SID856259

ID: ALA1348232

Chembl Id: CHEMBL1348232

PubChem CID: 135449532

Max Phase: Preclinical

Molecular Formula: C10H12N4O

Molecular Weight: 204.23

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  Cc1cc(O)nc(-n2nc(C)cc2C)n1

Standard InChI:  InChI=1S/C10H12N4O/c1-6-5-9(15)12-10(11-6)14-8(3)4-7(2)13-14/h4-5H,1-3H3,(H,11,12,15)

Standard InChI Key:  XIFVEJXUSTTZKD-UHFFFAOYSA-N

Alternative Forms

1. Parent:

   

   ALA1348232

   ---

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 204.23

Molecular Weight (Monoisotopic): 204.1011

AlogP: 1.29

#Rotatable Bonds: 1

Polar Surface Area: 63.83

Molecular Species: NEUTRAL

HBA: 5

HBD: 1

#RO5 Violations: 0

HBA (Lipinski): 5

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 12.65

CX Basic pKa: 2.33

CX LogP: 1.57

CX LogD: 1.57

Aromatic Rings: 2

Heavy Atoms: 15

QED Weighted: 0.76

Np Likeness Score: -2.47

References

1. PubChem BioAssay data set, 

2. KONISHI K, KURAGANO T.  (1990)  Fungicidal Activity of Pyrazolylpyrimidines,  15  (1): [10.1584/jpestics.15.13]

3. MMV Pathogen Box,  [10.6019/CHEMBL3637841]

4. Nathan group, Weill Cornell Medical College; Barry Lab, NIAID NIH; Winzeler lab, UCSD; Laboratory of Microbiology, Parasitology and Hygiene (LMPH), Univ. of Antwerp; London School of Hygiene and Tropical Medicine; Parasite Chemotherapy Unit at Swiss Tropical and Public Health Institute; Huston group at the University of Vermont; Castellanos group at UTMB, Galveston, Texas; Sakanari Lab, Univ. of Calif. San Francisco; Townson (Simon) Lab, Imperial College London; Fidelis Cho-Ngwa Lab, University of Buea, Buea, Cameroon; Laboratory of Molecular Parasitology at the New York Blood Center; Bickle Lab, London School of Hygiene and Tropical Medicine; Keiser Lab, Swiss Tropical and Public Health Institute; Caffrey group at the Center for Discovery and Innovation in Parasitic Diseases, Skaggs School of Pharmacy and Pharmaceutical Sciences, UC San Diego; University of Cape Town; Shanmugam group at CSIR-National Chemical Laboratory, Pune (India); Novartis Institute for Tropical Disease-Singapore; Abbvie. MMV Pathogen Box Bioactivity Data,  [10.6019/CHEMBL3832761]

5. Anna Ehmann. The Australian National University Dept Of Immunology Pathogen Box Compounds Screened,  [10.6019/CHEMBL3987221]

6. Sarink, M; Mykytyn, A; Tielens, A; van Hellemond, J. Naegleria gruberi Pathogen Box compounds screening,  [10.6019/CHEMBL4513101]

7. Johannes Zuegg, Alysha Elliott, Maite Amado, Emma Cowie, Ali Hinton, Geraldine Kaeslin, Angela Kavanagh, Anne Kunert, Gabriell Lowe, Soumya Ramu, Janet Reid, Robin Trauer, Mathilde Desselle, Ruth Neale, Karl Hansford, Mark Blascovich, Matthew Cooper. CO-ADD screening of MMV (CH) - MMV compounds,  [10.6019/CHEMBL4513149]

8. Poirier, Marion, Pujol-Gimenez, Jonai, Manatschal, Cristina, Buhlmann, Sven, Embaby, Ahmed, Javor, Sacha, Hediger, Matthias A., Reymond, Jean-Louis.  (2020)  Pyrazolyl-pyrimidones inhibit the function of human solute carrier protein SLC11A2 (hDMT1) by metal chelation,  11  (9): [PMID:33479694] [10.1039/d0md00085j]

9. Soares de Melo C,Singh V,Myrick A,Simelane SB,Taylor D,Brunschwig C,Lawrence N,Schnappinger D,Engelhart CA,Kumar A,Parish T,Su Q,Myers TG,Boshoff HIM,Barry CE,Sirgel FA,van Helden PD,Buchanan KI,Bayliss T,Green SR,Ray PC,Wyatt PG,Basarab GS,Eyermann CJ,Chibale K,Ghorpade SR.  (2021)  Antitubercular 2-Pyrazolylpyrimidinones: Structure-Activity Relationship and Mode-of-Action Studies.,  64  (1.0): [PMID:33395287] [10.1021/acs.jmedchem.0c01727]

Source

Source(4):

• Scientific Literature
• PubChem BioAssays
• MMV Pathogen Box
• CO-ADD antimicrobial screening data