136 Results for "

M5

" in MedChemExpress (MCE) Product Catalog:
Products (136)

136 Results for "M5" in MCE Product Catalog:

Cat. No.: HY-122510
CAS No.: 4438-22-6
Synonyms: Atropine oxidation
Target:  

Parasite

Research Areas:  

Neurological Disease

Atropine Oxide (Atropine oxidation), a derivative of Atropine, acts as a competitive antagonist to the muscarinic acetylcholine receptors M1, M2, M3, M4, and M5, and is utilized in the treatment of specific nerve agent and pesticide poisonings.
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Cat. No.: HY-122510A
CAS No.: 4574-60-1
Synonyms: Atropine oxidation hydrochloride
Target:  

mAChR

Atropine Oxide (Atropine oxidation) hydrochloride, a derivative of Atropine, acts as a competitive antagonist to the muscarinic acetylcholine receptors M1, M2, M3, M4, and M5, and is utilized in the treatment of specific nerve agent and pesticide poisonings .
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Cat. No.: HY-12567A
CAS No.: 1488362-56-6
Purity:  98.19%
Synonyms: (R)-VU0483253
Target:  

Drug Isomer

Research Areas:  

Others

(R)-ML375 ((R)-VU0483253) is an enantiomer of ML375 (HY-12567). (R)-ML375 is devoid of M5 mAChR activity (hM5, IC50>30 μM) .
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Cat. No.: HY-167849
CAS No.: 2409055-48-5
Synonyms: BBI-4000 tosylate
Target:  

mAChR

Research Areas:  

Neurological Disease

Sofpironium (BBI 4000) tosylate is an anticholinergic agent used in the study of primary axillary hyperhidrosis (PAH). Sofpironium tosylate reduces sweating by inhibiting M3 muscarinic receptors in eccrine glands at the application site. Sofpironium tosylate also has a high afnity for the M1, M2, M4 and M5 subtypes .
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Cat. No.: HY-19752
CAS No.: 1135681-23-0
Synonyms: CID-25010775 free base
Target:  

mAChR

Research Areas:  

Neurological Disease

VU0357017 (CID-25010775) is a potent, selective and brain-penetrant allosteric agonist of M1 muscarinic acetylcholine receptor, with an EC50 of 477 nM. VU0357017 is highly selective for M1 and has no activity at M2-M5 up to the highest concentrations tested (30 μM). VU0357017 can be used for the research of Alzheimer’s disease and schizophrenia .
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Cat. No.: HY-B0406AR
CAS No.: 590-63-6
Synonyms: Carbamyl-β-methylcholine chloride (Standard)
Research Areas:  

Neurological Disease Cancer

Bethanechol (chloride) (Standard) is the analytical standard of Bethanechol (chloride). This product is intended for research and analytical applications. Bethanechol chloride (Carbamyl-β-methylcholine chloride), a parasympathomimetic agent, is a mAChR agonist that exerts its effects via directly stimulating the mAChR (M1, M2, M3, M4, and M5) of the parasympathetic nervous system .
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Cat. No.: HY-186205
CAS No.: 1299471-83-2
Target:  

Drug Metabolite

Research Areas:  

Cancer

(Rac)-EGC-M5 is an orally active metabolite of green tea Catechin (EGC) (HY-N0898). (Rac)-EGC-M5 enhances the activity of CD4 + T cells. (Rac)-EGC-M5 boosts the cytotoxic activity of NK cells in vivo. (Rac)-EGC-M5 can be used in cancer-related research .
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Cat. No.: HY-76570A
CAS No.: 250214-40-5
Synonyms: (Rac)-Desfesoterodine hydrochloride; (Rac)-PNU-200577 hydrochloride
Target:  

mAChR

Research Areas:  

