NP-MRD: Showing NP-Card for Inubosin B (NP0013763)

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Record Information

Version

2.0

Created at

2021-01-05 23:03:31 UTC

Updated at

2021-07-15 17:15:23 UTC

NP-MRD ID

NP0013763

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Inubosin B

Provided By

NPAtlas

Description

Inubosin B is found in Streptomyces sp. IFM 11440. Inubosin B was first documented in 2015 (PMID: 25621736). Based on a literature review very few articles have been published on 2-(hydroxymethyl)acridin-4-ol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242119493D          

 28 30  0  0  0  0            999 V2000
   -4.5195   -1.4465    0.4327 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2774   -0.1070    0.2848 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8403    0.2288    0.1948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4876    1.5544    0.0442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1581    1.9325   -0.0460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8457    3.2904   -0.1984 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1453    0.9909    0.0124 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1469    1.3172   -0.0711 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1497    0.4500   -0.0200 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4865    0.7818   -0.1057 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4990   -0.1303   -0.0503 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1795   -1.4605    0.0995 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8360   -1.8286    0.1892 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8280   -0.8896    0.1309 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5184   -1.2786    0.2215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4881   -0.3371    0.1629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8221   -0.6905    0.2507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3334   -1.8118    1.3136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8308    0.2763   -0.6091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6694    0.4441    1.1870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2771    2.3101   -0.0036 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0898    3.6183   -0.2683 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7560    1.8251   -0.2239 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5511    0.1167   -0.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9486   -2.2397    0.1505 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5766   -2.8850    0.3084 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2089   -2.3104    0.3401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0800   -1.7211    0.3672 H   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  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  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17  3  1  0  0  0  0
 16  7  1  0  0  0  0
 14  9  1  0  0  0  0
  1 18  1  0  0  0  0
  2 19  1  0  0  0  0
  2 20  1  0  0  0  0
  4 21  1  0  0  0  0
  6 22  1  0  0  0  0
 10 23  1  0  0  0  0
 11 24  1  0  0  0  0
 12 25  1  0  0  0  0
 13 26  1  0  0  0  0
 15 27  1  0  0  0  0
 17 28  1  0  0  0  0
M  END


  Mrv1652306242119493D          

 28 30  0  0  0  0            999 V2000
   -4.5195   -1.4465    0.4327 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2774   -0.1070    0.2848 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8403    0.2288    0.1948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4876    1.5544    0.0442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1581    1.9325   -0.0460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8457    3.2904   -0.1984 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1453    0.9909    0.0124 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1469    1.3172   -0.0711 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1497    0.4500   -0.0200 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4865    0.7818   -0.1057 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4990   -0.1303   -0.0503 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1795   -1.4605    0.0995 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8360   -1.8286    0.1892 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8280   -0.8896    0.1309 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5184   -1.2786    0.2215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4881   -0.3371    0.1629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8221   -0.6905    0.2507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3334   -1.8118    1.3136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8308    0.2763   -0.6091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6694    0.4441    1.1870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2771    2.3101   -0.0036 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0898    3.6183   -0.2683 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7560    1.8251   -0.2239 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5511    0.1167   -0.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9486   -2.2397    0.1505 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5766   -2.8850    0.3084 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2089   -2.3104    0.3401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0800   -1.7211    0.3672 H   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  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  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17  3  1  0  0  0  0
 16  7  1  0  0  0  0
 14  9  1  0  0  0  0
  1 18  1  0  0  0  0
  2 19  1  0  0  0  0
  2 20  1  0  0  0  0
  4 21  1  0  0  0  0
  6 22  1  0  0  0  0
 10 23  1  0  0  0  0
 11 24  1  0  0  0  0
 12 25  1  0  0  0  0
 13 26  1  0  0  0  0
 15 27  1  0  0  0  0
 17 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0013763

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2N=C3C([H])=C([H])C([H])=C([H])C3=C([H])C2=C([H])C(=C1[H])C([H])([H])O[H]

> <INCHI_IDENTIFIER>
InChI=1S/C14H11NO2/c16-8-9-5-11-7-10-3-1-2-4-12(10)15-14(11)13(17)6-9/h1-7,16-17H,8H2

> <INCHI_KEY>
KJKXFKGBQVVKAX-UHFFFAOYSA-N

> <FORMULA>
C14H11NO2

> <MOLECULAR_WEIGHT>
225.247

> <EXACT_MASS>
225.078978598

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
28

> <JCHEM_AVERAGE_POLARIZABILITY>
24.218539088965933

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(hydroxymethyl)acridin-4-ol

> <ALOGPS_LOGP>
2.54

> <JCHEM_LOGP>
2.4353124646666666

> <ALOGPS_LOGS>
-3.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.980645973680765

