NP-MRD: Showing NP-Card for 2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-n-[1,4,7,14-tetrahydroxy-3,6,9-triisopropyl-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3h,6h,9h,12h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid (NP0268896)

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Record Information

Version

2.0

Created at

2022-09-08 14:10:19 UTC

Updated at

2022-09-08 14:10:19 UTC

NP-MRD ID

NP0268896

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-n-[1,4,7,14-tetrahydroxy-3,6,9-triisopropyl-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3h,6h,9h,12h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid

Description

2-[(1-Hydroxy-2-phenylethylidene)amino]-3-methyl-N-[1,4,7,14-tetrahydroxy-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3,6,9-tris(propan-2-yl)-3H,6H,9H,10H,12H,13H,16H,17H,19H,20H,21H,21aH-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating. Based on a literature review very few articles have been published on 2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-N-[1,4,7,14-tetrahydroxy-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3,6,9-tris(propan-2-yl)-3H,6H,9H,10H,12H,13H,16H,17H,19H,20H,21H,21aH-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082216102D          

 59 61  0  0  0  0            999 V2000
    4.7002    0.2880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2648   -0.3135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6075   -0.8122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0681   -0.1254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6327   -0.7269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4359   -0.5387    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.6746    0.2510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1100    0.8525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4778    0.4392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6993    1.2339    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.4982    1.4395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0758    0.8503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7197    2.2342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5187    2.4398    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.0962    1.8507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8747    1.0559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8952    2.0562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4727    1.4671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2717    1.6727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8492    1.0835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6277    0.2888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8288    0.0832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2512    0.6724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1422    2.8234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3636    3.6181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3432    2.6178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1236   -0.1916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7806   -0.9419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9457   -0.2609    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1339   -1.0641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8944   -1.3840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4281   -1.4913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0687   -2.0112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9388   -2.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8392   -1.7163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1297   -2.3434    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.3264   -2.5315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7618   -1.9300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0878   -3.3213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6524   -3.9228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4137   -4.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4556   -3.7346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2845   -3.5094    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.0459   -4.2992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6105   -4.9007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2426   -4.4874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0040   -5.2771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5686   -5.8786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2007   -5.4653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6780   -3.8858    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9167   -3.0961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7199   -2.9079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3521   -2.4945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5273   -2.5116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2562   -1.7324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9134   -1.2338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5907   -1.7048    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3940   -1.5166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9586   -2.1182    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
 10  9  1  4  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 14 13  1  4  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 13 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
  9 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 36 32  1  4  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 43 39  1  4  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
 50 46  1  4  0  0  0
 50 51  2  0  0  0  0
 51 52  1  0  0  0  0
 51 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 53 57  1  0  0  0  0
 57 58  1  0  0  0  0
  5 58  1  0  0  0  0
 58 59  2  0  0  0  0
M  END

     RDKit          3D

126128  0  0  0  0  0  0  0  0999 V2000
    0.7666    6.5391    1.8483 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0190    5.1339    1.3070 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4433    5.0298    0.9148 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0029    4.9010    0.2505 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1252    3.5313   -0.4084 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0131    2.5868    0.6720 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4538    1.3915    0.7114 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2378    0.5761    1.8424 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2284    0.8111   -0.4049 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6191    1.1390   -0.2936 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3356    1.0832    0.6882 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8394    0.6384    1.9848 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7970    1.4294    0.8067 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4980    0.5884    1.5929 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1203   -0.1534    2.2616 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8207   -0.0833    3.7143 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1618   -1.1530    1.9248 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0368   -1.6967    0.5753 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9682   -1.3508   -0.3935 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8218   -1.9216   -1.6578 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7977   -2.7875   -1.9334 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8764   -3.1225   -0.9631 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9974   -2.5759    0.2945 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3244    1.7014   -0.5747 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8004    2.0443   -0.5329 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0054    0.5657   -1.4917 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0910   -0.7201   -0.4137 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3866   -1.0985   -1.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.8234   -3.2361    0.6661 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1288   -4.5844    0.7434 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2063   -4.6023    0.0398 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1715   -4.9794    2.1899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0809   -3.3423    1.3134 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2548   -3.1864    0.8886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3499   -3.3437    1.7127 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5370   -2.8146   -0.5473 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3303   -4.1366   -1.3284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3223   -5.1398   -0.7938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6191   -3.9109   -2.8041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8885   -2.4851   -0.7575 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6645   -1.5567   -0.6803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0200   -1.7562   -1.0302 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3751   -0.1365   -0.2373 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.6866    0.6635   -0.3481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7538    0.0259    0.5297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2063    0.7108   -1.7611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3447    0.3985   -0.9727 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4623    1.2028   -1.1340 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.9483    2.3423   -0.3181 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -2.3156    3.3390   -1.2043 N   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5150    3.4338   -2.6718 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4180    6.7039    2.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3088    6.7223    2.0222 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1386    7.2353    1.0552 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8375    4.4536    2.1999 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6897    4.2305    0.1864 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0380    4.7630    1.8363 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8480    6.0196    0.6037 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0885    5.6397   -0.5812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9992    5.0283    0.6922 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1251    3.3999   -0.8442 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2278    0.9775    2.7728 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8805    1.2173   -1.3924 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7369    1.3806    2.6810 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7990    2.4973    1.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7440    0.8848    4.0584 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.1473   -1.9802    2.6872 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.7973    2.6230   -0.9779 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1311    1.8711    0.5174 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9824    3.0672   -0.8835 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2978    1.3430   -1.2378 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3350    0.8916   -2.3336 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9455    0.1106   -1.9082 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4693   -0.2193   -0.9276 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1347   -1.1257   -0.5283 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6335   -2.1156   -2.0656 H   0  0  0  0  0  0  0  0  0  0  0  0
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 35100  1  0
M  END


