11 Results for "

halflives

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "halflives" in MCE Product Catalog:

Cat. No.: HY-12410
CAS No.: 1557232-32-2
Purity:  ≥95.0%
Target:  

Itk

Research Areas:  

Inflammation/Immunology

GNE-9822 is a potent, orally active and selective ITK inhibitor with a Ki value of 0.7 nM, and an EC50 value of 354.5 nM. GNE-9822 has good ADME properties. GNE-9822 can be used in research of asthma .
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Cat. No.: HY-175207
CAS No.: 3109469-27-1
Target:  

Glycosidase

Research Areas:  

Cancer

CHI3L1-IN-3 is a CHI3L1 inhibitor. CHI3L1-IN-3 binds to CHI3L1 with Kds of 13.76 μM and 13.5 μM in MST and SPR assays, respectively. CHI3L1-IN-3 demonstrates extended plasma half-lives and microsomal stability, along with reduced intrinsic clearance. CHI3L1-IN-3 induces dose-dependent cytotoxicity, reduces spheroid mass and inhibits migration in a 3D multicellular glioblastoma (GBM) spheroid model. CHI3L1-IN-3 can be used for the study of GBM .
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Cat. No.: HY-139980
CAS No.: 2768712-71-4
Purity:  99.94%
Target:  

CDK

Research Areas:  

Cancer

CDK9-IN-13 (compound 38) is potent and selective CDK9 inhibitor, with an IC50 of <3 nM. CDK9-IN-13 exhibits short half-lives in rodents .
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Cat. No.: HY-128268
CAS No.: 735303-62-5
Target:  

Parasite

Research Areas:  

Infection

PFK-IN-1 (compound 1) is a phosphofructokinase (PFK) inhibitor, with IC50 values of 0.41 and 0.23 μM against T.brucei and T.cruzi PFK, respectively, and an ED50 of 15.18 μg/mL for T.brucei. The half-lives of PFK-IN-1 in rat and mouse liver microsomes are 9.7 and 408 minutes, respectively .
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Cat. No.: HY-148177
CAS No.: 1821293-40-6
Synonyms: ZY-19489; MMV 253; AZ13721412
Target:  

Parasite

Research Areas:  

Infection

Sutidiazine (ZY-19489) is an orally active and antimalarial agent. Sutidiazine inhibits parasitemia-induced infection. Sutidiazine shows short half-lives (approximately 7 h) and an exposure effect .
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Cat. No.: HY-W040303
CAS No.: 98967-40-9
Synonyms: DE-498; XRD-498
Research Areas:  

Others

Flumetsulam is pre- and postemergence herbicide, which is susceptible to dissipate in corn ecosystem with half-live less than 8.7 days .
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Cat. No.: HY-W040303R
CAS No.: 98967-40-9
Synonyms: DE-498 (Standard); XRD-498 (Standard)
Research Areas:  

Others

Flumetsulam (Standard) is the analytical standard of Flumetsulam. This product is intended for research and analytical applications. Flumetsulam is pre- and postemergence herbicide, which is susceptible to dissipate in corn ecosystem with half-live less than 8.7 days .
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Cat. No.: HY-164815
CAS No.: 104732-22-1
Synonyms: Tianeptine metabolite MC5
Target:  

Drug Metabolite

Research Areas:  

Neurological Disease

S 8849-1 (free base) (Tianeptine metabolite MC5) is a Tianeptine (HY-90003) metabolite that is found in plasma. The mean elimination half-lives of S 8849-1 (free base) is 7.53 h in rats. S 8849-1 (free base) is promising for research of antidepressants .
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Cat. No.: HY-123639
CAS No.: 261766-32-9
Synonyms: N-(2-Phenylethyl)-indomethacin amide
Target:  

COX

Research Areas:  

Inflammation/Immunology Cancer

LM-4108 (N-(2-Phenylethyl)-indomethacin amide) is a selective and orally active COX-2 inhibitor with an IC50 of 0.06 μM for purified human COX-2. LM-4108 shows anti-inflammatory activity and may be effective in prevention of cancer. Half-lives for the disappearance of 10 μM LM-4108 in rat, human, and mouse liver microsomes were 11 min, 21 min, and 51 min, respectively .
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Cat. No.: HY-166341S
CAS No.: 1330822-91-7
Synonyms: Tianeptine metabolite MC5-d4
S 8849-1-d4 (free base) (Tianeptine metabolite MC5-d4) is deuterium labeled S 8849-1 (free base). S 8849-1 (free base) (Tianeptine metabolite MC5) is a Tianeptine (HY-90003) metabolite that is found in plasma. The mean elimination half-lives of S 8849-1 (free base) is 7.53 h in rats. S 8849-1 (free base) is promising for research of antidepressants .
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Cat. No.: HY-147740
CAS No.: 70492-21-6
Research Areas:  

Cancer

WEHI-150 is a replica of mitoxantrone, is a portent DNA interstrand crosslinkhalf-lives of 12.5 h. WEHI-150 forms covalent adducts at CpG sequences and exhibits a preference for methylated CpG sites. Formaldehyde-activated WEHI-150 induces DNA interstrand crosslinks. Formaldehyde-activated WEHI-150 shows Concentration-dependent transcription blockages. WEHI-150 can mediate covalent adducts that are independent of interactions with the N-2 of guanine and is capable of adduct formation at novel DNA sequences .
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