27 Results for "

prove

" in MedChemExpress (MCE) Product Catalog:
Products (27)

27 Results for "prove" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-B0136
CAS No.: 91832-40-5
Synonyms: FK-482; CI-983
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

Cefdinir (FK-482) is a semi-synthetic, broad-spectrum antibiotic in the third generation of the cephalosporin class, which is proved to be effective for infections caused by several Gram-negative and Gram-positive bacteria. Cefdinir can be used for the research of common bacterial infections of the ear, sinus, throat, and skin .
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3
3 Cited Publications
Cat. No.: HY-12659
CAS No.: 1192189-69-7
Purity:  99.54%
Target:  

LIM Kinase (LIMK) ROCK PKA

Research Areas:  

Endocrinology

LX7101 is a potent LIM-kinase, ROCK and PKA inhibitor with IC50s of 24 nM, 1.6 nM, 10 nM and <1 nM for LIMK1, LIMK2, ROCK2 and PKA, respectively. LX7101 proves significantly selective for LIMK2 with IC50 values of 4.3 nM and 32 nM for LIMK2 and LIMK1 at 2 μM ATP, respectively. LX7101 has the potential for ocular hypertension and associated glaucoma research .
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1
1 Cited Publications
Cat. No.: HY-116874
CAS No.: 74115-08-5
Purity:  98.66%
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

SKF 83822 is an atypical agonist of dopamine D1 receptor. SKF 83822 activates adenylyl cyclase (AC), but not phospholipase C (PLC). SKF 83822 is also proved to stimulate AC via cAMP production. SKF 83822 can be used for research of schizophrenia .
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Cat. No.: HY-125776
CAS No.: 143390-89-0
Purity:  ≥99.0%
Synonyms: BAS 490 F
Kresoxim-methyl (BAS 490 F), a Strobilurin-based fungicide, inhibits the respiration at the complex III (cytochrome bc1 complex). Kresoxim-methyl binds to complex III from yeast with an apparent Kd of 0.07 μM proving a high affinity for this enzyme .
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Cat. No.: HY-136375
CAS No.: 21725-46-2
Purity:  99.73%
Research Areas:  

Others

Cyanazine, a triazine herbicide cyanazine, is used to control a variety of grass weeds and broadleaf weed. Cyanazine is proved non-genotoxic .
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Cat. No.: HY-135158
CAS No.: 20488-27-1
Purity:  99.53%
Synonyms: Val-Pro; H-Val-Pro-OH
Target:  

Peptides

Research Areas:  

Others

Prolylvaline (Pro-Val) is a proline-valine dipeptide that can be used to bind fluorescein isothiocyanate (FITC). Prolylvaline has specific imprinting effects in Tetrahymena, inducing negative imprinting. Using protozoan organisms, proline dipeptides containing different partner amino acids can be distinguished from dipeptides with opposite amino acid positions .
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Cat. No.: HY-106784A
CAS No.: 92284-99-6
(E)-Ajoene is a oxygenated ajoene and organosulfur compound, which can be acquired via allicin decomposing. The polysulfides from garlic can be converted by human red blood cells into hydrogen sulfide (H2S) and allyl glutathione. (E)-Ajoene has been proved to show neuroprotective effects against ischemic damage. (E)-Ajoene is orally active to inhibit lipid peroxidation. (E)-Ajoene increases the number of cresyl violet-positive neurons and decreases the number of reactive gliosis in the CA1 region .
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Cat. No.: HY-W103463
CAS No.: 4641-57-0
Synonyms: 1-Phenylpyrrolidin-2-one
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

1-Phenyl-2-pyrrolidinone (1-Phenylpyrrolidin-2-one) is a phenyl analogue of GABA with sedative effect, decreasing the exploratory behavior of rats at 50-100 mg/kg (i.v.). 1-Phenyl-2-pyrrolidinone also has been proved to inhibit emotional reactions in dogs and cats. 1-Phenyl-2-pyrrolidinone induces decreases in the pressor reaction to emotional stress without accompanied by normalization of the function of baroreceptor reflexes .
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Cat. No.: HY-B0371B
CAS No.: 109351-34-0
Target:  

Adrenergic Receptor

Research Areas:  

Endocrinology

(R)-Terazosin is an active R-enantiomer of Terazosin. (R)-Terazosin is a potent α1-adrenoceptor antagonist with Ki values of 6.51 nM, 1.01 nM and 1.97 nM for α1a, α1b and α1d-adrenoceptor, respectively .
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Cat. No.: HY-B0590D
CAS No.: 1026016-84-1
Synonyms: (-)-TBZ; (3S,11bS)-TBZ; (3S,11bS)-Tetrabenazine
Target:  