  Mrv1652309082216102D          

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M  END
> <DATABASE_ID>
NP0268896

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC1N=C(O)C(N=C(O)C(N=C(O)CC2=CC=CC=C2)C(C)C)C(C)OC(=O)C(N=C(O)C(N=C(O)C(N=C(O)C2CCCN2C1=O)C(C)C)C(C)C)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C43H67N7O9/c1-22(2)20-29-42(57)50-19-15-18-30(50)37(52)46-33(24(5)6)39(54)47-34(25(7)8)40(55)48-35(26(9)10)43(58)59-27(11)36(41(56)44-29)49-38(53)32(23(3)4)45-31(51)21-28-16-13-12-14-17-28/h12-14,16-17,22-27,29-30,32-36H,15,18-21H2,1-11H3,(H,44,56)(H,45,51)(H,46,52)(H,47,54)(H,48,55)(H,49,53)

> <INCHI_KEY>
RSWKXBQPPHRRRM-UHFFFAOYSA-N

> <FORMULA>
C43H67N7O9

> <MOLECULAR_WEIGHT>
826.049

> <EXACT_MASS>
825.500026765

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
126

> <JCHEM_AVERAGE_POLARIZABILITY>
87.66291668491057

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-N-[1,4,7,14-tetrahydroxy-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3,6,9-tris(propan-2-yl)-3H,6H,9H,10H,12H,13H,16H,17H,19H,20H,21H,21aH-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid

> <JCHEM_LOGP>
7.549007671352025

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
3.504767843188239

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.0323731202016835

> <JCHEM_PKA_STRONGEST_BASIC>
1.8563941634492378

> <JCHEM_POLAR_SURFACE_AREA>
242.14999999999995

> <JCHEM_REFRACTIVITY>
221.39300000000017

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-N-[1,4,7,14-tetrahydroxy-3,6,9-triisopropyl-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3H,6H,9H,12H,13H,16H,19H,20H,21H,21aH-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       8.774   0.538   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.828  -0.585   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.601  -1.516   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.327  -0.234   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.381  -1.357   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      13.880  -1.006   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      14.326   0.469   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      13.272   1.591   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      15.825   0.820   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      16.239   2.303   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      17.730   2.687   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      18.808   1.587   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      18.143   4.171   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      19.635   4.554   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      20.713   3.455   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      20.300   1.971   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      22.204   3.838   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      23.282   2.739   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      24.774   3.122   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      25.852   2.023   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      25.438   0.539   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      23.947   0.155   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      22.869   1.255   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.065   5.270   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      17.479   6.754   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.574   4.887   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      17.031  -0.358   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      16.390  -1.758   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      18.565  -0.487   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      18.917  -1.986   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      20.336  -2.584   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      17.599  -2.784   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      18.795  -3.754   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      18.552  -5.275   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      20.233  -3.204   0.000  0.00  0.00           C+0
HETATM   36  N   UNK     0      17.042  -4.374   0.000  0.00  0.00           N+0
HETATM   37  C   UNK     0      15.543  -4.726   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      14.489  -3.603   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      15.097  -6.200   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      16.151  -7.323   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      15.706  -8.797   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      17.651  -6.971   0.000  0.00  0.00           C+0
HETATM   43  N   UNK     0      13.598  -6.551   0.000  0.00  0.00           N+0
HETATM   44  C   UNK     0      13.152  -8.025   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      14.206  -9.148   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      11.653  -8.376   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      11.207  -9.851   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      12.261 -10.973   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       9.708 -10.202   0.000  0.00  0.00           C+0
HETATM   50  N   UNK     0      10.599  -7.254   0.000  0.00  0.00           N+0
HETATM   51  C   UNK     0      11.044  -5.779   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      12.544  -5.428   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0       9.991  -4.656   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       8.451  -4.688   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0       7.945  -3.234   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       9.172  -2.303   0.000  0.00  0.00           C+0
HETATM   57  N   UNK     0      10.436  -3.182   0.000  0.00  0.00           N+0
HETATM   58  C   UNK     0      11.935  -2.831   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0      12.989  -3.954   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   58                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   27                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   24                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   18                                                       
CONECT   24   13   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27    9   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   36                                                  
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   32   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   43                                                  
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   39   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47   50                                                  
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47                                                            
CONECT   50   46   51                                                       
CONECT   51   50   52   53                                                  
CONECT   52   51                                                            
CONECT   53   51   54   57                                                  
CONECT   54   53   55                                                       
CONECT   55   54   56                                                       
CONECT   56   55   57                                                       
CONECT   57   56   53   58                                                  
CONECT   58   57    5   59                                                  
CONECT   59   58                                                            
MASTER        0    0    0    0    0    0    0    0   59    0  122    0
END

