10039 Results for "

Selectivity

" in MedChemExpress (MCE) Product Catalog:
Products (10039)

10039 Results for "Selectivity" in MCE Product Catalog:

Cat. No.: HY-10794R
CAS No.: 915191-42-3
MF498 (Standard) is the analytical standard of MF498 (HY-10794). This product is intended for research and analytical applications. MF498 is a selective and orally active E prostanoid Receptor 4 (EP4) antagonist with a Ki value of 0.7 nM. MF498 can be used in the research of inflammation, such as rheumatoid and osteoarthritis .
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Cat. No.: HY-10800
CAS No.: 876922-98-4
Research Areas:  

Neurological Disease

GSK-588045 is a potent 5-HT(1A/B/D) receptor antagonist. GSK-588045 shows high degree of selectivity over human ether-a-go-go related gene (hERG) potassium channels. GSK-588045 can be used for the research of neurological disease, such as depression and anxiety .
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Cat. No.: HY-108243R
CAS No.: 1034148-04-3
AZD5423 (Standard) is the analytical standard of AZD5423 (HY-108243). This product is intended for research and analytical applications. AZD5423 is an inhaled, potent, selective, and non-steroidal glucocorticoid receptor (GR) modulator (SGRM) . AZD5423 effectively reduces allergen-induced responses in subjects with mild allergic asthma .
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Cat. No.: HY-108318R
CAS No.: 213743-31-8
Synonyms: KIN 001-51 (Standard)
RK-24466 (Standard) is the analytical standard of RK-24466 (HY-108318). This product is intended for research and analytical applications. RK-24466 (KiN 001-51) is a potent and selective Lck inhibitor; inhibits Lck (64-509) and LckCD isoforms with IC50s of less than 1 and 2 nM, respectively.
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Cat. No.: HY-108329R
CAS No.: 1883711-97-4
AM-0902 (Standard) is the analytical standard of AM-0902 (HY-108329). This product is intended for research and analytical applications. AM-0902 is a potent, selective transient receptor potential A1 (TRPA1) antagonist with IC50s of 71 and 131 nM for rTRPA1 and hTRPA1, respectively.
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Cat. No.: HY-10840
CAS No.: 518336-59-9
Target:  

PPAR

Research Areas:  

Metabolic Disease

PPARδ agonist 14 (Cpd 33) is a selective PPARδ agonist with an EC50 of 3 nM for PPARδ. PPARδ agonist 14 shows no cross-activity against PPARα and PPARγ. PPARδ agonist 14 can be used for research on PPARδ-related metabolic diseases .
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Cat. No.: HY-108411R
CAS No.: 87233-61-2
Emedastine (Standard) is the analytical standard of Emedastine. This product is intended for research and analytical applications. Emedastine is an orally active, selective and high affinity histamine H1 receptor antagonist with a Ki value of 1.3 nM. Emedastine is a benzimidazole derivative with potent antiallergic properties and used for allergic rhinitis, allergic skin diseases and allergic conjunctivitis .
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Cat. No.: HY-108449R
CAS No.: 68489-09-8
Synonyms: WS-12 (Standard); AR-15512 (Standard); AVX-012 (Standard)
Research Areas:  

Neurological Disease

Acoltremon (Standard) is the analytical standard of Acoltremon (HY-108449). This product is intended for research and analytical applications. Acoltremon (WS-12; AR-15512) is a potent and selective TRPM8 agonist, the menthol derivative, as a cooling agent. Acoltremon shows analgesic effect, and can be used in chronic neuropathic pain research .
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Cat. No.: HY-108488R
CAS No.: 1380088-03-8
Target:  

Reference Standards Src

Research Areas:  

Cancer

KB SRC 4 (Standard) is the analytical standard of KB SRC 4 (HY-108488). This product is intended for research and analytical applications. KB SRC 4 is a potent, and highly selective c-Src inhibitor, with a Ki of 44 nM and a Kd of 86 nM, and shows no inhibition on c-Abl up to 125 μM; KB SRC 4 has antitumor activity.
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Cat. No.: HY-108497
CAS No.: 217480-26-7
Purity:  95.42%
Target:  

Somatostatin Receptor

Research Areas:  

Neurological Disease Cancer

L-803087 is a potent and selective somatostatin sst4 receptor agonist with a Ki of 0.7 nM. L-803087 is >280-fold higher than other somatostatin receptors. L-803087 facilitates AMPA-mediated hippocampal synaptic responses in vitro and increases kainate-induced seizures in mice .
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Cat. No.: HY-108509
CAS No.: 105565-55-7
Purity:  98.02%
Synonyms: BMY-14802-1; BMS 181100 hydrochloride
BMY-14802 hydrochloride (BMY-14802-1) is a selective and orally active sigma receptor antagonist with an IC50 of 112 nM. BMY-14802 hydrochloride is also a 5-HT1A and adrenergic α1 receptors agonist. BMY-14802 hydrochloride has antipsychotic effects .
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Cat. No.: HY-108553
CAS No.: 126463-64-7
Target:  

