30 Results for "

warfarin

" in MedChemExpress (MCE) Product Catalog:
Products (30)

30 Results for "warfarin" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-N6678
CAS No.: 5975-78-0
Zearalanone is a reductive metabolite of Zearalenone (HY-103447). Zearalanone binds to serum albumin across multiple species. Zearalanone enhances the binding affinity of Warfarin (HY-B0687) to serum albumin .
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Cat. No.: HY-W015998
CAS No.: 5543-58-8
(R)-(+)-Warfarin is an orally active chiral 4-hydroxycoumarin compound with vitamin K epoxide reductase (VKOR) inhibitory activity and cytochrome P450 substrate activity . (R)-(+)-Warfarin undergoes stereoselective metabolism via CYP1A2 to form 6-Hydroxywarfarin and 8-Hydroxywarfarin, and is metabolized via CYP3A4 to produce 10-Hydroxywarfarin (HY-134999). (R)-(+)-Warfarin can be used for the research of thromboembolic diseases .
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Cat. No.: HY-B1042
CAS No.: 1949-20-8
Synonyms: SKF-9976 citrate; AF-438 citrate
Target:  

Cytochrome P450

Research Areas:  

Inflammation/Immunology

Oxolamine citrate (SKF-9976 citrate) is an orally active antitussive. Oxolamine citrate can inhibit CYP2B1/2. Oxolamine citrate has anti-inflammatory effects on the respiratory organs of guinea pigs. Oxolamine citrate increases the AUC of Warfarin (HY-B0687) and prolongs its terminal half-life. Oxolamine citrate can be used in respiratory disease research .
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Cat. No.: HY-139167
CAS No.: 17834-03-6
Purity:  99.39%
Synonyms: warfarin RC15
Target:  

Drug Derivative

Research Areas:  

Others

7-Hydroxywarfarin is a Warfarin analog with anticoagulant activity .
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Cat. No.: HY-W015998S
CAS No.: 773005-79-1
(R)-(+)-Warfarin-d5 is the deuterated-labeled (R)-(+)-Warfarin (HY-W015998). (R)-(+)-Warfarin is an orally active chiral 4-hydroxycoumarin compound with vitamin K epoxide reductase (VKOR) inhibitory activity and cytochrome P450 substrate activity . (R)-(+)-Warfarin undergoes stereoselective metabolism via CYP1A2 to form 6-Hydroxywarfarin and 8-Hydroxywarfarin, and is metabolized via CYP3A4 to produce 10-Hydroxywarfarin (HY-134999). (R)-(+)-Warfarin can be used for the research of thromboembolic diseases .
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Cat. No.: HY-128720
CAS No.: 759-65-9
Purity:  ≥95.0%
Diethyl oxalpropionate is an intermediate for poly((R,S)-3,3-dimethylmalic acid) (PDMMLA) derivative synthesis. PDMMLA derivative can be used in synthesis of nanoparticles and study of warfarin encapsulation and controlled release .
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Cat. No.: HY-NP002C
CAS No.: 9048-46-8
Rabbit Serum Albumin (globulin free) is a plasma protein derived from rabbits. Rabbit Serum Albumin (globulin-free) can stereoselectively bind to a variety of bioactive molecules. Rabbit Serum Albumin (globulin free) acts as the allergen Ory c RSA with cross-reactivity to other mammalian serum albumins. Rabbit Serum Albumin (globulin free) can be used for the research of allergy .
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Cat. No.: HY-113958
CAS No.: 104653-34-1
Synonyms: LM-2219
Target:  

VD/VDR

Research Areas:  

Others

Difethialone (LM-2219) is an anticoagulant rodenticide. Difethialone shows high rodenticide activity in warfarin-sensitive and resistant strains of rats and mice. Difethialone interferes with the circulation of vitamin K in the liver, preventing the synthesis of coagulation factors, resulting in the inability of the blood to coagulate properly, ultimately causing internal bleeding and death. Difethialone can be used in studies of ecological impacts .
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Cat. No.: HY-132569S
CAS No.: 94820-66-3
8-Hydroxy warfarin-d5 can be used as an internal standard for the quantification of Warfarin and its known metabolites .
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Cat. No.: HY-113958R
CAS No.: 104653-34-1
Synonyms: LM-2219 (Standard)
Research Areas:  

Others

Difethialone (Standard) is the analytical standard of Difethialone. This product is intended for research and analytical applications. Difethialone (LM-2219) is an anticoagulant rodenticide. Difethialone shows high rodenticide activity in warfarin-sensitive and resistant strains of rats and mice. Difethialone interferes with the circulation of vitamin K in the liver, preventing the synthesis of coagulation factors, resulting in the inability of the blood to coagulate properly, ultimately causing internal bleeding and death. Difethialone can be used in studies of ecological impacts .
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Cat. No.: HY-W741611
CAS No.: 67588-18-5
Synonyms: NSC 289346
Target:  

Drug Metabolite

Research Areas:  

