NP-MRD: Showing NP-Card for [26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid (NP0190144)

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Record Information

Version

2.0

Created at

2022-09-04 06:45:40 UTC

Updated at

2022-09-04 06:45:41 UTC

NP-MRD ID

NP0190144

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid

Description

2-[26-(Carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]Tetratriacontan-9-yl]acetic acid belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups. [26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid is found in Cryptoporus volvatus. 2-[26-(Carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]Tetratriacontan-9-yl]acetic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171515392D          

 58 62  0  0  0  0            999 V2000
   10.8267    3.3413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5664    2.5585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7582    2.3925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2104    3.0094    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4979    1.6097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2357    1.2406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8397    0.6785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2608   -0.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4567    0.1537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2145    0.9423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8948   -0.4504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1371   -1.2391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9412   -1.4236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1834   -2.2123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5266   -2.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9875   -2.3968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5494   -1.7927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3071   -1.0041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5030   -0.8195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6989   -0.6350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7050   -3.1153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0628   -3.6331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3007   -3.9490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5049   -4.7483    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4804   -4.0374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4512   -4.8619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1505   -5.2995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8792   -4.9125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1213   -6.1239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6685   -3.8911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9307   -3.5220    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3267   -2.9600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9056   -2.2506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0904   -2.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7929   -3.1471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5728   -1.7352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8703   -0.9658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6855   -0.8387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9830   -0.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3111   -0.5480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7981    0.0579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3158   -0.5845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0182   -1.3540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2031   -1.4811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3879   -1.6082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4613    0.8339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1036    1.3517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8657    1.6676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6615    2.4669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6860    1.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7152    2.5804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0158    3.0180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2872    2.6311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0451    3.8425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4081   -4.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9559   -5.2908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6000   -4.8399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3396   -5.6227    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  2  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  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  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
  8 19  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  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
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 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
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 33 44  1  0  0  0  0
 38 44  1  0  0  0  0
 44 45  1  0  0  0  0
 39 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 48 50  1  0  0  0  0
  5 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52 53  2  0  0  0  0
 52 54  1  0  0  0  0
 30 55  1  0  0  0  0
 55 56  2  0  0  0  0
 55 57  1  0  0  0  0
 57 58  1  0  0  0  0
M  END

     RDKit          3D

122126  0  0  0  0  0  0  0  0999 V2000
   -5.7486   -0.8415    1.9795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7660   -0.1469    1.4186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8487    0.5978    2.3128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5252    0.9215    1.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5392    1.3982    0.2962 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9612    2.7877    0.1456 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8523    3.5367    1.4305 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7191    3.6520   -0.8321 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1947    3.6576   -0.6592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7953    2.3463   -0.2156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8331    1.2122   -0.4288 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6210    1.1082   -1.9330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5347   -0.0731   -0.0293 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7612   -1.2872   -0.5588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2174   -1.9430    0.5063 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1169   -3.3269    0.3769 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8405   -3.7640   -0.9933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6735   -3.0463   -2.0022 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7406   -5.1485   -1.2639 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4756   -5.6239   -2.5805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0822   -3.7812    1.3911 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7746   -5.2326    1.3607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9724   -6.0194    1.6559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9948   -7.2902    1.5079 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1356   -5.4468    2.1082 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8878   -2.9074    1.4031 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5710   -2.4601    2.5549 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1363   -2.5567    0.3413 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7344   -3.2288   -0.4935 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1759   -3.0627   -0.0676 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3031   -3.8350    1.2309 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0087   -3.7793   -1.1044 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4496   -2.9305   -2.2351 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8260   -1.5821   -2.3534 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6768   -0.8054   -1.0708 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3717   -0.0591   -1.2119 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7837    0.2040   -1.0249 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6127    1.3957   -0.1417 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6931    2.3366   -0.4951 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1483    3.6258   -0.5600 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0897    4.0381    0.5028 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6148    5.1998    0.4411 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4368    3.2397    1.5666 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3567    3.7124    2.5584 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0785    4.6947   -0.5715 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6700    5.1052    0.8359 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8387    6.3314    0.8125 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4011    6.8568    1.8485 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5447    6.9036   -0.4124 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9317    4.4196   -1.4476 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0624    4.6762   -2.6910 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2208    3.9186   -0.9727 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5313    2.6746   -0.4223 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.1890    0.1303   -1.2250 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1639   -1.4488    0.2581 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8867   -1.7013    0.9411 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6175   -1.6628    0.1632 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4246   -1.3904    1.3236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9062   -0.8860    3.0288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3489    1.4651    2.7927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6599   -0.1019    3.1838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8662    0.0137    1.8493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0459    1.6628    2.4092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8156    0.7258   -0.2600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7308    4.6277    1.1511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7848    3.5209    2.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9543    3.3115    2.0394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3791    4.7112   -0.5939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3587    3.5123   -1.8758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6363    4.0146   -1.6320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5096    4.4457    0.0876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6621    2.1487   -0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2480    2.3804    0.7809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5650    0.8977   -2.1768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0443    1.9861   -2.4796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1902    0.2405   -2.3811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5529   -0.0120   -0.5183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4795   -1.8692   -1.1480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9643   -0.8672   -1.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1229   -3.7010    0.6519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9298   -6.6352   -2.7244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3791   -5.6898   -2.7164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8680   -4.8990   -3.3345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5889   -3.6218    2.4022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2453   -5.5981    0.4611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0538   -5.4197    2.2111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4723   -5.5294    3.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5500   -4.3206   -0.3707 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5748   -3.0678   -1.5738 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4541   -4.5749    1.3596 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004171515392D          

