83 Results for "

V2

" in MedChemExpress (MCE) Product Catalog:
Products (83)

83 Results for "V2" in MCE Product Catalog:

Cat. No.: HY-18344
CAS No.: 185913-78-4
Synonyms: SR 121463
Target:  

Vasopressin Receptor

Research Areas:  

Metabolic Disease

Satavaptan (SR 121463) is an antagonist for vasopressin V2 receptor. Satavaptan regulates the vasopressin regulated phosphopeptides and vasopressin-mediated signaling pathway. Satavaptan is potential in ameliorating hyponatremia .
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Cat. No.: HY-109133
CAS No.: 1914998-56-3
Synonyms: BAY 1753011
Pecavaptan, a chemical probe, is an orally active and dual antagonist of V1a/V2 receptor (Ki=0.5 nM and 0.6 nM for human, respectively). Pecavaptan promotes an increase in urine production, which reduces the associated symptoms of water retention and edema .
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Cat. No.: HY-P0049A
CAS No.: 75499-44-4
Synonyms: Arg8-vasopressin diacetate; AVP diacetate; ADH
Research Areas:  

Neurological Disease Cancer

Argipressin (diacetate) (AVP (diacetate), also known as antidiuretic hormone (ADH)) is a 9 amino acid neuropeptide secreted by the posterior pituitary. Argipressin (diacetate) (AVP (diacetate)) can regulate the biological effects of fluid balance, osmolality and cardiovascular through three separate G-protein coupled receptors (GPCRs), namely Avpr1a (V1a), Avpr1b (V1b) and Avpr2 (V2). Argipressin (diacetate) (AVP (diacetate)) also have potentially important effects on centrally regulated metabolic processes .
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Cat. No.: HY-RS03483
Research Areas:  

Others

CYP4V2 Human Pre-designed siRNA Set A contains three designed siRNAs for CYP4V2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P0272A
CAS No.: 1610056-01-3
Target:  

HIV

Research Areas:  

Infection

Peptide T (TFA) is an octapeptide from the V2 region of HIV-1 gp120. Peptide T is a ligand for the CD4 receptor and prevents binding of HIV to the CD4 receptor.
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Cat. No.: HY-18346R
CAS No.: 137975-06-5
Synonyms: OPC-31260 (Standard)
Mozavaptan (Standard) is the analytical standard of Mozavaptan. This product is intended for research and analytical applications. Mozavaptan (OPC-31260) is a benzazepine derivative and a potent, selective, competitive and orally active vasopressin V2 receptor antagonist with an IC50 of 14 nM. Mozavaptan shows ~85-fold selectivity for V2 receptor over V1 receptor (IC50 of 1.2 μM), and can antagonize the antidiuretic action of arginine vasopressin (AVP) in vivo. Mozavaptan has the potential for hyponatremia, syndrome of inappropriate antidiuretic hormone (SIADH), and congestive heart failure treatment [2].
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Cat. No.: HY-185971
Target:  

mRNA

Research Areas:  

Others

PiggyBac mRNA V2 (N1-methyl-pseudouridine) is an enzyme encoding PiggyBac transposase, mediating efficient transgene integration and scarless excision, used for transgenic and cell engineering.
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Cat. No.: HY-185969
Target:  

mRNA

Research Areas:  

Others

Cre mRNA V2 (N1-methyl-pseudouridine) is an enzyme encoding Cre recombinase that recognizes the loxP site to mediate recombination, used for conditional gene knockout and lineage tracing.
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Cat. No.: HY-157220
CAS No.: 942619-79-6
Purity:  99.85%
Target:  

Vasopressin Receptor

Research Areas:  

Cardiovascular Disease

Tolvaptan phosphate ester sodium, a prodrug of Tolvaptan (HY-17000), can be used in the study of cardiac edema. Tolvaptan is a selective, competitive and orally active vasopressin receptor 2 (V2R) antagonist with an IC50 of 1.28 μM for the inhibition of arginine vasopressin (AVP)-induced platelet aggregation [2].
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Cat. No.: HY-P1390A
Target:  

Vasopressin Receptor

Research Areas:  

Endocrinology

d[Cha4]-AVP TFA is a potent and selective vasopressin (AVP) V1b receptor agonist with a Ki of 1.2 nM for human V1b receptor. d[Cha4]-AVP TFA shows more selective for V1b receptor than human V1a receptor, V2 receptor, and oxytocin receptors [2].
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Cat. No.: HY-185968
Target:  

mRNA

Research Areas:  

