71 Results for "

PET tracer

" in MedChemExpress (MCE) Product Catalog:
Products (71)

71 Results for "PET tracer" in MCE Product Catalog:

86
86 Publications Verification
Cat. No.: HY-42110
CAS No.: 1977-07-7
Target:  

mAChR

Research Areas:  

Neurological Disease

Deschloroclozapine, a metabolite of Clozapine, is a highly potent muscarinic DREADDs agonist, with blood-brain barrier permeability. Deschloroclozapine binds to DREADD receptor subtypes hM3Dq and hM4Di with Ki of 6.3 and 4.2 nM, respectively. [ 11C]-Deschloroclozapine is developed as a promising PET tracer for DREADD imaging .
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86
86 Publications Verification
Cat. No.: HY-42110A
Target:  

mAChR

Research Areas:  

Neurological Disease

Deschloroclozapine dihydrochloride, a metabolite of Clozapine, is a highly potent muscarinic DREADDs agonist, with blood-brain barrier permeability. Deschloroclozapine dihydrochloride binds to DREADD receptor subtypes hM3Dq and hM4Di with Ki of 6.3 and 4.2 nM, respectively. [ 11C]-Deschloroclozapine dihydrochloride is developed as a promising PET tracer for DREADD imaging .
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2
2 Cited Publications
Cat. No.: HY-101184
CAS No.: 1415379-56-4
Purity:  99.21%
Synonyms: AV-1451
Target:  

Tau Protein

Research Areas:  

Neurological Disease

T807 a novel tau positron emission tomography (PET) tracer.
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1
1 Cited Publications
Cat. No.: HY-125399
CAS No.: 1366302-52-4
Purity:  99.74%
Synonyms: HBED-CC-PSMA
Research Areas:  

Cancer

PSMA-11 is a small molecule ligand that targets prostate-specific membrane antigen (PSMA) and has the ability to inhibit PSMA activity. PSMA-11 can be used to synthesize 68Ga-PSMA-11, a positron emission tomography (PET) tracer that can be used to image advanced prostate cancer .
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Cat. No.: HY-147173
CAS No.: 2374782-76-8
Purity:  99.82%
Target:  

FAP

Research Areas:  

Cancer

FAPI-74 is a PET (positron emission tomography) tracer targeting the fibroblast activation protein (FAP). FAPI-74 can be used for FAP-positive tumor research .
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Cat. No.: HY-114616
CAS No.: 1565796-97-5
Purity:  93.06%
Research Areas:  

Neurological Disease

PBB3 is a tracer of tau PET. PBB3 can be used to detect levels of tau protein in Alzheimer's disease and non-Alzheimer's disease .
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Cat. No.: HY-126192
CAS No.: 566169-93-5
Purity:  ≥95.0%
Synonyms: PiB; 6-OH-BTA-1
Pittsburgh Compound B (PiB) is a blood-brain barrier-permeable, specific deposition PET tracer that binds to Aβ(1-40) fibrils with a Ki value of 678.4 nM. Through click chemical modification (a clickable Pittsburgh Compound B derivative is prepared by introducing a PEG3 linker and an alkynyl group at the 6-hydroxy site of Pittsburgh Compound B, followed by covalent conjugation with azide-labeled fluorescent dyes or affinity tags via copper-catalyzed azide-alkyne cycloaddition (CuAAC)), Pittsburgh Compound B and its conjugates can be used for fluorescence imaging, ultrastructural studies, and enrichment and characterization of Aβ complexes. Pittsburgh Compound B is applicable to Alzheimer's disease research .
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Cat. No.: HY-101185
CAS No.: 1320211-61-7
Target:  

Tau Protein

Research Areas:  

Neurological Disease

T808 is a selective tau protein-targeting ligand. T808 can be used to synthesize [ 18F]-T808, a highly selective tau protein positron emission tomography (PET) tracer. T808 can also be used to synthesize [ 3H]-T808, a marker for in vitro experiments. T808 can be used for the research of alzheimer’s disease .
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Cat. No.: HY-175748
CAS No.: 3056154-69-6
MK-7337 is an α-synuclein ligand with an affinity of < 1 nM. MK-7337 labeled with 11C can be used as a PET tracer for neurodegenerative disorders like Parkinson’s disease imagination .
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Cat. No.: HY-119190
CAS No.: 2055776-17-3
Purity:  98.23%
Research Areas:  

