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Cat. No. | Product Name | Target | Signaling Pathways |
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T27189 |
DL-threo dihydrosphingosine
DL-Safingol,DTD,DL threo dihydrosphingosine |
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DL-threo dihydrosphingosine is a cell-permeable inhibitor of the extracellular signal-regulated kinase (ERK) signalling cassette in mammalian cells. DL-threo dihydrosphingosine is effective against both growth factor- and G-protein-dependent activation of | |||
T83978 |
Safingol hydrochloride
SPC 100270 hydrochloride,L-threo-dihydrosphingosine hydrochloride |
PI3K; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
Safingol hydrochloride (L-threo-dihydrosphingosine hydrochloride) 是蛋白激酶 C 特异性抑制剂,通过抑制 PKC 和 PI3-激酶途径诱导实体瘤细胞自噬,诱导癌细胞死亡。Safingol hydrochloride 抑制 PKC 和 PI3k。 | |||
T39401 |
Sphinganine 1-phosphate
D-erythro-Dihydrosphingosine 1-phosphate,Sphinganine 1-phosphate |
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Sphinganine 1-phosphate, also known as D-erythro-Dihydrosphingosine 1-phosphate, is a polar sphingolipid metabolite. It plays a crucial role in regulating various cellular processes including cell migration, differentiation, survival, and complex physiological processes. | |||
T37454 |
C16 dihydro Ceramide (d18:0/16:0)
Ceramide (d18:0/16:0),Cer(d18:0/16:0),N-hexadecanoyl-D-erythro-Dihydrosphingosine,N-Palmitoyl Sphinganine |
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C16 dihydro Ceramide is a bioactive sphingolipid and precursor in the de novo synthesis of C16 ceramide (d18:0/16:0) that lacks the 4,5-trans double bond.[1] C16 dihydro Ceramide (0-46 nM) inhibits C16 ceramide-induced membrane permeabilization, measured as cytochrome C oxidation, in rat liver mitochondria in a concentration-dependent manner. It also inhibits C16 ceramide-induced channel formation in liposomes. C16 dihydro ceramide is biologically inactive as a single agent, lacking the ability ... | |||
T36833 |
A6770
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A6770 is an inhibitor of sphingosine-1-phosphate (S1P) lyase.1It induces accumulation of [3H]sphinganine-1-phosphate ([3H]dhS1P), an S1P lyase substrate, in IT-79MTNC3 cells that endogenously express high levels of S1P lyase (EC50= <0.01 μM), an effect that is reduced in the presence of vitamin B6(EC50= <100 μM). 1.Ohtoyo, M., Tamura, M., Machinaga, N., et al.Scintillation proximity assay to detect the changes in cellular dihydrosphingosine 1-phosphate levelsLipids51(10)1207-1216(2016) |
Cat. No. | Product Name | Target | Signaling Pathways |
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T22723 |
Dihydrosphingosine
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Others | Others |
Dihydrosphingosine is a Protein kinase C inhibitor. | |||
T13632 |
D-Erythro-dihydrosphingosine
Dihydrosphingosine,Octadecasphinganine,D-赤式-C 18 - 二氢-D-神经鞘氨醇,C18-Dihydrosphingosine,D-erythro-Sphinganine |
Phospholipase; Endogenous Metabolite | Metabolism |
D-Erythro-dihydrosphingosine (C18-Dihydrosphingosine) 可抑制花生四烯酸的释放和cPLA2α活性。 |