NP-MRD: Showing NP-Card for (1s,4s,5s,7r,8s,10e,12r,13s,16r,17s)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0⁵,⁷]nonadeca-10,14,18-trien-2-one (NP0200538)

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Record Information

Version

2.0

Created at

2022-09-04 19:24:08 UTC

Updated at

2022-09-04 19:24:08 UTC

NP-MRD ID

NP0200538

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4s,5s,7r,8s,10e,12r,13s,16r,17s)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0⁵,⁷]nonadeca-10,14,18-trien-2-one

Description

Alachalasin A belongs to the class of organic compounds known as alachalasins. These are cytochalasans with a structure in which the hydrogenated isoindole bears a methyl group. (1s,4s,5s,7r,8s,10e,12r,13s,16r,17s)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0⁵,⁷]nonadeca-10,14,18-trien-2-one is found in Schizothecium vesticola. Based on a literature review very few articles have been published on Alachalasin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042221242D          

 28 31  0  0  1  0            999 V2000
   -0.9089   -2.4986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0822   -2.2769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1305   -1.4798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4971   -0.8972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9271   -1.2654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3008   -0.5299    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9059    0.2367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1158   -0.6580    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1447   -1.4145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9910   -1.6390    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5111   -1.8481    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3719   -1.5758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6963   -2.3599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8204   -0.8834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6176   -1.0961    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0111   -0.2949    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6616   -1.9199    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2977   -1.1866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4669   -1.7402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2198   -2.5274    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0598   -3.3818    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7044   -3.9497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2632   -3.5962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6791   -3.0135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8825   -3.2279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2985   -2.6452    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5018   -2.8596    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2232   -3.6733    0.0000 O   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
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 11  9  1  1  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 20 19  1  6  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 26 25  1  1  0  0  0
 11 26  1  0  0  0  0
 26 27  1  0  0  0  0
  2 27  1  0  0  0  0
 27 28  1  6  0  0  0
M  END

     RDKit          3D

 59 62  0  0  0  0  0  0  0  0999 V2000
   -3.8632    3.0217   -0.3726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9565    1.8941   -0.0245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3709    0.6525   -0.0042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8012    0.3978   -0.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5523   -0.5330    0.3262 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6455   -1.4379   -0.9053 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2377   -2.8346   -0.7015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8395   -0.6352   -1.7790 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9518    0.0766   -1.1603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1174    0.9096   -1.9552 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0162   -0.1522    0.2742 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3134   -1.2685    0.8725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0048   -1.9002    1.7385 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0213   -1.8439    0.7164 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6395   -1.8543   -0.6246 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5505   -3.2172   -1.0743 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0569   -1.4569   -0.7283 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6663   -2.0616   -2.0252 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7437   -2.0124    0.4961 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8222   -0.6236   -0.0330 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4788    0.4612    0.9152 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5508    1.5687    0.9926 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2090    1.2150    0.5504 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4138    1.4476    1.7721 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1186    1.3898    1.9730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0104    1.0909    1.1310 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5569    2.2307    0.3099 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6254    3.3379    1.1911 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3202    3.9444   -0.5907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4857    3.2031    0.5510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5134    2.7800   -1.2365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1269   -0.6224   -0.1242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4751    1.0880    0.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9616    0.5979   -1.4308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7908   -1.0290    1.2574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6797   -1.4022   -1.3325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6595   -3.4697   -1.5479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7332   -3.3054    0.1984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1613   -3.0147   -0.7509 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3414    0.5157   -2.7707 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9977   -2.9327    1.0806 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7453   -1.4569    1.4878 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0752   -1.3622   -1.4380 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1351   -3.7490   -0.4718 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7821   -2.1169   -1.8965 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4710   -1.3411   -2.8177 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2996   -3.0719   -2.1818 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9314   -0.5431   -0.3002 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4743    0.0813    1.9559 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3203    2.2230    1.8329 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4911    2.1014    0.0330 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5214    1.0410    1.0793 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4325    2.2571    0.1608 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7237    0.7239   -0.2702 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0825    1.7172    2.6363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1505    1.6400    3.0645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8974    0.9222    1.8609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9401    2.5476   -0.5187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3375    4.1709    0.7486 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 11  9  1  6
 11  5  1  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
  2  1  1  0
  2 27  1  0
 27 28  1  0
 27 26  1  0
 26 25  1  0
 25 24  2  0
 24 23  1  0
 23 21  1  0
 21 22  1  0
 21 20  1  0
 20 19  1  0
 19 17  1  0
 17 18  1  6
 17 15  1  0
 15 16  1  0
 15 14  1  0
 14 12  1  0
 12 13  2  0
  5  6  1  0
 17 20  1  0
 26 11  1  0
 12 11  1  0
  7 37  1  0
  7 38  1  0
  7 39  1  0
  6 36  1  6
 10 40  1  0
  5 35  1  1
  4 32  1  0
  4 33  1  0
  4 34  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 27 58  1  6
 28 59  1  0
 26 57  1  1
 25 56  1  0
 24 55  1  0
 23 53  1  0
 23 54  1  0
 21 49  1  1
 22 50  1  0
 22 51  1  0
 22 52  1  0
 20 48  1  6
 18 45  1  0
 18 46  1  0
 18 47  1  0
 15 43  1  6
 16 44  1  0
 14 41  1  0
 14 42  1  0
M  END