Neurological Disease

PF-06445974, a promising positron emission tomography (PET) lead, has exquisite potency at PDE4B with an IC50 <1 nM. The IC50 values are 36, 4.7 and 17 nM for PDE4D, PDE4A and PDE4C, respectively. PF-06445974 has good selectivity over PDE4D, excellent brain permeability, and a high level of specific binding in the "cold tracer" study .
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Cat. No.: HY-139048
CAS No.: 1639210-26-6
Purity:  ≥98.0%
Target:  

iGluR

Research Areas:  

Neurological Disease

Fluoroethylnormemantine, a derivative of Memantine, is an antagonist of the N-methyl-D-aspartate (NMDA) receptor. [ 18F]-Fluoroethylnormemantine can be used as a positron emission tomography (PET) tracer. Fluoroethylnormemantine exhibits anti-amnesic, neuroprotective, antidepressant-like and fear-attenuating effects .
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Cat. No.: HY-179492
CAS No.: 3033951-64-0
Target:  

hnRNP

Research Areas:  

Neurological Disease

ACI-19278 is a TDP-43 PET tracer with an average Kd of 25 nM. ACI-19278 only binds to pathological TDP-43 aggregates and does not cross-react with Aβ, Tau, etc. [ 18F]ACI-19278 successfully visualized the TDP-43 pathology in the human brain through positron emission computed tomography. ACI-19278 can be used for in vivo diagnosis of TDP-43 protein lesions .
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Cat. No.: HY-177459
Target:  

FAP

Research Areas:  

Cancer

DOTA-2P(FAPI)2 is a dimeric FAP (fibroblast activation protein) that can be used as a PET imaging agent and a tracer for tumor therapy .
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Cat. No.: HY-173291
CAS No.: 3063166-64-0
Target:  

Tau Protein

Research Areas:  

Neurological Disease

Tau ligand-1 (Compound 75) is a ligand for aggregated tau protein that can penetrate the blood-brain barrier . In tissues from patients with Alzheimer's disease, progressive supranuclear palsy, corticobasal degeneration, and Pick's disease, Tau ligand-1 exhibits high affinity for aggregated tau protein, with equilibrium dissociation constant (KD) values ranging from 1 to 3.8 nM . Tau ligand-1 can serve as a potential positron emission tomography (PET) tracer and holds promise for application in positron emission tomography imaging studies of tau-related diseases in the central nervous system .
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Cat. No.: HY-W007746
CAS No.: 141091-37-4
Target:  

Drug Intermediate

Research Areas:  

Others

1-Cyclohexeneboronic acid pinacol ester (Compound 4) is an organoboron ester that can be used in the synthesis of PET tracers .
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Cat. No.: HY-110141
CAS No.: 924298-51-1
Purity:  98.02%
Target:  

mGluR

Research Areas:  

Others

ABP688 is a high affinity human mGluR5 antagonist with anKi of 1.7 nM. Radioisotope-labeled ABP688 can be used as a PET tracer for clinical imaging of the mGlu5 receptor .
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Cat. No.: HY-128642
CAS No.: 2370952-98-8
Purity:  98.94%
Target:  

FAP

Research Areas:  

Cancer

FAPI-2 is a quinoline-based fibroblast activation protein (FAP)-targeting ligand that can be labeled as 68Ga-FAPI-2 and used as a PET tracer for cancer diagnosis. FAPI-2 has advantages such as fast tracer kinetics, no need for fasting preparation, and being unaffected by blood glucose .
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Cat. No.: HY-175229
CAS No.: 3066073-36-4
Target:  

PSMA

Research Areas:  

Cancer

PSMA ligand 1 (Compound 1c) is a PSMA ligand with an IC50 of 26.74 nM. The [ 18F]-labeled PSMA ligand 1 can serve as a PSMA PET tracer and is used in research on the diagnosis of prostate cancer .
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Cat. No.: HY-141464
CAS No.: 131287-39-3
Purity:  95.03%
Synonyms: Fmoc-Asn(Ac3AcNH-beta-Glc)-OH
Research Areas:  

Cancer

Fmoc-L-Asn(beta-D-GlcNAc(Ac)3)-OH (Fmoc-Asn(Ac3AcNH-beta-Glc)-OH) can be used in the synthesis of silicon-fluoride acceptor (SiFA) derivatized octreotate derivatives. SiFA-octreotate analogues, as tumor imaging agents, are useful tool for the research of positron emission tomography (PET) .
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Cat. No.: HY-163281
CAS No.: 1839622-49-9
Research Areas:  

Cancer

FSY-OSO2F is (S)-2-amino-3-(4-((fluorosulfonyl) oxy) phenyl) propanoic acid. The radiolabeled form of FSY-OSO2F, ([ 18F]FSY-OSO2F), serves as a PET tracer that is taken up by cancer cells. FSY-OSO2F can be used in research related to cancer and PET imaging .
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