NP-MRD: Showing NP-Card for 9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-6-(sec-butyl)-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one (NP0219467)

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Record Information

Version

2.0

Created at

2022-09-05 20:28:00 UTC

Updated at

2022-09-05 20:28:01 UTC

NP-MRD ID

NP0219467

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-6-(sec-butyl)-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one

Description

6-(Butan-2-yl)-9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]Tricosane]-5',10',12',16'-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. 9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-6-(sec-butyl)-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one is found in Streptomyces avermitilis. 6-(Butan-2-yl)-9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]Tricosane]-5',10',12',16'-tetraen-3'-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 04121520472D          

 52 56  0  0  0  0            999 V2000
   11.5067   -2.6498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7607   -2.2974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0826   -2.7672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1504   -3.5895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3366   -2.4149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6584   -2.8847    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9125   -2.5323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1665   -2.1800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4884   -2.6498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5562   -3.4720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3022   -3.8244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3700   -4.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6918   -5.1164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9459   -4.7640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8781   -3.9418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2677   -5.2339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3355   -6.0561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6574   -6.5259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7252   -7.3481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0471   -7.8180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1149   -8.6402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8608   -8.9925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3011   -7.4656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6230   -7.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2333   -6.6434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4873   -6.2910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9114   -6.1735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5218   -4.8815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4539   -4.0593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8436   -5.3513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0977   -4.9990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0298   -4.1767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7080   -3.7069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5186   -3.5535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6402   -2.8847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9620   -3.3545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8942   -2.5323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8264   -1.7101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0804   -1.3578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4023   -1.8276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5045   -1.2403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2505   -1.5927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3183   -2.4149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0643   -2.7672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1321   -3.5895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7424   -2.2974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4367   -0.4181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9803   -3.3545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8447   -1.7101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5228   -1.2403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2688   -1.5927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9469   -1.1228    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
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  4  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 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  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 18 27  1  0  0  0  0
 16 28  1  0  0  0  0
 28 29  1  0  0  0  0
 30 28  1  4  0  0  0
 30 31  2  0  0  0  0
 32 31  1  4  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 38 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 35 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
  9 46  1  0  0  0  0
 41 47  1  0  0  0  0
 11 48  1  0  0  0  0
  7 48  1  0  0  0  0
  7 49  1  0  0  0  0
 49 50  2  0  0  0  0
 50 51  1  0  0  0  0
  5 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END


  Mrv0541 04121520472D          

 52 56  0  0  0  0            999 V2000
   11.5067   -2.6498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7607   -2.2974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0826   -2.7672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1504   -3.5895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3366   -2.4149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6584   -2.8847    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9125   -2.5323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1665   -2.1800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4884   -2.6498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5562   -3.4720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3022   -3.8244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3700   -4.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6918   -5.1164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9459   -4.7640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8781   -3.9418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2677   -5.2339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3355   -6.0561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6574   -6.5259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7252   -7.3481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0471   -7.8180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1149   -8.6402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8608   -8.9925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3011   -7.4656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6230   -7.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2333   -6.6434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4873   -6.2910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9114   -6.1735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5218   -4.8815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4539   -4.0593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8436   -5.3513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0977   -4.9990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0298   -4.1767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7080   -3.7069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5186   -3.5535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6402   -2.8847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9620   -3.3545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8942   -2.5323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8264   -1.7101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0804   -1.3578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4023   -1.8276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5045   -1.2403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2505   -1.5927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3183   -2.4149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0643   -2.7672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1321   -3.5895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7424   -2.2974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4367   -0.4181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9803   -3.3545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8447   -1.7101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5228   -1.2403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2688   -1.5927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9469   -1.1228    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
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  4  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 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  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 18 27  1  0  0  0  0
 16 28  1  0  0  0  0
 28 29  1  0  0  0  0
 30 28  1  4  0  0  0
 30 31  2  0  0  0  0
 32 31  1  4  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 38 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 35 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
  9 46  1  0  0  0  0
 41 47  1  0  0  0  0
 11 48  1  0  0  0  0
  7 48  1  0  0  0  0
  7 49  1  0  0  0  0
 49 50  2  0  0  0  0
 50 51  1  0  0  0  0
  5 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0219467

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C1OC2(CC3CC(CC=C(C)C(OC4CC(OC)C(O)C(C)O4)C(C)C=CC=C(C)C4(O)CC(OC)C(C)=CC4C(=O)O3)O2)C=CC1C

> <INCHI_IDENTIFIER>
InChI=1S/C42H64O10/c1-11-24(2)39-27(5)17-18-41(52-39)22-32-20-31(51-41)16-15-26(4)38(50-36-21-34(46-9)37(43)30(8)48-36)25(3)13-12-14-29(7)42(45)23-35(47-10)28(6)19-33(42)40(44)49-32/h12-15,17-19,24-25,27,30-39,43,45H,11,16,20-23H2,1-10H3

