NP-MRD: Showing NP-Card for (2s,3s)-n-[(2s)-1-[(3s,7s,10s,13e)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid (NP0156969)

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Record Information

Version

2.0

Created at

2022-09-02 14:15:41 UTC

Updated at

2022-09-02 14:15:42 UTC

NP-MRD ID

NP0156969

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3s)-n-[(2s)-1-[(3s,7s,10s,13e)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid

Description

Paliurine A belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds. (2s,3s)-n-[(2s)-1-[(3s,7s,10s,13e)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid is found in Paliurus ramosissimus. Based on a literature review very few articles have been published on Paliurine A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022216152D          

 48 51  0  0  1  0            999 V2000
    3.5899    5.9908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2620    5.5123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1838    4.6911    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8559    4.2127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4334    4.3482    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3552    3.5269    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0273    3.0485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7777    3.3914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9490    2.2272    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2142    1.8521    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3439    1.0374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1589    0.9089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5328    1.6443    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3476    1.7740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6426    2.5445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8673    1.1333    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5722    0.3629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0919   -0.2779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9067   -0.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4264   -0.7889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1313   -1.5594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3166   -1.6891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7969   -1.0483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6820    1.2630    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9771    2.0334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4574    2.6742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7918    2.1631    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0869    2.9336    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.9016    3.0633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5672    3.5743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8622    4.3447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3115    1.5224    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.1262    1.6521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0165    0.7520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8167    1.0598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9955    1.1381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3054    0.6859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5688    1.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2529    2.1636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8852    1.6337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8161    1.9433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1823    3.3196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9327    3.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0109    4.4837    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7613    4.8266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8395    5.6479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  4  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  9 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
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 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 16 24  1  1  0  0  0
 24 25  2  0  0  0  0
 25 26  1  4  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 27 32  1  6  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 10 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  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  1  0  0  0  0
 39 42  1  0  0  0  0
 42 43  2  0  0  0  0
 36 43  1  0  0  0  0
 42 44  1  0  0  0  0
 44 45  2  0  0  0  0
 46 45  1  4  0  0  0
 46 47  2  0  0  0  0
  5 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END

     RDKit          3D

 99102  0  0  0  0  0  0  0  0999 V2000
    5.3361    3.1877   -3.1944 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0674    2.3177   -1.9856 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7127    1.7000   -2.0106 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5832    2.6799   -2.1337 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1987    4.1535   -3.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4088    3.5156   -2.8753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4486    2.1406   -2.8505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2533   -0.4469   -0.6615 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4135   -0.9956   -0.6656 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0900    0.2787    1.3690 C   0  0  1  0  0  0  0  0  0  0  0  0
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 30 81  1  0
 28 76  1  1
 29 77  1  0
 29 78  1  0
 29 79  1  0
 27 75  1  6
 33 85  1  0
 33 86  1  0
 33 87  1  0
 34 88  1  0
 34 89  1  0
 34 90  1  0
 26 74  1  0
 16 66  1  6
 17 67  1  0
 17 68  1  0
 19 69  1  0
 20 70  1  0
 21 71  1  0
 22 72  1  0
 23 73  1  0
 12 64  1  0
 12 65  1  0
 11 62  1  0
 11 63  1  0
 10 61  1  6
 37 91  1  0
 38 92  1  0
 41 93  1  0
 41 94  1  0
 41 95  1  0
 43 96  1  0
 44 97  1  0
 45 98  1  0
 48 99  1  0
  5 58  1  1
  8 59  1  0
  9 60  1  1
  3 54  1  6
  4 55  1  0
  4 56  1  0
  4 57  1  0
  2 52  1  0
  2 53  1  0
  1 49  1  0
  1 50  1  0
  1 51  1  0
M  END


