NP-MRD: Showing NP-Card for Albucidin (NP0008322)

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Record Information

Version

2.0

Created at

2020-12-09 05:56:29 UTC

Updated at

2021-07-15 17:00:06 UTC

NP-MRD ID

NP0008322

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Albucidin

Provided By

NPAtlas

Description

Albucidin is found in Streptomyces and Streptomyces albus. Albucidin was first documented in 2009 (PMID: 19247393). Based on a literature review very few articles have been published on [4-(6-amino-9H-purin-9-yl)oxetan-2-yl]methanol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106093D          

 27 29  0  0  0  0            999 V2000
   -4.7098    0.8895    0.0523 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6900    0.0554   -0.4733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8671   -0.8050   -1.4700 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8150   -1.5490   -1.8861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5951   -1.4478   -1.3254 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3597   -0.5924   -0.3126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4325    0.1723    0.1183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9689    0.9391    1.1197 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6543    0.6797    1.3251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020   -0.2583    0.4402 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9999   -0.8351    0.2974 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0545   -0.3571    1.2350 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5350    0.4703    0.0574 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0211    0.3345   -0.0918 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4795    0.6407   -1.3658 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7673   -0.3253   -0.7642 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2430    0.6934    0.9251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9398    1.7570   -0.4716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0281   -2.2369   -2.7094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0657    1.1859    2.0906 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9542   -1.9598    0.2883 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7764   -1.1316    1.5664 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7669    0.2912    2.0593 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1442    1.5062    0.0691 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2865   -0.7175    0.1477 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4943    1.0126    0.6509 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3911    1.5879   -1.5727 H   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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  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
 13 16  1  0  0  0  0
  7  2  1  0  0  0  0
 16 11  1  0  0  0  0
 10  6  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  4 19  1  0  0  0  0
  9 20  1  0  0  0  0
 11 21  1  6  0  0  0
 12 22  1  0  0  0  0
 12 23  1  0  0  0  0
 13 24  1  1  0  0  0
 14 25  1  0  0  0  0
 14 26  1  0  0  0  0
 15 27  1  0  0  0  0
M  END


  Mrv1652306242106093D          

 27 29  0  0  0  0            999 V2000
   -4.7098    0.8895    0.0523 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6900    0.0554   -0.4733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8671   -0.8050   -1.4700 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8150   -1.5490   -1.8861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5951   -1.4478   -1.3254 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3597   -0.5924   -0.3126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4325    0.1723    0.1183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9689    0.9391    1.1197 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6543    0.6797    1.3251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020   -0.2583    0.4402 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9999   -0.8351    0.2974 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0545   -0.3571    1.2350 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5350    0.4703    0.0574 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0211    0.3345   -0.0918 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4795    0.6407   -1.3658 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7673   -0.3253   -0.7642 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2430    0.6934    0.9251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9398    1.7570   -0.4716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0281   -2.2369   -2.7094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0657    1.1859    2.0906 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9542   -1.9598    0.2883 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7764   -1.1316    1.5664 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7669    0.2912    2.0593 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1442    1.5062    0.0691 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2865   -0.7175    0.1477 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4943    1.0126    0.6509 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3911    1.5879   -1.5727 H   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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  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
 13 16  1  0  0  0  0
  7  2  1  0  0  0  0
 16 11  1  0  0  0  0
 10  6  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  4 19  1  0  0  0  0
  9 20  1  0  0  0  0
 11 21  1  6  0  0  0
 12 22  1  0  0  0  0
 12 23  1  0  0  0  0
 13 24  1  1  0  0  0
 14 25  1  0  0  0  0
 14 26  1  0  0  0  0
 15 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0008322

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@@]1([H])O[C@]([H])(N2C([H])=NC3=C2N=C([H])N=C3N([H])[H])C1([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C9H11N5O2/c10-8-7-9(12-3-11-8)14(4-13-7)6-1-5(2-15)16-6/h3-6,15H,1-2H2,(H2,10,11,12)/t5-,6-/m0/s1

> <INCHI_KEY>
QNROWADMDDKKHX-UHFFFAOYSA-N

> <FORMULA>
C9H11N5O2

> <MOLECULAR_WEIGHT>
221.22

> <EXACT_MASS>
221.091274614

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
27

> <JCHEM_AVERAGE_POLARIZABILITY>
21.831669828247176

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2S,4S)-4-(6-amino-9H-purin-9-yl)oxetan-2-yl]methanol

> <ALOGPS_LOGP>
-0.62

> <JCHEM_LOGP>
-0.5599908666666668

> <ALOGPS_LOGS>
-1.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.540032813449415