Neurological Disease

(Rac)-5-Hydroxymethyl Tolterodine ((Rac)-Desfesoterodine) hydrochloride, an active metabolite of Tolterodine, is a mAChR antagonist (Ki values of 2.3 nM, 2 nM, 2.5 nM, 2.8 nM, and 2.9 nM for M1, M2, M3, M4, and M5 receptors, respectively). (Rac)-5-Hydroxymethyl Tolterodine hydrochloride can be used for overactive bladder research .
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Cat. No.: HY-70053S
CAS No.: 1185237-08-4
(Rac)-Fesoterodine-d14 fumarate is a labelled racemic Fesoterodine. Fesoterodine is an orally active, nonsubtype selective, competitive muscarinic receptor (mAChR) antagonist with pKivalues of 8.0, 7.7, 7.4, 7.3, 7.5 for M1, M2, M3, M4, M5 receptors, respectively. Fesoterodine is used for the overactive bladder (OAB) .
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Cat. No.: HY-A0030R
CAS No.: 286930-03-8
Fesoterodine (fumarate) (Standard) is the analytical standard of Fesoterodine (fumarate). This product is intended for research and analytical applications. Fesoterodine Fumarate is an orally active, nonsubtype selective, competitive muscarinic receptor (mAChR) antagonist with pKi values of 8.0, 7.7, 7.4, 7.3, 7.5 for M1, M2, M3, M4, M5 receptors, respectively. Fesoterodine Fumarate is used for the overactive bladder (OAB) .
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Cat. No.: HY-W720879
CAS No.: 1126611-84-4
Fesoterodine-d3 is the deuterium labeled Fesoterodine (HY-70053). Fesoterodine is an orally active, nonsubtype selective, competitive muscarinic receptor (mAChR) antagonist with pKi values of 8.0, 7.7, 7.4, 7.3, 7.5 for M1, M2, M3, M4, M5 receptors, respectively. Fesoterodine is used for the overactive bladder (OAB) .
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Cat. No.: HY-76570S1
5-Hydroxymethyl Tolterodine-d14 (formate) is deuterium labeled (Rac)-5-Hydroxymethyl Tolterodine. (Rac)-5-Hydroxymethyl Tolterodine ((Rac)-Desfesoterodine), an active metabolite of Tolterodine, is a mAChR antagonist (Ki values of 2.3 nM, 2 nM, 2.5 nM, 2.8 nM, and 2.9 nM for M1, M2, M3, M4, and M5 receptors, respectively). (Rac)-5-Hydroxymethyl Tolterodine can be used for overactive bladder research .
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Cat. No.: HY-183959
CAS No.: 713099-37-7
Target:  

WDR5

Research Areas:  

Cancer

DC_M5_2 is a WD40 repeat domain protein 5 (WDR5) inhibitor with an IC50 of 9.63 μM and a KD of 13.8 μM. DC_M5_2 binds to the WDR5 pocket that interacts with the MLL1 peptide, blocking the WDR5-MLL1 protein-protein interaction . DC_M5_2 can be used in leukemia-related research .
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Cat. No.: HY-76570S
CAS No.: 1185071-13-9
Synonyms: (Rac)-Desfesoterodine-d14; (Rac)-PNU-200577-d14
(Rac)-5-Hydroxymethyl Tolterodine-d14 is the deuterium labeled (Rac)-5-Hydroxymethyl Tolterodine. (Rac)-5-Hydroxymethyl Tolterodine ((Rac)-Desfesoterodine), an active metabolite of Tolterodine, is a mAChR antagonist (Ki values of 2.3 nM, 2 nM, 2.5 nM, 2.8 nM, and 2.9 nM for M1, M2, M3, M4, and M5 receptors, respectively). (Rac)-5-Hydroxymethyl Tolterodine can be used for overactive bladder research .
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Cat. No.: HY-P75801
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: GSTM5; S-(Hydroxyalkyl)Glutathione Lyase M5; Glutathione S-Transferase Mu 5; Glutathione S-Aralkyltransferase M5; Glutathione S-Transferase M5; Glutathione S-Alkyltransferase M5; GST Class-Mu 5; Glutathione S-Aryltransferase M5; GSTM5-5; Glutathione S-Tra
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-W709579
CAS No.: 2207957-90-0
Target:  

Drug Metabolite

Research Areas:  

Others

AB-CHMINACA metabolite M5A is a metabolite of AB-CHMINACA in the liver.
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Cat. No.: HY-101281R
CAS No.: 2092923-21-0
Research Areas:  

Neurological Disease

VU 6008667 (Standard) is the analytical standard of VU 6008667 (HY-101281). This product is intended for research and analytical applications. VU 6008667 is a selective negative allosteric modulator of M5 NAM with IC50s of 1.2 μM and 1.6 μM for human M5 and rat M5, respectively. High CNS penetration .
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Cat. No.: HY-123778
CAS No.: 2222737-15-5
Target:  

mAChR

Research Areas:  

Neurological Disease

VU6007678 is a CNS-penetrant muscarinic acetylcholine receptor (mAChR) modulator. VU6007678 potentiates acetylcholine-mediated signaling at human M1, M3, M5 and rat M1, M3, M4, M5 muscarinic acetylcholine receptors. VU6007678 is applicable to research related to Alzheimer's disease, schizophrenia, and ischemic stroke .
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Cat. No.: HY-P810322
Synonyms: Muscarinic acetylcholine receptor M5, CHRM5

Host:  

Rabbit

Application:  

IHC-P, ELISA

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-12100S2
Synonyms: GSK573719A-d7
Umeclidinium bromide-d7 (GSK573719A-d7) is the deuterium labeled Umeclidinium bromide (HY-12100). Umeclidinium bromide is a novel mAChR antagonist. The affinity (Ki) of Umeclidinium bromide for the cloned human M1-M5 mAChRs ranges from 0.05 to 0.16 nM.
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