BDBM11325 Hydroxamate 7::N-hydroxy-2-[(1,1,2,2,3,3,4,4,4-nonafluorobutane)sulfonamido]acetamide

SMILES ONC(=O)CNS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F

InChI Key InChIKey=HJAQLIVSMXUHPV-UHFFFAOYSA-N

Data  10 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 11325   

TargetCarbonic anhydrase 2(Human)
Universita Degli Studi

LigandPNGBDBM11325(N-hydroxy-2-[(1,1,2,2,3,3,4,4,4-nonafluorobutane)s...)
Affinity DataKi:  15nMAssay Description:Initial rates of 4-nitrophenyl acetate hydrolysis catalyzed by different CA isozymes were monitored spectrophotometrically at 400 nm. A molar absorpt...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCarbonic anhydrase 4(Bovine)
Universita Degli Studi

LigandPNGBDBM11325(N-hydroxy-2-[(1,1,2,2,3,3,4,4,4-nonafluorobutane)s...)
Affinity DataKi:  16nMAssay Description:Initial rates of 4-nitrophenyl acetate hydrolysis catalyzed by different CA isozymes were monitored spectrophotometrically at 400 nm. A molar absorpt...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCarbonic anhydrase 1(Human)
Universita Degli Studi

LigandPNGBDBM11325(N-hydroxy-2-[(1,1,2,2,3,3,4,4,4-nonafluorobutane)s...)
Affinity DataKi:  18nM ΔG°:  -10.6kcal/molepH: 7.4 T: 2°CAssay Description:Initial rates of 4-nitrophenyl acetate hydrolysis catalyzed by different CA isozymes were monitored spectrophotometrically at 400 nm. A molar absorpt...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target72 kDa type IV collagenase(Human)
Universita Degli Studi

LigandPNGBDBM11325(N-hydroxy-2-[(1,1,2,2,3,3,4,4,4-nonafluorobutane)s...)
Affinity DataKi:  75nMAssay Description:Initial rates of 4-nitrophenyl acetate hydrolysis catalyzed by different CA isozymes were monitored spectrophotometrically at 400 nm. A molar absorpt...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target72 kDa type IV collagenase(Human)
Universita Degli Studi

LigandPNGBDBM11325(N-hydroxy-2-[(1,1,2,2,3,3,4,4,4-nonafluorobutane)s...)
Affinity DataKi:  76nMAssay Description:Inhibition of MMP2More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCollagenase ColG(Hathewaya histolytica)
Universita Degli Studi

LigandPNGBDBM11325(N-hydroxy-2-[(1,1,2,2,3,3,4,4,4-nonafluorobutane)s...)
Affinity DataKi:  80nMAssay Description:Initial rates of 4-nitrophenyl acetate hydrolysis catalyzed by different CA isozymes were monitored spectrophotometrically at 400 nm. A molar absorpt...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetMatrix metalloproteinase-9(Human)
Universita Degli Studi

LigandPNGBDBM11325(N-hydroxy-2-[(1,1,2,2,3,3,4,4,4-nonafluorobutane)s...)
Affinity DataKi:  125nMAssay Description:Initial rates of 4-nitrophenyl acetate hydrolysis catalyzed by different CA isozymes were monitored spectrophotometrically at 400 nm. A molar absorpt...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetMatrix metalloproteinase-9(Human)
Universita Degli Studi

LigandPNGBDBM11325(N-hydroxy-2-[(1,1,2,2,3,3,4,4,4-nonafluorobutane)s...)
Affinity DataKi:  126nMAssay Description:Inhibition of MMP9More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetNeutrophil collagenase(Human)
Universita Degli Studi

LigandPNGBDBM11325(N-hydroxy-2-[(1,1,2,2,3,3,4,4,4-nonafluorobutane)s...)
Affinity DataKi:  130nMAssay Description:Initial rates of 4-nitrophenyl acetate hydrolysis catalyzed by different CA isozymes were monitored spectrophotometrically at 400 nm. A molar absorpt...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetInterstitial collagenase(Human)
Universita Degli Studi

LigandPNGBDBM11325(N-hydroxy-2-[(1,1,2,2,3,3,4,4,4-nonafluorobutane)s...)
Affinity DataKi: >200nMAssay Description:Initial rates of 4-nitrophenyl acetate hydrolysis catalyzed by different CA isozymes were monitored spectrophotometrically at 400 nm. A molar absorpt...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed