NP-MRD: Showing NP-Card for n-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydroindole-2-carboximidic acid (NP0206745)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 03:06:39 UTC

Updated at

2022-09-05 03:06:39 UTC

NP-MRD ID

NP0206745

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydroindole-2-carboximidic acid

Description

N-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydro-1H-indole-2-carboximidic acid belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. N-acyl-alpha amino acids and derivatives are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom. Based on a literature review very few articles have been published on N-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydro-1H-indole-2-carboximidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052205062D          

 45 48  0  0  0  0            999 V2000
   -3.0225   -1.3057    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3080   -0.8932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3080   -0.0682    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5935   -1.3057    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8791   -0.8932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1646   -1.3057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5499   -0.8932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2644   -1.3057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9788   -0.8932    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9788   -0.0682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6933    0.3443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2644    0.3443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5107    0.0087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0413    0.6218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8663    0.6218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2788    1.3363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8663    2.0508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2788    2.7652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0413    2.0508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3712    1.3363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1781    1.1648    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7912    1.7168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5758    1.4619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6197    2.5238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2328    3.0758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0174    2.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6305    3.3729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4151    3.1180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5867    2.3110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9736    1.7590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1889    2.0139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8351    2.7787    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6635    3.5857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2766    4.1377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1211    3.8406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2926    4.6476    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7342    3.2886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5188    3.5435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1319    2.9915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9165    3.2464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0880    4.0534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8727    4.3084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4749    4.6054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6465    5.4124    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -1.6903    4.3505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 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
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  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  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
 32 24  1  4  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  2  0  0  0  0
 38 45  1  0  0  0  0
M  END

     RDKit          3D

 88 91  0  0  0  0  0  0  0  0999 V2000
   10.2113    1.3141    0.1220 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2021    2.3174   -0.1930 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.0402    2.8673   -0.3301 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9598    4.2237   -0.7539 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.8373    2.1759   -0.0742 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.6618    2.4600   -0.8234 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4818    1.6029   -0.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1132    1.7919    1.0269 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9249    0.8566    1.3245 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8264    1.0848    0.5758 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9269    1.0024   -0.1890 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0136    2.1015   -0.2981 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6089   -0.1398   -1.0827 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7225   -1.0819   -1.3214 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3638   -2.3508   -0.6088 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5575   -3.1826   -1.5813 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2176   -4.4734   -0.9126 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4383   -4.3670    0.5782 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6583   -5.3960    1.1562 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8195   -3.0501    1.1080 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3550   -1.8535    0.4569 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5636   -0.9809   -0.3267 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7619   -0.6555   -0.5559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0486    0.2596   -1.4261 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0138   -1.2125    0.0795 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3864   -2.4721   -0.6869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6039   -3.0603   -0.0735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4151   -3.7824    1.1038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4948   -4.3861    1.7111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7322   -4.2496    1.1217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9198   -3.5373   -0.0417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8386   -2.9371   -0.6436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0086   -0.3056    0.1571 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8929    0.4983    0.2243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6916    1.5498    1.2087 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1766    0.6206   -0.5258 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.2573    0.6020    0.3861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2345    1.9097   -1.2736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1408    3.1109   -0.4530 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9572    3.7872   -0.2410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9573    4.9068    0.5551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1056    5.3868    1.1572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0869    6.5142    1.9544 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2707    4.6958    0.9303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7509    5.2873    1.6883 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -6.3271    3.5679    0.1414 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8821    4.4716   -1.7611 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9771    5.0075   -0.0677 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8277    1.4586    0.6697 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8340    2.2448   -1.8973 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3511    3.5419   -0.7831 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7155    0.5504   -0.6312 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6167    1.9290   -1.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7577    2.8075    1.2362 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9046    1.4782    1.7355 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6798    0.9560    2.4313 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3395   -0.1916    1.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1393    2.7960   -1.0380 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1710    0.1555   -2.0489 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8337   -1.3062   -2.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6742   -0.6257   -0.9997 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2055   -2.8739   -0.1629 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1664   -3.3261   -2.5101 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6540   -2.6267   -1.8832 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8618   -5.2812   -1.3193 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1745   -4.7390   -1.1442 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4851   -4.4446    0.8818 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8956   -6.2790    0.8165 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1272   -3.0327    2.2092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2401   -3.2339    1.1366 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9613   -1.2571    1.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6630   -1.4918    1.1235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5826   -3.1905   -0.6490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6274   -2.1793   -1.7609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4570   -3.8975    1.5753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3509   -4.9575    2.6390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6066   -4.7127    1.5771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9234   -3.4471   -0.4889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9113   -2.3925   -1.5539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7726    1.8009    1.4919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3705   -0.1890   -1.2272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9208    0.5842    1.3341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1914    1.9762   -1.8758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4346    1.9707   -2.0660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0630    3.3975   -0.7221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0282    5.4339    0.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2478    7.0406    2.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2758    3.0533   -0.0100 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  1  0
  3  2  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  2  0
 25 33  1  0
 33 34  2  3
 34 35  1  0
 34 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 39 40  2  0
 40 41  1  0
 41 42  2  0
 42 43  1  0
 42 44  1  0
 44 45  1  0
 44 46  2  0
 22 13  1  0
 32 27  1  0
 46 39  1  0
 21 15  1  0
  4 47  1  0
  4 48  1  0
  2  1  1  0
  5 49  1  0
  6 50  1  0
  6 51  1  0
  7 52  1  0
  7 53  1  0
  8 54  1  0
  8 55  1  0
  9 56  1  0
  9 57  1  0
 12 58  1  0
 13 59  1  6
 14 60  1  0
 14 61  1  0
 15 62  1  1
 16 63  1  0
 16 64  1  0
 17 65  1  0
 17 66  1  0
 18 67  1  6
 19 68  1  0
 20 69  1  0
 20 70  1  0
 21 71  1  1
 25 72  1  1
 26 73  1  0
 26 74  1  0
 28 75  1  0
 29 76  1  0
 30 77  1  0
 31 78  1  0
 32 79  1  0
 35 80  1  0
 36 81  1  6
 37 82  1  0
 38 83  1  0
 38 84  1  0
 40 85  1  0
 41 86  1  0
 43 87  1  0
 46 88  1  0
M  END


