174 Results for "

ABT

" in MedChemExpress (MCE) Product Catalog:
Products (174)

174 Results for "ABT" in MCE Product Catalog:

Cat. No.: HY-14316A
CAS No.: 209326-19-2
Purity:  99.49%
Synonyms: Ebanicline dihydrochloride; ABT-594 dihydrochloride
Target:  

nAChR

Research Areas:  

Neurological Disease

Tebanicline dihydrochloride (Ebanicline dihydrochloride) is a nAChR modulator with potent, orally effective analgesic activity. It inhibits the binding of cytisine to α4β2 neuronal nAChRs with a Ki of 37 pM .
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Cat. No.: HY-14316B
CAS No.: 203564-54-9
Synonyms: Ebanicline hydrochloride; ABT-594 hydrochloride
Target:  

nAChR

Research Areas:  

Neurological Disease

Tebanicline hydrochloride (Ebanicline hydrochloride) is a nAChR modulator with potent, orally effective analgesic activity. Tebanicline hydrochloride inhibits the binding of cytisine to α4β2 neuronal nAChRs with a Ki of 37 pM .
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Cat. No.: HY-14316C
CAS No.: 198283-74-8
Synonyms: Ebanicline tosylate; ABT-594 tosylate
Target:  

nAChR

Research Areas:  

Neurological Disease

Tebanicline tosylate, an analogue of epibatidine, is a neuronal nicotinic acetylcholine receptor agonist. Tebanicline tosylate exhibits potent antinociceptive effects and has a high affinity for the α4β2 neuronal nicotinic acetylcholine receptor subunit in the central nervous system.
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Cat. No.: HY-10130R
CAS No.: 912445-05-7
Synonyms: ABT-888 dihydrochloride (Standard)
Research Areas:  

Cancer

Veliparib (dihydrochloride) (Standard) is the analytical standard of Veliparib (dihydrochloride) (HY-10130). This product is intended for research and analytical applications. Veliparib (dihydrochloride) is a potent inhibitor of PARP1 and PARP2 with Kis of 5.2 nM and 2.9 nM in cell-free assays, respectively.
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Cat. No.: HY-13997R
CAS No.: 1258226-87-7
Synonyms: ABT-267 (Standard)
Target:  

HCV Reference Standards

Research Areas:  

Infection

Ombitasvir (Standard) is the analytical standard of Ombitasvir. This product is intended for research and analytical applications. Ombitasvir is a potent inhibitor of the hepatitis C virus protein NS5A, with EC50s of 0.82 to 19.3 pM against HCV genotypes 1 to 5, and 366 pM against genotype 6a.
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Cat. No.: HY-160718
CAS No.: 171752-56-0
Synonyms: ABT-431; DAS-431
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Adrogolide is an A-86929 (HY-171472) prodrug and dopamine D1 receptor agonist. Adrogolide is converted rapidly in plasma to A-86929. Adrogolide improves behavioral disability and locomotor activity scores. Adrogolide can also attenuate the ability of Cocaine to induce Cocaine-seeking behavior. Adrogolide can be used in the research of Parkinson's disease .
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Cat. No.: HY-17634R
CAS No.: 1365970-03-1
Synonyms: ABT-493 (Standard)
Research Areas:  

Infection

Glecaprevir (Standard) is the analytical standard of Glecaprevir. This product is intended for research and analytical applications. Glecaprevir is a novel HCV NS3/4A protease inhibitor, with IC50 values ranging from 3.5 to 11.3 nM. Glecaprevir is also a SARS-CoV 3CLpro inhibitor with an IC50 of 4.09 μM .
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Cat. No.: HY-P99627
CAS No.: 1708936-80-4
Synonyms: NV-02; PG110; ABT-110

Target:  

Trk Receptor

Research Areas:  

Inflammation/Immunology

Frunevetmab (NV-02) is a felinized anti-nerve growth factor (NGF) monoclonal antibody with a Kd of 20 pM. Frunevetmab can effectively decrease osteoarthritis (OA) pain in cats .
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Cat. No.: HY-103389R
CAS No.: 1614-12-6
Synonyms: ABT (Standard); 3-Aminobenzotriazole (Standard)
Research Areas:  

Cancer

1-Aminobenzotriazole (Standard) is the analytical standard of 1-Aminobenzotriazole. This product is intended for research and analytical applications. 1-Aminobenzotriazole is a nonspecific and irreversible inhibitor of cytochrome P450 (P450).
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Cat. No.: HY-P99391B
CAS No.: 1781223-80-0
Synonyms: ABT-700 (WT IgG1); ABBV-400 Antibody (WT IgG1)
Target:  

c-Met/HGFR

Research Areas:  

