255 Results for "

local

" in MedChemExpress (MCE) Product Catalog:
Products (255)

255 Results for "local" in MCE Product Catalog:

21
21 Publications Verification
Art. -Nr.: HY-A0129
CAS. Nr.: 51-74-1
Synonyms: Histamine diphosphate
Histamine phosphate is the agonist for histamine receptor and a vasodilator. Histamine phosphate is an organic nitrogen compound that participates in local immune responses, regulates intestinal physiological functions, and acts as a neurotransmitter. Histamine phosphate affects p38 MAPK/Akt signaling pathway, exhibits antitumor, antioxidant and anti-inflammatory activities. Histamine phosphate can be used in the research of acute myeloid leukemia, malignant melanoma, and renal cell carcinoma .
loading...
    loading...
21
21 Publications Verification
Art. -Nr.: HY-B0722
CAS. Nr.: 56-92-8
Histamine dihydrochloride is the agonist for histamine receptor and a vasodilator. Histamine dihydrochloride is an organic nitrogen compound that participates in local immune responses, regulates intestinal physiological functions, and acts as a neurotransmitter. Histamine dihydrochloride affects p38 MAPK/Akt signaling pathway, exhibits antitumor, antioxidant and anti-inflammatory activities. Histamine dihydrochloride can be used in the research of acute myeloid leukemia, malignant melanoma, and renal cell carcinoma .
loading...
    loading...
21
21 Publications Verification
Art. -Nr.: HY-B1204
CAS. Nr.: 51-45-6
Synonyms: Ergamine
Histamine is the agonist for histamine receptor and a vasodilator. Histamine is an organic nitrogen compound that participates in local immune responses, regulates intestinal physiological functions, and acts as a neurotransmitter. Histamine affects p38 MAPK/Akt signaling pathway, exhibits antitumor, antioxidant and anti-inflammatory activities. Histamine can be used in the research of acute myeloid leukemia, malignant melanoma, and renal cell carcinoma .
loading...
    loading...
17
17 Cited Publications
Art. -Nr.: HY-12403A
CAS. Nr.: 2855063-75-9
Reinheit:  99.87%
Synonyms: TXA127 acetate; Angiotensin (1-7) acetate; Ang-(1-7) acetate
Angiotensin 1-7 (Ang-(1-7)) acetate is an endogenous heptapeptide from the renin-angiotensin system (RAS) with a cardioprotective role due to its anti-inflammatory and anti-fibrotic activities in cardiac cells. Angiotensin 1-7 acetate inhibits purified canine ACE activity (IC50=0.65 μM). Angiotensin 1-7 acetate acts as a local synergistic modulator of kinin-induced vasodilation by inhibiting ACE and releasing nitric oxide. Angiotensin 1-7 acetate blocks Ang II-induced smooth muscle cell proliferation and hypertrophy and shows antiangiogenic and growth-inhibitory effects on the endothelium .
loading...
    loading...
17
17 Cited Publications
Art. -Nr.: HY-12403
CAS. Nr.: 51833-78-4
Reinheit:  99.75%
Synonyms: TXA127; Angiotensin (1-7); Ang-(1-7)
Angiotensin 1-7 (Ang-(1-7)) is an endogenous heptapeptide from the renin-angiotensin system (RAS) with a cardioprotective role due to its anti-inflammatory and anti-fibrotic activities in cardiac cells. Angiotensin 1-7 inhibits purified canine ACE activity (IC50=0.65 μM). Angiotensin 1-7 acts as a local synergistic modulator of kinin-induced vasodilation by inhibiting ACE and releasing nitric oxide. Angiotensin 1-7 blocks Ang II-induced smooth muscle cell proliferation and hypertrophy and shows antiangiogenic and growth-inhibitory effects on the endothelium. Angiotensin 1-7 shows anti-inflammatory activity .
loading...
    loading...
9
9 Cited Publications
Art. -Nr.: HY-16714
CAS. Nr.: 33173-53-4
Synonyms: p-Azidophenylalanine; p-Azido-L-phenylalanine
Forschungsgebiete:  

Others

4-Azido-L-phenylalanine is an unnatural amino acid, which is used as an effective vibrational reporter of local protein environments. 4-Azido-L-phenylalanine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
loading...
    loading...
9
9 Cited Publications
Art. -Nr.: HY-16714A
CAS. Nr.: 34670-43-4
Synonyms: p-Azidophenylalanine hydrochloride; p-Azido-L-phenylalanine hydrochloride
Forschungsgebiete:  

Others

4-Azido-L-phenylalanine hydrochloride is an unnatural amino acid, which is used as an effective vibrational reporter of local protein environments. 4-Azido-L-phenylalanine (hydrochloride) is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
loading...
    loading...
8
8 Cited Publications
Art. -Nr.: HY-B0563C
CAS. Nr.: 854056-07-8
Ropivacaine mesylate is a long-acting amide local anaesthetic agent for a spinal block and effectively blocks neuropathic pain. Ropivacaine blocks impulse conduction via reversible inhibition of sodium ion influx in nerve fibressup . Ropivacaine is also an inhibitor of K2P (two-pore domain potassium channel) TREK-1 with an IC50 of 402.7 μM in COS-7 cell's membrane .
loading...
    loading...
7
7 Cited Publications
Art. -Nr.: HY-12754
CAS. Nr.: 1357171-62-0
Reinheit:  ≥98.0%
Synonyms: CID-46742353
Forschungsgebiete:  

