BackBack |Pangu Molecule Optimizer
C[N+](C)(C)c1cccc(C(O)(O)C(F)(F)F)c1
C[N+](C)(C)c1cccc(C(O)(O)C(F)(F)F)c1
Optimized 10
C[N+](C)(C)c1cccc(C2(O)CC(C(O)(O)C(F)(F)F)C2)c1
C15H21F3NO3+
MolWeight320.15
TPSA60.69
logP1.63
QED0.59
SAscore3.47
Similarity0.57
C[N+](C)(C)c1cccc(C(O)(N(O)c2ccccc2)C(F)(F)F)c1
C17H20F3N2O2+
MolWeight341.15
TPSA43.7
logP1.86
QED0.51
SAscore3.59
Similarity0.55
C[N+](C)(C)c1cccc(C(O)(O)C2CC(C(F)(F)C(F)(F)F)C(O)O2)c1
C16H21F5NO4+
MolWeight386.14
TPSA69.92
logP1.13
QED0.42
SAscore4.73
Similarity0.55
C[N+](C)(C)c1cccc(OC(O)(c2cccc(O)c2)C(F)(F)F)c1
C17H19F3NO3+
MolWeight342.13
TPSA49.69
logP3.13
QED0.66
SAscore3.51
Similarity0.53
C[N+](C)(C)c1cccc(C(O)(O)C(O)(O)c2ccc(F)cc2F)c1
C17H20F2NO4+
MolWeight340.14
TPSA80.92
logP0.91
QED0.5
SAscore3.19
Similarity0.51
C[N+](C)(C)c1cccc(C(O)(O)c2ccc(F)cc2)c1
C16H19FNO2+
MolWeight276.14
TPSA40.46
logP2.82
QED0.67
SAscore2.86
Similarity0.49
C[N+](C)(C)c1cccc(C2(O)CNC(=O)C2(O)C(F)(F)F)c1
C14H18F3N2O3+
MolWeight319.13
TPSA69.56
logP0.21
QED0.7
SAscore4.29
Similarity0.47
COC(O)(c1cccc([N+](C)(C)C)c1)N1CC(F)(F)C1=O
C14H19F2N2O3+
MolWeight301.14
TPSA49.77
logP0.83
QED0.51
SAscore4.17
Similarity0.46
CN(C)C1C=CC(=CC(O)(O)C(O)(O)c2cccc([N+](C)(C)C)c2)C=C1
C20H29N2O4+
MolWeight361.21
TPSA84.16
logP-0.19
QED0.46
SAscore3.99
Similarity0.44
C[N+](C)(C)c1cccc(C(O)(O)C(F)(F)F)c1OC(O)(O)C1(O)CC1
C15H21F3NO6+
MolWeight368.13
TPSA110.38
logP0.16
QED0.37
SAscore3.85
Similarity0.43
Huawei CloudSIMM
ADMET
Similarity:
Original Molecule
Optimized Molecule
Physicochemical PropertyOriginalOptimized
Molecular Weight (MW)250.24
???
Molecular Refractivity (MR)58.179
???
Volume211
???
Density1.186
???
pKa8.005
???
Check Acidbase
???
nHA2
???
nHD2
???
nRot2
???
nRing1
???
MaxRing6
???
nHet6
???
fChar1
???
nRig6
???
Flexibility0.333
???
Stereo Centers0
???
TPSA40.46
???
logS-2.222
???
logP1.583
???
Medicinal Chemistry
QED0.618
???
SAscore3.224
???
SCscore1.981
???
Fsp30.455
???
NPscore0.006
???
Lipinski RuleAccepted
???
Pfizer RuleRejected
???
GSK RuleAccepted
???
Golden TriangleAccepted
???
PAINS0 alert(s)
???
ALARM NMR Rule0 alert(s)
???
BMS Rule1 alert(s)
???
Chelator Rule0 alert(s)
???
Absorption
Caco-2 Permeability0.803
???
MDCK Permeability-8.1e-06
???
Pgp-inhibitor---
???
Pgp-substrate---
???
HIA---
???
F20%---
???
F30%---
???
Distribution
PPB48.506%
???
VD1.918
???
BBB Penetration--
???
Fu76.319%
???
Metabolism
CYP1A2 inhibitor---
???
CYP1A2 substrate+
???
CYP2C9 inhibitor---
???
CYP2C9 substrate--
???
CYP3A4 inhibitor---
???
CYP3A4 substrate--
???
Excretion
CL0.929
???
T1/20.062
???
Toxicity
hERG Blockers---
???
H-HT-
???
DILI---
???
AMES Toxicity+
???
FDAMDD++
???
Skin Sensitization++
???
Carcinogencity+
???
Eye Corrosion---
???
Eye Irritation+
???
Environmental Toxicity
Bioconcentration Factors0.754
???
IGC500.466
???
LC50FM4.553
???
LC50DM10.235
???
Tox21 Pathway
NR-AR---
???
NR-AR-LBD---
???
NR-AhR---
???
NR-Aromatase--
???
NR-ER---
???
NR-ER-LBD---
???
NR-PPAR-gamma---
???
SR-ARE---
???
SR-ATAD5---
???
SR-HSE---
???
SR-MMP---
???
SR-p53---
???
Toxicophore Rules
Acute Toxicity Rule0 alert(s)
???
Genotoxic Carcinogenicity Rule0 alert(s)
???
NonGenotoxic Carcinogenicity Rule0 alert(s)
???
Skin Sensitization Rule2 alert(s)
???
Aquatic Toxicity Rule1 alert(s)
???
NonBiodegradable Rule1 alert(s)
???
SureChEMBL Rule0 alert(s)
???
FAF-Drugs4 Rule2 alert(s)
???
Bioactivity
β-secretase 1 inhibitor---
???
HIV inhibitor---
???