23 Results for "

H1-5

" in MedChemExpress (MCE) Product Catalog:
Products (23)

23 Results for "H1-5" in MCE Product Catalog:

14
14 Publications Verification
Cat. No.: HY-14541
CAS No.: 132539-06-1
Purity:  99.96%
Synonyms: LY170053
Olanzapine (LY170053) is a selective, orally active monoaminergic antagonist with high affinity binding to serotonin H1, 5HT2A/2C, 5HT3, 5HT6 (Ki=7, 4, 11, 57, and 5 nM, respectively), dopamine D1-4 (Ki=11 to 31 nM), muscarinic M1-5 (Ki=1.9-25 nM), and adrenergic α1 receptor (Ki=19 nM). Olanzapine is an atypical antipsychotic .
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1
1 Cited Publications
Cat. No.: HY-W016622
CAS No.: 28940-11-6
Synonyms: 7-Methyl-2H-1,5-benzodioxepin-3(4H)-one
Watermelon ketone (7-Methyl-2H-1,5-benzodioxepin-3(4H)-one) is a compound with a fresh marine scent .
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Cat. No.: HY-B2169
CAS No.: 3575-80-2
Melperone is a butyrophenone with atypical antipsychotic properties. Melperone is a multireceptor antagonist with Kds of 102 nM, 180 nM, 180 nM, and 150 nM for 5-HT2A, dopamine D2, α1-adrenergic, and α2-adrenergic receptors, respectively. Melperone has weak binding to histamine H1, 5-HT2C, 5-HT1A, 5-HT1D, and muscarinic receptors, with Kd values ​​of 580 nM, 2100 nM, 2200 nM, 3400 nM, >10000 nM, respectively. Melperone is also a CYP2D6 inhibitor. Melperone can be used for the study of schizophrenia, and agitation in the elderly .
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Cat. No.: HY-14541R
CAS No.: 132539-06-1
Synonyms: LY170053 (Standard)
Olanzapine (Standard) is the analytical standard of Olanzapine. This product is intended for research and analytical applications. Olanzapine (LY170053) is a selective, orally active monoaminergic antagonist with high affinity binding to serotonin H1, 5HT2A/2C, 5HT3, 5HT6 (Ki=7, 4, 11, 57, and 5 nM, respectively), dopamine D1-4 (Ki=11 to 31 nM), muscarinic M1-5 (Ki=1.9-25 nM), and adrenergic α1 receptor (Ki=19 nM). Olanzapine is an atypical antipsychotic .
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Cat. No.: HY-178113
CAS No.: 1537192-10-1
Target:  

15-PGDH

Research Areas:  

Inflammation/Immunology

15-PGDH-IN-4 (Compound 40) is a 15-PGDH inhibitor with an IC50 of 1.2 nM against h15-PGDH. 15-PGDH-IN-4 functionally inhibits the activity of 15-PGDH. 15-PGDH-IN-4 can be used in the research of colitis .
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Cat. No.: HY-RS05950
Research Areas:  

Others

H1-5 Human Pre-designed siRNA Set A contains three designed siRNAs for H1-5 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P991067
CAS No.: 2724922-85-2
Synonyms: KP-104

Target:  

Complement System

Research Areas:  

Inflammation/Immunology

Vensobafusp alfa (KP-104) is a fusion protein composed of an IgG4 monoclonal antibody directed against terminal complement protein C5 fused to the complement factor H 1-5 domain (FH1-5). Vensobafusp alfa shows anti-inflammatory and immunomodulatory activities. The isotype control for Vensobafusp alfa can refer to Human IgG4 (S228P) kappa, Isotype Control (HY-P99003) . .
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Cat. No.: HY-14541S
CAS No.: 786686-79-1
Purity:  99.09%
Synonyms: LY170053-d3
Olanzapine-d3 (LY170053-d3) is the deuterium labeled Olanzapine. Olanzapine is a selective, orally active monoaminergic antagonist with high affinity binding to serotonin H1, 5HT2A/2C, 5HT3, 5HT6 (Ki=7, 4, 11, 57, and 5 nM, respectively), dopamine D1-4 (Ki=11 to 31 nM), muscarinic M1-5 (Ki=1.9-25 nM), and adrenergic α1 receptors (Ki=19 nM). Olanzapine is an atypical antipsychotic .
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Cat. No.: HY-118110
CAS No.: 322666-76-2
Purity:  99.92%
Target:  

Lipoxygenase

Research Areas:  

Inflammation/Immunology

MLS000545091 is a potent and selective lipoxygenase-2 (LOX-2) inhibitor with an IC50 value of 2.6 μM for h15-LOX-2 .
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Cat. No.: HY-20007
CAS No.: 69718-72-5
Target:  

Drug Intermediate

Research Areas:  

Others

2,3,4,5-Tetrahydro-1H-1,5-methano-3-benzazepine is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-20006
CAS No.: 230615-52-8
Target:  