Others

LbCas12a mRNA V2 (N1-methyl-pseudouridine) encodes the genera *Cas12a* (LbCas12a, formerly Cpf1), possessing TTTN PAM and staggered cleavage characteristics, and is used for gene editing.
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Cat. No.: HY-168742
Target:  

Vasopressin Receptor

Research Areas:  

Neurological Disease

V1a/V2 antagonist 1 (Compound 18j) is an orally active dual V1a and V2 receptor antagonist with high binding affinity for both receptors (Ki: 0.13 nM for hV1a, 0.53 nM for hV2 and 0.5 nM for mV1a; IC50: 2.2 nM for hV1a). V1a/V2 antagonist 1 inhibits Oxytocin (HY-17571)-induced scratching behavior in mice .
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Cat. No.: HY-185970
Target:  

mRNA

Research Areas:  

Others

PE2/PE3 mRNA V2 (N1-methyl-pseudouridine) is an enzyme encoding the primer editor PE2/PE3, enabling precise small-fragment editing without double-strand breaks, used for precise gene modification.
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Cat. No.: HY-121540
CAS No.: 877618-79-6
Target:  

Wnt

Research Areas:  

Cancer

IWP-2-V2 is a IWP-2 (HY-13912) analogue that retains activity against the Wnt/β-catenin pathway .
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Cat. No.: HY-14185R
CAS No.: 168079-32-1
Synonyms: VPA-985 (Standard); WAY-VPA 985 (Standard)
Lixivaptan (Standard) is the analytical standard of Lixivaptan. This product is intended for research and analytical applications. Lixivaptan (VPA-985, WAY-VPA 985) is an orally active and selective vasopressin receptor V2 antagonist, with IC50 values of 1.2 and 2.3 nM for human and rat V2, respectively.
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Cat. No.: HY-109181
CAS No.: 2379889-71-9
Synonyms: SK-1404; KRP-N118
Target:  

Vasopressin Receptor

Research Areas:  

Others

Lazuvapagon (SK-1404) is a vasopressin V2 receptor agonist for the research of nocturia .
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Cat. No.: HY-158163
CAS No.: 3038564-39-2
Target:  

Herbicide

Research Areas:  

Inflammation/Immunology

Herbicidal agent 4 (compound V-2) is an auxinic herbicidal agent. Herbicidal agent 4 may also be an immune activator while upregulating the defense genes and increasing content of jasmonic acid .
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Cat. No.: HY-123593R
CAS No.: 138470-70-9
Synonyms: OPC-31260 hydrochloride (Standard)
Mozavaptan (hydrochloride) (Standard) is the analytical standard of Mozavaptan (hydrochloride). This product is intended for research and analytical applications. Mozavaptan hydrochloride (OPC-31260 hydrochloride) is a benzazepine derivative and a potent, selective, competitive and orally active vasopressin V2 receptor antagonist with an IC50 of 14 nM. Mozavaptan hydrochloride shows ~85-fold selectivity for V2 receptor over V1 receptor (IC50 of 1.2 μM), and can antagonize the antidiuretic action of arginine vasopressin (AVP) in vivo. Mozavaptan hydrochloride has the potential for hyponatremia, syndrome of inappropriate antidiuretic hormone (SIADH), and congestive heart failure treatment [2].
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Cat. No.: HY-P1810
CAS No.: 1647119-71-8
Target:  

Vasopressin Receptor

Research Areas:  

Neurological Disease

c(Bua-Cpa-Thi-Val-Asn-Cys)-Pro-Agm is a is a potent, selective and short-acting peptidic V2 receptor (V2R) agonist with EC50s of 0.25 and 0.05 nM for hV2R and rV2R, respectively .
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Cat. No.: HY-18346S
CAS No.: 2750534-83-7
Synonyms: OPC-31260-d6
Mozavaptan-d6 (OPC-31260-d6) is the deuterium labeled Mozavaptan. Mozavaptan (OPC-31260) is a benzazepine derivative and a potent, selective, competitive and orally active vasopressin V2 receptor antagonist with an IC50 of 14 nM. Mozavaptan shows ~85-fold selectivity for V2 receptor over V1 receptor (IC50 of 1.2 μM), and can antagonize the antidiuretic action of arginine vasopressin (AVP) in vivo. Mozavaptan has the potential for hyponatremia, syndrome of inappropriate antidiuretic hormone (SIADH), and congestive heart failure treatment [2].
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