View in JSmol

Synonyms

Value	Source
2-[(1-Hydroxy-2-phenylethylidene)amino]-3-methyl-N-[1,4,7,14-tetrahydroxy-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3,6,9-tris(propan-2-yl)-3H,6H,9H,10H,12H,13H,16H,17H,19H,20H,21H,21ah-pyrrolo[2,1-L]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidate	Generator

Chemical Formula

C₄₃H₆₇N₇O₉

Average Mass

826.0490 Da

Monoisotopic Mass

825.50003 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)CC1N=C(O)C(N=C(O)C(N=C(O)CC2=CC=CC=C2)C(C)C)C(C)OC(=O)C(N=C(O)C(N=C(O)C(N=C(O)C2CCCN2C1=O)C(C)C)C(C)C)C(C)C

InChI Identifier

InChI=1S/C43H67N7O9/c1-22(2)20-29-42(57)50-19-15-18-30(50)37(52)46-33(24(5)6)39(54)47-34(25(7)8)40(55)48-35(26(9)10)43(58)59-27(11)36(41(56)44-29)49-38(53)32(23(3)4)45-31(51)21-28-16-13-12-14-17-28/h12-14,16-17,22-27,29-30,32-36H,15,18-21H2,1-11H3,(H,44,56)(H,45,51)(H,46,52)(H,47,54)(H,48,55)(H,49,53)

InChI Key

RSWKXBQPPHRRRM-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Peptidomimetics

Sub Class

Depsipeptides

Direct Parent

Cyclic depsipeptides

Alternative Parents

Substituents

Cyclic depsipeptide
Macrolide lactam
Alpha-amino acid ester
Valine or derivatives
Macrolactam
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
N-substituted-alpha-amino acid
Alpha-amino acid or derivatives
Phenylacetamide
Monocyclic benzene moiety
Fatty amide
N-acyl-amine
Fatty acyl
Benzenoid
Tertiary carboxylic acid amide
Pyrrolidine
Secondary carboxylic acid amide
Lactone
Lactam
Carboxamide group
Carboxylic acid ester
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Azacycle
Oxacycle
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Organonitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

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

78136573

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-n-[1,4,7,14-tetrahydroxy-3,6,9-triisopropyl-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3h,6h,9h,12h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid (NP0268896)

MOL for NP0268896 (2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-n-[1,4,7,14-tetrahydroxy-3,6,9-triisopropyl-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3h,6h,9h,12h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid)

3D MOL for NP0268896 (2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-n-[1,4,7,14-tetrahydroxy-3,6,9-triisopropyl-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3h,6h,9h,12h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid)

3D SDF for NP0268896 (2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-n-[1,4,7,14-tetrahydroxy-3,6,9-triisopropyl-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3h,6h,9h,12h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid)

3D-SDF for NP0268896 (2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-n-[1,4,7,14-tetrahydroxy-3,6,9-triisopropyl-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3h,6h,9h,12h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid)

PDB for NP0268896 (2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-n-[1,4,7,14-tetrahydroxy-3,6,9-triisopropyl-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3h,6h,9h,12h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid)

3D PDB for NP0268896 (2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-n-[1,4,7,14-tetrahydroxy-3,6,9-triisopropyl-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3h,6h,9h,12h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid)

SMILES for NP0268896 (2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-n-[1,4,7,14-tetrahydroxy-3,6,9-triisopropyl-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3h,6h,9h,12h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid)

INCHI for NP0268896 (2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-n-[1,4,7,14-tetrahydroxy-3,6,9-triisopropyl-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3h,6h,9h,12h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid)

Structure for NP0268896 (2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-n-[1,4,7,14-tetrahydroxy-3,6,9-triisopropyl-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3h,6h,9h,12h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid)

3D Structure for NP0268896 (2-[(1-hydroxy-2-phenylethylidene)amino]-3-methyl-n-[1,4,7,14-tetrahydroxy-3,6,9-triisopropyl-12-methyl-16-(2-methylpropyl)-10,17-dioxo-3h,6h,9h,12h,13h,16h,19h,20h,21h,21ah-pyrrolo[2,1-l]1-oxa-4,7,10,13,16-pentaazacyclononadecan-13-yl]butanimidic acid)