Metabolic Disease

Dehydro warfarin is a metabolite of (±)-warfarin. It is formed from (±)-warfarin by rat liver microsomes.
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Cat. No.: HY-159002S
Methyl-warfarin-d3 is a deuterated labeling methylated Warfarin (HY-B0687) .
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Cat. No.: HY-W742809
CAS No.: 63740-81-8
Target:  

Drug Derivative

Research Areas:  

Others

(S)-7-Hydroxywarfarin is the S stereoisomer of 7-Hydroxywarfarin (HY-139167). (S)-7-Hydroxywarfarin is the inactive, major metabolite of racemic Warfarin (HY-B0687) .
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Cat. No.: HY-116601
CAS No.: 17834-02-5
Target:  

Cytochrome P450

Research Areas:  

Others

6-Hydroxywarfarin is a metabolite of (+) -warfarin. 6-Hydroxywarfarin is a weaker vitamin K antagonist. 6-Hydroxywarfarin is metabolized by the cytochrome P450 isomer 2C9 (CYP2C9) .
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Cat. No.: HY-121814A
CAS No.: 66556-77-2
Synonyms: (R)-Acenocoumarin; (R)-Nicoumalone
Target:  

VD/VDR

Research Areas:  

Cardiovascular Disease

(R)-Acenocoumarol ((R)-Acenocoumarin; (R)-Nicoumalone) is a short-acting and orally active anticoagulant, like Warfarin (HY-B0687), works by inhibiting vitamin K epoxide reductase. (R)-Acenocoumarol has a greater in vivo anticoagulant potency than Warfarin. (R)-Acenocoumarol has a single chiral center that produces two different enantiomeric forms. (R)-Acenocoumarol has a longer plasma elimination half-life (6.6 h) and a slower plasma clearance rate (1.9 L/h) than the (S)-enantiomer, resulting in a stronger in vivo anticoagulant effect.
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Cat. No.: HY-134999
CAS No.: 83219-99-2
Research Areas:  

Metabolic Disease

10-Hydroxywarfarin, a metabolite of (R)-(+)-Warfarin (HY-W015998 ), is a CYP2C9 and vitamin K epoxide reductase complex 1 (VKOR) inhibitor with IC50s of 1.6 µM and 80 ng/mL, respectively .
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Cat. No.: HY-W739842
CAS No.: 17834-04-7
Synonyms: 8-OH warfarin
Target:  

Cytochrome P450

Research Areas:  

Cardiovascular Disease

8-Hydroxywarfarin (8-OH Warfarin) is a CYP2C9 inhibitor. 8-Hydroxywarfarin inactivates the anticoagulant activity of Warfarin (HY-B0687) via 8-hydroxylation. 8-Hydroxywarfarin serves as a glucuronidation substrate for UGT1A1, UGT1A8, UGT1A9, as well as wild-type/mutant UGT1A10. This reaction enhances its polarity, solubility and excretion efficiency, and the process is independent of phenylalanine 90 of UGT1A10. 8-Hydroxywarfarin can be used in studies related to thromboembolic diseases .
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Cat. No.: HY-B1717
CAS No.: 959-14-8
Target:  

Cytochrome P450

Research Areas:  

Inflammation/Immunology

Oxolamine (SKF-9976) is an orally active antitussive. Oxolamine can inhibit CYP2B1/2. Oxolamine has anti-inflammatory effects on the respiratory organs of guinea pigs. Oxolamine increases the AUC of Warfarin (HY-B0687) and prolongs its terminal half-life. Oxolamine can be used in respiratory disease research .
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Cat. No.: HY-113958S
CAS No.: 2714420-97-8
Synonyms: Baraki-d4; LM 2219-d4
Difethialone-d4 (Baraki-d4; LM 2219-d4) is the deuterium labeled Difethialone (HY-113958). Difethialone (LM-2219) is an anticoagulant rodenticide. Difethialone shows high rodenticide activity in warfarin-sensitive and resistant strains of rats and mice. Difethialone interferes with the circulation of vitamin K in the liver, preventing the synthesis of coagulation factors, resulting in the inability of the blood to coagulate properly, ultimately causing internal bleeding and death. Difethialone can be used in studies of ecological impacts .
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Cat. No.: HY-121535
CAS No.: 116476-16-5
Research Areas:  

Others

Levosemotiadil, an S-isomer of semotiadil, exhibits stronger binding affinity to human serum albumin (HSA) compared to its R-isomer counterpart. This study utilized high-performance frontal analysis (HPFA) to demonstrate that levosemotiadil binds approximately three times more strongly to HSA than semotiadil. The binding parameters were evaluated using Scatchard analysis, revealing specific interactions with the diazepam binding site on HSA. The presence of diazepam decreased the binding affinity of both enantiomers, while warfarin did not alter their binding characteristics. These findings highlight levosemotiadil's potential as a Ca- and Na-channel blocker with significant binding preferences for HSA, crucial for understanding its pharmacokinetics and therapeutic effects .
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