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.443572175190017

> <JCHEM_PKA_STRONGEST_BASIC>
5.100375414829846

> <JCHEM_POLAR_SURFACE_AREA>
53.35

> <JCHEM_REFRACTIVITY>
64.8543

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.22e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(hydroxymethyl)acridin-4-ol

> <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  O   UNK     0      -4.519  -1.446   0.433  0.00  0.00           O+0
HETATM    2  C   UNK     0      -4.277  -0.107   0.285  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.840   0.229   0.195  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.488   1.554   0.044  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.158   1.933  -0.046  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.846   3.290  -0.198  0.00  0.00           O+0
HETATM    7  C   UNK     0      -0.145   0.991   0.012  0.00  0.00           C+0
HETATM    8  N   UNK     0       1.147   1.317  -0.071  0.00  0.00           N+0
HETATM    9  C   UNK     0       2.150   0.450  -0.020  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.486   0.782  -0.106  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.499  -0.130  -0.050  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.180  -1.460   0.100  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.836  -1.829   0.189  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.828  -0.890   0.131  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.518  -1.279   0.222  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.488  -0.337   0.163  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.822  -0.691   0.251  0.00  0.00           C+0
HETATM   18  H   UNK     0      -4.333  -1.812   1.314  0.00  0.00           H+0
HETATM   19  H   UNK     0      -4.831   0.276  -0.609  0.00  0.00           H+0
HETATM   20  H   UNK     0      -4.669   0.444   1.187  0.00  0.00           H+0
HETATM   21  H   UNK     0      -3.277   2.310  -0.004  0.00  0.00           H+0
HETATM   22  H   UNK     0       0.090   3.618  -0.268  0.00  0.00           H+0
HETATM   23  H   UNK     0       3.756   1.825  -0.224  0.00  0.00           H+0
HETATM   24  H   UNK     0       5.551   0.117  -0.116  0.00  0.00           H+0
HETATM   25  H   UNK     0       4.949  -2.240   0.151  0.00  0.00           H+0
HETATM   26  H   UNK     0       2.577  -2.885   0.308  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.209  -2.310   0.340  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.080  -1.721   0.367  0.00  0.00           H+0
CONECT    1    2   18                                                       
CONECT    2    1    3   19   20                                             
CONECT    3    2    4   17                                                  
CONECT    4    3    5   21                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5   22                                                       
CONECT    7    5    8   16                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11   23                                                  
CONECT   11   10   12   24                                                  
CONECT   12   11   13   25                                                  
CONECT   13   12   14   26                                                  
CONECT   14   13   15    9                                                  
CONECT   15   14   16   27                                                  
CONECT   16   15   17    7                                                  
CONECT   17   16    3   28                                                  
CONECT   18    1                                                            
CONECT   19    2                                                            
CONECT   20    2                                                            
CONECT   21    4                                                            
CONECT   22    6                                                            
CONECT   23   10                                                            
CONECT   24   11                                                            
CONECT   25   12                                                            
CONECT   26   13                                                            
CONECT   27   15                                                            
CONECT   28   17                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₄H₁₁NO₂

Average Mass

225.2470 Da

Monoisotopic Mass

225.07898 Da

IUPAC Name

2-(hydroxymethyl)acridin-4-ol

Traditional Name

2-(hydroxymethyl)acridin-4-ol

CAS Registry Number

Not Available

SMILES

OCC1=CC2=CC3=CC=CC=C3N=C2C(O)=C1

InChI Identifier

InChI=1S/C14H11NO2/c16-8-9-5-11-7-10-3-1-2-4-12(10)15-14(11)13(17)6-9/h1-7,16-17H,8H2

InChI Key

KJKXFKGBQVVKAX-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 sp. IFM 11440	NPAtlas	25621736

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	2.54	ALOGPS
logP	2.44	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	9.44	ChemAxon
pKa (Strongest Basic)	5.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	53.35 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	64.85 m³·mol⁻¹	ChemAxon
Polarizability	24.22 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA007494

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

58965248

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

78318520

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Arai MA, Koryudzu K, Ishibashi M: Inubosins A, B, and C are acridine alkaloids isolated from a culture of Streptomyces sp. IFM 11440 with Ngn2 promoter activity. J Nat Prod. 2015 Feb 27;78(2):311-4. doi: 10.1021/np5006218. Epub 2015 Jan 26. [PubMed:25621736 ]

Showing NP-Card for Inubosin B (NP0013763)

MOL for NP0013763 (Inubosin B)

3D MOL for NP0013763 (Inubosin B)

3D SDF for NP0013763 (Inubosin B)

3D-SDF for NP0013763 (Inubosin B)

PDB for NP0013763 (Inubosin B)

3D PDB for NP0013763 (Inubosin B)

SMILES for NP0013763 (Inubosin B)

INCHI for NP0013763 (Inubosin B)

Structure for NP0013763 (Inubosin B)

3D Structure for NP0013763 (Inubosin B)