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M  END
> <DATABASE_ID>
NP0190144

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1OCC2C(=C)CCC3C(C)(CCCC23C)COC(=O)C(CC(O)=O)C(OCC2C(=C)CCC3C(C)(CCCC23C)COC(=O)C1CC(O)=O)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C44H64O14/c1-25-11-13-31-41(3)15-9-17-43(31,5)29(25)21-55-35(39(51)53-7)27(19-33(45)46)37(49)58-24-42(4)16-10-18-44(6)30(26(2)12-14-32(42)44)22-56-36(40(52)54-8)28(20-34(47)48)38(50)57-23-41/h27-32,35-36H,1-2,9-24H2,3-8H3,(H,45,46)(H,47,48)

> <INCHI_KEY>
OXFMLGZWGZNFCM-UHFFFAOYSA-N

> <FORMULA>
C44H64O14

> <MOLECULAR_WEIGHT>
816.982

> <EXACT_MASS>
816.429606741

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
122

> <JCHEM_AVERAGE_POLARIZABILITY>
85.92780904427718

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid

> <ALOGPS_LOGP>
3.65

> <JCHEM_LOGP>
5.333223576

> <ALOGPS_LOGS>
-5.73

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.460939153912462

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.858879166163839

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9240722879969376

> <JCHEM_POLAR_SURFACE_AREA>
198.26

> <JCHEM_REFRACTIVITY>
207.17160000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.53e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      20.210   6.237   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      19.724   4.776   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      18.215   4.466   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      17.193   5.618   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      17.729   3.005   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      19.107   2.316   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      20.234   1.267   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      21.020  -0.058   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      19.519   0.287   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      19.067   1.759   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      18.470  -0.841   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      18.923  -2.313   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      20.423  -2.657   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      20.876  -4.130   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      21.516  -5.530   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      22.377  -4.474   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      23.425  -3.346   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      22.973  -1.874   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      21.472  -1.530   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      19.971  -1.185   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      19.983  -5.815   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      18.784  -6.782   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      17.361  -7.371   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      17.742  -8.864   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      15.830  -7.536   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.775  -9.076   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      17.081  -9.892   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      18.441  -9.170   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      17.026 -11.431   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      14.314  -7.263   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      12.937  -6.574   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      11.810  -5.525   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.024  -4.201   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.502  -4.438   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.947  -5.875   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.536  -3.239   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       9.091  -1.803   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      10.613  -1.566   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      11.168  -0.129   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       9.914  -1.023   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      12.690   0.108   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      13.656  -1.091   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      13.101  -2.527   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      11.579  -2.765   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      10.057  -3.002   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      12.061   1.557   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      13.260   2.523   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      14.683   3.113   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      14.301   4.605   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      16.214   3.278   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      16.268   4.817   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      14.963   5.634   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      13.603   4.911   0.000  0.00  0.00           O+0