Proteasome Apoptosis

Research Areas:  

Cancer

Dihydroeponemycin, an analogue of the antitumor and antiangiogenic natural product eponemycin, selectively targets the 20S proteasome. Dihydroeponemycin covalently modifies a subset of catalytic proteasomal subunits, binding preferentially to the IFN-gamma-inducible subunits LMP2 and LMP7. Dihydroeponemycin-mediated proteasome inhibition induces a spindle-like cellular morphological change and apoptosis .
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Cat. No.: HY-108610C
CAS No.: 83542-43-2
Synonyms: (S)-ET-18-OCH3
Target:  

Apoptosis

Research Areas:  

Cancer

(S)-Edelfosine ((S)-ET-18-OCH3) is the (S)-enantiomer of Edelfosine (ET-18-OCH3) (HY-108610C). Edelfosine is a selective antitumour lipid targeting apoptosis through intracellular activation of Fas/CD95 Death receptor .
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Cat. No.: HY-108626
CAS No.: 1345964-89-7
Purity:  99.59%
Synonyms: NCGC84
Research Areas:  

Neurological Disease

ML154 (NCGC84) is a selective, brain-penetrant and non-peptide neuropeptide S receptor (NPSR) antagonist with a pA2 of 9.98. ML154 potently inhibits NPS-stimulated cellular calcium, cAMP, and ERK phosphorylation responses with IC50 values of 36.5 nM, 22.1 nM, and 9.3 nM, respectively .
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Cat. No.: HY-108658
CAS No.: 630103-23-0
Purity:  99.85%
Target:  

P2Y Receptor

Research Areas:  

Cardiovascular Disease

MRS2500 tetraammonium is a potent, selective and stable antagonist of the P2Y1 receptor (Ki=0.78 nM for recombinant human P2Y1 receptor). MRS2500 tetraammonium inhibits the ADP-induced aggregation of human platelets with an IC50 value of 0.95 nM. Antithrombotic activity .
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Cat. No.: HY-108703AR
CAS No.: 2133294-96-7
Synonyms: PXT002331 monohydrochloride (Standard)
Research Areas:  

Neurological Disease

Foliglurax monohydrochloride (Standard) is the analytical standard of Foliglurax (monohydrochloride) (HY-108703A). This product is intended for research and analytical applications. Foliglurax monohydrochloride (PXT002331 monohydrochloride) is a highly selective and potent, brain-penetrant metabotropic glutamate receptor 4 positive allosteric modulator (mGluR4 PAM) , with an EC50 of 79 nM . AntiparKinsonian effect .
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Cat. No.: HY-108912R
CAS No.: 221529-58-4
Synonyms: CAY10441 (Standard)
RO1138452 (Standard) is the analytical standard of RO1138452. This product is intended for research and analytical applications. RO1138452 is a potent and selective IP (prostacyclin) receptor antagonist. RO1138452 displays high affinity for IP receptors. In human platelets, pKi is 9.3±0.1; in a recombinant IP receptor system, pKi is 8.7±0.06.
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Cat. No.: HY-109024R
CAS No.: 1228088-30-9
Synonyms: RG7314 (Standard)
Balovaptan (Standard) is the analytical standard of Balovaptan (HY-109024). This product is intended for research and analytical applications. Balovaptan (RG7314) is an orally available, selective brain-penetrant vasopressin 1a (hV1a) receptor antagonist, with Kis of 1 and 39 nM for human (hV1a) and mouse (mV1a) receptors, and is used for the research of autism.
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Cat. No.: HY-109045
CAS No.: 1075798-37-6
Synonyms: BTA074; AP 611074
Target:  

E1/E2/E3 Enzyme HPV

Research Areas:  

Infection

Teslexivir (BTA074) is a potent antiviral agent. Teslexivir is a potent and selective inhibitor of the interaction between two essential viral proteins, E1 and E2, an association that is a necessary step in the DNA replication and thus viral production for Human Papilloma Virus (HPV) 6 and 11. Teslexivir can be used for condyloma research .
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Cat. No.: HY-109045A
CAS No.: 1075281-70-7
Purity:  99.34%
Synonyms: BTA074 hydrochloride; AP 611074 hydrochloride
Target:  

E1/E2/E3 Enzyme HPV

Research Areas:  

Infection

Teslexivir (BTA074) hydrochloride is a potent antiviral agent. Teslexivir hydrochloride is a potent and selective inhibitor of the interaction between two essential viral proteins, E1 and E2, an association that is a necessary step in the DNA replication and thus viral production for Human Papilloma Virus (HPV) 6 and 11. Teslexivir hydrochloride can be used for condyloma research .
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