  Mrv1652309052205062D          

 45 48  0  0  0  0            999 V2000
   -3.0225   -1.3057    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3080   -0.8932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3080   -0.0682    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5935   -1.3057    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8791   -0.8932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1646   -1.3057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5499   -0.8932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2644   -1.3057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9788   -0.8932    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9788   -0.0682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6933    0.3443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2644    0.3443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5107    0.0087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0413    0.6218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8663    0.6218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2788    1.3363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8663    2.0508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2788    2.7652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0413    2.0508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3712    1.3363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1781    1.1648    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7912    1.7168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5758    1.4619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6197    2.5238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2328    3.0758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0174    2.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6305    3.3729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4151    3.1180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5867    2.3110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9736    1.7590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1889    2.0139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8351    2.7787    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6635    3.5857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2766    4.1377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1211    3.8406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2926    4.6476    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7342    3.2886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5188    3.5435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1319    2.9915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9165    3.2464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0880    4.0534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8727    4.3084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4749    4.6054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6465    5.4124    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -1.6903    4.3505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 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
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  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  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
 32 24  1  4  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  2  0  0  0  0
 38 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0206745

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NC(=N)NCCCCN=C(O)C1CC2CCC(O)CC2N1C(=O)C(CC1=CC=CC=C1)N=C(O)C(O)CC1=CC=C(O)C(Cl)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C32H43ClN6O6/c33-23-14-20(8-11-27(23)41)16-28(42)30(44)38-24(15-19-6-2-1-3-7-19)31(45)39-25-18-22(40)10-9-21(25)17-26(39)29(43)36-12-4-5-13-37-32(34)35/h1-3,6-8,11,14,21-22,24-26,28,40-42H,4-5,9-10,12-13,15-18H2,(H,36,43)(H,38,44)(H4,34,35,37)

> <INCHI_KEY>
LNFDGLKYPWLQGX-UHFFFAOYSA-N

> <FORMULA>
C32H43ClN6O6

> <MOLECULAR_WEIGHT>
643.18

> <EXACT_MASS>
642.2932608

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
69.10423439642462

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydro-1H-indole-2-carboximidic acid

