NP-MRD: Showing NP-Card for (6s)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid (NP0224315)

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Record Information

Version

2.0

Created at

2022-09-06 02:38:36 UTC

Updated at

2022-09-06 02:38:36 UTC

NP-MRD ID

NP0224315

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(6s)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid

Description

N-methyl-valyl-amiclenomycin, also known as BA 2, belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms. (6s)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid was first documented in 1993 (PMID: 7681541). Based on a literature review very few articles have been published on N-methyl-valyl-amiclenomycin.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 49  0  0  0  0  0  0  0  0999 V2000
   -1.5955   -2.2905   -2.7144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9605   -2.6447   -1.5188 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6447   -1.6158   -0.5535 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1823   -2.2647    0.6481 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9352   -0.8905   -0.2338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7045   -0.8115   -1.1904 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2737   -0.3287    1.0773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6157    0.3364    1.0400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7319    1.4848    0.1077 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8010    2.6097    0.4218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7721    3.6006   -0.3836 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9735    2.6511    1.5203 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3486   -0.6963   -1.1697 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5594   -1.5353   -1.5535 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7508    0.4951   -0.3512 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3798    0.2473    0.9605 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6622    1.5934    1.5593 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8309    2.1742    1.5721 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9708    1.4658    0.9556 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3385    1.9438   -0.3462 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7814   -0.0001    0.9238 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5977   -0.5949    0.9252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1681   -2.9539   -3.5370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6874   -2.5411   -2.7489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3925   -1.2768   -3.0540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3108   -3.5154   -1.0880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0605   -2.5473    1.1815 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2499   -3.1748    0.3761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3523   -1.1299    1.8683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5221    0.4096    1.3837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8354    0.7283    2.0773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4011   -0.4290    0.8705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5736    1.2585   -0.9554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7785    1.9151    0.2528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3757    2.5705    2.4575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0698   -0.2836   -2.0965 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5267   -2.5212   -1.0632 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4255   -1.7816   -2.6498 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4988   -0.9910   -1.4958 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5043    1.0635   -0.9944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0898    1.1817   -0.2704 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6907   -0.2572    1.6633 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8255    2.1042    2.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0138    3.1454    2.0088 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8577    1.6563    1.6287 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5689    2.2792   -0.9326 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2210    2.4636   -0.3896 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6594   -0.6241    0.8975 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5456   -1.6785    0.9054 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 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
  3  5  1  1
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 12  1  0
 10 11  2  0
 22 16  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  4 27  1  0
  4 28  1  0
 13 36  1  6
 14 37  1  0
 14 38  1  0
 14 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  1
 17 43  1  0
 18 44  1  0
 19 45  1  1
 20 46  1  0
 20 47  1  0
 21 48  1  0
 22 49  1  0
  7 29  1  0
  7 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 12 35  1  0
M  END


  Mrv1652309062204382D          

 22 22  0  0  1  0            999 V2000
    1.2375    2.5855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8250    3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  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  2  0  0  0  0
 10 12  1  0  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 16 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0224315

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN[C@@](N)(C(C)CC1C=CC(N)C=C1)C(=O)CCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H27N3O3/c1-11(10-12-6-8-13(17)9-7-12)16(18,19-2)14(20)4-3-5-15(21)22/h6-9,11-13,19H,3-5,10,17-18H2,1-2H3,(H,21,22)/t11?,12?,13?,16-/m0/s1

> <INCHI_KEY>
IYJXSJJCXYNKBU-NPQGJGQUSA-N

> <FORMULA>
C16H27N3O3

> <MOLECULAR_WEIGHT>
309.41

> <EXACT_MASS>
309.205241741

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
33.29245493656553

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(6S)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid

> <JCHEM_LOGP>
-1.098211415213816

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
17.557430685017508

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.092454686254636

> <JCHEM_PKA_STRONGEST_BASIC>
9.122792433256395

> <JCHEM_POLAR_SURFACE_AREA>
118.44

> <JCHEM_REFRACTIVITY>
87.5716

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(6S)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       2.310   4.826   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       1.540   6.160   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0      -1.540   6.160   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       0.000   7.700   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.334   8.470   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -1.334   8.470   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334  10.010   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.667  10.780   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.667  12.320   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -4.001  13.090   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      -1.334  13.090   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       1.334  -2.310   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5   13                                             
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    3   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   16                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   44    0
END

View in JSmol

Synonyms

Value	Source
BA 2	MeSH
BA-2	MeSH

Chemical Formula

C₁₆H₂₇N₃O₃

Average Mass

309.4100 Da

Monoisotopic Mass

309.20524 Da

IUPAC Name

(6S)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid

Traditional Name

(6S)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid

CAS Registry Number

Not Available

SMILES

CN[C@@](N)(C(C)CC1C=CC(N)C=C1)C(=O)CCCC(O)=O

InChI Identifier

InChI=1S/C16H27N3O3/c1-11(10-12-6-8-13(17)9-7-12)16(18,19-2)14(20)4-3-5-15(21)22/h6-9,11-13,19H,3-5,10,17-18H2,1-2H3,(H,21,22)/t11?,12?,13?,16-/m0/s1

InChI Key

IYJXSJJCXYNKBU-NPQGJGQUSA-N

Experimental Spectra

Not Available

Predicted Spectra

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

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Medium-chain fatty acids

Alternative Parents

Substituents

Medium-chain fatty acid
Branched fatty acid
Amino fatty acid
Amino acid
Ketone
Amino acid or derivatives
Secondary amine
Monocarboxylic acid or derivatives
Secondary aliphatic amine
Carboxylic acid
Carboxylic acid derivative
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 homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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	-1.1	ChemAxon
pKa (Strongest Acidic)	4.09	ChemAxon
pKa (Strongest Basic)	9.12	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	118.44 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	87.57 m³·mol⁻¹	ChemAxon
Polarizability	33.29 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

132621

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

150455

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Yamada T, Osawa T, Kawakishi S, Udaka S, Ohta T: Antimutagenic effects of N-methyl-valyl-amiclenomycin (BA-2) isolated from the metabolites of Streptomyces sp. Mutat Res. 1993 Apr;286(2):293-7. doi: 10.1016/0027-5107(93)90194-k. [PubMed:7681541 ]
LOTUS database [Link]

Showing NP-Card for (6s)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid (NP0224315)

MOL for NP0224315 ((6s)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid)

3D MOL for NP0224315 ((6s)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid)

3D SDF for NP0224315 ((6s)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid)

3D-SDF for NP0224315 ((6s)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid)

PDB for NP0224315 ((6s)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid)

3D PDB for NP0224315 ((6s)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid)

SMILES for NP0224315 ((6s)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid)

INCHI for NP0224315 ((6s)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid)

Structure for NP0224315 ((6s)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid)

3D Structure for NP0224315 ((6s)-6-amino-8-(4-aminocyclohexa-2,5-dien-1-yl)-7-methyl-6-(methylamino)-5-oxooctanoic acid)