NP-MRD: Showing NP-Card for Circinamide (NP0069713)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 15:04:16 UTC

Updated at

2022-04-28 15:04:16 UTC

NP-MRD ID

NP0069713

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Circinamide

Description

(2S,3S)-3-{[(1R,2R)-1-[bis(4-aminobutyl)carbamoyl]-2-methylbutyl]-C-hydroxycarbonimidoyl}oxirane-2-carboxylic acid belongs to the class of organic compounds known as isoleucine and derivatives. Isoleucine and derivatives are compounds containing isoleucine or a derivative thereof resulting from reaction of isoleucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Circinamide is found in Anabaena circinalis. Based on a literature review very few articles have been published on (2S,3S)-3-{[(1R,2R)-1-[bis(4-aminobutyl)carbamoyl]-2-methylbutyl]-C-hydroxycarbonimidoyl}oxirane-2-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282217042D          

 27 27  0  0  1  0            999 V2000
   -0.1105   -6.1283    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8250   -5.7158    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1105   -5.3033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -6.4302    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -5.0013    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875   -5.0013    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3000   -5.7158    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1250   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3000   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3000   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1250   -4.2868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875   -3.5724    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3000   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1250   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5375   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3625   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7750   -1.4289    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -2.1434    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -6.8427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -6.8427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -7.5572    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
  1  3  1  0  0  0  0
  2  4  1  1  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 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
 14 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
  1 25  1  6  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END

     RDKit          3D

 61 61  0  0  0  0  0  0  0  0999 V2000
    2.8215   -0.0018   -3.7785 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6017   -0.5893   -2.3989 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4966    0.1787   -1.7562 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2496    0.0791   -2.5439 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2544   -0.2241   -0.3051 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4716    0.0253    0.4619 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1859   -1.0150    1.0999 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8184   -2.2146    1.0464 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4103   -0.7131    1.8634 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6390   -1.4227    3.0508 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5054   -1.7378    1.9878 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9020   -1.3145    2.1024 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8323   -2.0807    1.7794 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2084   -0.0474    2.5748 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1481    0.6560    0.1736 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4041    1.8883    0.4342 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1884    0.2419    0.3721 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1548    1.2157    0.7687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7640    1.8072   -0.4963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8095    2.8594   -0.1402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3860    3.4176   -1.4230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3558    4.0323   -2.2427 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5192   -1.1357    0.1837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3716   -2.0132    1.3816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2584   -1.6787    2.5424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7269   -1.8156    2.1994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0316   -3.1976    1.8111 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8005   -0.2616   -4.2084 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0027   -0.4275   -4.4283 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6355    1.1102   -3.7829 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5617   -0.5241   -1.8553 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2957   -1.6592   -2.5599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8628    1.2528   -1.6689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5760    0.5542   -1.9638 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0499   -0.9929   -2.7502 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4120    0.6039   -3.5111 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0389   -1.2879   -0.2802 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7971    1.0123    0.5212 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7711    0.3391    1.9347 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3457   -2.7576    1.6036 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5571    0.4034    3.1793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6629    2.0826    1.3181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9729    0.9026    1.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0204    2.2974   -1.1391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2701    1.0304   -1.0795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3388    3.6719    0.4392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6019    2.3770    0.4306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1968    4.1417   -1.2026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8303    2.5957   -2.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8284    4.2934   -3.1524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0069    4.9271   -1.8330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9396   -1.6155   -0.6632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5864   -1.2637   -0.1659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6479   -3.0706    1.0881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2999   -2.1117    1.7106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0877   -2.3767    3.4044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0852   -0.6508    2.9040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0102   -1.1575    1.3694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3042   -1.5592    3.1032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8973   -3.2889    0.7761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3499   -3.7896    2.3412 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
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 14  1  0
 12 13  2  0
  5 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 17 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 11  9  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  1
  4 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  6
  6 38  1  0
  9 39  1  1
 11 40  1  6
 14 41  1  0
 18 42  1  0
 18 43  1  0
 19 44  1  0
 19 45  1  0
 20 46  1  0
 20 47  1  0
 21 48  1  0
 21 49  1  0
 22 50  1  0
 22 51  1  0
 23 52  1  0
 23 53  1  0
 24 54  1  0
 24 55  1  0
 25 56  1  0
 25 57  1  0
 26 58  1  0
 26 59  1  0
 27 60  1  0
 27 61  1  0
M  END


  Mrv1652304282217042D          

 27 27  0  0  1  0            999 V2000
   -0.1105   -6.1283    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8250   -5.7158    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1105   -5.3033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -6.4302    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -5.0013    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875   -5.0013    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3000   -5.7158    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1250   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3000   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3000   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1250   -4.2868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875   -3.5724    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3000   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1250   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5375   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3625   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7750   -1.4289    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -2.1434    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -6.8427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -6.8427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -7.5572    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
  1  3  1  0  0  0  0
  2  4  1  1  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 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
 14 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
  1 25  1  6  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0069713

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H](C)[C@@H](NC(=O)[C@H]1O[C@@H]1C(O)=O)C(=O)N(CCCCN)CCCCN

