14 results for "Compounds for HSC Proliferation and Renewal" in 产品

Compounds for HSC Proliferation and Renewal

Hematopoietic stem cells (HSCs) reside in the bone marrow and generate two progenitor cell lineages: myeloid and lymphoid cells. The myeloid cells include erythrocytes, platelets, neutrophils, basophils, eosinophils, monocytes/ macrophages, and dendritic cells. The lymphoid cells comprise natural killer cells, B and T lymphocytes.

Figure 1: Model of the hematopoietic hierarchy. HSCs have the potential to both self-renew and differentiate. Multipotent progenitors give rise to all ...

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Potent, selective inhibitor of TGF-βRI, ALK4 and ALK7

GMP Version Available: TB1614-GMP
GMP
Chemical Name: 4-[4-(1,3-benzodioxol-5-yl)-5-(2-pyridinyl)-1H-imidazol-2-yl]benzamide
Purity: ≥99%
dopaminergic neurons derived from hiPSCs using SB 431542
(2)
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Highly selective GSK-3 inhibitor; acts as Wnt activator

GMP Version Available: TB4423-GMP
GMP
Alternate Names: CHIR99021,CT99021
Chemical Name: 6-[[2-[[4-(2,4-Dichlorophenyl)-5-(5-methyl-1H-imidazol-2-yl)-2-pyrimidinyl]amino]ethyl]amino]-3-pyridinecarbonitrile
Purity: ≥98%
Cardiomyocyte derived from human induced pluripotent stem cells (hiPSCs) using CHIR 99021.
(2)
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Promotes HSCs expansion; increases HSCs engraftment; also endogenous prostaglandin

Alternate Names: PGE2
Chemical Name: (5Z,11α,13E,15S)-11,15-Dihydroxy-9-oxo-prosta-5,13-dien-1-oic acid
Purity: ≥98%
Promotes HSCs expansion; increases HSCs engraftment; also endogenous prostaglandin
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Selective inhibitor of p38 MAPK

Alternate Names: Adezmapimod
Chemical Name: 4-[5-(4-Fluorophenyl)-2-[4-(methylsulfonyl)phenyl]-1H-imidazol-4-yl]pyridine
Purity: ≥98%
Selective inhibitor of p38 MAPK
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Glutathione (GSH) precursor; neuroprotective

Chemical Name: (2R)-2-(Acetylamino)-3-mercaptopropanamide
Glutathione (GSH) precursor; neuroprotective
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Potent GSK-3 inhibitor; also inhibits cdks

Alternate Names: 6BIO
Chemical Name: (2'Z,3'E)-6-Bromoindirubin-3'-oxime
Purity: ≥98%
Potent GSK-3 inhibitor; also inhibits cdks
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Potent aryl hydrocarbon receptor (AhR) antagonist

Chemical Name: 1-Methyl-N-[2-methyl-4-[2-(2-methylphenyl)diazenyl]phenyl-1H-pyrazole-5-carboxamide
Purity: ≥98%
Potent aryl hydrocarbon receptor (AhR) antagonist
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PARP-1 inhibitor

Chemical Name: Pyridine-3-carboxamide
Purity: ≥99%
iPSC-derived Human Intestinal Organoid
(5)
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Synthetic prostaglandin E2 (Cat. No. 2296) derivative; regulates HSC development

Chemical Name: (5Z,11α,13E,15R)-11,15-Dihydroxy-16,16-dimethyl-9-oxo-prosta-5,13-dien-1oic acid
Purity: ≥95%
Synthetic prostaglandin E2 (Cat. No. 2296) derivative; regulates HSC development
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Aryl hydrocarbon receptor (AhR) antagonist; promotes HSC expansion and engraftment

Chemical Name: 4-[2-[[2-Benzo[b]thien-3-yl-9-(1-methylethyl)-9H-purin-6-yl]amino]ethyl]phenol
Purity: ≥98%
Aryl hydrocarbon receptor (AhR) antagonist; promotes HSC expansion and engraftment
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Dipeptidyl peptidase IV (DPP-IV) inhibitor

Alternate Names: Ile-Pro-Ile
Chemical Name: L-Isoleucyl-L-prolyl-L-isoleucine
Purity: ≥98%
Dipeptidyl peptidase IV (DPP-IV) inhibitor
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BET bromodomain inhibitor; arrests cell cycle at G1 phase

Alternate Names: TEN 010
Chemical Name: (6S)-4-(4-Chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetamide
Purity: ≥98%
BET bromodomain inhibitor; arrests cell cycle at G1 phase
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Sterile-filtered 10 mM solution of CHIR 99021 pre-dissolved in DMSO

Chemical Name: 6-[[2-[[4-(2,4-Dichlorophenyl)-5-(5-methyl-1H-imidazol-2-yl)-2-pyrimidinyl]amino]ethyl]amino]-3-pyridinecarbonitrile
Purity: ≥97%
Sterile-filtered 10mM solution of CHIR 99021 pre-dissolved in water
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Potent integrin inhibitor (αvβ3/αvβ6); also improves stem cell attachment in 3D cell culture scaffolds

Purity: ≥95%
Potent integrin inhibitor (αVβ3/αVβ5); also improves stem cell attachment in 3D cell culture scaffolds
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