16 results for "Other Differentiation Compounds" in 产品

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Other Differentiation Compounds

SB 431542

Catalog #: 1614
(13)
Citations (2378)
Product Documents

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)

TPPB

Catalog #: 5343
Citations (29)
Product Documents

High affinity PKC activator; also APP modulator

Chemical Name: (2E,4E)-N-[(2S,5S)-1,2,3,4,5,6-Hexahydro-5-(hydroxymethyl)-1-methyl-2-(1-methylethyl)-3-oxo-1,4-benzodiazocin-8-yl]-5-[4-(trifluoromethyl)phenyl]-2,4-pentadienamide
Purity: ≥98%
High affinity PKC activator; also APP modulator

T3

Catalog #: 6666
Citations (6)
Product Documents

Thyroid hormone; also promotes differentiation of oligodendroglial precursor cells

Chemical Name: O-(4-Hydroxy-3-iodophenyl-3,5-diiodo-L-tyrosine
Purity: ≥98%
Thyroid hormone; also promotes differentiation of oligodendroglial precursor cells

AGN 193109

Catalog #: 5758
(1)
Citations (26)
Product Documents

High affinity pan-RAR antagonist

Chemical Name: 4-[2-[5,6-Dihydro-5,5-dimethyl-8-(4-methylphenyl)-2-naphthalenyl]ethynyl]benzoic acid
Purity: ≥98%
High affinity pan-RAR antagonist

CH 223191

Catalog #: 3858
(1)
Citations (56)
Product Documents

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

Rosiglitazone

Catalog #: 5325
(1)
Citations (55)
Product Documents

Potent and selective PPARγ agonist; antidiabetic agent

Alternate Names: BRL 49653
Chemical Name: 5-[[4-[2-(Methyl-2-pyridinylamino)ethoxy]phenyl]methyl]-2,4-thiazolidinedione
Purity: ≥98%
Potent and selective PPARγ agonist; antidiabetic agent

Clemastine fumarate

Catalog #: 1453
Citations (9)
Product Documents

H1 antagonist

Chemical Name: (2R)-2-[2-[(1R)-1-(4-Chlorophenylethoxy]ethyl]-1-methyl-2-pyrrolidine fumarate
Purity: ≥98%
H1 antagonist

Ketoconazole

Catalog #: 1103
Citations (20)
Product Documents

Cytochrome P450c17 inhibitor

Chemical Name: cis-1-Acetyl-4-[4-[[2-(2,4-dichlorophenyl)-2-(1H-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl] methoxy]phenyl]piperazine
Purity: ≥98%
Cytochrome P450c17 inhibitor

SIS3

Catalog #: 5291
Citations (35)
Product Documents

Selective Smad3 inhibitor; inhibits TGF-βR1 signaling

Chemical Name: 1,2,3,4-Tetrahydro-6,7-dimethoxy-2-[(2E)-3-(1-phenyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-1-oxo-2-propenyl]-isoquinoline hydrochloride
Purity: ≥97%
Selective Smad3 inhibitor; inhibits TGF-βR1 signaling

AS 1842856

Catalog #: 4265
Citations (6)
Product Documents

Potent and selective Foxo1 inhibitor; orally bioavailable

Chemical Name: 5-Amino-7-(cyclohexylamino)-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
Purity: ≥98%
Potent and selective Foxo1 inhibitor; orally bioavailable

FM19G11

Catalog #: 6653
(1)
Product Documents

HIF α-subunit inhibitor

Chemical Name: 2-Oxo-2-(p-tolyl)ethyl 3-(2,4-dinitrobenzamido)benzoate
Purity: ≥98%
HIF α-subunit inhibitor

NNMTi

Catalog #: 6900
Citations (2)
Product Documents

Nicotinamide N-methyltransferase (NNMT) inhibitor; promotes myoblast differentiation

Chemical Name: 5-Amino-1-methylquinolinium iodide
Purity: ≥97%
Nicotinamide N-methyltransferase (NNMT) inhibitor; promotes myoblast differentiation

Hh-Ag1.5

Catalog #: 7807
Product Documents

Potent and high affinity Smo receptor agonist

Chemical Name: 3-Chloro-4,7-difluoro-N-[trans-4-(methylamino)cyclohexyl]-N-[[3-(4-pyridinyl)phenyl]methyl]benzo[b]thiophene-2-carboxamide
Purity: ≥98%
Potent and high affinity Smo receptor agonist

N-Acetylcysteine

Catalog #: 7874
(1)
Citations (61)
Product Documents

Glutathione (GSH) precursor; maintains stem cell function in culture.

Chemical Name: (2R)-2-Acetamido-3-sulfanylpropanoic acid
Purity: ≥98%
Adult Stem Cell-derived Lung Organoids
(5)

CEPT Cocktail Kit

Catalog #: 7991
(1)
Citations (7)
Product Documents

Cell culture supplement for improving stem cell survival

cept-cocktail-product-image

HG-9-91-01

Catalog #: 8985
Product Documents

Potent pan-salt inducible kinases (SIK1, SIK2 and SIK3) inhibitor. Also inhibits Lat-B-induced EP differentiation via nuclear YAP1 accumulation.

Alternate Names: SIK inhibitor 1
Chemical Name: 1-(2,4-Dimethoxyphenyl)-3-(2,6-dimethylphenyl)-1-(6-((4-(4-methylpiperazin-1-yl)phenyl)amino)pyrimidin-4-yl)urea
Purity: ≥98%
Potent pan-salt inducible kinases (SIK1, SIK2 and SIK3) inhibitor. Also inhibits Lat-B-induced EP differentiation via nuclear YAP1 accumulation.
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