  Mrv1652309042221242D          

 28 31  0  0  1  0            999 V2000
   -0.9089   -2.4986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0822   -2.2769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1305   -1.4798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4971   -0.8972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9271   -1.2654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3008   -0.5299    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9059    0.2367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1158   -0.6580    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1447   -1.4145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9910   -1.6390    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5111   -1.8481    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3719   -1.5758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6963   -2.3599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8204   -0.8834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6176   -1.0961    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0111   -0.2949    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6616   -1.9199    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2977   -1.1866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4669   -1.7402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2198   -2.5274    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0598   -3.3818    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7044   -3.9497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2632   -3.5962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6791   -3.0135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8825   -3.2279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2985   -2.6452    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5018   -2.8596    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2232   -3.6733    0.0000 O   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
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 11  9  1  1  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 20 19  1  6  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 26 25  1  1  0  0  0
 11 26  1  0  0  0  0
 26 27  1  0  0  0  0
  2 27  1  0  0  0  0
 27 28  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0200538

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C22H31NO5/c1-10-7-6-8-14-18(26)12(3)11(2)17-13(4)23-20(27)22(14,17)16(25)9-15(24)21(5)19(10)28-21/h6,8,10,13-15,17-19,24,26H,7,9H2,1-5H3,(H,23,27)/b8-6+/t10-,13-,14-,15-,17-,18+,19+,21-,22+/m0/s1

> <INCHI_KEY>
YXPDKMSUYDWDKY-UPYKMMFCSA-N

> <FORMULA>
C22H31NO5

> <MOLECULAR_WEIGHT>
389.492

> <EXACT_MASS>
389.220223102

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
41.841739215566676

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,4S,5S,7R,8S,10E,12R,13S,16R,17S)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0^{1,16}.0^{5,7}]nonadeca-10,14,18-trien-2-one

> <JCHEM_LOGP>
0.5913866463926847

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.264190063336738

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.7042987860906

> <JCHEM_PKA_STRONGEST_BASIC>
5.466257105995265

> <JCHEM_POLAR_SURFACE_AREA>
102.65

> <JCHEM_REFRACTIVITY>
105.8658

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4S,5S,7R,8S,10E,12R,13S,16R,17S)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0^{1,16}.0^{5,7}]nonadeca-10,14,18-trien-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.697  -4.664   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.153  -4.250   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.244  -2.762   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.928  -1.675   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.731  -2.362   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.428  -0.989   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.691   0.442   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       3.950  -1.228   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       4.003  -2.640   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.583  -3.059   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.821  -3.450   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.428  -2.942   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.033  -4.405   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.265  -1.649   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.753  -2.046   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.487  -0.551   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.835  -3.584   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.022  -2.215   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.338  -3.248   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.877  -4.718   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.578  -6.313   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.782  -7.373   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.091  -6.713   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.001  -5.625   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.514  -6.025   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.424  -4.938   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.937  -5.338   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.417  -6.857   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   27                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   11                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9    5   12   26                                             
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   17   21                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   11   27                                                  
CONECT   27   26    2   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₁NO₅

Average Mass

389.4920 Da

Monoisotopic Mass

389.22022 Da

IUPAC Name

(1S,4S,5S,7R,8S,10E,12R,13S,16R,17S)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0^{1,16}.0^{5,7}]nonadeca-10,14,18-trien-2-one

Traditional Name

(1S,4S,5S,7R,8S,10E,12R,13S,16R,17S)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0^{1,16}.0^{5,7}]nonadeca-10,14,18-trien-2-one

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C22H31NO5/c1-10-7-6-8-14-18(26)12(3)11(2)17-13(4)23-20(27)22(14,17)16(25)9-15(24)21(5)19(10)28-21/h6,8,10,13-15,17-19,24,26H,7,9H2,1-5H3,(H,23,27)/b8-6+/t10-,13-,14-,15-,17-,18+,19+,21-,22+/m0/s1

InChI Key

YXPDKMSUYDWDKY-UPYKMMFCSA-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

Species Name	Source	Reference
Schizothecium vesticola	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alachalasins. These are cytochalasans with a structure in which the hydrogenated isoindole bears a methyl group.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Cytochalasans

Sub Class

Alachalasins

Direct Parent

Alachalasins

Alternative Parents

Substituents

Carbocyclic alachalasin skeleton
Isoindolone
Isoindoline
Isoindole or derivatives
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 oxygen compound
Organic nitrogen compound
Organic oxide
Hydrocarbon derivative
Alcohol
Organonitrogen compound
Organooxygen compound
Carbonyl group
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	0.59	ChemAxon
pKa (Strongest Acidic)	2.7	ChemAxon
pKa (Strongest Basic)	5.47	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	102.65 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	105.87 m³·mol⁻¹	ChemAxon
Polarizability	41.84 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

78437879

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24882543

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,5s,7r,8s,10e,12r,13s,16r,17s)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0⁵,⁷]nonadeca-10,14,18-trien-2-one (NP0200538)

MOL for NP0200538 ((1s,4s,5s,7r,8s,10e,12r,13s,16r,17s)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0⁵,⁷]nonadeca-10,14,18-trien-2-one)

3D MOL for NP0200538 ((1s,4s,5s,7r,8s,10e,12r,13s,16r,17s)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0⁵,⁷]nonadeca-10,14,18-trien-2-one)

3D SDF for NP0200538 ((1s,4s,5s,7r,8s,10e,12r,13s,16r,17s)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0⁵,⁷]nonadeca-10,14,18-trien-2-one)

3D-SDF for NP0200538 ((1s,4s,5s,7r,8s,10e,12r,13s,16r,17s)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0⁵,⁷]nonadeca-10,14,18-trien-2-one)

PDB for NP0200538 ((1s,4s,5s,7r,8s,10e,12r,13s,16r,17s)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0⁵,⁷]nonadeca-10,14,18-trien-2-one)

3D PDB for NP0200538 ((1s,4s,5s,7r,8s,10e,12r,13s,16r,17s)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0⁵,⁷]nonadeca-10,14,18-trien-2-one)

SMILES for NP0200538 ((1s,4s,5s,7r,8s,10e,12r,13s,16r,17s)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0⁵,⁷]nonadeca-10,14,18-trien-2-one)

INCHI for NP0200538 ((1s,4s,5s,7r,8s,10e,12r,13s,16r,17s)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0⁵,⁷]nonadeca-10,14,18-trien-2-one)

Structure for NP0200538 ((1s,4s,5s,7r,8s,10e,12r,13s,16r,17s)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0⁵,⁷]nonadeca-10,14,18-trien-2-one)

3D Structure for NP0200538 ((1s,4s,5s,7r,8s,10e,12r,13s,16r,17s)-4,13,19-trihydroxy-5,8,14,15,17-pentamethyl-6-oxa-18-azatetracyclo[10.7.0.0¹,¹⁶.0⁵,⁷]nonadeca-10,14,18-trien-2-one)