Cancer

Telisotuzumab (WT IgG1) is a monoclonal antibody that retains the natural wild-type IgG1 Fc structure without engineering modification. Telisotuzumab (HY-P99391) is a humanized IgG1 anti-c-Met monoclonal antibody whose Fc hinge region has been engineered to introduce additional cysteine ​​coupling sites for targeted drug conjugation .
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Cat. No.: HY-124540B
CAS No.: 1258641-38-1
Purity:  98.79%
Target:  

nAChR

Research Areas:  

Neurological Disease

(Rac)-ABT-202 dihydrochloride is a racemate of ABT-202. ABT-202 is an agonist of nicotinic acetylcholine receptors (nAChRs) and can be used as an analgesic .
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Cat. No.: HY-10635AR
CAS No.: 808756-70-9
(S)-ABT-102 (Standard) is the analytical standard of (S)-ABT-102 (HY-10635A). This product is intended for research and analytical applications. (S)-ABT-102 is a TRPV1 Antagonist, with an IC50 of 123 nM. (S)-ABT-102 has analgesic activity .
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Cat. No.: HY-10635A
CAS No.: 808756-70-9
Target:  

TRP Channel

Research Areas:  

Inflammation/Immunology Cancer

(S)-ABT-102 is a TRPV1 Antagonist, with an IC50 of 123 nM. (S)-ABT-102 has analgesic activity .
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Cat. No.: HY-131001
Target:  

nAChR

Research Areas:  

Neurological Disease

DPNB-ABT594 is a nitrobenzyl-caged ABT594 (HY-14316A) and activates nAChRs containing the α4β2 subunits with good selectivity than the α7 subunit. DPNB-ABT594 can be used to map the distribution of nAChRs on neurons of the medial habenula (MHb) and helps to gain a deeper understanding of the nAChR-mediated Ca 2+ signalling in the MHb .
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Cat. No.: HY-14588A
CAS No.: 1798014-18-2
Synonyms: (rel)-ABT-378
Target:  

Drug Intermediate

Research Areas:  

Others

rel-Lopinavir ((rel)-ABT-378) is a drug impurity.
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Cat. No.: HY-131232
CAS No.: 2365172-82-1
Purity:  98.64%
Synonyms: Desmorpholinyl ABT-263-NH-Me
Desmorpholinyl navitoclax-NH-Me (Desmorpholinyl ABT-263-NH-Me) is an N-methylamino-substituted derivative of Navitoclax (HY-10087) and a BCL-XL-targeting PROTAC precursor. Desmorpholinyl navitoclax-NH-Me is used for the synthesis of BCL-XL-targeting PROTACs and related research .
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Cat. No.: HY-14588S
CAS No.: 1322625-54-6
Synonyms: (rel)-ABT-378-d8
(rel)-Lopinavir-d8 ((rel)-ABT-378-d8) is the deuterium labeled Lopinavir (HY-14588) . Lopinavir (ABT-378) is a highly potent, selective peptidomimetic inhibitor of the HIV-1 protease, with Kis of 1.3 to 3.6 pM for wild-type and mutant HIV protease. Lopinavir acts by arresting maturation of HIV-1 thereby blocking its infectivity . Lopinavir is also a SARS-CoV 3CL pro inhibitor with an IC50 of 14.2 μM .
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Cat. No.: HY-90001S3
CAS No.: 1217720-20-1
Synonyms: rel-ABT 538-d6; rel-RTV-d6
rel-Ritonavir-d6 (rel-ABT 538-d6) is the deuterium labeled rel-Ritonavir. rel-Ritonavir is a relative configuration of Ritonavir (HY-90001). Ritonavir (ABT 538) is an inhibitor of HIV protease used to study of HIV infection and AIDS. Ritonavir is also a SARS-CoV 3CLpro inhibitor with an IC50 of 1.61 μM .
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Cat. No.: HY-109001A
CAS No.: 2221010-57-5
Purity:  ≥98.0%
Synonyms: (1S,2R)-ABT-957
Target:  

Proteasome

Research Areas:  

Neurological Disease

(1S,2R)-Alicapistat ((1S,2R)-ABT-957) is an orally active selective inhibitor of human calpains 1 and 2 for the potential application of Alzheimer's disease (AD) . (1S,2R)-Alicapistat mitigates the metabolic liability of carbonyl reduction and inhibits calpain 1 with an IC50 value of 395 nM .
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Cat. No.: HY-167869
CAS No.: 819058-88-3
Target:  

Drug Metabolite

Research Areas:  

Others

A-849529 is an acid metabolite of ABT-869 (HY-50751). ABT-869 is a potent and orally active multi-target inhibitor of VEGFR and PDGFR family .
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