  Mrv1652309022216152D          

 48 51  0  0  1  0            999 V2000
    3.5899    5.9908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2620    5.5123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1838    4.6911    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8559    4.2127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4334    4.3482    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3552    3.5269    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0273    3.0485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7777    3.3914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9490    2.2272    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2142    1.8521    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3439    1.0374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1589    0.9089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5328    1.6443    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3476    1.7740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6426    2.5445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8673    1.1333    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5722    0.3629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0919   -0.2779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9067   -0.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4264   -0.7889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1313   -1.5594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3166   -1.6891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7969   -1.0483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6820    1.2630    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9771    2.0334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4574    2.6742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7918    2.1631    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0869    2.9336    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.9016    3.0633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5672    3.5743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8622    4.3447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3115    1.5224    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.1262    1.6521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0165    0.7520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8167    1.0598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9955    1.1381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3054    0.6859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5688    1.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5222    1.8810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2529    2.1636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8852    1.6337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1040    2.4983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8161    1.9433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1823    3.3196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9327    3.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0109    4.4837    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7613    4.8266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8395    5.6479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  4  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  9 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  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
 16 24  1  1  0  0  0
 24 25  2  0  0  0  0
 25 26  1  4  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 27 32  1  6  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 10 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  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  1  0  0  0  0
 39 42  1  0  0  0  0
 42 43  2  0  0  0  0
 36 43  1  0  0  0  0
 42 44  1  0  0  0  0
 44 45  2  0  0  0  0
 46 45  1  4  0  0  0
 46 47  2  0  0  0  0
  5 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0156969

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)[C@H](N(C)C)C(O)=N[C@@H](CC1=CC=CC=C1)C(=O)N1CC[C@@H]2OC3=CC=C(OC)C(=C3)\C=C\N=C(O)[C@@H](N=C(O)[C@@H]12)[C@@H](C)CC

> <INCHI_IDENTIFIER>
InChI=1S/C37H51N5O6/c1-8-23(3)31-34(43)38-19-17-26-22-27(15-16-29(26)47-7)48-30-18-20-42(33(30)36(45)40-31)37(46)28(21-25-13-11-10-12-14-25)39-35(44)32(41(5)6)24(4)9-2/h10-17,19,22-24,28,30-33H,8-9,18,20-21H2,1-7H3,(H,38,43)(H,39,44)(H,40,45)/b19-17+/t23-,24-,28-,30-,31-,32-,33-/m0/s1

> <INCHI_KEY>
IQWOZPMCQYCQOS-WQKKCOBFSA-N

> <FORMULA>
C37H51N5O6

> <MOLECULAR_WEIGHT>
661.844

> <EXACT_MASS>
661.383934382

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
99

> <JCHEM_AVERAGE_POLARIZABILITY>
71.67722136703992

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S)-N-[(2S)-1-[(3S,7S,10S,13E)-10-[(2S)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0^{3,7}]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid

> <ALOGPS_LOGP>
4.30

> <JCHEM_LOGP>
-1.7305927657334856

> <ALOGPS_LOGS>
-5.04

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
-4.735855718718271

> <JCHEM_PKA_STRONGEST_ACIDIC>
-7.741851408347569

> <JCHEM_PKA_STRONGEST_BASIC>
14.951405660103424

> <JCHEM_POLAR_SURFACE_AREA>
139.78

> <JCHEM_REFRACTIVITY>
185.6878

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.08e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S)-N-[(2S)-1-[(3S,7S,10S,13E)-10-[(2S)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0^{3,7}]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       6.701  11.183   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.956  10.290   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.810   8.757   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.064   7.864   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.409   8.117   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       6.263   6.584   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       7.518   5.691   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.918   6.331   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       7.372   4.157   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.000   3.457   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.242   1.936   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.763   1.697   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       8.461   3.069   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       9.982   3.312   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      10.533   4.750   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      10.952   2.115   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.402   0.677   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.372  -0.519   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.892  -0.277   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.863  -1.473   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.312  -2.911   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.791  -3.153   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.821  -1.957   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0      12.473   2.358   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0      13.024   3.796   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      12.054   4.992   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      14.545   4.038   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      15.095   5.476   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      16.616   5.718   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      14.125   6.672   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      14.676   8.110   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0      15.515   2.842   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0      17.036   3.084   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      14.964   1.404   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       5.258   1.978   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       3.725   2.124   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.437   1.280   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       1.062   1.974   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       0.975   3.511   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -0.472   4.039   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -1.652   3.050   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       2.061   4.664   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       3.390   3.628   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       2.207   6.197   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       3.608   6.837   0.000  0.00  0.00           C+0
HETATM   46  N   UNK     0       3.754   8.370   0.000  0.00  0.00           N+0
HETATM   47  C   UNK     0       5.154   9.010   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       5.300  10.543   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   47                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   13                                                  
CONECT   10    9   11   35                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    9   14                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   24                                                  
CONECT   17   16   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   16   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   32                                                  
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30                                                            
CONECT   32   27   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   10   36                                                       
CONECT   36   35   37   43                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   42                                                  
CONECT   40   39   41                                                       
CONECT   41   40                                                            
CONECT   42   39   43   44                                                  
CONECT   43   42   36                                                       
CONECT   44   42   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46    5   48                                                  
CONECT   48   47                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₅₁N₅O₆

