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(2S,3aR,9bR)-6-((3,5-bis(trifluoromethyl)benzyl)oxy)-7,8-dihydroxy-2-propyl-3,3a-dihydro-2H-furo[3,2-c]isochromen-5(9bH)-one ID: ALA4878350
PubChem CID: 164626650
Max Phase: Preclinical
Molecular Formula: C23H20F6O6
Molecular Weight: 506.40
Molecule Type: Unknown
Associated Items:
Names and Identifiers Canonical SMILES: CCC[C@H]1C[C@H]2OC(=O)c3c(cc(O)c(O)c3OCc3cc(C(F)(F)F)cc(C(F)(F)F)c3)[C@H]2O1
Standard InChI: InChI=1S/C23H20F6O6/c1-2-3-13-7-16-19(34-13)14-8-15(30)18(31)20(17(14)21(32)35-16)33-9-10-4-11(22(24,25)26)6-12(5-10)23(27,28)29/h4-6,8,13,16,19,30-31H,2-3,7,9H2,1H3/t13-,16+,19+/m0/s1
Standard InChI Key: CUQWLLJOYDZRSI-URKNILKWSA-N
Molfile:
RDKit 2D
37 40 0 0 0 0 0 0 0 0999 V2000
27.8154 -3.9623 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
28.2321 -4.6790 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
28.6444 -3.9598 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
24.9531 -5.4080 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
25.3697 -4.6956 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
24.5443 -4.6910 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
25.3891 -8.8079 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
25.3880 -9.6353 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
26.1027 -10.0481 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
26.1009 -8.3952 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
26.8162 -8.8042 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
26.8151 -9.6327 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
28.2478 -8.8063 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
27.5304 -8.3887 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
28.2467 -9.6348 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
27.5282 -10.0458 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
27.6972 -10.8562 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
28.5201 -10.9458 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
28.8596 -10.1910 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
27.5304 -7.5638 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
28.9570 -9.2162 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
26.9405 -10.6287 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
28.9298 -11.6619 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.7548 -11.6650 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
30.1646 -12.3810 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
26.0985 -7.5702 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
24.6746 -8.3956 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
24.6731 -10.0472 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
26.8117 -7.1556 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
26.8092 -6.3306 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
27.5243 -5.9205 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
27.5222 -5.0963 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
26.8059 -4.6851 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
26.0904 -5.1042 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
26.0960 -5.9270 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
25.3679 -3.8715 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
28.9510 -5.0928 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
2 1 1 0
3 2 1 0
5 4 1 0
6 5 1 0
7 8 2 0
8 9 1 0
9 12 2 0
11 10 2 0
10 7 1 0
11 12 1 0
11 14 1 0
12 16 1 0
15 13 1 0
13 14 1 0
15 16 1 0
16 17 1 0
17 18 1 0
18 19 1 0
19 15 1 0
14 20 2 0
15 21 1 1
16 22 1 1
18 23 1 6
23 24 1 0
24 25 1 0
10 26 1 0
7 27 1 0
8 28 1 0
26 29 1 0
29 30 1 0
30 31 2 0
31 32 1 0
32 33 2 0
33 34 1 0
34 35 2 0
35 30 1 0
34 5 1 0
5 36 1 0
32 2 1 0
2 37 1 0
M END Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: UnknownTopical: 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: 506.40Molecular Weight (Monoisotopic): 506.1164AlogP: 5.88#Rotatable Bonds: 5Polar Surface Area: 85.22Molecular Species: NEUTRALHBA: 6HBD: 2#RO5 Violations: 2HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 2CX Acidic pKa: 8.53CX Basic pKa: ┄CX LogP: 5.59CX LogD: 5.56Aromatic Rings: 2Heavy Atoms: 35QED Weighted: 0.30Np Likeness Score: 1.08
References 1. Coronado L, Zhang XQ, Dorta D, Escala N, Pineda LM, Ng MG, Del Olmo E, Wang CY, Gu YC, Shao CL, Spadafora C.. (2021) Semisynthesis, Antiplasmodial Activity, and Mechanism of Action Studies of Isocoumarin Derivatives., 84 (5.0): [PMID:33979168 ] [10.1021/acs.jnatprod.0c01032 ]