Drug Intermediate

Research Areas:  

Others

2,3,4,5-Tetrahydro-1H-1,5-methano-3-benzazepine hydrochlortde is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-116919
CAS No.: 511306-37-9
Target:  

Lipoxygenase

Research Areas:  

Cardiovascular Disease

MLS000536924 is a potent and selective inhibitor of human epithelial 15-lipoxygenase-2 with competitive activity. MLS000536924 exhibits more than 50-fold selectivity in inhibiting h15-LOX-2 and can be effectively applied to study its role in atherosclerosis, cystic fibrosis, and ferroptosis. The binding mode of MLS000536924 shows stronger restriction of protein movement than other inhibitors, further verifying its higher biological activity .
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Cat. No.: HY-153930
CAS No.: 478040-08-3
Target:  

Lipoxygenase

Research Areas:  

Inflammation/Immunology

h15-LOX-2 inhibitor 1 (Comp 105) is a human epithelial 15-lipoxygenase-2 (h15-LOX-2) inhibitor with IC50 of 0.34 μM .
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Cat. No.: HY-14541A
CAS No.: 783334-36-1
Synonyms: LY170053 hydrochloride
Olanzapine hydrochloride is a selective, orally active monoaminergic antagonist with high affinity binding to serotonin H1, 5HT2A/2C, 5HT3, 5HT6 (Ki=7, 4, 11, 57, and 5 nM, respectively), dopamine D1-4 (Ki=11 to 31 nM), muscarinic M1-5 (Ki=1.9-25 nM), and adrenergic α1 receptor (Ki=19 nM). Olanzapine hydrochloride is an atypical antipsychotic .
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Cat. No.: HY-103109
CAS No.: 1622-79-3
Melperone hydrochloride is a butyrophenone with atypical antipsychotic properties. Melperone hydrochloride is a multireceptor antagonist with Kds of 102 nM, 180 nM, 180 nM, and 150 nM for 5-HT2A, dopamine D2, α1-adrenergic, and α2-adrenergic receptors, respectively. Melperone hydrochloride has weak binding to histamine H1, 5-HT2C, 5-HT1A, 5-HT1D, and muscarinic receptors, with Kd values ​​of 580 nM, 2100 nM, 2200 nM, 3400 nM, >10000 nM, respectively. Melperone hydrochloride is also a CYP2D6 inhibitor. Melperone hydrochloride can be used for the study of schizophrenia, and agitation in the elderly .
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Cat. No.: HY-B2169S2
CAS No.: 1219798-80-7
Melperone-d4 hydrochloride is the deuterium labeled Melperone hydrochloride (HY-103109) . Melperone hydrochloride is a butyrophenone with atypical antipsychotic properties. Melperone hydrochloride is a multireceptor antagonist with Kds of 102 nM, 180 nM, 180 nM, and 150 nM for 5-HT2A, dopamine D2, α1-adrenergic, and α2-adrenergic receptors, respectively. Melperone hydrochloride has weak binding to histamine H1, 5-HT2C, 5-HT1A, 5-HT1D, and muscarinic receptors, with Kd values ​​of 580 nM, 2100 nM, 2200 nM, 3400 nM, >10000 nM, respectively. Melperone hydrochloride is also a CYP2D6 inhibitor. Melperone hydrochloride can be used for the study of schizophrenia, and agitation in the elderly .
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Cat. No.: HY-161908
CAS No.: 1164515-84-7
Target:  

Lipoxygenase

Research Areas:  

Inflammation/Immunology

h15-LOX-2 inhibitor 3 (Compound 13) is an inhibitor of h15-LOX, with IC50 and Ki values of 25 μM and 15.1 μM, respectively .
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Cat. No.: HY-161907
Target:  

Lipoxygenase

Research Areas:  

Inflammation/Immunology

h15-LOX-2 inhibitor 2 (Compound 10) is an inhibitor of h15-LOX, with IC50 and Ki values of 26.9 μM and 16.4 μM, respectively .
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Cat. No.: HY-116124
CAS No.: 123673-33-6
Target:  

Lipoxygenase

Research Areas:  

Others

17(S)-HpDHA is the main 15-Lipoxygenase (LOX) isoenzyme: h15-LOX-1 and h15-LOX-2 and docosahexaenoic acid (DHA). product. 17(S)-HpDHA negatively regulates epoxide synthesis via allosteric regulation. 17(S)-HpDHA also inhibits platelet aggregation with an EC50 of approximately 1 μM .
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Cat. No.: HY-W016622R
CAS No.: 28940-11-6
Synonyms: 7-Methyl-2H-1,5-benzodioxepin-3(4H)-one (Standard)
Research Areas:  

Others

Watermelon ketone (Standard) is the analytical standard of Watermelon ketone (HY-W016622). This product is intended for research and analytical applications. Watermelon ketone (7-Methyl-2H-1,5-benzodioxepin-3(4H)-one) is a compound with a fresh marine scent.
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