HETATM   54  O   UNK     0      15.017   7.173   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0      13.829  -8.725   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      14.851  -9.876   0.000  0.00  0.00           O+0
HETATM   57  O   UNK     0      12.320  -9.034   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0      11.834 -10.496   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   50                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   19                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15   16   21                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18    8   13   20                                             
CONECT   20   19                                                            
CONECT   21   14   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   25   31   55                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   44                                                  
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   44                                                  
CONECT   39   38   40   41   46                                             
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   33   38   45                                             
CONECT   45   44                                                            
CONECT   46   39   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48    5   51                                                  
CONECT   51   50   52                                                       
CONECT   52   51   53   54                                                  
CONECT   53   52                                                            
CONECT   54   52                                                            
CONECT   55   30   56   57                                                  
CONECT   56   55                                                            
CONECT   57   55   58                                                       
CONECT   58   57                                                            
MASTER        0    0    0    0    0    0    0    0   58    0  124    0
END

View in JSmol

Synonyms

Value	Source
2-[26-(Carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0,.0,.0,]tetratriacontan-9-yl]acetate	Generator
2-[26-(Carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetate	Generator

Chemical Formula

C₄₄H₆₄O₁₄

Average Mass

816.9820 Da

Monoisotopic Mass

816.42961 Da

IUPAC Name

2-[26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

COC(=O)C1OCC2C(=C)CCC3C(C)(CCCC23C)COC(=O)C(CC(O)=O)C(OCC2C(=C)CCC3C(C)(CCCC23C)COC(=O)C1CC(O)=O)C(=O)OC

InChI Identifier

InChI=1S/C44H64O14/c1-25-11-13-31-41(3)15-9-17-43(31,5)29(25)21-55-35(39(51)53-7)27(19-33(45)46)37(49)58-24-42(4)16-10-18-44(6)30(26(2)12-14-32(42)44)22-56-36(40(52)54-8)28(20-34(47)48)38(50)57-23-41/h27-32,35-36H,1-2,9-24H2,3-8H3,(H,45,46)(H,47,48)

InChI Key

OXFMLGZWGZNFCM-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
Cryptoporus volvatus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Hexacarboxylic acids and derivatives

Direct Parent

Hexacarboxylic acids and derivatives

Alternative Parents

Substituents

Hexacarboxylic acid or derivatives
Macrolide
Methyl ester
Carboxylic acid ester
Lactone
Carboxylic acid
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	3.65	ALOGPS
logP	5.33	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	3.86	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	198.26 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	207.17 m³·mol⁻¹	ChemAxon
Polarizability	85.93 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

73228378

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid (NP0190144)

MOL for NP0190144 ([26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid)

3D MOL for NP0190144 ([26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid)

3D SDF for NP0190144 ([26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid)

3D-SDF for NP0190144 ([26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid)

PDB for NP0190144 ([26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid)

3D PDB for NP0190144 ([26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid)

SMILES for NP0190144 ([26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid)

INCHI for NP0190144 ([26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid)

Structure for NP0190144 ([26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid)

3D Structure for NP0190144 ([26-(carboxymethyl)-10,27-bis(methoxycarbonyl)-1,5,18,22-tetramethyl-14,31-dimethylidene-8,25-dioxo-7,11,24,28-tetraoxapentacyclo[28.4.0.0⁵,³⁴.0¹³,¹⁸.0¹⁷,²²]tetratriacontan-9-yl]acetic acid)