12 Results for "

AM1

" in MedChemExpress (MCE) Product Catalog:
Products (12)

12 Results for "AM1" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-10302
CAS No.: 957116-20-0
Purity:  98.02%
Target:  

CGRP Receptor

Research Areas:  

Neurological Disease

MK-3207 (Hydrochloride) is a potent and orally bioavailable CGRP receptor antagonist with IC50 of 0.12 nM and Ki of 0.024 nM, and is highly selective versus human AM1, AM2, CTR, and AMY3.
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1
1 Cited Publications
Cat. No.: HY-P1455A
Synonyms: Human adrenomedullin-(1-52)-NH2 TFA
Target:  

Inhibitory Antibodies

Research Areas:  

Cancer

Adrenomedullin (AM) (1-52), human (TFA) affects cell proliferation and angiogenesis in cancer.
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1
1 Cited Publications
Cat. No.: HY-P1455
CAS No.: 148498-78-6
Synonyms: Human adrenomedullin-(1-52)-NH2
Target:  

Inhibitory Antibodies

Research Areas:  

Cancer

Adrenomedullin (AM) (1-52), human is a 52-amino acid peptide, which affects cell proliferation and angiogenesis in cancer.
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Cat. No.: HY-129148
CAS No.: 149507-55-1
Synonyms: GAAM1
Ganoderic acid AM1 (GAAM1) is a natural product that can be found in ganoderma lucidum. Ganoderic acid AM1 shows cytotoxicity with an IC50 value of 19.8 µM for HeLa cells [1].
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Cat. No.: HY-171012
CAS No.: 21829-22-1
Synonyms: NSC 335504
Target:  

STING

Research Areas:  

Inflammation/Immunology

Clonixeril (NSC 335504) is a non-nucleotide hSTING modulator. Clonixeril has weak agonist activity at micromolar concentrations and results in antagonism of the hSTING WT pathway at low femtomolar (10 -15 M) and in some cases even attomolar (10 -18 M) concentrations. Clonixeril reduces hSTING oligomerization at a concentration of 1 aM-1 pM [1].
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Cat. No.: HY-147910
CAS No.: 2499489-76-6
Carpro-AM1 is a dual-acting FAAH/substrate-selective COX inhibitor with an IC50 value of 94 nM for FAAH [1].
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Cat. No.: HY-N11472
CAS No.: 41545-37-3
Synonyms: RhAMnocitrin-3-O-β-D-glucopyranoside
Rhamnocitrin 3-glucoside (Rhamnocitrin-3-O-β-D-glucopyranoside) is a natural product that can be isolated from Astragalus membranaceus (Fisch.) Bge. var. mongholicus (Bge.) Hsiao (AM) .
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Cat. No.: HY-D3422
Target:  

Fluorescent Dye

Research Areas:  

Others

AM1-44 is a fixable, cationic styryl fluorescent dye primarily used for labeling nerve terminals and synaptic vesicles. In its free state, AM1-44 exhibits extremely weak fluorescence; upon insertion into the cell membrane, its fluorescence increases, and after endocytosis into vesicles and release via exocytosis, its fluorescence decreases. Therefore, it can be used to study synaptic activity, synaptic vesicle cycling, neurotransmitter release, and synaptic plasticity (Ex/Em = 480/598-600 nm in membrane environment) [1] .
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Cat. No.: HY-D1637
CAS No.: 172646-43-4
Target:  

Fluorescent Dye

Research Areas:  

Others

5-Nitro BAPTA tetramethyl ester is a calcium chelator. 5-Nitro BAPTA tetramethyl ester involves in the two-photon probe synthesis, and is used for real-time imaging of intracellular calcium ions, calcium waves monitoring at a depth of 100-300 μm in liver tissues for 1100-4000 s. 5-Nitro BAPTA tetramethyl ester, together with fluorescent compound 2-Me-substituted TM, can be used to form a red fluorescent probe (CaTM-2 AM) .
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Cat. No.: HY-187523
CAS No.: 3120945-90-3
Synonyms: para-MLL
Target:  

Endogenous Metabolite

Research Areas:  

Others

Methylolanthanin (para-MLL) is a natural small-molecule metallophore identified in the culture supernatant of Methylobacterium extorquens AM1. Methylolanthanin binds lanthanide metal ions such as La 3+, Nd 3+ and Lu 3+. It is applicable to studies related to lanthanide metabolism, bacterial metallophores, metal homeostasis and methylotrophic metabolism [1] .
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Cat. No.: HY-10302R
CAS No.: 957116-20-0
Research Areas:  

Neurological Disease

MK-3207 hydrochloride (Standard) is the analytical standard of MK-3207 hydrochloride (HY-10302). This product is intended for research and analytical applications. MK-3207 hydrochloride is a potent and orally bioavailable CGRP receptor antagonist with IC50 of 0.12 nM and Ki of 0.024 nM, and is highly selective versus human AM1, AM2, CTR, and AMY3.
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Cat. No.: HY-183142
CAS No.: 2252341-45-8
Target:  

CGRP Receptor

Research Areas:  

Cancer

CLR/RAMP3-receptor antagonist-1 is a selective antagonist of the CLR/RAMP3 receptor (CLR/RAMP3, AM2 receptor), with pIC50 values of 5.86, 9.21 and 9.07 against AM1 (CLR/RAMP2), AM2 (CLR/RAMP3) and CGRP (CLR/RAMP1) receptors, respectively. CLR/RAMP3-receptor antagonist-1 reduces the levels of pancreatic cancer progression markers, induces apoptosis in vitro, and prolongs survival in mouse models of pancreatic cancer. CLR/RAMP3-receptor antagonist-1 can be used in pancreatic cancer-related research [1].
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