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N-(3-(cyclopentyloxy)-4-(5-phenylfuran-2-yl)phenyl)picolinimidamide methanesulfonate ID: ALA3794259
PubChem CID: 127029136
Max Phase: Preclinical
Molecular Formula: C28H29N3O5S
Molecular Weight: 423.52
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: CS(=O)(=O)O.N=C(Nc1ccc(-c2ccc(-c3ccccc3)o2)c(OC2CCCC2)c1)c1ccccn1
Standard InChI: InChI=1S/C27H25N3O2.CH4O3S/c28-27(23-12-6-7-17-29-23)30-20-13-14-22(26(18-20)31-21-10-4-5-11-21)25-16-15-24(32-25)19-8-2-1-3-9-19;1-5(2,3)4/h1-3,6-9,12-18,21H,4-5,10-11H2,(H2,28,30);1H3,(H,2,3,4)
Standard InChI Key: MSUZZWXAWDLCKP-UHFFFAOYSA-N
Molfile:
RDKit 2D
37 40 0 0 0 0 0 0 0 0999 V2000
9.2520 -0.3644 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
10.2915 0.2353 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
11.3309 -0.3644 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
10.2915 1.4353 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.2915 -0.9647 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1.2990 -0.7500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.2990 0.7500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.0000 1.5000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.2990 0.7500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.2990 -0.7500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.0000 -1.5000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5972 1.5031 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
2.5951 3.0039 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.8933 3.7570 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.5548 3.6021 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
3.8933 5.2571 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1924 6.0071 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.4914 5.2571 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.4915 3.7571 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1925 3.0071 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-2.5987 -1.5004 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.9511 -0.8815 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-4.9530 -1.9978 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.2010 -3.2957 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.7343 -2.9815 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.4458 -1.8433 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.1563 -0.5279 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.6557 -0.4862 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.4415 -1.7638 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.7279 -3.0832 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.2285 -3.1250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.0031 -3.0008 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1.3039 -3.7494 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.4469 -5.2297 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.9152 -5.5365 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.6607 -4.2349 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6532 -3.1236 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2 1 2 0
3 2 2 0
4 2 1 0
2 5 1 0
6 7 2 0
7 8 1 0
8 9 2 0
9 10 1 0
10 11 2 0
11 6 1 0
7 12 1 0
12 13 1 0
13 14 1 0
13 15 2 0
14 16 2 0
16 17 1 0
17 18 2 0
18 19 1 0
19 20 2 0
20 14 1 0
21 22 1 0
22 23 1 0
23 24 2 0
24 25 1 0
25 21 2 0
10 21 1 0
26 27 2 0
27 28 1 0
28 29 2 0
29 30 1 0
30 31 2 0
31 26 1 0
23 26 1 0
11 32 1 0
32 33 1 0
33 34 1 0
34 35 1 0
35 36 1 0
36 37 1 0
37 33 1 0
M END Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 423.52Molecular Weight (Monoisotopic): 423.1947AlogP: 6.77#Rotatable Bonds: 6Polar Surface Area: 71.14Molecular Species: NEUTRALHBA: 4HBD: 2#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 1CX Acidic pKa: ┄CX Basic pKa: 5.29CX LogP: 5.72CX LogD: 5.71Aromatic Rings: 4Heavy Atoms: 32QED Weighted: 0.27Np Likeness Score: -0.57
References 1. Zhu X, Farahat AA, Mattamana M, Joice A, Pandharkar T, Holt E, Banerjee M, Gragg JL, Hu L, Kumar A, Yang S, Wang MZ, Boykin DW, Werbovetz KA.. (2016) Synthesis and pharmacological evaluation of mono-arylimidamides as antileishmanial agents., 26 (10): [PMID:27048943 ] [10.1016/j.bmcl.2016.03.082 ]