Average Mass

661.8440 Da

Monoisotopic Mass

661.38393 Da

IUPAC Name

(2S,3S)-N-[(2S)-1-[(3S,7S,10S,13E)-10-[(2S)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0^{3,7}]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

CC[C@H](C)[C@H](N(C)C)C(O)=N[C@@H](CC1=CC=CC=C1)C(=O)N1CC[C@@H]2OC3=CC=C(OC)C(=C3)\C=C\N=C(O)[C@@H](N=C(O)[C@@H]12)[C@@H](C)CC

InChI Identifier

InChI=1S/C37H51N5O6/c1-8-23(3)31-34(43)38-19-17-26-22-27(15-16-29(26)47-7)48-30-18-20-42(33(30)36(45)40-31)37(46)28(21-25-13-11-10-12-14-25)39-35(44)32(41(5)6)24(4)9-2/h10-17,19,22-24,28,30-33H,8-9,18,20-21H2,1-7H3,(H,38,43)(H,39,44)(H,40,45)/b19-17+/t23-,24-,28-,30-,31-,32-,33-/m0/s1

InChI Key

IQWOZPMCQYCQOS-WQKKCOBFSA-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
Paliurus ramosissimus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Cyclic alpha peptide
Isoleucine or derivatives
N-acyl-alpha amino acid or derivatives
Macrolactam
Alpha-amino acid amide
Alpha-amino acid or derivatives
Amphetamine or derivatives
Anisole
Phenol ether
N-acylpyrrolidine
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
N-acyl-amine
Fatty acyl
Fatty amide
Tertiary carboxylic acid amide
Pyrrolidine
Carboxamide group
Amino acid or derivatives
Lactam
Tertiary aliphatic amine
Secondary carboxylic acid amide
Tertiary amine
Organoheterocyclic compound
Oxacycle
Ether
Azacycle
Organic nitrogen compound
Carbonyl group
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Amine
Organopnictogen 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	4.3	ALOGPS
logP	-1.7	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	-7.7	ChemAxon
pKa (Strongest Basic)	14.95	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	139.78 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	185.69 m³·mol⁻¹	ChemAxon
Polarizability	71.68 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

C00027461

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

101063131

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3s)-n-[(2s)-1-[(3s,7s,10s,13e)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid (NP0156969)

MOL for NP0156969 ((2s,3s)-n-[(2s)-1-[(3s,7s,10s,13e)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid)

3D MOL for NP0156969 ((2s,3s)-n-[(2s)-1-[(3s,7s,10s,13e)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid)

3D SDF for NP0156969 ((2s,3s)-n-[(2s)-1-[(3s,7s,10s,13e)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid)

3D-SDF for NP0156969 ((2s,3s)-n-[(2s)-1-[(3s,7s,10s,13e)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid)

PDB for NP0156969 ((2s,3s)-n-[(2s)-1-[(3s,7s,10s,13e)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid)

3D PDB for NP0156969 ((2s,3s)-n-[(2s)-1-[(3s,7s,10s,13e)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid)

SMILES for NP0156969 ((2s,3s)-n-[(2s)-1-[(3s,7s,10s,13e)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid)

INCHI for NP0156969 ((2s,3s)-n-[(2s)-1-[(3s,7s,10s,13e)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid)

Structure for NP0156969 ((2s,3s)-n-[(2s)-1-[(3s,7s,10s,13e)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid)

3D Structure for NP0156969 ((2s,3s)-n-[(2s)-1-[(3s,7s,10s,13e)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanimidic acid)