NP-MRD: Showing NP-Card for n-(3-{n-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid (NP0145801)

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Record Information

Version

2.0

Created at

2022-09-02 01:04:38 UTC

Updated at

2022-09-02 01:04:39 UTC

NP-MRD ID

NP0145801

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-(3-{n-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid

Description

N-(3-{N-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid belongs to the class of organic compounds known as tertiary carboxylic acid amides. Tertiary carboxylic acid amides are compounds containing an amide derivative of carboxylic acid, with the general structure RN(R1)C(R2)=O (R1-R2 any atom but H). n-(3-{n-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid is found in Neopetrosia chaliniformis. N-(3-{N-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261505352D          

 29 29  0  0  0  0            999 V2000
   -4.3025   -5.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5880   -5.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5880   -4.3419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8736   -5.5794    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1591   -5.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4446   -5.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7302   -5.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0157   -5.5794    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6988   -5.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4133   -5.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1277   -5.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8422   -5.5794    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9889   -4.7676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8064   -4.6562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1648   -5.3993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9848   -5.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0962   -6.5945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8598   -6.9068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9711   -7.7242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3188   -8.2294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5552   -7.9171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9029   -8.4222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1393   -8.1099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0280   -7.2924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2644   -6.9801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1531   -6.1627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0157   -6.4044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6988   -6.8169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7302   -6.8169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21 20  1  4  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 12 26  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 74 74  0  0  0  0  0  0  0  0999 V2000
    7.6607   -0.9575   -1.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9878    0.5514   -1.8262 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7160    0.8207   -3.0248 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9417    0.9408   -0.6430 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.8864    1.3994    0.7430 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8369    0.3674    1.3443 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4881    0.7104    0.7324 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5014   -0.2964    1.0834 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9179   -1.1955    0.0946 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6747   -0.6019   -0.6042 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.4869    2.3311   -0.6690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7775    2.3180   -1.3960 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9551    2.3420   -0.3968 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2226    2.2558   -1.1490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2900    1.5322   -0.7335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3171    0.7511    0.5174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3168   -0.7505    0.2152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5318   -1.0456   -1.0154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1022   -2.4830   -1.1196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5664   -2.5296   -1.3259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9403   -2.7767   -0.0083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7272   -1.9909    0.3541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4730   -0.8402   -0.5630 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0311   -0.3340    2.4244 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4411    0.6810    3.4174 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2476   -1.2335    2.8315 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6619   -1.3367   -0.9202 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6066   -0.8043   -2.3787 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9289   -1.4159   -2.6157 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5100    2.2008   -1.0207 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8472    1.2105    1.1842 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4775    2.3489    0.9563 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9410    0.3426    2.3913 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2054   -0.6261    0.9529 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1452    1.7038    1.0265 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6212    0.6466   -0.3730 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7440   -2.1598    0.5422 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7050   -1.3501   -0.6987 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3664   -1.3117   -1.3666 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1090    0.3704   -1.0316 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4885   -1.2727    0.9766 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0588    0.4143    1.1822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8649    0.8271   -1.9990 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4955    1.5963   -1.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0226    3.3517   -0.8368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6868    2.3368    0.4445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9187    3.2631   -2.0088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9023    1.5037   -2.1231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8337    1.4725    0.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8826    3.3022    0.1620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3234    2.8113   -2.0705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1444    1.5252   -1.3771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2872    0.9428    1.0831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5130    0.9607    1.1938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3484   -1.0949    0.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8270   -1.2361    1.0912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6312   -0.3835   -1.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0787   -0.8088   -1.9663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3669   -2.9681   -0.1750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5622   -2.9723   -1.9872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3105   -3.3366   -2.0712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3368   -1.5947   -1.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7127   -2.7228    0.8066 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.8467   -2.6618    0.3933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4677   -0.2839   -0.6175 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.9501    0.1435    4.2766 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4590    1.1016    3.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0220    1.5311    3.0744 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  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  1  0
 11 12  1  0
 12 26  1  0
 26 25  1  0
 25 24  1  0
 24 23  1  0
 23 22  1  0
 22 21  1  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 17  2  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
  8 27  1  0
 27 28  1  0
 27 29  2  0
 13 12  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  6 37  1  0
  7 38  1  0
  7 39  1  0
  9 40  1  0
  9 41  1  0
 10 42  1  0
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 11 45  1  0
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 19 56  1  0
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 15 51  1  0
 14 48  1  0
 14 49  1  0
 13 46  1  0
 13 47  1  0
 28 72  1  0
 28 73  1  0
 28 74  1  0
M  END


