NP-MRD: Showing NP-Card for 8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol (NP0263505)

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Record Information

Version

2.0

Created at

2022-09-08 06:42:38 UTC

Updated at

2022-09-08 06:42:38 UTC

NP-MRD ID

NP0263505

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol

Description

Pithecolobine belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides. 8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol is found in Samanea saman. 8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol was first documented in 1991 (PMID: 1725878). Based on a literature review very few articles have been published on Pithecolobine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082208422D          

 27 27  0  0  0  0            999 V2000
   -4.1421   -4.0372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4276   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7131   -4.0372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9986   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2842   -4.0372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5697   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1448   -4.0372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8592   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5737   -4.0372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2882   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4349   -3.6378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2524   -3.5265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6428   -2.7997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6108   -4.2695    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4308   -4.6472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5421   -5.4647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3057   -5.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4171   -6.5945    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7648   -7.0996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8761   -7.9171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2239   -8.4222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4603   -8.1099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3489   -7.2924    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5853   -6.9801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4740   -6.1627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7104   -5.8504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5991   -5.0329    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  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
 12 14  2  0  0  0  0
 14 15  1  4  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
 20 21  1  0  0  0  0
 21 22  1  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
 26 27  1  0  0  0  0
 10 27  1  0  0  0  0
M  END

     RDKit          3D

 73 73  0  0  0  0  0  0  0  0999 V2000
    8.2435    1.3842   -1.2680 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0076    0.0131   -0.7087 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0022    0.0038    0.4302 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6790    0.5252   -0.0395 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6623    0.5326    1.0641 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3828   -0.8161    1.6541 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8621   -1.7798    0.6164 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5825   -1.3126   -0.0340 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4815   -1.1372    0.9649 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2115   -0.6822    0.2790 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3957    0.6200   -0.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8816    1.2525   -0.8360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0830    1.4882   -2.2100 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8221    1.6074   -0.0739 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9449    1.5175    1.3364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7367    2.6788    1.9208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1472    2.6517    1.3621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6461    1.2697    1.4016 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0660    1.2063    1.2423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5284    0.1344    0.2939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1040    0.3705   -1.1233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7877   -0.8908   -1.8626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3630   -1.0723   -2.0691 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8269   -2.1562   -1.2768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3661   -2.3055   -1.6477 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4729   -2.2369   -0.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1785   -1.6718   -0.7218 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.6947    2.1852   -0.7333 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9032    1.4138   -2.3252 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3264    1.6333   -1.1885 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6529   -0.6901   -1.4869 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9633   -0.4217   -0.3116 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8756   -1.0849    0.6820 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3601    0.5124    1.3239 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2875   -0.1221   -0.8658 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7766    1.5846   -0.3864 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6929    0.9083    0.6329 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0210    1.2435    1.8447 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3529   -1.2421    2.0053 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6457   -0.7461    2.4661 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6787   -1.9135   -0.1331 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6547   -2.7825    1.0516 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7547   -0.3876   -0.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3337   -2.1019   -0.7984 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3202   -2.0933    1.5030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8184   -0.3771    1.7050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5784   -0.6834    1.0366 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8866    1.3184    0.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0715    0.5230   -1.2753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9047    1.0709   -2.6280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5113    0.6065    1.6167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9357    1.5679    1.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8353    2.5264    3.0181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2916    3.6508    1.7080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0895    3.0277    0.3184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8212    3.3235    1.9054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3822    0.9240    2.3662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4314    2.2131    0.9572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5481    0.9762    2.2333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6447    0.0776    0.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1073   -0.8297    0.6584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9732    0.8747   -1.6419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2632    1.0729   -1.2238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2363   -1.7441   -1.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2682   -0.9149   -2.8643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8312   -0.1882   -1.9544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9583   -1.9807   -0.1872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4111   -3.0666   -1.5265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0266   -1.5193   -2.3544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2303   -3.2761   -2.1934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9337   -1.6719    0.3950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3275   -3.2795   -0.0749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0859   -1.3230   -1.6830 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  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 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 10  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  0
  7 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  0
  9 46  1  0
 10 47  1  1
 11 48  1  0
 11 49  1  0
 13 50  1  0
 15 51  1  0
 15 52  1  0
 16 53  1  0
 16 54  1  0
 17 55  1  0
 17 56  1  0
 18 57  1  0
 19 58  1  0
 19 59  1  0
 20 60  1  0
 20 61  1  0
 21 62  1  0
 21 63  1  0
 22 64  1  0
 22 65  1  0
 23 66  1  0
 24 67  1  0
 24 68  1  0
 25 69  1  0
 25 70  1  0
 26 71  1  0
 26 72  1  0
 27 73  1  0
M  END