Monoamine Transporter

Research Areas:  

Neurological Disease

(-)-Tetrabenazine ((-)-TBZ; compound 13) is an enantiomer of Tetrabenazine (HY-B0590). (+)-Tetrabenazine proves 3-fold more active than (-)-Tetrabenazine in inhibiting vesicular monoamine transporter 2 (VMAT2) .
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Cat. No.: HY-N15154
CAS No.: 587014-85-5
Tasiamide B is a Cathepsin D inhibitor, which is a linear peptide found in the marine cyanobacteria Symploca sp.. Tasiamide B is proved as a good template for the development of aspartic proteases inhibitors. Tasiamide B is effective against skin cancer by strongly interacting with the target protein HSP90 .
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Cat. No.: HY-147709
CAS No.: 2569221-17-4
Target:  

Tyrosinase

Research Areas:  

Others

Compound 4B proved to be the most effective tyrosinase inhibitor (ic50= 3.80 μ M) It also showed good antioxidant activity.
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Cat. No.: HY-136375S
CAS No.: 1190003-29-2
Cyanazine-d5 is deuterium labeled Cyanazine. Cyanazine, a triazine herbicide cyanazine, is used to control a variety of grass weeds and broadleaf weed. Cyanazine is proved non-genotoxic .
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Cat. No.: HY-136375R
CAS No.: 21725-46-2
Research Areas:  

Others

Cyanazine (Standard) is the analytical standard of Cyanazine. This product is intended for research and analytical applications. Cyanazine, a triazine herbicide cyanazine, is used to control a variety of grass weeds and broadleaf weed. Cyanazine is proved non-genotoxic .
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Cat. No.: HY-N10322
CAS No.: 641-90-7
2-Hydroxyemodin is an active metabolite of emodin in the hepatic microsomes. Emodin is an anthraquinone present in fungal metabolites and constituent of rhubarb. 2-Hydroxyemodin proves to be mutagenic to Salmonella typhimurium TA1537 in the absence of activation system .
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Cat. No.: HY-154910
CAS No.: 1021920-32-0
Purity:  98.49%
Target:  

mTOR

Research Areas:  

Cancer

CC214-1 is a potentially efficacious mTOR inhibitor that induces autophagy ,with an IC50 is 0.002 μM. CC214-1 proved to be useful as an in vitro tool compound for the exploration of mTOR kinase biology. CC214-1 can be used for Glioblastoma study .
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Cat. No.: HY-147707
CAS No.: 2772693-05-5
Target:  

Cannabinoid Receptor

Research Areas:  

Others

Hexyl resorcinol derivative 29 has been proved to be a CB2 selective competitive antagonist / reverse agonist with good potency. Olivanol and 5- (2-methyloctane-2-yl) resorcinol derivatives 23 and 24 showed significant antinociceptive activity. Compound 24 was shown to activate cannabinoid and TRPV1 receptors.
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Cat. No.: HY-125776R
CAS No.: 143390-89-0
Synonyms: BAS 490 F (Standard)
Kresoxim-methyl (Standard) is the analytical standard of Kresoxim-methyl. This product is intended for research and analytical applications. Kresoxim-methyl (BAS 490 F), a Strobilurin-based fungicide, inhibits the respiration at the complex III (cytochrome bc1 complex). Kresoxim-methyl binds to complex III from yeast with an apparent Kd of 0.07 μM proving a high affinity for this enzyme .
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Cat. No.: HY-B0136R
CAS No.: 91832-40-5
Synonyms: FK-482 (Standard); CI-983 (Standard)
Research Areas:  

Infection

Cefdinir (Standard) is the analytical standard of Cefdinir. This product is intended for research and analytical applications. Cefdinir (FK-482) is a semi-synthetic, broad-spectrum antibiotic in the third generation of the cephalosporin class, which is proved to be effective for infections caused by several Gram-negative and Gram-positive bacteria. Cefdinir can be used for the research of common bacterial infections of the ear, sinus, throat, and skin .
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Cat. No.: HY-12659B
CAS No.: 2319882-48-7
Target:  

LIM Kinase (LIMK) ROCK PKA

Research Areas:  

Endocrinology

LX7101 monohydrochloride is a potent LIM-kinase, ROCK and PKA inhibitor with IC50s of 24 nM, 1.6 nM, 10 nM and <1 nM for LIMK1, LIMK2, ROCK2 and PKA, respectively. LX7101 monohydrochloride proves significantly selective for LIMK2 with IC50 values of 4.3 nM and 32 nM for LIMK2 and LIMK1 at 2 μM ATP, respectively. LX7101 monohydrochloride has the potential for ocular hypertension and associated glaucoma research .
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