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Compound InformationSONAR Target prediction
Name:

Acetohexamide

Unique Identifier:Prest3
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:C15H20N2O4S
Molecular Weight:304.238 g/mol
X log p:6.772  (online calculus)
Lipinksi Failures1
TPSA76.66
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:6
Rotatable Bond Count:6
Canonical Smiles:CC(=O)c1ccc(cc1)S(=O)(=O)NC(=O)NC1CCCCC1
Generic_name:Acetohexamide
Chemical_iupac_name:1-(4-acetylphenyl)sulfonyl-3-cyclohexyl-urea
Drug_type:Approved Drug
Pharmgkb_id:PA448023
Kegg_compound_id:C06806
Drugbank_id:APRD00773
Melting_point:188-190 oC
H2o_solubility:3430 mg/L
Logp:2.954
Cas_registry_number:968-81-0
Drug_category:Hypoglycemic Agents; Sulfonylureas; ATC:A10BB31
Indication:Used in the management of diabetes mellitus type 2 (adult-onset).
Pharmacology:Acetohexamide is an intermediate-acting, first-generation oral sulfonylurea. It
lowers blood sugar by stimulating the pancreatic beta cells to secrete insulin and
by helping the body use insulin efficiently. The pancreas must produce insulin for
this medication to work. Acetohexamide has one-third the potency of chlorpropamide,
and twice the potency of tolbutamide; however, similar hypoglycemic efficacy occurs
with equipotent dosage of sulfonylureas.
Mechanism_of_action:Sulfonylureas such as acetohexamide bind to an ATP-dependent K+ channel
on the cell membrane of pancreatic beta cells. This inhibits a tonic,
hyperpolarizing outflux of potassium, which causes the electric potential over the
membrane to become more positive. This depolarization opens voltage-gated
Ca2+ channels. The rise in intracellular calcium leads to increased
fusion of insulin granulae with the cell membrane, and therefore increased secretion
of (pro)insulin.
Organisms_affected:Humans and other mammals

Found: 3 nonactive as graph: single | with analogs 2 3 Next >> 
Species: 9606
Condition: TMPPre001
Replicates: 2
Raw OD Value: r im 2109.0000±0
Normalized OD Score: sc h 1.0146±0
Z-Score: 0.3291±0
p-Value: 0.742104
Z-Factor: -6.48492
Fitness Defect: 0.2983
Bioactivity Statement: Nonactive
Experimental Conditions
Library:Prestwick
Plate Number and Position:1|F6
Drug Concentration:50.00 nM
OD Absorbance:0 nm
Robot Temperature:23.50 Celcius
Date:2006-10-10 YYYY-MM-DD
Plate CH Control (+):1020±963.92163
Plate DMSO Control (-):2084±569.64618
Plate Z-Factor:-4.4103
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DBLink | Rows returned: 1
1989 1-(4-acetylphenyl)sulfonyl-3-cyclohexyl-urea

internal high similarity DBLink | Rows returned: 0

active | Cluster 5012 | Additional Members: 11 | Rows returned: 1
Prest1231 0.48936170212766

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