BackBack |Pangu Molecule Optimizer
CCc1cc2ccc(CN3CCN(c4ccc(C(=O)NC)nc4)CC3)cc2[nH]c1=O
CCc1cc2ccc(CN3CCN(c4ccc(C(=O)NC)nc4)CC3)cc2[nH]c1=O
Optimized 10
CCc1cc2ccc(CN3CCCc4cc(C(=O)NC)ncc43)cc2[nH]c1=O
C22H24N4O2
MolWeight376.46
TPSA78.09
logP2.8
QED0.73
SAscore2.61
Similarity0.61
CCc1cc2ccc(CN3CCN(c4cc(C)c(C(=O)NC)s4)CC3)cc2[nH]1
C22H28N4OS
MolWeight396.56
TPSA51.37
logP3.78
QED0.69
SAscore2.63
Similarity0.57
CCc1ccc(N2CCN(Cc3ccc4c(c3)c(C(=O)NC)nn4C)CC2)cn1
C22H28N6O
MolWeight392.51
TPSA66.29
logP2.21
QED0.72
SAscore2.47
Similarity0.56
CCNC(=O)c1cccc(CN2CCN(c3ccc4cc(CC)[nH]c4c3)CC2)n1
C23H29N5O
MolWeight391.52
TPSA64.26
logP3.2
QED0.68
SAscore2.43
Similarity0.55
CCc1ccc2cc(CN3CCN(c4cc(C(=O)NC)[nH]c4C)CC3)cnc2c1
C23H29N5O
MolWeight391.52
TPSA64.26
logP3.12
QED0.7
SAscore2.63
Similarity0.54
CCc1cc2ccc(CN3CCN(c4ccc(NC)nc4NC)C(=O)C3)cc2[nH]c1=O
C23H28N6O2
MolWeight420.52
TPSA93.36
logP2.42
QED0.57
SAscore2.77
Similarity0.53
CCc1ccc(CN2CCN(c3ncc(SC)nc3C)CC2)cc1C(=O)NC
C21H29N5OS
MolWeight399.56
TPSA61.36
logP2.75
QED0.75
SAscore2.64
Similarity0.49
CCc1cc2ccc(C(=O)N3CCCN(Cc4ccc(C(=O)NC)o4)CC3)cc2[nH]1
C23H28N4O3
MolWeight408.5
TPSA81.58
logP3.03
QED0.68
SAscore2.47
Similarity0.46
C=Cc1ccc(N2CCN(CC(=O)NCc3cccc(C(=O)NC)c3)CC2)cn1
C22H27N5O2
MolWeight393.49
TPSA77.57
logP1.52
QED0.75
SAscore2.33
Similarity0.46
CCc1ccc(N2CCN(CC(=O)NCc3ccc4c(c3)C(C)N=C4)CC2)cc1O
C24H30N4O2
MolWeight406.53
TPSA68.17
logP2.89
QED0.77
SAscore3.13
Similarity0.45
Total 161764 visits to this website since August 23rd, 2021
©2021 Huaweicloud.com 版权所有免责声明数据来源声明
Huawei CloudSIMM
ADMET
Similarity:
Original Molecule
Optimized Molecule
Physicochemical PropertyOriginalOptimized
Molecular Weight (MW)405.5
???
Molecular Refractivity (MR)119.064
???
Volume375
???
Density1.081
???
pKa5.255
???
Check Acidbase
???
nHA5
???
nHD2
???
nRot5
???
nRing4
???
MaxRing10
???
nHet7
???
fChar0
???
nRig25
???
Flexibility0.2
???
Stereo Centers0
???
TPSA81.33
???
logS-2.975
???
logP2.167
???
Medicinal Chemistry
QED0.68
???
SAscore2.395
???
SCscore4.824
???
Fsp30.348
???
NPscore-1.549
???
Lipinski RuleAccepted
???
Pfizer RuleAccepted
???
GSK RuleRejected
???
Golden TriangleAccepted
???
PAINS0 alert(s)
???
ALARM NMR Rule1 alert(s)
???
BMS Rule0 alert(s)
???
Chelator Rule0 alert(s)
???
Absorption
Caco-2 Permeability0.692
???
MDCK Permeability2.7e-06
???
Pgp-inhibitor---
???
Pgp-substrate+++
???
HIA+++
???
F20%+++
???
F30%+++
???
Distribution
PPB84.366%
???
VD0.645
???
BBB Penetration+++
???
Fu26.252%
???
Metabolism
CYP1A2 inhibitor--
???
CYP1A2 substrate+++
???
CYP2C9 inhibitor--
???
CYP2C9 substrate---
???
CYP3A4 inhibitor+
???
CYP3A4 substrate++
???
Excretion
CL0.776
???
T1/20.135
???
Toxicity
hERG Blockers+++
???
H-HT++
???
DILI+
???
AMES Toxicity---
???
FDAMDD+++
???
Skin Sensitization--
???
Carcinogencity-
???
Eye Corrosion---
???
Eye Irritation---
???
Environmental Toxicity
Bioconcentration Factors0.392
???
IGC501.387
???
LC50FM5.146
???
LC50DM6.652
???
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 Rule1 alert(s)
???
NonGenotoxic Carcinogenicity Rule0 alert(s)
???
Skin Sensitization Rule0 alert(s)
???
Aquatic Toxicity Rule0 alert(s)
???
NonBiodegradable Rule1 alert(s)
???
SureChEMBL Rule0 alert(s)
???
FAF-Drugs4 Rule1 alert(s)
???
Bioactivity
β-secretase 1 inhibitor--
???
HIV inhibitor---
???