> <JCHEM_LOGP>
-0.2769377926920703

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
3.6686899874497114

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.975962541331824

> <JCHEM_PKA_STRONGEST_BASIC>
12.05792365539392

> <JCHEM_POLAR_SURFACE_AREA>
208.07999999999996

> <JCHEM_REFRACTIVITY>
180.9232

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydroindole-2-carboximidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  N   UNK     0      -5.642  -2.437   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0      -4.308  -1.667   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      -4.308  -0.127   0.000  0.00  0.00           N+0
HETATM    4  N   UNK     0      -2.975  -2.437   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0      -1.641  -1.667   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.307  -2.437   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.026  -1.667   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.360  -2.437   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       3.694  -1.667   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       3.694  -0.127   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.028   0.643   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.360   0.643   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.953   0.016   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.077   1.161   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.617   1.161   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.387   2.494   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.617   3.828   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.387   5.162   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.077   3.828   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.693   2.494   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       2.199   2.174   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       3.344   3.205   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.808   2.729   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.023   4.711   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.168   5.742   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.632   5.266   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.777   6.296   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.242   5.820   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.562   4.314   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.417   3.283   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.953   3.759   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0       1.559   5.187   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0       1.239   6.693   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       2.383   7.724   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -0.226   7.169   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -0.546   8.676   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -1.370   6.139   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -2.835   6.615   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -3.980   5.584   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -5.444   6.060   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -5.764   7.566   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      -7.229   8.042   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      -4.620   8.597   0.000  0.00  0.00           C+0
HETATM   44 Cl   UNK     0      -4.940  10.103   0.000  0.00  0.00          Cl+0
HETATM   45  C   UNK     0      -3.155   8.121   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   21                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   14   21                                                  
CONECT   21   20   12   22                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   32                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   26                                                       
CONECT   32   24   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39   45                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   38                                                       
MASTER        0    0    0    0    0    0    0    0   45    0   96    0
END

View in JSmol

Synonyms

Value	Source
N-(4-Carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydro-1H-indole-2-carboximidate	Generator

Chemical Formula

C₃₂H₄₃ClN₆O₆

Average Mass

643.1800 Da

Monoisotopic Mass

642.29326 Da

IUPAC Name

N-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydro-1H-indole-2-carboximidic acid

Traditional Name

N-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydroindole-2-carboximidic acid

CAS Registry Number

Not Available

SMILES

NC(=N)NCCCCN=C(O)C1CC2CCC(O)CC2N1C(=O)C(CC1=CC=CC=C1)N=C(O)C(O)CC1=CC=C(O)C(Cl)=C1

InChI Identifier

InChI=1S/C32H43ClN6O6/c33-23-14-20(8-11-27(23)41)16-28(42)30(44)38-24(15-19-6-2-1-3-7-19)31(45)39-25-18-22(40)10-9-21(25)17-26(39)29(43)36-12-4-5-13-37-32(34)35/h1-3,6-8,11,14,21-22,24-26,28,40-42H,4-5,9-10,12-13,15-18H2,(H,36,43)(H,38,44)(H4,34,35,37)

InChI Key

LNFDGLKYPWLQGX-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 n-acyl-alpha amino acids and derivatives. N-acyl-alpha amino acids and derivatives are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

N-acyl-alpha amino acids and derivatives

Alternative Parents

Substituents

N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
Amphetamine or derivatives
Indole or derivatives
2-halophenol
N-acylpyrrolidine
2-chlorophenol
1-hydroxy-2-unsubstituted benzenoid
Chlorobenzene
Halobenzene
Phenol
Aryl chloride
Aryl halide
Monocyclic benzene moiety
Benzenoid
Tertiary carboxylic acid amide
Pyrrolidine
Cyclic alcohol
Secondary alcohol
Carboxamide group
Guanidine
Carboximidamide
Carboximidic acid
Carboximidic acid derivative
Propargyl-type 1,3-dipolar organic compound
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Organohalogen compound
Organopnictogen compound
Organochloride
Organooxygen compound
Carbonyl group
Organonitrogen compound
Organic oxide
Hydrocarbon derivative
Imine
Alcohol
Organic nitrogen compound
Organic oxygen 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
logP	-0.28	ChemAxon
pKa (Strongest Acidic)	2.98	ChemAxon
pKa (Strongest Basic)	12.06	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	208.08 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	180.92 m³·mol⁻¹	ChemAxon
Polarizability	69.1 Å³	ChemAxon
Number of Rings	4	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

163038832

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydroindole-2-carboximidic acid (NP0206745)

MOL for NP0206745 (n-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydroindole-2-carboximidic acid)

3D MOL for NP0206745 (n-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydroindole-2-carboximidic acid)

3D SDF for NP0206745 (n-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydroindole-2-carboximidic acid)

3D-SDF for NP0206745 (n-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydroindole-2-carboximidic acid)

PDB for NP0206745 (n-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydroindole-2-carboximidic acid)

3D PDB for NP0206745 (n-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydroindole-2-carboximidic acid)

SMILES for NP0206745 (n-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydroindole-2-carboximidic acid)

INCHI for NP0206745 (n-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydroindole-2-carboximidic acid)

Structure for NP0206745 (n-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydroindole-2-carboximidic acid)

3D Structure for NP0206745 (n-(4-carbamimidamidobutyl)-1-(2-{[3-(3-chloro-4-hydroxyphenyl)-1,2-dihydroxypropylidene]amino}-3-phenylpropanoyl)-6-hydroxy-octahydroindole-2-carboximidic acid)