> <INCHI_KEY>
CAJDUHQNQRQATN-UHFFFAOYSA-N

> <FORMULA>
C42H64O10

> <MOLECULAR_WEIGHT>
728.964

> <EXACT_MASS>
728.449948261

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
116

> <JCHEM_AVERAGE_POLARIZABILITY>
81.92592725143086

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-(butan-2-yl)-9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one

> <ALOGPS_LOGP>
5.13

> <JCHEM_LOGP>
6.481082806333333

> <ALOGPS_LOGS>
-5.61

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.730323892876104

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.056900390979408

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4233721636613117

> <JCHEM_POLAR_SURFACE_AREA>
122.14000000000001

> <JCHEM_REFRACTIVITY>
202.4592000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.81e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-6-(sec-butyl)-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-APR-15         0                                  
HETATM    1  C   UNK     0      21.479  -4.946   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      20.087  -4.289   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      18.821  -5.166   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      18.947  -6.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.428  -4.508   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      16.162  -5.385   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      14.770  -4.727   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.378  -4.069   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.112  -4.946   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.238  -6.481   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.631  -7.139   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.757  -8.674   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.491  -9.551   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.099  -8.893   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.972  -7.358   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.833  -9.770   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       9.960 -11.305   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       8.694 -12.182   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.820 -13.716   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.555 -14.594   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.681 -16.128   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.074 -16.786   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.162 -13.936   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.896 -14.813   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.035 -12.401   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.643 -11.743   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.301 -11.524   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.441  -9.112   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.314  -7.577   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.175  -9.989   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.782  -9.331   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.656  -7.797   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.922  -6.920   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       8.435  -6.633   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.795  -5.385   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       5.529  -6.262   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       5.403  -4.727   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.276  -3.192   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       3.883  -2.534   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       2.618  -3.411   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.542  -2.315   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       7.934  -2.973   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       8.061  -4.508   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       9.453  -5.166   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       9.580  -6.700   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      10.719  -4.289   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       6.415  -0.780   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      14.897  -6.262   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      14.643  -3.192   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      15.909  -2.315   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      17.302  -2.973   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      18.568  -2.096   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   51                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   48   49                                             
CONECT    8    7    9                                                       
CONECT    9    8   10   46                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   48                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   28                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   27                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   18                                                       
CONECT   28   16   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   37   43                                             
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39   41                                                  
CONECT   39   38   40                                                       
CONECT   40   39                                                            
CONECT   41   38   42   47                                                  
CONECT   42   41   43                                                       
CONECT   43   42   35   44                                                  
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44    9                                                       
CONECT   47   41                                                            
CONECT   48   11    7                                                       
CONECT   49    7   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50    5   52                                                  
CONECT   52   51                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  112    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₂H₆₄O₁₀

Average Mass

728.9640 Da

Monoisotopic Mass

728.44995 Da

IUPAC Name

6-(butan-2-yl)-9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one

Traditional Name

CAS Registry Number

Not Available

SMILES

CCC(C)C1OC2(CC3CC(CC=C(C)C(OC4CC(OC)C(O)C(C)O4)C(C)C=CC=C(C)C4(O)CC(OC)C(C)=CC4C(=O)O3)O2)C=CC1C

InChI Identifier

InChI=1S/C42H64O10/c1-11-24(2)39-27(5)17-18-41(52-39)22-32-20-31(51-41)16-15-26(4)38(50-36-21-34(46-9)37(43)30(8)48-36)25(3)13-12-14-29(7)42(45)23-35(47-10)28(6)19-33(42)40(44)49-32/h12-15,17-19,24-25,27,30-39,43,45H,11,16,20-23H2,1-10H3

InChI Key

CAJDUHQNQRQATN-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Streptomyces avermitilis	LOTUS Database	35616633

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
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Ketal
Monosaccharide
Oxane
Pyran
Tertiary alcohol
Secondary alcohol
Carboxylic acid ester
Lactone
Acetal
Carboxylic acid derivative
Dialkyl ether
Ether
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Oxacycle
Carbonyl group
Organic oxygen compound
Organic oxide
Alcohol
Hydrocarbon derivative
Organooxygen compound
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	5.13	ALOGPS
logP	6.48	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	13.06	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	122.14 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	202.46 m³·mol⁻¹	ChemAxon
Polarizability	81.93 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

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 9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-6-(sec-butyl)-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one (NP0219467)

MOL for NP0219467 (9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-6-(sec-butyl)-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

3D MOL for NP0219467 (9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-6-(sec-butyl)-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

3D SDF for NP0219467 (9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-6-(sec-butyl)-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

3D-SDF for NP0219467 (9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-6-(sec-butyl)-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

PDB for NP0219467 (9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-6-(sec-butyl)-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

3D PDB for NP0219467 (9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-6-(sec-butyl)-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

SMILES for NP0219467 (9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-6-(sec-butyl)-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

INCHI for NP0219467 (9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-6-(sec-butyl)-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

Structure for NP0219467 (9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-6-(sec-butyl)-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

3D Structure for NP0219467 (9'-hydroxy-15'-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-7'-methoxy-5,6',10',14',16'-pentamethyl-6-(sec-butyl)-5,6-dihydro-2',20'-dioxaspiro[pyran-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)