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Guanfacine
Guanfacine
United States Biological

Centrally acting a-adrenoceptor agonist. Antihypertensive. Form: White Solid Melting Point: 208-211 degrees C Solubility: Unstable in methanol solution

Zoxazolamine
Zoxazolamine
United States Biological

Centrally acting myorelaxant; formerly used as an antispasmodic and uricosuric. Used as a tool for assessing hepatic cytochrome P-450 activity in rodents....

rac Guaifenesin-d5
rac Guaifenesin-d5
United States Biological

Centrally acting muscle relaxant with expectorant properties. Form: White Solid Melting Point: 79-81 degrees C Solubility: Dichloromethane, Ethyl Acetate,...

CENPH, Recombinant, Human, aa136-247, His-tag (Centromere Protein H, CENP-H, Interphase Centromere Complex Protein 35, ICEN35)
CENPH, Recombinant, Human, aa136-247, His-tag (Centromere Protein H, CENP-H, Interphase Centromere Complex Protein 35, ICEN35)
United States Biological

CENPH, belongs to the centromere protein H family. This protein is component of the CENPA-NAC (nucleosome-associated) complex that plays a central role in...

YM201636, Phosphoinositide Kinase Inhibitor (6-Amino-N-(3-(4-(4-morpholinyl)pyrido[3?2?:4,5]furo[3,2-d]pyrimidin-2-yl)phenyl)-3-pyridine carboxamide)
YM201636, Phosphoinositide Kinase Inhibitor (6-Amino-N-(3-(4-(4-morpholinyl)pyrido[3?2?:4,5]furo[3,2-d]pyrimidin-2-yl)phenyl)-3-pyridine carboxamide)
United States Biological

Cell-permeable. YM-201636 is a selective inhibitor of phosphoinositide kinase (PIK) PIKfyve (IC503nM). It inhibits p110a at higher concentration (IC50=3uM)....

Salermide (N-?[3-?[[(2-?hydroxy-?1-?naphthalenyl)methylene]amino]phenyl]-?a-?methyl-?benzeneacetamide)
Salermide (N-?[3-?[[(2-?hydroxy-?1-?naphthalenyl)methylene]amino]phenyl]-?a-?methyl-?benzeneacetamide)
United States Biological

Cell-permeable. Salermide is an inhibitor of SIRT1 and SIRT2. In vitro, Salermide has a stronger inhibitory effect on SIRT2 than on SIRT1. It induces massive...

LDN 57444, UCH-L1 Inhibitor (5-Chloro-1-[(2,5-dichlorophenyl)met
hyl]-1H-indole-2,3-dione 3-(O-acetyloxime))
LDN 57444, UCH-L1 Inhibitor (5-Chloro-1-[(2,5-dichlorophenyl)met hyl]-1H-indole-2,3-dione 3-(O-acetyloxime))
United States Biological

Cell-permeable. LDN-57444 is a potent, reversible, competitive and active site-directed inhibitor of UCHL1 (Ki = 0.4uM). Decreases proteasome activity and...

Glibenclamide (5-Chloro-N-[4-(cyclohexylureidosulfonyl)phenethyl]-2-methoxybenzamide, Glyburide, N-p-[2-(5-Chloro-2-methoxybenzamido)ethyl]benzenesulfonyl-N?-cyclohexylurea)
Glibenclamide (5-Chloro-N-[4-(cyclohexylureidosulfonyl)phenethyl]-2-methoxybenzamide, Glyburide, N-p-[2-(5-Chloro-2-methoxybenzamido)ethyl]benzenesulfonyl-N?-cyclohexylurea)
United States Biological

Cell-permeable. An anti-diabetic agent. ATP-sensitive potassium channel (KATP) blocker. Inhibits KATP currents in the pancreatic beta cells causing an...

Pioglitazone (5-?[[4-?[2-?(5-?ethyl-?2-?pyridinyl)ethoxy]phenyl]methyl]-?2,?4-?thiazolidinedione)
Pioglitazone (5-?[[4-?[2-?(5-?ethyl-?2-?pyridinyl)ethoxy]phenyl]methyl]-?2,?4-?thiazolidinedione)
United States Biological

Cell-permeable. A thiazolidinedione (TZD) derivative that acts as a selective peroxisome proliferator-activated receptor gamma (PPARg) agonist (EC50 =...

