NP-MRD: Showing NP-Card for methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate (NP0314567)

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Record Information

Version

2.0

Created at

2022-09-11 12:43:59 UTC

Updated at

2022-09-11 12:43:59 UTC

NP-MRD ID

NP0314567

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate

Description

Methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]Hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate is found in Fusarium tricinctum. Methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]Hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201500182D          

 30 31  0  0  0  0            999 V2000
   -7.3124   -0.8752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9768   -0.1215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1563   -0.0352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6714   -0.7027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8208    0.7184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3057    1.3859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9701    2.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0003    0.8047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5154    0.1372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8509   -0.6164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6949    0.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2100   -0.4440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3895   -0.3577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9046   -1.0252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0841   -0.9389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5992   -1.6064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347   -2.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2213   -1.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7062   -2.1876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5569   -0.7665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1576   -0.3540    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5569    0.0585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3415    0.3135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0059    1.0671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0560    0.7260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7704    0.3135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4849    0.7260    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8264   -0.3540    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3415   -1.0214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5964   -1.8060    0.0000 O   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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  4  0  0  0
  8  5  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 11  9  1  4  0  0  0
 11 12  2  0  0  0  0
 13 12  1  4  0  0  0
 13 14  2  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 22  1  0  0  0  0
 22 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
 26 27  1  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  0  0  0  0
 20 29  1  0  0  0  0
 29 30  2  0  0  0  0
M  END

     RDKit          3D

 57 58  0  0  0  0  0  0  0  0999 V2000
   -8.7820    1.5464    1.1913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3437    1.4516    1.1650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6411    0.4934    0.4728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2421    0.6080    0.6047 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1576   -0.0197    0.1696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2679   -1.1919   -0.7139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8938    0.5094    0.6122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6720    0.2625    0.4681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9571   -0.7358   -0.2607 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3894   -0.8153   -0.2740 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2599    0.0723    0.4266 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5633   -0.0264    0.3960 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2801    1.0430    1.2302 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3846   -0.9715   -0.3248 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8763   -1.8383   -1.0533 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8639   -0.9386   -0.2203 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4632   -1.9054   -1.1675 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8331   -0.5040   -1.0773 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1094   -0.3363   -0.2916 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.1948   -0.9247   -0.9576 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4739    1.0600    0.0625 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6701    1.9072   -1.1527 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5707    2.0570   -1.9676 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8734   -1.1553    0.8773 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4918   -1.1086    1.1458 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8790   -1.1839    2.2146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4606   -0.4319   -0.2423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7443   -0.2938   -0.1818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0896   -1.4876   -1.0149 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0216   -2.3093   -1.6554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3358    0.7075    1.6685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2368    1.8096    0.2054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0525    2.4208    1.8996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7762    2.2003    1.7400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9177    1.4993    1.2836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8031   -2.0171   -0.1659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7685   -0.8788   -1.6666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3379   -1.6537   -1.0451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0665    1.4415    1.3089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9632    0.9889    1.0399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4325   -1.4957   -0.8503 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7961   -1.6408   -0.8813 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8390    0.8893    1.0304 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1110    0.8874    2.2883 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7746    2.0111    0.9375 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3143    1.1269    0.8971 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7647   -0.0096   -2.0786 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7919   -1.3052   -0.2899 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7450    1.5067    0.7764 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4455    1.0128    0.6045 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0694    2.9285   -0.8629 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4823    1.4934   -1.8162 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8255    2.4724   -1.4792 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5884   -1.6692    1.4085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7436   -3.3859   -1.6131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0310   -2.1317   -1.2373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9858   -2.0408   -2.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
 30 29  1  0
 29 27  1  0
 27 28  2  0
 27  3  1  0
  3  2  2  0
  2  1  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 16 14  1  1
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  6
 19 21  1  0
 21 22  1  0
 22 23  1  0
 19 24  1  0
 24 25  1  0
 25 26  2  0
 18 16  1  0
 25 16  1  0
 30 55  1  0
 30 56  1  0
 30 57  1  0
  2 34  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 35  1  0
  6 36  1  0
  6 37  1  0
  6 38  1  0
  7 39  1  0
  8 40  1  0
  9 41  1  0
 10 42  1  0
 11 43  1  0
 13 44  1  0
 13 45  1  0
 13 46  1  0
 18 47  1  6
 20 48  1  0
 21 49  1  0
 21 50  1  0
 22 51  1  0
 22 52  1  0
 23 53  1  0
 24 54  1  0
M  END


  Mrv1533004201500182D          

 30 31  0  0  0  0            999 V2000
   -7.3124   -0.8752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9768   -0.1215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1563   -0.0352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6714   -0.7027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8208    0.7184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3057    1.3859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9701    2.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0003    0.8047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5154    0.1372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8509   -0.6164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6949    0.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2100   -0.4440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3895   -0.3577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9046   -1.0252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0841   -0.9389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5992   -1.6064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347   -2.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2213   -1.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7062   -2.1876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5569   -0.7665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1576   -0.3540    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5569    0.0585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3415    0.3135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0059    1.0671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0560    0.7260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7704    0.3135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4849    0.7260    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8264   -0.3540    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3415   -1.0214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5964   -1.8060    0.0000 O   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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  4  0  0  0
  8  5  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 11  9  1  4  0  0  0
 11 12  2  0  0  0  0
 13 12  1  4  0  0  0
 13 14  2  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 22  1  0  0  0  0
 22 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
 26 27  1  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  0  0  0  0
 20 29  1  0  0  0  0
 29 30  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0314567

