NP-MRD: Showing NP-Card for n-{11,18-dihydroxy-16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosa-10,17-dien-12-yl}ethanimidic acid (NP0324645)

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Record Information

Version

2.0

Created at

2022-09-12 04:51:23 UTC

Updated at

2022-09-12 04:51:23 UTC

NP-MRD ID

NP0324645

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-{11,18-dihydroxy-16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosa-10,17-dien-12-yl}ethanimidic acid

Description

N-{11,18-dihydroxy-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-16-(propan-2-yl)-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]Pentacosa-10,17-dien-12-yl}ethanimidic acid belongs to the class of organic compounds known as steroidal glycosides. These are sterol lipids containing a carbohydrate moiety glycosidically linked to the steroid skeleton. n-{11,18-dihydroxy-16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosa-10,17-dien-12-yl}ethanimidic acid is found in Aspergillus carneus. N-{11,18-dihydroxy-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-16-(propan-2-yl)-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]Pentacosa-10,17-dien-12-yl}ethanimidic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251506522D          

 52 55  0  0  0  0            999 V2000
    2.9857   -3.7580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1189   -2.9439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4804   -2.4214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6135   -1.6073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9750   -1.0848    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2033   -1.3766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0702   -2.1908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5648   -0.8542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2004   -1.1626    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8501   -0.6542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6152   -0.9626    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7346    0.1627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6717    0.0423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4757    0.2272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2259    0.7364    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7483    1.3749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5388    2.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5170    1.0754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3745    1.3577    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0130    0.8353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8799    0.0211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7847    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9179    1.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2794    2.4636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5077    2.1719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8692    2.6943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0023    3.5085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3638    4.0309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5921    3.7391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7740    3.8002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4126    3.2778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4232    0.6046    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2901   -0.2096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1949    0.8964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3281    1.7106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8334    0.3740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6489    0.4989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0198   -0.2380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4335   -0.8185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7003   -0.4402    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9286   -0.7320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1049   -0.6846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7954   -1.5462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3114   -2.1899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8586   -2.8795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0628   -2.6620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0237   -1.8379    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3852   -1.3155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5184   -0.5013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    1.9001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3892    2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8359    2.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  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
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  2  0  0  0  0
 24 31  1  0  0  0  0
 22 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 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
 36 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 43 47  1  0  0  0  0
 47 48  1  0  0  0  0
  4 48  1  0  0  0  0
 48 49  2  0  0  0  0
 18 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  1  0  0  0  0
M  END

     RDKit          3D

106109  0  0  0  0  0  0  0  0999 V2000
   -6.3266    1.9376   -0.9147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9629    0.5149   -1.1831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6164    0.2872   -1.7582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4531    0.7583   -0.9076 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4282    0.1375    0.3756 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0944   -1.1804    0.6636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3956   -1.5755    1.8603 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4578   -2.1982   -0.1619 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3593   -2.9736   -0.9915 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1922   -3.2202   -2.3675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1585   -4.0207   -3.1393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1967   -2.7484   -2.9560 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6401   -3.1633    0.7232 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5247   -4.3226    1.1562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5772   -3.6991    0.0277 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7520   -3.4402    0.0677 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3632   -3.3071   -1.0534 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5918   -3.2925    1.2681 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9547   -4.7493    1.6410 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6824   -5.4656    0.5645 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7134   -5.4874    2.0962 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7446   -2.4667    1.1540 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0333   -1.1465    1.5000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9392   -0.9949    2.4306 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5152    0.1458    1.0197 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4106    0.2482   -0.5130 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7347    0.1080   -1.1487 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4944    1.2406   -1.3398 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7497    1.1415   -1.9447 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2399   -0.0648   -2.3524 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.4887   -1.2034   -2.1663 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2362   -1.0950   -1.5612 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.5551    2.3497    3.1219 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6941    3.1510    1.2504 C   0  0  2  0  0  0  0  0  0  0  0  0
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    1.9834    5.4684    1.0120 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6130    4.7709   -0.2968 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7888    3.6727    0.2534 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4928    3.2339   -0.0845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7113    3.0008   -1.3291 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6619    2.9932    0.7982 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7923    4.1347    1.8235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5869    5.1735    1.0558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6558    4.3190    0.4811 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3502    2.2078   -0.9398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7077    2.7606   -2.0542 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.6633    2.3924   -0.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2188   -3.3938   -0.5310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1287   -4.1471   -2.6179 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.4076   -5.1463    0.4210 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8812   -3.0309    2.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6269   -4.6554    2.5269 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1440    4.3405    2.3662 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1819    6.1991    1.2424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9352    5.9861    0.8428 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6778    2.0135    1.2672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8121    4.5751    2.0544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2689    3.8140    2.7462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0348    5.8853    1.7982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9770    5.6643    0.3005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0913    4.8474   -0.3901 H   0  0  0  0  0  0  0  0  0  0  0  0
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 22 79  1  0
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 36 92  1  0
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 46100  1  1
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 47102  1  0
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 49105  1  0
 49106  1  0
 19 72  1  0
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 20 75  1  0
 21 76  1  0
 21 77  1  0
 21 78  1  0
M  END