  Mrv1533004261505352D          

 29 29  0  0  0  0            999 V2000
   -4.3025   -5.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5880   -5.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5880   -4.3419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8736   -5.5794    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1591   -5.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4446   -5.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7302   -5.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0157   -5.5794    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6988   -5.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4133   -5.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1277   -5.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8422   -5.5794    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9889   -4.7676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8064   -4.6562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1648   -5.3993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9848   -5.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0962   -6.5945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8598   -6.9068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9711   -7.7242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3188   -8.2294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5552   -7.9171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9029   -8.4222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1393   -8.1099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0280   -7.2924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2644   -6.9801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1531   -6.1627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0157   -6.4044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6988   -6.8169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7302   -6.8169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 17 18  1  0  0  0  0
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 21 20  1  4  0  0  0
 21 22  2  0  0  0  0
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 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 12 26  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0145801

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)NCCCN(CCCN1CCCCCCCCC=CCCCC1)C(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H45N3O2/c1-23(28)25-17-15-21-27(24(2)29)22-16-20-26-18-13-11-9-7-5-3-4-6-8-10-12-14-19-26/h5,7H,3-4,6,8-22H2,1-2H3,(H,25,28)

> <INCHI_KEY>
NRDQQWPDWIXTER-UHFFFAOYSA-N

> <FORMULA>
C24H45N3O2

> <MOLECULAR_WEIGHT>
407.643

> <EXACT_MASS>
407.351177701

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
50.99594546738717

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-(3-{N-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)acetamide

> <ALOGPS_LOGP>
5.53

> <JCHEM_LOGP>
3.067053057999998

> <ALOGPS_LOGS>
-5.15

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.96511750729183

> <JCHEM_PKA_STRONGEST_BASIC>
10.10849230332167

> <JCHEM_POLAR_SURFACE_AREA>
52.650000000000006

> <JCHEM_REFRACTIVITY>
124.0704

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.91e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-(3-{N-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)acetamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0      -8.031 -10.415   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.698  -9.645   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -6.698  -8.105   0.000  0.00  0.00           O+0
HETATM    4  N   UNK     0      -5.364 -10.415   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0      -4.030  -9.645   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.697 -10.415   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.363  -9.645   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0      -0.029 -10.415   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       1.304  -9.645   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.638 -10.415   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.972  -9.645   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       5.305 -10.415   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       5.579  -8.899   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.105  -8.692   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.774 -10.079   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.305 -10.784   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.513 -12.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.938 -12.893   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.146 -14.419   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.928 -15.362   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.503 -14.779   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.285 -15.721   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.860 -15.138   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.652 -13.613   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.227 -13.030   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.019 -11.504   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.029 -11.955   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.304 -12.725   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -1.363 -12.725   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   27                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   26                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   12                                                       
CONECT   27    8   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   58    0
END

View in JSmol

Synonyms

Value	Source
N-(3-{N-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidate	Generator

Chemical Formula

C₂₄H₄₅N₃O₂

Average Mass

407.6430 Da

Monoisotopic Mass

407.35118 Da

IUPAC Name

N-(3-{N-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)acetamide

Traditional Name

N-(3-{N-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)acetamide

CAS Registry Number

Not Available

SMILES

CC(=O)NCCCN(CCCN1CCCCCCCCC=CCCCC1)C(C)=O

InChI Identifier

InChI=1S/C24H45N3O2/c1-23(28)25-17-15-21-27(24(2)29)22-16-20-26-18-13-11-9-7-5-3-4-6-8-10-12-14-19-26/h5,7H,3-4,6,8-22H2,1-2H3,(H,25,28)

InChI Key

NRDQQWPDWIXTER-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Neopetrosia chaliniformis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tertiary carboxylic acid amides. Tertiary carboxylic acid amides are compounds containing an amide derivative of carboxylic acid, with the general structure RN(R1)C(R2)=O (R1-R2 any atom but H).

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Carboxylic acid derivatives

Direct Parent

Tertiary carboxylic acid amides

Alternative Parents

Substituents

Tertiary carboxylic acid amide
Acetamide
Amino acid or derivatives
Tertiary amine
Tertiary aliphatic amine
Carboximidic acid
Carboximidic acid derivative
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Organoheterocyclic compound
Azacycle
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic nitrogen compound
Carbonyl group
Hydrocarbon derivative
Amine
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	5.53	ALOGPS
logP	3.07	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	15.97	ChemAxon
pKa (Strongest Basic)	10.11	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	52.65 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	124.07 m³·mol⁻¹	ChemAxon
Polarizability	51 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-(3-{n-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid (NP0145801)

MOL for NP0145801 (n-(3-{n-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid)

3D MOL for NP0145801 (n-(3-{n-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid)

3D SDF for NP0145801 (n-(3-{n-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid)

3D-SDF for NP0145801 (n-(3-{n-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid)

PDB for NP0145801 (n-(3-{n-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid)

3D PDB for NP0145801 (n-(3-{n-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid)

SMILES for NP0145801 (n-(3-{n-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid)

INCHI for NP0145801 (n-(3-{n-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid)

Structure for NP0145801 (n-(3-{n-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid)

3D Structure for NP0145801 (n-(3-{n-[3-(1-azacyclopentadec-6-en-1-yl)propyl]acetamido}propyl)ethanimidic acid)