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Results for "

g 15

" in TargetMol Product Catalog

Inhibitors & Agonists
68
Peptide Products
3
Inhibitory Antibodies
3
PROTAC Products
17
Natural Products
7
Recombinant Protein
26
Isotope Products
2
Antibody Products
34
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4
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1
ADC/ADC Related
1

G15

T73891161002-05-6

G15 is a cell-permeable non-steroidal antagonist of GPER (Ki = 20 nM)

Estrogen Receptor/ERR

In Stock

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Cited

Cross-linked dextran G 15

TCL-0049111081-40-6

Cross-linked dextran G 15 is a hydrophilic gel used as a gel filtration medium (spherical protein separation range: >1500 Da; polysaccharide separation range: >1500 Da).

Inquiry Price

7-10 days

Size

QTY

KRAS G12C inhibitor 15

T117692349393-21-9

KRAS G12C inhibitor 15 is a potent inhibitor of the KRAS G12C protein.

Ras

$2,120

10-14 weeks

Size

QTY

KRAS G12D inhibitor 15

T746072763155-39-9

KRAS G12D inhibitor 15 is a potent and specific inhibitor targeting the KRAS G12D mutation, showing potential for research into various diseases and disorders, including cancer and its metastases [1].

Kras Others Ras

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Anti-Mouse TL1A/TNFSF15 Antibody (5G4.6)

T9901A-549

Anti-Mouse TL1A/TNFSF15 Antibody (5G4.6) is an IgG antibody inhibitor derived from the American hamster, specifically targeting the mouse TL1A/TNFSF15.

TNF

$182

2-4 weeks

Size

QTY

Cross-linked dextran G 150

TCL-0041412774-36-6

Cross-linked dextran G 150 is a hydrophilic gel used as a gel filtration medium, with a particle size range of 40-120 μm and suitable for separating spherical proteins within a molecular weight range of 5k-300k Da.

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Tezepelumab

Tezepelumab-ekko, MEDI 19929, AMG 157

T773591572943-04-4

Tezepelumab (AMG 157) is a humanized monoclonal antibody (IgG2λ) targeting TSLP that prevents TSLP from interacting with its heterodimer receptor. Tezepelumab can be used to study advanced asthma disease.

Others

$1,060

In Stock

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Medifoxamine

Medifoxamina, LG-152, LG152, LG 152

T2444432359-34-5In house

Medifoxamine (LG 152) is a selective non-monoamine oxidase inhibitor that exhibits antidepressant activity through inhibition of 5 HT reuptake.Medifoxamine preferentially inhibits dopamine reuptake.

Dopamine Receptor Monoamine Oxidase

$100

In Stock

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Sembragiline

RO-4602522, RO4602522, RG-1577, RG1577, EVT-302, EVT302

T28750676479-06-4In house

Sembragiline (EVT-302) is a selective MAO-B inhibitor for the study of Alzheimer's disease (AD).

MAO Monoamine Oxidase Reactive Oxygen Species ROS

$998

In Stock

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QTY

ARRY-403

ARRY-403, ARRY403, ARRY 403, AMG-151, AMG151, AMG 151

T301421138669-65-4In house

ARRY-403 is a novel glucokinase activator that reduces fasting and postprandial blood glucose in patients with type 2 diabetes.

Endogenous Metabolite Glucokinase

$415

In Stock

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G150

T113442369751-30-2

G150 inhibited interferon expression triggered by DSDNA with IC50 of 10.2 nM.G150 is an effective and highly selective inhibitor of human cyclic GMP-AMP synthase (H-CGAS).

cGAS DNA

$128

In Stock

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HO-PEG15-OH

T1549028821-35-4

HO-PEG15-OH, a PEG-based linker for PROTACs, crucially joins two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation through the ubiquitin-proteasome system within cells.

Others PROTAC Linker

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Amino-PEG15-amine

H2N-PEG15-CH2CH2NH2

T17414

Amino-PEG15-amine is a PEG-based linker for PROTACs, joining two essential ligands necessary for forming PROTAC molecules and enabling selective protein degradation through the ubiquitin-proteasome system within cells.

Others PROTAC Linker

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Azido-PEG15-azide

T17487

Azido-PEG15-azide is a PEG-based linker for PROTACs, joining two essential ligands crucial for forming PROTAC molecules, thereby enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Others PROTAC Linker

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Azido-PEG15-t-butyl ester

T17488

Azido-PEG15-t-butyl ester is a polyethylene glycol (PEG) derived linker, specifically designed for the synthesis of proteolysis-targeting chimeras (PROTACs) [1].

Others PROTAC Linker

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PD153035 hydrochloride

ZM 252868 HCl, Tyrphostin AG 1517, SU-5271 Hcl, PD153035 HCl, AG 1517 Hcl

T1761183322-45-4

PD153035 hydrochloride (ZM 252868) is a effective and selective inhibitor of EGFR (Ki: 5.2 pM, IC50: 29 pM); few influence against FGFR, PGDFR, InsR, CSF-1, and Src.

EGFR

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Bis-PEG15-acid

T17620

Bis-PEG15-acid, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Others PROTAC Linker

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Boc-NH-PEG15-azide

T17670

Boc-NH-PEG15-azide, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation via the ubiquitin-proteasome system within cells.

Others PROTAC Linker

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Boc-NH-PEG15-NH2

T176712222566-55-2

Boc-NH-PEG15-NH2 is a PEG-based linker for PROTACs that joins two essential ligands, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.

Others PROTAC Linker

5 days

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Cbz-N-PEG15-amine

T17715

Cbz-N-PEG15-amine is a PEG-based linker for PROTACs that integrates two essential ligands, crucial for forming PROTAC molecules, enabling selective protein degradation via the ubiquitin-proteasome system within cells.

Others PROTAC Linker

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Fmoc-NH-PEG15-CH2CH2COOH

T179682378590-46-4

Fmoc-NH-PEG15-CH2CH2COOH is a PEG-based PROTAC linker used for PROTAC synthesis [1].

Others PROTAC Linker

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m-PEG15-alcohol

T181492258654-78-1

m-PEG15-alcohol is a PEG-based linker for PROTACs, joining two essential ligands [crucial for forming PROTAC molecules], and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Others PROTAC Linker

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m-PEG15-NHS ester

T18150

m-PEG15-NHS ester is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules, and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Others PROTAC Linker

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AG1557

AG-1557, AG 1557

T2034189290-58-2

AG1557 (AG-1557) is an inhibitor of the epidermal growth factor receptor (EGFR) tyrosine kinase (pIC50: 8.194).

EGFR Potassium Channel

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