Qvd Apexbio

LH 21

C3642-5 5 mg
EUR 345
Description: IC50: 631 ±98 and 690 ± 41 nM for human and rat CB1 receptors, respectivelyLH 21 is a CB1 antagonist. The endogenous cannabinoid system plays a critical modulatory role in feeding behavior and metabolism, acting at both peripheral and central levels.

Apexbio Reagents Laboratories manufactures the qvd apexbio reagents distributed by Genprice. The Qvd Apexbio reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact Apexbio Reagents. Other Qvd products are available in stock. Specificity: Qvd Category: Apexbio

ML-211

10 mg
EUR 270
Description: IC50: LYPLA1 (17 nM) and the related LYPLA2 (30 nM)ML-211 is a dual inhibitor of LYPLA1 and the related LYPLA2.Lysophospholipase 1 (LYPLA1), a protein palmitoyl thioesterase, is responsible for depalmitoylation of the oncogene HRas.

ML-211

25 mg
EUR 519
Description: IC50: LYPLA1 (17 nM) and the related LYPLA2 (30 nM)ML-211 is a dual inhibitor of LYPLA1 and the related LYPLA2.Lysophospholipase 1 (LYPLA1), a protein palmitoyl thioesterase, is responsible for depalmitoylation of the oncogene HRas.

ML-211

5 mg
EUR 174
Description: IC50: LYPLA1 (17 nM) and the related LYPLA2 (30 nM)ML-211 is a dual inhibitor of LYPLA1 and the related LYPLA2.Lysophospholipase 1 (LYPLA1), a protein palmitoyl thioesterase, is responsible for depalmitoylation of the oncogene HRas.

Stachydrine (hydrochloride)

100 mg
EUR 119
Description: Stachydrine is an anti-metastatic agent.Stachydrine, a pyrrolidine betaine, was first isolated from seed husk and the pulp of the fruit of C. Leonurus, and many other Asian plants and fruits.

Stachydrine (hydrochloride)

1 g
EUR 467
Description: Stachydrine is an anti-metastatic agent.Stachydrine, a pyrrolidine betaine, was first isolated from seed husk and the pulp of the fruit of C. Leonurus, and many other Asian plants and fruits.

Stachydrine (hydrochloride)

250 mg
EUR 206
Description: Stachydrine is an anti-metastatic agent.Stachydrine, a pyrrolidine betaine, was first isolated from seed husk and the pulp of the fruit of C. Leonurus, and many other Asian plants and fruits.

Stachydrine (hydrochloride)

500 mg
EUR 328
Description: Stachydrine is an anti-metastatic agent.Stachydrine, a pyrrolidine betaine, was first isolated from seed husk and the pulp of the fruit of C. Leonurus, and many other Asian plants and fruits.

Human Samples information

Stachydrine (hydrochloride)

C3648-100 100 mg
EUR 119
Description: Stachydrine is an anti-metastatic agent.Stachydrine, a pyrrolidine betaine, was first isolated from seed husk and the pulp of the fruit of C. Leonurus, and many other Asian plants and fruits.

Stachydrine (hydrochloride)

C3648-1000 1 g
EUR 467
Description: Stachydrine is an anti-metastatic agent.Stachydrine, a pyrrolidine betaine, was first isolated from seed husk and the pulp of the fruit of C. Leonurus, and many other Asian plants and fruits.

Stachydrine (hydrochloride)

C3648-250 250 mg
EUR 206
Description: Stachydrine is an anti-metastatic agent.Stachydrine, a pyrrolidine betaine, was first isolated from seed husk and the pulp of the fruit of C. Leonurus, and many other Asian plants and fruits.

Stachydrine (hydrochloride)

C3648-500 500 mg
EUR 328
Description: Stachydrine is an anti-metastatic agent.Stachydrine, a pyrrolidine betaine, was first isolated from seed husk and the pulp of the fruit of C. Leonurus, and many other Asian plants and fruits.

