NP-MRD: Showing NP-Card for (1s,4s,8s,9e,11r,12s,14r,15s,16r,17s)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-9,18-dien-2-one (NP0267315)

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Record Information

Version

2.0

Created at

2022-09-08 12:03:40 UTC

Updated at

2022-09-08 12:03:40 UTC

NP-MRD ID

NP0267315

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4s,8s,9e,11r,12s,14r,15s,16r,17s)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-9,18-dien-2-one

Description

(1S,4S,8S,11R,12S,14R,15S,16R,17S)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]Nonadeca-9,18-dien-2-one belongs to the class of organic compounds known as aspochalasins. These are cytochalasans with a structure in which the hydrogenated isoindole bears a 2-methylpropyl group. Based on a literature review very few articles have been published on (1S,4S,8S,11R,12S,14R,15S,16R,17S)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]Nonadeca-9,18-dien-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082214032D          

 28 31  0  0  1  0            999 V2000
    3.1501   -4.3590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6790   -3.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8569   -3.7511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0376   -2.9187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8334   -2.0768    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0441   -1.8370    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1203   -1.0838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1900   -0.8377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8078   -0.7422    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9176   -0.8926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7092    0.0158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3775   -1.5162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6175   -1.1952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1587   -1.6259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6879   -0.3732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1751    0.3698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4961    1.1298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3147    1.2318    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6114    2.0399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8124    0.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6311    0.6758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1288    0.0178    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9474    0.1198    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7661    0.2218    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4451   -0.5382    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1241   -1.2982    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7580   -1.8594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3054   -1.4002    0.0000 C   0  0  1  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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  7  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 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  6  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 22 21  1  1  0  0  0
  9 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 25 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28  5  1  1  0  0  0
  9 28  1  0  0  0  0
M  END

     RDKit          3D

 61 64  0  0  0  0  0  0  0  0999 V2000
   -4.9799    0.5499   -0.6393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6610    1.2682   -0.7833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0192    2.7550   -0.9376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7992    1.1555    0.4266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4117   -0.2039    0.8335 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5714   -0.2672    2.0098 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3465   -0.5143    1.7434 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6268   -0.6185    2.7429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1661   -0.6567    0.2888 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2344    0.6596   -0.2642 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0535    0.9313   -1.4368 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9701    1.6625    0.5427 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1565    2.2631   -0.1451 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1880    3.6365    0.1195 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4384    1.7021    0.4356 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5001    1.4474   -0.5630 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0848    0.0452   -0.5096 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3120   -0.7842   -1.4970 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4259   -0.1841   -2.8018 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8624   -0.9322   -1.2098 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1233   -1.6371   -0.4054 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6879   -1.7909   -0.1149 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5601   -2.7429    1.1003 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0782   -4.0197    0.9184 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8604   -2.9426    1.3337 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7534   -2.5116    0.2203 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1851   -2.8158    0.6880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5918   -1.0200   -0.1012 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7569    1.0890   -1.2557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9571   -0.4811   -1.0398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2636    0.5931    0.4326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1437    1.0197   -1.7308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6412    3.1157   -0.1169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0365    3.2938   -1.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4979    2.8332   -1.9390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3949    1.6598    1.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9361    1.8414    0.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3625   -0.7384    1.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6615   -0.0521    3.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3332    1.1562    1.4586 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2998    2.4747    0.9104 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1162    2.1785   -1.2464 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3206    4.0698    0.0421 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1769    0.7151    0.9147 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8355    2.3171    1.2563 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0761    1.6683   -1.5752 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3036    2.2206   -0.4328 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1129   -0.3671    0.4940 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1371    0.1130   -0.8557 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8920   -1.7091   -1.6957 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6025    0.2863   -2.9903 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3999   -0.1589   -1.9427 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6215   -2.3529    0.3151 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2071   -2.3852   -0.9184 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3427   -2.6420    1.8408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2786   -3.2021    2.3254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6561   -3.1321   -0.7149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9415   -2.3614    0.0554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3217   -3.9326    0.5598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2997   -2.6608    1.7768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8009   -0.9039   -1.1563 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  9  7  1  1
  9 28  1  0
 28 26  1  0
 26 27  1  0
 26 25  1  0
 25 24  1  0
 24 23  1  0
 23 22  1  0
 22 21  1  0
 21 20  2  0
 20 18  1  0
 18 19  1  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15 13  1  0
 13 14  1  0
 13 12  1  0
 12 10  1  0
 10 11  2  0
 28  5  1  0
 23 25  1  0
 22  9  1  0
 10  9  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  1
  8 39  1  0
 28 61  1  6
 26 57  1  6
 27 58  1  0
 27 59  1  0
 27 60  1  0
 25 56  1  1
 23 55  1  1
 22 54  1  6
 21 53  1  0
 20 52  1  0
 18 50  1  6
 19 51  1  0
 17 48  1  0
 17 49  1  0
 16 46  1  0
 16 47  1  0
 15 44  1  0
 15 45  1  0
 13 42  1  6
 14 43  1  0
 12 40  1  0
 12 41  1  0
M  END


  Mrv1652309082214032D          

 28 31  0  0  1  0            999 V2000
    3.1501   -4.3590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6790   -3.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8569   -3.7511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0376   -2.9187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8334   -2.0768    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0441   -1.8370    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1203   -1.0838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1900   -0.8377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8078   -0.7422    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9176   -0.8926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7092    0.0158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3775   -1.5162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6175   -1.1952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1587   -1.6259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6879   -0.3732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1751    0.3698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4961    1.1298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3147    1.2318    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6114    2.0399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8124    0.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6311    0.6758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1288    0.0178    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9474    0.1198    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7661    0.2218    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4451   -0.5382    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1241   -1.2982    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7580   -1.8594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3054   -1.4002    0.0000 C   0  0  1  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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  7  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 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  6  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 22 21  1  1  0  0  0
  9 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 25 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28  5  1  1  0  0  0
  9 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0267315