  Mrv1533004251506522D          

 52 55  0  0  0  0            999 V2000
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    2.6135   -1.6073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.2033   -1.3766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0702   -2.1908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5648   -0.8542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2004   -1.1626    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8501   -0.6542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6152   -0.9626    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7346    0.1627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6717    0.0423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4757    0.2272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2259    0.7364    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7483    1.3749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3745    1.3577    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0130    0.8353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8799    0.0211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7847    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9179    1.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2794    2.4636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5077    2.1719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8692    2.6943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0023    3.5085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3638    4.0309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5921    3.7391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7740    3.8002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4126    3.2778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4232    0.6046    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2901   -0.2096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1949    0.8964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3281    1.7106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8334    0.3740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6489    0.4989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0198   -0.2380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4335   -0.8185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7003   -0.4402    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9286   -0.7320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1049   -0.6846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7954   -1.5462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3114   -2.1899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8586   -2.8795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0628   -2.6620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0237   -1.8379    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3852   -1.3155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5184   -0.5013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    1.9001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3892    2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8359    2.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  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
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  2  0  0  0  0
 24 31  1  0  0  0  0
 22 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 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
 36 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 43 47  1  0  0  0  0
 47 48  1  0  0  0  0
  4 48  1  0  0  0  0
 48 49  2  0  0  0  0
 18 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0324645

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC1NC(=O)C(NC(C)=O)C(C)OC(=O)C(NC(=O)C(CC2=CC=C(OC)C=C2)N(C)C(=O)C2CCCN2C(=O)C2CCCN2C1=O)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C37H54N6O9/c1-8-11-26-34(47)42-18-10-13-28(42)36(49)43-19-9-12-27(43)35(48)41(6)29(20-24-14-16-25(51-7)17-15-24)32(45)40-30(21(2)3)37(50)52-22(4)31(33(46)39-26)38-23(5)44/h14-17,21-22,26-31H,8-13,18-20H2,1-7H3,(H,38,44)(H,39,46)(H,40,45)

> <INCHI_KEY>
WQYQLZJEDBPTDY-UHFFFAOYSA-N

> <FORMULA>
C37H54N6O9

> <MOLECULAR_WEIGHT>
726.872

> <EXACT_MASS>
726.395227343

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
106

> <JCHEM_AVERAGE_POLARIZABILITY>
76.3492533490278

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-{19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,11,15,18,21-hexaoxo-16-(propan-2-yl)-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosan-12-yl}acetamide

> <ALOGPS_LOGP>
2.04

> <JCHEM_LOGP>
0.7139250886666649

> <ALOGPS_LOGS>
-3.52

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.094627027111583

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.643056598892882

> <JCHEM_PKA_STRONGEST_BASIC>
-1.8169849746022018

> <JCHEM_POLAR_SURFACE_AREA>
183.76

> <JCHEM_REFRACTIVITY>
188.37610000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.22e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-{16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,11,15,18,21-hexaoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosan-12-yl}acetamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       5.573  -7.015   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.822  -5.495   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.630  -4.520   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.879  -3.000   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       3.687  -2.025   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       2.246  -2.570   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.998  -4.089   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.054  -1.594   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -0.374  -2.170   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -1.587  -1.221   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -3.015  -1.797   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.371   0.304   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.254   0.079   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.755   0.424   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.422   1.375   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.397   2.567   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.006   4.056   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.832   2.007   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       4.432   2.534   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       5.624   1.559   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.376   0.039   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.065   2.104   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.313   3.624   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.122   4.599   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.681   4.054   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.489   5.029   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.738   6.549   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.546   7.524   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.105   6.980   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.178   7.094   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.370   6.119   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0       8.257   1.129   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0       8.008  -0.391   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.697   1.673   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       9.946   3.193   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      10.889   0.698   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      12.411   0.931   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      13.104  -0.444   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      12.009  -1.528   0.000  0.00  0.00           C+0
HETATM   40  N   UNK     0      10.641  -0.822   0.000  0.00  0.00           N+0
HETATM   41  C   UNK     0       9.200  -1.366   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       7.663  -1.278   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       8.951  -2.886   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       9.915  -4.088   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       9.069  -5.375   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       7.584  -4.969   0.000  0.00  0.00           C+0
HETATM   47  N   UNK     0       7.511  -3.431   0.000  0.00  0.00           N+0
HETATM   48  C   UNK     0       6.319  -2.456   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       6.568  -0.936   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       2.873   3.547   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       2.593   5.061   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       1.560   4.352   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   48                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    8   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   50                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   32                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   31                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   30                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   27   31                                                       
CONECT   31   30   24                                                       
CONECT   32   22   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   40                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   36   41                                                  
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44   47                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   43   48                                                  
CONECT   48   47    4   49                                                  
CONECT   49   48                                                            
CONECT   50   18   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  110    0
END