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C(=CC)C=C(C)C=CC=CC=C(C)C(=O)C12OC1C(O)(CCO)NC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H27NO7/c1-5-16(18(26)29-4)13-14(2)9-7-6-8-10-15(3)17(25)22-19(30-22)21(28,11-12-24)23-20(22)27/h5-10,13,19,24,28H,11-12H2,1-4H3,(H,23,27)

> <INCHI_KEY>
OHWILISHWFHITP-UHFFFAOYSA-N

> <FORMULA>
C22H27NO7

> <MOLECULAR_WEIGHT>
417.458

> <EXACT_MASS>
417.178752213

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
44.61376249771926

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 2-ethylidene-11-[4-hydroxy-4-(2-hydroxyethyl)-2-oxo-6-oxa-3-azabicyclo[3.1.0]hexan-1-yl]-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate

> <ALOGPS_LOGP>
2.19

> <JCHEM_LOGP>
2.2911527173333344

> <ALOGPS_LOGS>
-4.44

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.671114038000042

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.208607841680964

> <JCHEM_PKA_STRONGEST_BASIC>
-2.4354784299534646

> <JCHEM_POLAR_SURFACE_AREA>
125.46000000000001

> <JCHEM_REFRACTIVITY>
113.92869999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.52e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-ethylidene-11-[4-hydroxy-4-(2-hydroxyethyl)-2-oxo-6-oxa-3-azabicyclo[3.1.0]hexan-1-yl]-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0     -13.650  -1.634   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0     -13.023  -0.227   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0     -11.492  -0.066   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0     -10.587  -1.312   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0     -10.865   1.341   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -11.771   2.587   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -11.144   3.994   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -9.334   1.502   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -8.429   0.256   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -9.055  -1.151   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.897   0.417   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.992  -0.829   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.460  -0.668   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.555  -1.914   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.024  -1.753   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.118  -2.999   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.745  -4.405   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.413  -2.838   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.318  -4.083   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.039  -1.431   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.294  -0.661   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.039   0.109   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.504   0.585   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.878   1.992   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.838   1.355   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.171   0.585   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.505   1.355   0.000  0.00  0.00           O+0
HETATM   28  N   UNK     0       3.409  -0.661   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0       2.504  -1.907   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.980  -3.371   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    5    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22   29                                             
CONECT   21   20   22                                                       
CONECT   22   21   20   23                                                  
CONECT   23   22   24   25   28                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   23   29                                                       
CONECT   29   28   20   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   62    0
END

View in JSmol

Synonyms

Value	Source
Methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoic acid	Generator

Chemical Formula

C₂₂H₂₇NO₇

Average Mass

417.4580 Da

Monoisotopic Mass

417.17875 Da

IUPAC Name

methyl 2-ethylidene-11-[4-hydroxy-4-(2-hydroxyethyl)-2-oxo-6-oxa-3-azabicyclo[3.1.0]hexan-1-yl]-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate

Traditional Name

methyl 2-ethylidene-11-[4-hydroxy-4-(2-hydroxyethyl)-2-oxo-6-oxa-3-azabicyclo[3.1.0]hexan-1-yl]-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate

CAS Registry Number

Not Available

SMILES

COC(=O)C(=CC)C=C(C)C=CC=CC=C(C)C(=O)C12OC1C(O)(CCO)NC2=O

InChI Identifier

InChI=1S/C22H27NO7/c1-5-16(18(26)29-4)13-14(2)9-7-6-8-10-15(3)17(25)22-19(30-22)21(28,11-12-24)23-20(22)27/h5-10,13,19,24,28H,11-12H2,1-4H3,(H,23,27)

InChI Key

OHWILISHWFHITP-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

Species Name	Source	Reference
Fusarium tricinctum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acid esters

Direct Parent

Fatty acid esters

Alternative Parents

Substituents

Fatty acid ester
B'-hydroxy-alpha,beta-unsaturated-ketone
Para-oxazine
Alpha-branched alpha,beta-unsaturated-ketone
Acryloyl-group
Enone
Pyrroline
Cyclic carboximidic acid
Alpha,beta-unsaturated ketone
Methyl ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Ketone
Alkanolamine
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Oxacycle
Azacycle
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
Organic oxide
Organonitrogen compound
Organooxygen compound
Primary alcohol
Alcohol
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	2.19	ALOGPS
logP	2.29	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	10.21	ChemAxon
pKa (Strongest Basic)	-2.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	125.46 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	113.93 m³·mol⁻¹	ChemAxon
Polarizability	44.61 Å³	ChemAxon
Number of Rings	2	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

85045822

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate (NP0314567)

MOL for NP0314567 (methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate)

3D MOL for NP0314567 (methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate)

3D SDF for NP0314567 (methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate)

3D-SDF for NP0314567 (methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate)

PDB for NP0314567 (methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate)

3D PDB for NP0314567 (methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate)

SMILES for NP0314567 (methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate)

INCHI for NP0314567 (methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate)

Structure for NP0314567 (methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate)

3D Structure for NP0314567 (methyl 11-[2,4-dihydroxy-4-(2-hydroxyethyl)-6-oxa-3-azabicyclo[3.1.0]hex-2-en-1-yl]-2-ethylidene-4,10-dimethyl-11-oxoundeca-3,5,7,9-tetraenoate)