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C[C@@H]1N=C(O)[C@]23[C@H]1[C@H](C)[C@H]1O[C@H]1[C@@H]2\C=C\[C@@H](O)CCC[C@H](O)CC3=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H33NO5/c1-11(2)9-16-18-12(3)19-20(28-19)15-8-7-13(24)5-4-6-14(25)10-17(26)22(15,18)21(27)23-16/h7-8,11-16,18-20,24-25H,4-6,9-10H2,1-3H3,(H,23,27)/b8-7+/t12-,13-,14-,15-,16-,18-,19+,20-,22+/m0/s1

> <INCHI_KEY>
GNNKACUJOHRGTR-QOYOXESOSA-N

> <FORMULA>
C22H33NO5

> <MOLECULAR_WEIGHT>
391.508

> <EXACT_MASS>
391.235873167

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
42.3704803170107

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,4S,8S,9E,11R,12S,14R,15S,16R,17S)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0^{1,16}.0^{12,14}]nonadeca-9,18-dien-2-one

> <JCHEM_LOGP>
1.1590835103375163

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.047441437613593

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.784926299380534

> <JCHEM_PKA_STRONGEST_BASIC>
5.51417807414657

> <JCHEM_POLAR_SURFACE_AREA>
102.65000000000002

> <JCHEM_REFRACTIVITY>
105.5286

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4S,8S,9E,11R,12S,14R,15S,16R,17S)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0^{1,16}.0^{12,14}]nonadeca-9,18-dien-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       5.880  -8.137   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.001  -6.873   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.466  -7.002   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.670  -5.448   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.289  -3.877   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       3.816  -3.429   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       3.958  -2.023   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.221  -1.564   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.241  -1.385   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.579  -1.666   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.190   0.029   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.571  -2.830   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.153  -2.231   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.296  -3.035   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.284  -0.697   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.327   0.690   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.926   2.109   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.454   2.299   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.008   3.808   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.383   1.071   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.911   1.262   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.840   0.033   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.369   0.224   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.897   0.414   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.298  -1.005   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.698  -2.423   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.882  -3.471   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.170  -2.614   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   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    9   23                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23   25                                                       
CONECT   25   24   23   26                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26    5    9                                                  
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₃NO₅

Average Mass

391.5080 Da

Monoisotopic Mass

391.23587 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)C[C@@H]1N=C(O)[C@]23[C@H]1[C@H](C)[C@H]1O[C@H]1[C@@H]2\C=C\[C@@H](O)CCC[C@H](O)CC3=O

InChI Identifier

InChI=1S/C22H33NO5/c1-11(2)9-16-18-12(3)19-20(28-19)15-8-7-13(24)5-4-6-14(25)10-17(26)22(15,18)21(27)23-16/h7-8,11-16,18-20,24-25H,4-6,9-10H2,1-3H3,(H,23,27)/b8-7+/t12-,13-,14-,15-,16-,18-,19+,20-,22+/m0/s1

InChI Key

GNNKACUJOHRGTR-QOYOXESOSA-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 aspochalasins. These are cytochalasans with a structure in which the hydrogenated isoindole bears a 2-methylpropyl group.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Cytochalasans

Sub Class

Aspochalasins

Direct Parent

Aspochalasins

Alternative Parents

Substituents

Aspochalasin skeleton
Carbocyclic aspochalasin skeleton
Isoindolone
Isoindoline
Isoindole or derivatives
Oxepane
2-pyrrolidone
Pyrrolidone
Pyrrolidine
Carboxamide group
Ketone
Lactam
Secondary carboxylic acid amide
Secondary alcohol
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Oxacycle
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Organonitrogen compound
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

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

27024392

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44607389

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,4s,8s,9e,11r,12s,14r,15s,16r,17s)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-9,18-dien-2-one (NP0267315)

MOL for NP0267315 ((1s,4s,8s,9e,11r,12s,14r,15s,16r,17s)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-9,18-dien-2-one)

3D MOL for NP0267315 ((1s,4s,8s,9e,11r,12s,14r,15s,16r,17s)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-9,18-dien-2-one)

3D SDF for NP0267315 ((1s,4s,8s,9e,11r,12s,14r,15s,16r,17s)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-9,18-dien-2-one)

3D-SDF for NP0267315 ((1s,4s,8s,9e,11r,12s,14r,15s,16r,17s)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-9,18-dien-2-one)

PDB for NP0267315 ((1s,4s,8s,9e,11r,12s,14r,15s,16r,17s)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-9,18-dien-2-one)

3D PDB for NP0267315 ((1s,4s,8s,9e,11r,12s,14r,15s,16r,17s)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-9,18-dien-2-one)

SMILES for NP0267315 ((1s,4s,8s,9e,11r,12s,14r,15s,16r,17s)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-9,18-dien-2-one)

INCHI for NP0267315 ((1s,4s,8s,9e,11r,12s,14r,15s,16r,17s)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-9,18-dien-2-one)

Structure for NP0267315 ((1s,4s,8s,9e,11r,12s,14r,15s,16r,17s)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-9,18-dien-2-one)

3D Structure for NP0267315 ((1s,4s,8s,9e,11r,12s,14r,15s,16r,17s)-4,8,19-trihydroxy-15-methyl-17-(2-methylpropyl)-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-9,18-dien-2-one)