View in JSmol

Synonyms

Value	Source
N-{11,18-dihydroxy-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-16-(propan-2-yl)-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosa-10,17-dien-12-yl}ethanimidate	Generator

Chemical Formula

C₃₇H₅₄N₆O₉

Average Mass

726.8720 Da

Monoisotopic Mass

726.39523 Da

IUPAC Name

N-{19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,11,15,18,21-hexaoxo-16-(propan-2-yl)-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosan-12-yl}acetamide

Traditional Name

N-{16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,11,15,18,21-hexaoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosan-12-yl}acetamide

CAS Registry Number

Not Available

SMILES

CCCC1NC(=O)C(NC(C)=O)C(C)OC(=O)C(NC(=O)C(CC2=CC=C(OC)C=C2)N(C)C(=O)C2CCCN2C(=O)C2CCCN2C1=O)C(C)C

InChI Identifier

InChI=1S/C37H54N6O9/c1-8-11-26-34(47)42-18-10-13-28(42)36(49)43-19-9-12-27(43)35(48)41(6)29(20-24-14-16-25(51-7)17-15-24)32(45)40-30(21(2)3)37(50)52-22(4)31(33(46)39-26)38-23(5)44/h14-17,21-22,26-31H,8-13,18-20H2,1-7H3,(H,38,44)(H,39,46)(H,40,45)

InChI Key

WQYQLZJEDBPTDY-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
Aspergillus carneus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroidal glycosides. These are sterol lipids containing a carbohydrate moiety glycosidically linked to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Steroidal glycosides

Alternative Parents

Substituents

Steroidal glycoside
Oligosaccharide
20-oxosteroid
Pregnane-skeleton
Steroid ester
14-hydroxysteroid
Hydroxysteroid
Oxosteroid
17-hydroxysteroid
Delta-5-steroid
Glycosyl compound
O-glycosyl compound
Oxane
Alpha-hydroxy ketone
Cyclic alcohol
Tertiary alcohol
Secondary alcohol
Carboxylic acid ester
Ketone
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Acetal
Dialkyl ether
Ether
Monocarboxylic acid or derivatives
Alcohol
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
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	2.04	ALOGPS
logP	0.71	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	11.64	ChemAxon
pKa (Strongest Basic)	-1.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	183.76 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	188.38 m³·mol⁻¹	ChemAxon
Polarizability	76.35 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	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

73837654

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-{11,18-dihydroxy-16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosa-10,17-dien-12-yl}ethanimidic acid (NP0324645)

MOL for NP0324645 (n-{11,18-dihydroxy-16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosa-10,17-dien-12-yl}ethanimidic acid)

3D MOL for NP0324645 (n-{11,18-dihydroxy-16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosa-10,17-dien-12-yl}ethanimidic acid)

3D SDF for NP0324645 (n-{11,18-dihydroxy-16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosa-10,17-dien-12-yl}ethanimidic acid)

3D-SDF for NP0324645 (n-{11,18-dihydroxy-16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosa-10,17-dien-12-yl}ethanimidic acid)

PDB for NP0324645 (n-{11,18-dihydroxy-16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosa-10,17-dien-12-yl}ethanimidic acid)

3D PDB for NP0324645 (n-{11,18-dihydroxy-16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosa-10,17-dien-12-yl}ethanimidic acid)

SMILES for NP0324645 (n-{11,18-dihydroxy-16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosa-10,17-dien-12-yl}ethanimidic acid)

INCHI for NP0324645 (n-{11,18-dihydroxy-16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosa-10,17-dien-12-yl}ethanimidic acid)

Structure for NP0324645 (n-{11,18-dihydroxy-16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosa-10,17-dien-12-yl}ethanimidic acid)

3D Structure for NP0324645 (n-{11,18-dihydroxy-16-isopropyl-19-[(4-methoxyphenyl)methyl]-13,20-dimethyl-2,8,15,21-tetraoxo-9-propyl-14-oxa-1,7,10,17,20-pentaazatricyclo[20.3.0.0³,⁷]pentacosa-10,17-dien-12-yl}ethanimidic acid)