Inhibitor information

Natural Products
ZC100960
Molecular Formula
C12H16N2O2S
Molecular Weight
252.093248752 g/mol
Structure
IUPAC Name
(3Z)-6,6-dimethyl-3-[[(3S)-2-thioxopyrrolidin-3-yl]methylene]piperidine-2,4-dione
InChI
InChI=1S/C12H16N2O2S/c1-12(2)6-9(15)8(10(16)14-12)5-7-3-4-13-11(7)17/h5,7H,3-4,6H2,1-2H3,(H,13,17)(H,14,16)/b8-5-/t7-/m0/s1
InChI Key
SFOQPFHYQQRLHU-BJMRUTCWSA-N
SMILES
CC1(C)CC(=O)/C(=C/[C@@H]2CCNC2=S)C(=O)N1
Source
ZINC000005734401

Warheads

Acrylamide
Michael Acceptor


ADMET Property

Physicochemical Property

Property Value Property Value
Heavy Atom Count 17 Ring Count 2
Heteroatom Count 5 Rotatable Bond Count 1
Hydrogen Bond Acceptor Count 3 Hydrogen Bond Donor Count 2
Topological Polar Surface Area 58.2 LogP 0.84
LogS -1.467 LogD 1.018


Absorption

Property Value Property Value
Pgp inhibitor 0.01 Pgp substrate 0.044
HIA 0.965 F20 % 0.993
F30 % 0.571 Caco-2 -5.284
MDCK -5.455


Distribution

Property Value Property Value
BBB Penetration 0.997 PPB 52.677
VD 0.757 Fu 0.039


Metabolism

Property Value Property Value
CYP1A2 inhibitor 0.001 CYP1A2 substrate 0.431
CYP2A6 substrate 0.732 CYP2B6 substrate 0.586
CYP2C19 inhibitor 0.142 CYP2C19 substrate 0.808
CYP2C8 substrate 0.472 CYP2C9 inhibitor 0.159
CYP2C9 substrate 0.747 CYP2D6 inhibitor 0.006
CYP2D6 substrate 0.651 CYP2E1 substrate 0.359
CYP3A4 inhibitor 0.013 CYP3A4 substrate 0.829


Excretion

Property Value Property Value
T1/2 0.68 CL 8.03


Toxicity

Property Value Property Value
hERG Blockers 0.039 Hepatotoxicity 0.388
Mutagenicity 0.947 Rat Oral Acute Toxicity 0.673
FDAMDD 0.414 Skin Sensitization 0.996
Carcinogenicity 0.998 Eye Corrosion 0.001
Eye Irritation 0.155 Respiratory Toxicity 0.9


Environmental Toxicity

Property Value Property Value
Bioconcentration Factors -0.527 IGC50 1.294
LC50FM 0.731 LC50DM 3.981


Tox21 Pathway

Property Value Property Value
NR-AR 0.103 NR-AR-LBD 0.345
NR-AhR 0.016 NR-Aromatase 0.009
NR-ER 0.204 NR-ER-LBD 0.313
NR-PPAR-gamma 0.67 SR-ARE 0.067
SR-ATAD5 0.441 SR-HSE 0.528
SR-MMP 0.01 SR-p53 0.188