BackBack |Pangu Molecule Optimizer
Cc1n(CCCCCCCCCCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)cc[n+]1Cc1c(Cl)cccc1Cl.[I-]
Cc1n(CCCCCCCCCCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)cc[n+]1Cc1c(Cl)cccc1Cl.[I-]
Optimized 10
Cc1n(CCCCCCCCCCC(F)(F)C(F)(F)F)cc[n+]1CC(=O)O
C18H28F5N2O2+
MolWeight399.21
TPSA46.11
logP3.87
QED0.29
SAscore2.98
Similarity0.49
Cc1n(CCCCCCC(F)(F)C(F)(F)F)cc[n+]1Cc1ccccc1
C19H24F5N2+
MolWeight375.19
TPSA8.81
logP4.25
QED0.32
SAscore2.75
Similarity0.46
Cc1n(CCCCCCCCCCC(F)(F)C(F)(F)CO)cc2[n+]1CCO2
C19H31F4N2O2+
MolWeight395.23
TPSA38.27
logP3.44
QED0.31
SAscore3.53
Similarity0.37
Cc1n(CCCCCCC(F)(F)C(F)(F)F)cc[n+]1C1C=CN=C1
C16H21F5N3+
MolWeight350.17
TPSA21.17
logP3.12
QED0.38
SAscore4.16
Similarity0.37
CCC(F)(F)C(F)(F)CCCCCCCCCN1CC=[N+](C(F)(F)F)C1
C17H28F7N2+
MolWeight393.21
TPSA6.25
logP5.21
QED0.18
SAscore3.54
Similarity0.37
Cc1n(CCCCCCCC(F)(F)C(F)F)cc[n+]1-c1cc[nH]c1
C17H24F4N3+
MolWeight346.19
TPSA24.6
logP3.91
QED0.37
SAscore3.56
Similarity0.33
Cc1n(CCCCCCC(F)(F)C(F)(F)F)cc2[n+]1CC2
C14H20F5N2+
MolWeight311.15
TPSA8.81
logP3.6
QED0.41
SAscore3.48
Similarity0.32
Cc1[nH]n(CCCCCCCCC(F)(F)C(F)CF)c1C(F)(F)F
C15H23F7N2
MolWeight364.17
TPSA20.72
logP5.24
QED0.38
SAscore3.81
Similarity0.31
CC1N(CCCCCCCCCC(F)(F)C(=O)O)C=[N+]1C(F)(F)F
C15H24F5N2O2+
MolWeight359.18
TPSA43.55
logP3.65
QED0.26
SAscore3.85
Similarity0.3
Cc1n(CCCCCCCC2CCC(F)(F)CC2)cc[n+]1C(F)(F)F
C18H28F5N2+
MolWeight367.22
TPSA8.81
logP5.21
QED0.32
SAscore3.28
Similarity0.28
Huawei CloudSIMM
ADMET
Similarity:
Original Molecule
Optimized Molecule
Physicochemical PropertyOriginalOptimized
Molecular Weight (MW)791.35
???
Molecular Refractivity (MR)136.941
???
Volume533
???
Density1.485
???
pKa5.095
???
Check Acidbase
???
nHA1
???
nHD0
???
nRot17
???
nRing2
???
MaxRing6
???
nHet16
???
fChar0
???
nRig11
???
Flexibility1.545
???
Stereo Centers0
???
TPSA8.81
???
logS-4.665
???
logP7.448
???
Medicinal Chemistry
QED0.068
???
SAscore3.372
???
SCscore3.428
???
Fsp30.667
???
NPscore-0.353
???
Lipinski RuleRejected
???
Pfizer RuleRejected
???
GSK RuleRejected
???
Golden TriangleRejected
???
PAINS0 alert(s)
???
ALARM NMR Rule0 alert(s)
???
BMS Rule1 alert(s)
???
Chelator Rule0 alert(s)
???
Absorption
Caco-2 Permeability0.354
???
MDCK Permeability-2.3e-05
???
Pgp-inhibitor+++
???
Pgp-substrate+++
???
HIA--
???
F20%---
???
F30%---
???
Distribution
PPB81.201%
???
VD0.518
???
BBB Penetration---
???
Fu0.000%
???
Metabolism
CYP1A2 inhibitor-
???
CYP1A2 substrate++
???
CYP2C9 inhibitor-
???
CYP2C9 substrate--
???
CYP3A4 inhibitor-
???
CYP3A4 substrate++
???
Excretion
CL1.903
???
T1/20.984
???
Toxicity
hERG Blockers+++
???
H-HT--
???
DILI+++
???
AMES Toxicity---
???
FDAMDD++
???
Skin Sensitization--
???
Carcinogencity--
???
Eye Corrosion---
???
Eye Irritation---
???
Environmental Toxicity
Bioconcentration Factors0.461
???
IGC502.52
???
LC50FM5.764
???
LC50DM4.267
???
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 Rule0 alert(s)
???
Aquatic Toxicity Rule2 alert(s)
???
NonBiodegradable Rule2 alert(s)
???
SureChEMBL Rule4 alert(s)
???
FAF-Drugs4 Rule1 alert(s)
???
Bioactivity
β-secretase 1 inhibitor+
???
HIV inhibitor---
???