16 Results for "

Hv1

" in MedChemExpress (MCE) Product Catalog:
Products (16)

16 Results for "Hv1" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-12981
CAS No.: 920022-47-5
Purity:  99.92%
Synonyms: RO5028442
RG7713 (RO5028442) is a highly potent, selective and brain-penetrant Vasopressin 1a (V1a) receptor antagonist with Kis of 1 nM (hV1a) and 39 nM (mV1a).
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Cat. No.: HY-109024
CAS No.: 1228088-30-9
Purity:  99.89%
Synonyms: RG7314
Balovaptan (RG7314) is an orally available, selective brain-penetrant vasopressin 1a (hV1a) receptor antagonist, with Kis of 1 and 39 nM for human (hV1a) and mouse (mV1a) receptors, and is used for the research of autism.
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Cat. No.: HY-P5142
CAS No.: 193981-10-1
Synonyms: ω-ACTX-Hv1; ω-Atracotoxin-Hv1
ω-Hexatoxin-Hv1a (ω-ACTX-Hv1; ω-Atracotoxin-HV1) is an orally active insecticidal neurotoxin containing an inhibitor cystine knot motif and a selective calcium channel inhibitor. ω-Hexatoxin-Hv1a blocks L-type voltage-dependent Ca 2+ channels and reduces intracellular calcium ion concentration, thereby decreasing apoptosis, necroptosis and oxidative stress, and promoting cell recovery and energy level elevation. ω-Hexatoxin-Hv1a causes larval paralysis and death by impairing neurotransmission in the central nervous system of insects. It shows high injectable toxicity against insects of multiple orders, but exhibits weak oral toxicity. ω-Hexatoxin-Hv1a is widely applicable to studies related to ischemia-reperfusion injury, atopic dermatitis, and ischemic injury of cardiomyocytes and neurons [1] .
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Cat. No.: HY-163696A
CAS No.: 1609461-57-5
Target:  

Proton Pump

Research Areas:  

Others Neurological Disease Cancer

HV1-IN-1 hydrochloride is an inhibitor of the human voltage-gated proton channel (hHV1). HV1-IN-1 hydrochloride works by binding to the VSD of the HV1 channel. The VSD is a component of the HV1 channel that is responsible for detecting changes in membrane potential and triggering the opening of the channel. HV1-IN-1 hydrochloride can be used in the study of cancer, neuroinflammation and immune response [1].
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Cat. No.: HY-D1560
CAS No.: 438476-80-3
Target:  

Fluorescent Dye

Research Areas:  

Others

FG 488 DHPE is a lipid-coupled fluorochrome, has be used as a fluorophore Oregon Green 488. FG 488 DHPE monitors acidification of lipid vesicles with λex/λem=508/534 nm.FG 488 DHPE is also used for Hv1-induced proton translocation quantificatio with λex/λem=508/534 nm as well [1] .
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Cat. No.: HY-175003
CAS No.: 3097367-11-5
Target:  

Proton Pump

Research Areas:  

Cancer

HV1-IN-2 (Compound 14c) is a human voltage-gated proton channel (HV1) inhibitor with an IC50 of 2.14 μM. HV1-IN-2 has a potent anticancer activity with significant antiproliferative effects against THP-1 and MCF-7 cells. HV1-IN-2 can be used for cancers research, such as colorectal tumours, leukaemia, and breast cancer [1].
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Cat. No.: HY-P5142A
Synonyms: ω-ACTX-Hv1 TFA; ω-Atracotoxin-Hv1 TFA
ω-Hexatoxin-Hv1a (ω-ACTX-Hv1; ω-Atracotoxin-HV1) TFA is an orally active insecticidal neurotoxin containing an inhibitor cystine knot motif and a selective calcium channel inhibitor. ω-Hexatoxin-Hv1a TFA blocks L-type voltage-dependent Ca 2+ channels and reduces intracellular calcium ion concentration, thereby decreasing apoptosis, necroptosis and oxidative stress, and promoting cell recovery and energy level elevation. ω-Hexatoxin-Hv1a TFA causes larval paralysis and death by impairing neurotransmission in the central nervous system of insects. It shows high injectable toxicity against insects of multiple orders, but exhibits weak oral toxicity. ω-Hexatoxin-Hv1a TFA is widely applicable to studies related to ischemia-reperfusion injury, atopic dermatitis, and ischemic injury of cardiomyocytes and neurons [1] .
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Cat. No.: HY-RS06494
Research Areas:  

Others

HVCN1 Human Pre-designed siRNA Set A contains three designed siRNAs for HVCN1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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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 [1].
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Cat. No.: HY-162118
CAS No.: 2355304-05-9
Target:  

Vasopressin Receptor

Research Areas:  

Neurological Disease

RGH-122 (compound 43) is an orally active, potent, selective, and hV1a receptor antagonist with Ki value of 0.3 nM and IC50 of 0.9 nM. RGH-122 showes microsomal stability with CLint value of 13/28/25 μL/min/mg [1].
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Cat. No.: HY-W283930
CAS No.: 132858-26-5
YHV98-4 is a selective, blood-brain barrier-permeable Hv1 inhibitor with an IC50 of 0.7 μM. YHV98-4 reduces ROS production and restores the SHP-1-pAKT signaling pathway. YHV98-4 decreases the spread of hyperphosphorylated Tau protein. YHV98-4 alleviates inflammation and produces analgesic effects. YHV98-4 improves cognitive function in mouse models of Alzheimer's disease. YHV98-4 can be used in research related to inflammatory pain, neuropathic pain and Alzheimer's disease [1] .
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Cat. No.: HY-109024R
CAS No.: 1228088-30-9
Synonyms: RG7314 (Standard)
Balovaptan (Standard) is the analytical standard of Balovaptan (HY-109024). This product is intended for research and analytical applications. Balovaptan (RG7314) is an orally available, selective brain-penetrant vasopressin 1a (hV1a) receptor antagonist, with Kis of 1 and 39 nM for human (hV1a) and mouse (mV1a) receptors, and is used for the research of autism.
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Cat. No.: HY-RS22565
Research Areas:  

Others

Hvcn1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Hvcn1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P88397
Synonyms: CD111; CLPED1; ED4; HIgR; Hv1S; HvEC; nectin-1; OFC7; PRR; PRR1; PVRL1; PVRR; PVRR1; SK-12

Host:  

Mouse

Application:  

WB, IHC-P, ICC/IF

Reactivity:  

Human

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Cat. No.: HY-P88397A
Synonyms: CD111; CLPED1; ED4; HIgR; Hv1S; HvEC; nectin-1; OFC7; PRR; PRR1; PVRL1; PVRR; PVRR1; SK-12

Host:  

Mouse

Application:  

IHC-P, ICC/IF

Reactivity:  

Human

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Cat. No.: HY-P72932
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: CEACAM1; CD66a; Prev. BGP; Biliary Glycoprotein 1; BGP1; CEACAM1 Protein; Carcinoembryonic Antigen-Related Cell Adhesion Molecule 1 (Biliary Glycoprotein); Antigen CD66; Carcinoembryonic Antigen Related Cell Adhesion Molecule 1; BGP-1; Cell Adhesion Molec
Species:  
Human
Source:  
HEK293
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