  Mrv1652309082208422D          

 27 27  0  0  0  0            999 V2000
   -4.1421   -4.0372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4276   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7131   -4.0372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9986   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2842   -4.0372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5697   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1448   -4.0372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8592   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5737   -4.0372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2882   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4349   -3.6378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2524   -3.5265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6428   -2.7997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6108   -4.2695    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4308   -4.6472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5421   -5.4647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3057   -5.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4171   -6.5945    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7648   -7.0996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8761   -7.9171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2239   -8.4222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4603   -8.1099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3489   -7.2924    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5853   -6.9801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4740   -6.1627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7104   -5.8504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5991   -5.0329    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  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
 12 14  2  0  0  0  0
 14 15  1  4  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
 20 21  1  0  0  0  0
 21 22  1  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
 26 27  1  0  0  0  0
 10 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0263505

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCC1CC(O)=NCCCNCCCCNCCCN1

> <INCHI_IDENTIFIER>
InChI=1S/C22H46N4O/c1-2-3-4-5-6-7-8-13-21-20-22(27)26-19-12-17-24-15-10-9-14-23-16-11-18-25-21/h21,23-25H,2-20H2,1H3,(H,26,27)

> <INCHI_KEY>
QEGMJRQKNQFEEZ-UHFFFAOYSA-N

> <FORMULA>
C22H46N4O

> <MOLECULAR_WEIGHT>
382.637

> <EXACT_MASS>
382.367162117

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
48.98229444775962

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol

> <JCHEM_LOGP>
0.8014385484105351

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
3

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.935252862138363

> <JCHEM_PKA_STRONGEST_BASIC>
10.92843410558254

> <JCHEM_POLAR_SURFACE_AREA>
68.68

> <JCHEM_REFRACTIVITY>
116.58839999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
pithecolobine

> <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      -7.732  -7.536   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.398  -8.306   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.064  -7.536   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.731  -8.306   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.397  -7.536   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.063  -8.306   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.270  -7.536   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.604  -8.306   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.938  -7.536   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.271  -8.306   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.545  -6.791   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.071  -6.583   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.800  -5.226   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0       6.740  -7.970   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       8.271  -8.675   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.479 -10.201   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.904 -10.784   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0      10.112 -12.310   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       8.894 -13.253   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.102 -14.779   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.885 -15.721   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.459 -15.138   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       6.251 -13.613   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       4.826 -13.030   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.618 -11.504   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.193 -10.921   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0       2.985  -9.395   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    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   27                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   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   27                                                       
CONECT   27   26   10                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₄₆N₄O

Average Mass

382.6370 Da

Monoisotopic Mass

382.36716 Da

IUPAC Name

8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol

Traditional Name

pithecolobine

CAS Registry Number

Not Available

SMILES

CCCCCCCCCC1CC(O)=NCCCNCCCCNCCCN1

InChI Identifier

InChI=1S/C22H46N4O/c1-2-3-4-5-6-7-8-13-21-20-22(27)26-19-12-17-24-15-10-9-14-23-16-11-18-25-21/h21,23-25H,2-20H2,1H3,(H,26,27)

InChI Key

QEGMJRQKNQFEEZ-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
Samanea saman	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolactams

Sub Class

Not Available

Direct Parent

Macrolactams

Alternative Parents

Substituents

Macrolactam
Beta amino acid or derivatives
Amino acid or derivatives
Carboxamide group
Lactam
Secondary carboxylic acid amide
Carboxylic acid derivative
Secondary aliphatic amine
Secondary amine
Azacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Amine
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
Organic oxygen compound
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

azamacrocycle (CHEBI:8253 )
keratan 6'-sulfate (CHEBI:8253 )

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	0.8	ChemAxon
pKa (Strongest Acidic)	3.94	ChemAxon
pKa (Strongest Basic)	10.93	ChemAxon
Physiological Charge	3	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	68.68 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	116.59 m³·mol⁻¹	ChemAxon
Polarizability	48.98 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

C00002357

Chemspider ID

391179

KEGG Compound ID

C10611

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

442870

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Mar W, Tan GT, Cordell GA, Pezzuto JM, Jurcic K, Offermann F, Redl K, Steinke B, Wagner H: Biological activity of novel macrocyclic alkaloids (budmunchiamines) from Albizia amara detected on the basis of interaction with DNA. J Nat Prod. 1991 Nov-Dec;54(6):1531-42. doi: 10.1021/np50078a007. [PubMed:1725878 ]
LOTUS database [Link]

Showing NP-Card for 8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol (NP0263505)

MOL for NP0263505 (8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol)

3D MOL for NP0263505 (8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol)

3D SDF for NP0263505 (8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol)

3D-SDF for NP0263505 (8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol)

PDB for NP0263505 (8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol)

3D PDB for NP0263505 (8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol)

SMILES for NP0263505 (8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol)

INCHI for NP0263505 (8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol)

Structure for NP0263505 (8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol)

3D Structure for NP0263505 (8-nonyl-1,5,9,13-tetraazacycloheptadec-5-en-6-ol)