Cancer

ML228 (CID-46742353) is a potent the Hypoxia Inducible Factor (HIF) pathway activator with EC50 of 1 μM. ML228 potently activates HIF in vitro as well as its downstream target VEGF .
loading...
    loading...
4
4 Cited Publications
Art. -Nr.: HY-B0405
CAS. Nr.: 38396-39-3
Bupivacaine is a NMDA receptor inhibitor. Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels with the IC50 of 69.5 μM. Bupivacaine can be used for the research of chronic pain .
loading...
    loading...
4
4 Cited Publications
Art. -Nr.: HY-B0405A
CAS. Nr.: 18010-40-7
Bupivacaine hydrochloride is a NMDA receptor inhibitor.Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels with the IC50 of 69.5 μM. Bupivacaine hydrochloride can be used for the research of chronic pain .
loading...
    loading...
4
4 Cited Publications
Art. -Nr.: HY-12424
CAS. Nr.: 221877-54-9
Reinheit:  ≥98.0%
Synonyms: ABT-578; A 179578
Zotarolimus (ABT-578) is a derivative of Rapamycin (HY-10219), with anti-proliferative activity. Zotarolimus is an immunosuppressant. Zotarolimus is developed specifically for local delivery from stents for the prevention of coronary artery restenosis .
loading...
    loading...
4
4 Cited Publications
Art. -Nr.: HY-D0913
CAS. Nr.: 73043-80-8
Synonyms: 1M7
1-Methyl-7-nitroisatoic anhydride (1M7) is a reagent that detects local nucleotide flexibility, for probing 2'-hydroxyl reactivity, can be used for RNA structure analysis .
loading...
    loading...
3
3 Cited Publications
Art. -Nr.: HY-N0839
CAS. Nr.: 631-01-6
Synonyms: Quillaja sapogenin
Quillaic acid (Quillaja sapogenin)It is an anti-gastric cancer and anti-proliferation agent that can promote apoptosis of cancer cells. (apoptosis). Quillaic acidAlso has analgesic and local anti-inflammatory activity .
loading...
    loading...
3
3 Cited Publications
Art. -Nr.: HY-Y1314
CAS. Nr.: 67-71-0
Dimethyl sulfone (Methyl Sulfonyl Methane) is a metabolic product of endogenous methanethiol metabolism and intestinal bacterial metabolism. Dimethyl sulfone inhibits choriocapillary endothelial (CCE) cell proliferation, also has many biological effects, including antiinflammatory, antioxidant, and local anesthetic effects that could be neuroprotective .
loading...
    loading...
3
3 Cited Publications
Art. -Nr.: HY-B0379A
CAS. Nr.: 50-42-0
Target:  

nAChR

Forschungsgebiete:  

Neurological Disease

Adiphenine hydrochloride is a non-competitive inhibitor of nicotinic acetylcholine receptor (nAChR), with an IC50s of 1.9, 1.8, 3.7, and 6.3 μM for α1, α3β4, α4β2, and α4β4, respectively. Adiphenine hydrochloride has anticonvulsant effects .
loading...
    loading...
3
3 Cited Publications
Art. -Nr.: HY-66012
CAS. Nr.: 5875-06-9
Synonyms: Proxymetacaine hydrochloride
Target:  

Sodium Channel

Forschungsgebiete:  

Neurological Disease

Proparacaine (Proxymetacaine) hydrochloride is a local anesthetic. Proparacaine hydrochloride blocks voltage-gated sodium channels on neuronal cell membranes, thereby inhibiting signal conduction and nociceptive signal transmission. Proparacaine hydrochloride blocks nociceptive signals in the eye and induces ocular muscle relaxation to reduce eye movement during surgery. Proparacaine hydrochloride is used in research related to cataracts .
loading...
    loading...
2
2 Cited Publications
Art. -Nr.: HY-B1704
CAS. Nr.: 53179-07-0
Forschungsgebiete:  

Neurological Disease

Nisoxetine is a potent and selective inhibitor of noradrenaline transporter (NET), with a Kd of 0.76 nM. Nisoxetine is an antidepressant and local anesthetic, it can block voltage-gated sodium channels .
loading...
    loading...
2
2 Cited Publications
Art. -Nr.: HY-14839
CAS. Nr.: 223488-57-1
Reinheit:  99.78%
Synonyms: CP-533536 free acid
Evatanepag (CP-533536) is a non-prostanoid, potent and selective EP2 receptor agonist. Evatanepag can induce local bone formation in vivo. Evatanepag can be used in the research of fractures, bone defects, asthma .
loading...
    loading...
2
2 Cited Publications
Art. -Nr.: HY-B1704A
CAS. Nr.: 57754-86-6
Forschungsgebiete:  

Neurological Disease

Nisoxetine hydrochloride is a potent and selective inhibitor of noradrenaline transporter (NET), with a Kd of 0.76 nM. Nisoxetine hydrochloride is an antidepressant and local anesthetic, it can block voltage-gated sodium channels .
loading...
    loading...