> <INCHI_IDENTIFIER>
InChI=1S/C18H34N4O5/c1-3-12(2)13(21-16(23)14-15(27-14)18(25)26)17(24)22(10-6-4-8-19)11-7-5-9-20/h12-15H,3-11,19-20H2,1-2H3,(H,21,23)(H,25,26)/t12-,13-,14+,15+/m1/s1

> <INCHI_KEY>
YBKILQBWFWGLMQ-KBXIAJHMSA-N

> <FORMULA>
C18H34N4O5

> <MOLECULAR_WEIGHT>
386.493

> <EXACT_MASS>
386.252920211

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
42.125110199009455

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S)-3-{[(1R,2R)-1-[bis(4-aminobutyl)carbamoyl]-2-methylbutyl]carbamoyl}oxirane-2-carboxylic acid

> <JCHEM_LOGP>
-3.226726912110905

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
12.516112082310993

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.2451037285026145

> <JCHEM_PKA_STRONGEST_BASIC>
10.203026601343554

> <JCHEM_POLAR_SURFACE_AREA>
147.98

> <JCHEM_REFRACTIVITY>
100.13249999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S)-3-{[(1R,2R)-1-[bis(4-aminobutyl)carbamoyl]-2-methylbutyl]carbamoyl}oxirane-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -0.206 -11.439   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.540 -10.669   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.206  -9.899   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -3.080 -10.669   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -3.850 -12.003   0.000  0.00  0.00           O+0
HETATM    6  N   UNK     0      -3.850  -9.336   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      -5.390  -9.336   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -6.160 -10.669   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -7.700 -10.669   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.390 -12.003   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.160 -13.337   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -6.160  -8.002   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -7.700  -8.002   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0      -5.390  -6.668   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      -6.160  -5.335   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -7.700  -5.335   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -8.470  -4.001   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -10.010  -4.001   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0     -10.780  -2.667   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0      -3.850  -6.668   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.080  -5.335   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.540  -5.335   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.770  -4.001   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0       0.770  -4.001   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0       0.564 -12.773   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.104 -12.773   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -0.206 -14.107   0.000  0.00  0.00           O+0
CONECT    1    2    3   25                                                  
CONECT    2    1    3    4                                                  
CONECT    3    2    1                                                       
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10                                                            
CONECT   12    7   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   14   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25    1   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   54    0
END

View in JSmol

Synonyms

Value	Source
(2S,3S)-3-{[(1R,2R)-1-[bis(4-aminobutyl)carbamoyl]-2-methylbutyl]-C-hydroxycarbonimidoyl}oxirane-2-carboxylate	Generator

Chemical Formula

C₁₈H₃₄N₄O₅

Average Mass

386.4930 Da

Monoisotopic Mass

386.25292 Da

IUPAC Name

(2S,3S)-3-{[(1R,2R)-1-[bis(4-aminobutyl)carbamoyl]-2-methylbutyl]carbamoyl}oxirane-2-carboxylic acid

Traditional Name

(2S,3S)-3-{[(1R,2R)-1-[bis(4-aminobutyl)carbamoyl]-2-methylbutyl]carbamoyl}oxirane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC[C@@H](C)[C@@H](NC(=O)[C@H]1O[C@@H]1C(O)=O)C(=O)N(CCCCN)CCCCN

InChI Identifier

InChI=1S/C18H34N4O5/c1-3-12(2)13(21-16(23)14-15(27-14)18(25)26)17(24)22(10-6-4-8-19)11-7-5-9-20/h12-15H,3-11,19-20H2,1-2H3,(H,21,23)(H,25,26)/t12-,13-,14+,15+/m1/s1

InChI Key

YBKILQBWFWGLMQ-KBXIAJHMSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Anabaena circinalis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoleucine and derivatives. Isoleucine and derivatives are compounds containing isoleucine or a derivative thereof resulting from reaction of isoleucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Isoleucine and derivatives

Alternative Parents

Substituents

Isoleucine or derivatives
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
Oxirane carboxylic acid or derivatives
Oxirane carboxylic acid
N-acyl-amine
Tertiary carboxylic acid amide
Amino acid
Carboxamide group
Oxacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid
Carboximidic acid derivative
Carboximidic acid
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary amine
Organooxygen compound
Organonitrogen compound
Primary aliphatic amine
Carbonyl group
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	-3.2	ChemAxon
pKa (Strongest Acidic)	3.25	ChemAxon
pKa (Strongest Basic)	10.2	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	147.98 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	100.13 m³·mol⁻¹	ChemAxon
Polarizability	42.13 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

163106680

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Circinamide (NP0069713)

MOL for NP0069713 (Circinamide)

3D MOL for NP0069713 (Circinamide)

3D SDF for NP0069713 (Circinamide)

3D-SDF for NP0069713 (Circinamide)

PDB for NP0069713 (Circinamide)

3D PDB for NP0069713 (Circinamide)

SMILES for NP0069713 (Circinamide)

INCHI for NP0069713 (Circinamide)

Structure for NP0069713 (Circinamide)

3D Structure for NP0069713 (Circinamide)