Ceranib-2

C3649-10 10 mg
EUR 179
Description: IC50: 28 ?MCeranib-2 is an inhibitor of cellular ceramidase activity.Ceramidase catalyzes the hydrolysis of the N-acyl linkage between the fatty acid and sphingosine base in ceramide to produce sphingosine and a free fatty acid.

Ceranib-2

C3649-25 25 mg
EUR 357
Description: IC50: 28 ?MCeranib-2 is an inhibitor of cellular ceramidase activity.Ceramidase catalyzes the hydrolysis of the N-acyl linkage between the fatty acid and sphingosine base in ceramide to produce sphingosine and a free fatty acid.

Ceranib-2

C3649-5 5 mg
EUR 118
Description: IC50: 28 ?MCeranib-2 is an inhibitor of cellular ceramidase activity.Ceramidase catalyzes the hydrolysis of the N-acyl linkage between the fatty acid and sphingosine base in ceramide to produce sphingosine and a free fatty acid.

Ceranib-2

C3649-50 50 mg
EUR 595
Description: IC50: 28 ?MCeranib-2 is an inhibitor of cellular ceramidase activity.Ceramidase catalyzes the hydrolysis of the N-acyl linkage between the fatty acid and sphingosine base in ceramide to produce sphingosine and a free fatty acid.

ALK5 Inhibitor II (hydrochloride)

C3656-10 10 mg
EUR 176
Description: IC50: 4, 18, and 23 nM for ALK5 autophosphorylation, TGF-? cellular assay, and ALK5 binding in HepG2 cells, respectivelyALK5 Inhibitor II is an ALK5 inhibitor.The TGF-beta family of cytokines signal via serine/threonine kinase transmembrane type I and type II receptors.

ALK5 Inhibitor II (hydrochloride)

C3656-25 25 mg
EUR 321
Description: IC50: 4, 18, and 23 nM for ALK5 autophosphorylation, TGF-? cellular assay, and ALK5 binding in HepG2 cells, respectivelyALK5 Inhibitor II is an ALK5 inhibitor.The TGF-beta family of cytokines signal via serine/threonine kinase transmembrane type I and type II receptors.

ALK5 Inhibitor II (hydrochloride)

C3656-5 5 mg
EUR 122
Description: IC50: 4, 18, and 23 nM for ALK5 autophosphorylation, TGF-? cellular assay, and ALK5 binding in HepG2 cells, respectivelyALK5 Inhibitor II is an ALK5 inhibitor.The TGF-beta family of cytokines signal via serine/threonine kinase transmembrane type I and type II receptors.

WWL123

C3661-10 10 mg
EUR 316
Description: IC50: 0.43 ?MWWL123 is a brain-penetrant inhibitor of ABHD6.

WWL123

C3661-25 25 mg
EUR 634
Description: IC50: 0.43 ?MWWL123 is a brain-penetrant inhibitor of ABHD6.

WWL123

C3661-5 5 mg
EUR 200
Description: IC50: 0.43 ?MWWL123 is a brain-penetrant inhibitor of ABHD6.

GSK6853

C3668-10 10 mg
EUR 290
Description: pIC50: 8.1GSK6853 is a BRPF1 inhibitor.The BRPF (Bromodomain and PHD Fingercontaining) protein family are key scaffolding proteins for assembly of MYST histone acetyltransferase complexes.

GSK6853

C3668-100 100 mg
EUR 1091
Description: pIC50: 8.1GSK6853 is a BRPF1 inhibitor.The BRPF (Bromodomain and PHD Fingercontaining) protein family are key scaffolding proteins for assembly of MYST histone acetyltransferase complexes.

GSK6853

C3668-5 5 mg
EUR 186
Description: pIC50: 8.1GSK6853 is a BRPF1 inhibitor.The BRPF (Bromodomain and PHD Fingercontaining) protein family are key scaffolding proteins for assembly of MYST histone acetyltransferase complexes.