3.5498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6961   -2.9778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9034   -3.2066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3089   -2.6345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5163   -2.8633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0782   -2.2913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8708   -2.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1200   -1.4905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4745   -0.9184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9126   -1.2617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8942   -2.1769    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 13 11  1  4  0  0  0
 13 14  2  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
 15 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
 21 22  1  4  0  0  0
  9 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
  5 28  1  0  0  0  0
  9 28  1  0  0  0  0
 20 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0277332

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC1NC(=O)C23OC(=O)C=CC4OC4CCC(C)=CC2C=C(C)C(C)C13

> <INCHI_IDENTIFIER>
InChI=1S/C24H33NO4/c1-13(2)10-18-22-16(5)15(4)12-17-11-14(3)6-7-19-20(28-19)8-9-21(26)29-24(17,22)23(27)25-18/h8-9,11-13,16-20,22H,6-7,10H2,1-5H3,(H,25,27)

> <INCHI_KEY>
VJOXDHDYUAEUMO-UHFFFAOYSA-N

> <FORMULA>
C24H33NO4

> <MOLECULAR_WEIGHT>
399.531

> <EXACT_MASS>
399.240958547

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
44.69163729644893

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14-triene-3,20-dione

> <ALOGPS_LOGP>
3.67

> <JCHEM_LOGP>
3.9654661123333335

> <ALOGPS_LOGS>
-4.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.077259755949573

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.944192714493688

> <JCHEM_PKA_STRONGEST_BASIC>
-4.185456619282407

> <JCHEM_POLAR_SURFACE_AREA>
67.92999999999999

> <JCHEM_REFRACTIVITY>
113.51020000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.12e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14-triene-3,20-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0       1.739   3.055   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.465   1.696   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.004   1.645   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.651   0.389   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.376  -0.970   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       3.902  -1.181   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       3.790  -2.487   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       5.557  -3.370   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.813  -3.423   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.293  -2.996   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.663  -1.501   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.553  -0.433   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.142  -1.074   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.252  -2.142   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.882  -3.636   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.362  -3.209   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.992  -4.704   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.622  -6.199   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.142  -6.626   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.033  -5.558   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.553  -5.986   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.443  -4.918   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.964  -5.345   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.146  -4.277   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.625  -4.704   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.224  -2.782   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.886  -1.714   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.704  -2.355   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.403  -4.064   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   28                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   22   28                                             
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15   17                                                       
CONECT   17   16   15   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   29                                                  
CONECT   21   20   22                                                       
CONECT   22   21    9   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26    5    9                                                  
CONECT   29   20                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₃NO₄

Average Mass

399.5310 Da

Monoisotopic Mass

399.24096 Da

IUPAC Name

11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14-triene-3,20-dione

Traditional Name

11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14-triene-3,20-dione

CAS Registry Number

Not Available

SMILES

CC(C)CC1NC(=O)C23OC(=O)C=CC4OC4CCC(C)=CC2C=C(C)C(C)C13

InChI Identifier

InChI=1S/C24H33NO4/c1-13(2)10-18-22-16(5)15(4)12-17-11-14(3)6-7-19-20(28-19)8-9-21(26)29-24(17,22)23(27)25-18/h8-9,11-13,16-20,22H,6-7,10H2,1-5H3,(H,25,27)

InChI Key

VJOXDHDYUAEUMO-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 macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Isoindole or derivatives
Pyrroline
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Cyclic carboximidic acid
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Oxacycle
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carbonyl group
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	3.67	ALOGPS
logP	3.97	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	13.94	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	67.93 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	113.51 m³·mol⁻¹	ChemAxon
Polarizability	44.69 Å³	ChemAxon
Number of Rings	4	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

85050591

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 20-hydroxy-11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14,19-tetraen-3-one (NP0277332)

MOL for NP0277332 (20-hydroxy-11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14,19-tetraen-3-one)

3D MOL for NP0277332 (20-hydroxy-11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14,19-tetraen-3-one)

3D SDF for NP0277332 (20-hydroxy-11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14,19-tetraen-3-one)

3D-SDF for NP0277332 (20-hydroxy-11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14,19-tetraen-3-one)

PDB for NP0277332 (20-hydroxy-11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14,19-tetraen-3-one)

3D PDB for NP0277332 (20-hydroxy-11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14,19-tetraen-3-one)

SMILES for NP0277332 (20-hydroxy-11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14,19-tetraen-3-one)

INCHI for NP0277332 (20-hydroxy-11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14,19-tetraen-3-one)

Structure for NP0277332 (20-hydroxy-11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14,19-tetraen-3-one)

3D Structure for NP0277332 (20-hydroxy-11,15,16-trimethyl-18-(2-methylpropyl)-2,7-dioxa-19-azatetracyclo[11.7.0.0¹,¹⁷.0⁶,⁸]icosa-4,11,14,19-tetraen-3-one)