GO? 6976 (5,6,7,13-Tetrahydro-13-methyl-5-oxo-12H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-12-propanenitrile, Go6976, PD 406976)
GO? 6976 (5,6,7,13-Tetrahydro-13-methyl-5-oxo-12H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-12-propanenitrile, Go6976, PD 406976)
United States Biological

Cell-permeable. A potent protein kinase C (PKC) inhibitor (IC50 = 7.9nM). In vitro, discriminates between Ca2+- dependent and -independent isoforms of PKC;...

Z-VAD-FMK (Cell permeable) (Z-VAD(OMe)-FMK, pan-Caspase Inhibitor, Z-Val-Ala-DL-Asp(OMe)-fluoromethylketone, Benzyloxycarbonyl-Val-Ala-DL-Asp(OMe)-fluoromethylketone)
Z-VAD-FMK (Cell permeable) (Z-VAD(OMe)-FMK, pan-Caspase Inhibitor, Z-Val-Ala-DL-Asp(OMe)-fluoromethylketone, Benzyloxycarbonyl-Val-Ala-DL-Asp(OMe)-fluoromethylketone)
United States Biological

Cell-permeable, non-selective broad-spectrum caspase inhibitor. Binds irreversibly to the catalytic site of caspase proteases. The peptide is O-methylated in...

Cellobionic Acid Ammonium
Cellobionic Acid Ammonium
United States Biological

Cellobionic acid is produced by ozonization of Cellobiose. Cellobionic acid was not a good substrate for b-Glucosidase. The lactonized carboxyl group...

SB203580 (4-(4-Fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl)1H-imidazole)
SB203580 (4-(4-Fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl)1H-imidazole)
United States Biological

Cell permeable, specific p38 MAP kinase inhibitor. Binds to the ATP binding site of p38 MAP kinase. T cell proliferation inhibitor. IL-2 production...

Compound E ((2S)-2-(amino)-N-propanamide)
Compound E ((2S)-2-(amino)-N-propanamide)
United States Biological

Cell permeable, potent, selective, non-transition state and non-competitive gamma-secretase inhibitor. Notch processing inhibitor. Only weakly affects...

Jasplakinolide (Jaspamide, NSC 613009)
Jasplakinolide (Jaspamide, NSC 613009)
United States Biological

Cell permeable, non-fluorescent F-actin probe. Potent inducer of actin polymerization and stabilization. Competes with phallotoxins for actin binding....

Compound 34 ((2S,3R)-3-(3,4-Difluorophenyl)-2-(4-fluorophenyl)-4-hydroxy-N-((3S)-2-oxo-5-phenyl-2,3-1H-benzodiazepin-3-yl)butyramide)
Compound 34 ((2S,3R)-3-(3,4-Difluorophenyl)-2-(4-fluorophenyl)-4-hydroxy-N-((3S)-2-oxo-5-phenyl-2,3-1H-benzodiazepin-3-yl)butyramide)
United States Biological

Cell permeable, highly potent inhibitor of gamma-secretase (IC50 = 0.06nM). Storage and Stability: Short-term Storage: +4 degrees C Long-term Storage: -20...

IBMX (3-Isobutyl 1-methylxanthine, NSC 165960, EINECS 249-259-3)
IBMX (3-Isobutyl 1-methylxanthine, NSC 165960, EINECS 249-259-3)
United States Biological

Cell permeable, competitive, non-specific cAMP and cGMP phosphodiesterase inhibitor. Increases cAMP levels that activate PKA, leading to decreased...

MnTBAP chloride (Manganese (III) tetrakis (4-benzoic acid)porphyrin chloride)
MnTBAP chloride (Manganese (III) tetrakis (4-benzoic acid)porphyrin chloride)
United States Biological

Cell permeable superoxide dismutase (SOD) mimetic. Potent inhibitor of peroxynitrite-induced oxidative reactions (peroxynitrite scavenger), but not a...

MnTMPyP pentachloride (Manganese (III) tetrakis (1-methyl-4-pyridyl)porphyrin . 5Cl-)
MnTMPyP pentachloride (Manganese (III) tetrakis (1-methyl-4-pyridyl)porphyrin . 5Cl-)
United States Biological

Cell permeable superoxide dismutase (SOD) mimetic. Peroxynitrite scavenger. Displays a protective effect against H2O2 mediated injury. Neuroprotective....

Cyclopamine (11-Deoxyjervine, 11-Deoxojervine, HSDB 3505)
Cyclopamine (11-Deoxyjervine, 11-Deoxojervine, HSDB 3505)
United States Biological

Cell permeable steroidal alkaloid. Specific sonic hedgehog signaling (Shh) pathway inhibitor. Directly interacts/inhibits Smo (smoothened). Teratogenic and...

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