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.665181678651297

> <JCHEM_PKA_STRONGEST_BASIC>
3.9409201553456916

> <JCHEM_POLAR_SURFACE_AREA>
99.08000000000001

> <JCHEM_REFRACTIVITY>
55.72240000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.84e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2S,4S)-4-(6-aminopurin-9-yl)oxetan-2-yl]methanol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  N   UNK     0      -4.710   0.890   0.052  0.00  0.00           N+0
HETATM    2  C   UNK     0      -3.690   0.055  -0.473  0.00  0.00           C+0
HETATM    3  N   UNK     0      -3.867  -0.805  -1.470  0.00  0.00           N+0
HETATM    4  C   UNK     0      -2.815  -1.549  -1.886  0.00  0.00           C+0
HETATM    5  N   UNK     0      -1.595  -1.448  -1.325  0.00  0.00           N+0
HETATM    6  C   UNK     0      -1.360  -0.592  -0.313  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.433   0.172   0.118  0.00  0.00           C+0
HETATM    8  N   UNK     0      -1.969   0.939   1.120  0.00  0.00           N+0
HETATM    9  C   UNK     0      -0.654   0.680   1.325  0.00  0.00           C+0
HETATM   10  N   UNK     0      -0.302  -0.258   0.440  0.00  0.00           N+0
HETATM   11  C   UNK     0       1.000  -0.835   0.297  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.054  -0.357   1.235  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.535   0.470   0.057  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.021   0.335  -0.092  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.479   0.641  -1.366  0.00  0.00           O+0
HETATM   16  O   UNK     0       1.767  -0.325  -0.764  0.00  0.00           O+0
HETATM   17  H   UNK     0      -5.243   0.693   0.925  0.00  0.00           H+0
HETATM   18  H   UNK     0      -4.940   1.757  -0.472  0.00  0.00           H+0
HETATM   19  H   UNK     0      -3.028  -2.237  -2.709  0.00  0.00           H+0
HETATM   20  H   UNK     0      -0.066   1.186   2.091  0.00  0.00           H+0
HETATM   21  H   UNK     0       0.954  -1.960   0.288  0.00  0.00           H+0
HETATM   22  H   UNK     0       2.776  -1.132   1.566  0.00  0.00           H+0
HETATM   23  H   UNK     0       1.767   0.291   2.059  0.00  0.00           H+0
HETATM   24  H   UNK     0       2.144   1.506   0.069  0.00  0.00           H+0
HETATM   25  H   UNK     0       4.287  -0.718   0.148  0.00  0.00           H+0
HETATM   26  H   UNK     0       4.494   1.013   0.651  0.00  0.00           H+0
HETATM   27  H   UNK     0       4.391   1.588  -1.573  0.00  0.00           H+0
CONECT    1    2   17   18                                                  
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   19                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   10                                                  
CONECT    7    6    8    2                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   20                                                  
CONECT   10    9   11    6                                                  
CONECT   11   10   12   16   21                                             
CONECT   12   11   13   22   23                                             
CONECT   13   12   14   16   24                                             
CONECT   14   13   15   25   26                                             
CONECT   15   14   27                                                       
CONECT   16   13   11                                                       
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    4                                                            
CONECT   20    9                                                            
CONECT   21   11                                                            
CONECT   22   12                                                            
CONECT   23   12                                                            
CONECT   24   13                                                            
CONECT   25   14                                                            
CONECT   26   14                                                            
CONECT   27   15                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₉H₁₁N₅O₂

Average Mass

221.2200 Da

Monoisotopic Mass

221.09127 Da

IUPAC Name

[(2S,4S)-4-(6-amino-9H-purin-9-yl)oxetan-2-yl]methanol

Traditional Name

[(2S,4S)-4-(6-aminopurin-9-yl)oxetan-2-yl]methanol

CAS Registry Number

Not Available

SMILES

NC1=NC=NC2=C1N=CN2C1CC(CO)O1

InChI Identifier

InChI=1S/C9H11N5O2/c10-8-7-9(12-3-11-8)14(4-13-7)6-1-5(2-15)16-6/h3-6,15H,1-2H2,(H2,10,11,12)

InChI Key

QNROWADMDDKKHX-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, 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
Streptomyces	NPAtlas	19247393
Streptomyces albus	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	-0.62	ALOGPS
logP	-0.56	ChemAxon
logS	-1.4	ALOGPS
pKa (Strongest Acidic)	14.67	ChemAxon
pKa (Strongest Basic)	3.94	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	99.08 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	55.72 m³·mol⁻¹	ChemAxon
Polarizability	21.83 Å³	ChemAxon
Number of Rings	3	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

NPAtlas ID

NPA018537

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

28286259

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71340416

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Hahn DR, Graupner PR, Chapin E, Gray J, Heim D, Gilbert JR, Gerwick BC: Albucidin: a novel bleaching herbicide from Streptomyces albus subsp. chlorinus NRRL B-24108. J Antibiot (Tokyo). 2009 Apr;62(4):191-4. doi: 10.1038/ja.2009.11. Epub 2009 Feb 27. [PubMed:19247393 ]

Showing NP-Card for Albucidin (NP0008322)

MOL for NP0008322 (Albucidin)

3D MOL for NP0008322 (Albucidin)

3D SDF for NP0008322 (Albucidin)

3D-SDF for NP0008322 (Albucidin)

PDB for NP0008322 (Albucidin)

3D PDB for NP0008322 (Albucidin)

SMILES for NP0008322 (Albucidin)

INCHI for NP0008322 (Albucidin)

Structure for NP0008322 (Albucidin)

3D Structure for NP0008322 (Albucidin)