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Results for "

16:0 dgs

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    111
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16:0 DGS
16:0 DGS, 1,2-Dipalmitoyl-sn-glycero-3-succinate
T205587108032-13-9
16:0 DGS (1,2-Dipalmitoyl-sn-glycero-3-succinate) can be used in the preparation of pH-sensitive liposomes.
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c16 ceramide
Palmitoyl Ceramide, N-Palmitoylsphingosine, N-acylsphingosine, C16 Ceramide (d18:1 16:0)
T3756224696-26-2
C16 Ceramide (Palmitoyl Ceramide) is a naturally occurring small molecule that activates p53 by directly and selectively binding to it.
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TargetMol | Inhibitor Hot
Antennapedia Peptide TFA
Antennapedia Peptide(TFA), Antennapedia Peptide TFA(188842-14-0 free base)
TP1318
Antennapedia Peptide TFA (188842-14-0 free base), a peptide of 16 amino acids, is a member of the family of Cell-penetrating peptides, originally derived from the 60 amino acid long homeodomain of the Drosophila transcription factor Antennapedia.
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Cardiolipin (16:0/18:1/16:0/18:1) sodium
16:0-18:1 Cardiolipin sodium
T2032642260669-35-8
Cardiolipin (16:0 18:1 16:0 18:1) (16:0-18:1 Cardiolipin) sodium is an anionic phospholipid composed of long-chain fatty acid palmitic acid and monounsaturated fatty acid oleic acid. This compound can be utilized in the synthesis of nanodisk lipid bilayers for in situ mass spectrometry applications.
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Hexadecenyl-2-hydroxy-sn-glycero-3-PC
Lysophosphatidylcholine 16:0p 0:0, C16(Plasm) LPC
T20359597802-53-4
Hexadecenyl-2-hydroxy-sn-glycero-3-PC (C16(Plasm) LPC) is a phosphatidylcholine. It can extend the lag phase of α-synuclein aggregation, making it valuable for Parkinson's disease research.
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16:0 Phosphatidylpropanol
16:0 Phosphatidylpropanol, 1,2-Dipalmitoyl-sn-glycero-3-phosphopropanol sodium
T20513292609-91-1
16:0 Phosphatidylpropanol (1,2-Dipalmitoyl-sn-glycero-3-phosphopropanol) sodium is a phosphatidyl alcohol featuring a propanol head group.
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DPCB
DPCB, 16:0 CB
T2052381394812-57-7
DPCB (16:0 CB) is a zwitterionic lipidoid capable of forming lipid membranes.
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Urotensin-II receptor antagonist-1
T2053471034708-07-0
Urotensin-II receptor antagonist-1 (compound 1) is a human Urotensin II receptor antagonist with low oral bioavailability (F=0-3% in rats) and a Ki of 16 nM in HEK293 cells expressing human recombinant UT receptors. It inhibits cytochrome P450 enzymes (IC50=0.75 μM for CYP2D6; 1.4 μM for CYP3A4), suppresses κ opioid receptors (EC50=3.2 μM), and targets cardiac sodium channels (Ki=2.5 μM).
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10-14 weeks
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16:0 Phosphatidylmethanol sodium
16:0 Phosphatidylmethanol sodium, 1,2-Dipalmitoyl-sn-glycero-3-phosphomethanol sodium
T20534892609-89-7
16:0 Phosphatidylmethanol (1,2-Dipalmitoyl-sn-glycero-3-phosphomethanol) sodium is a phospholipid alcohol featuring a methanol head group.
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16:0 Cyclic LPA ammonium
1-Palmitoyl-sn-glycero-2,3-cyclic-phosphate ammonium, 16:0 Cyclic LPA ammonium
T205552799268-71-6
16:0 Cyclic LPA (1-Palmitoyl-sn-glycero-2,3-cyclic-phosphate) ammonium is a type of palmitoyl cyclic lysophosphatidic acid.
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C16 Lactosylceramide (d18:1/16:0)
T358044201-62-1
C16 Lactosylceramide is an endogenous bioactive sphingolipid. It forms membrane microdomains with Lyn kinase and the αi subunits of inhibitory G protein-coupled receptors (GPCRs), suggesting a role in cell signaling. Plasma levels of C16 lactosylceramide are elevated in insulin-resistant cattle. C16 Lactosylceramide is also upregulated in a mouse model of Niemann-Pick type C1 disease, a neurodegenerative cholesterol-sphingolipid lysosomal storage disorder.
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C16 Sphingomyelin (d18:1/16:0)
Sphingomyelin 16:0, N-Palmitoyl-D-sphingomyelin
T358056254-89-3
C16 Sphingomyelin (d18:1 16:0) (N-Palmitoyl-D-sphingomyelin) is a phospholipid analog of phospholipid bilayer membranes, which can be used to study biofilm activity.
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13C C16 Sphingomyelin (d18:1/16:0)
T36149144236-99-7
13C C16 Sphingomyelin is an isotopically enriched form of C16 sphingomyelin with carbon-13 occurring on the fatty acid portion. It is intended for use as an internal standard for the quantification of C16 sphingomyelin by GC- or LC-MS. C16 Sphingomyelin is a form of sphingomyelin containing palmitate (16:0) at the variable acylation position. It is the most common form of sphingomyelin found in eggs and is less abundant in the brain and in milk. C16 Sphingomyelin interacts with cholesterol in ordered lipid domains (lipid rafts). Sphingomyelinases remove phosphorylcholine from C16 sphingomyelin to produce C16 ceramide. While ceramides commonly induce apoptosis, ceramides with different fatty acid chain lengths might direct distinct functions and, in some cases, reduce apoptosis.
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DL-erythro/threo Sphinganine (d16:0)
DL-erythro threo Sphinganine (d16:0)
T3661350731-08-3
DL-erythro/threo Sphinganine (d16:0) is a sphingolipid that is decreased in rats following long-term, low-dose administration of dimethoate and is used as a biomarker for dimethoate exposure. It has been found in the fermentation broth of Bacterium SRCnm, which has antimicrobial and antioxidant activities. This product is a mixture of sphinganine (d16:0), L-erythro sphinganine (d16:0), D-threo sphinganine (d16:0), and L-threo sphinganine (d16:0).
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C16 Globotriaosylceramide (d18:1/16:0)
C16 Globotriaosylceramide (d18:1 16:0)
T36859137896-85-6
C16 globotriaosylceramide is an endogenous sphingolipid found in mammalian cell membranes that is synthesized from C16 lactosylceramide . C16 globotriaosylceramide acts as a receptor for Shiga toxin in B cell-derived Raji cells and THP-1 monocytes. It accumulates in endothelial cells, pericytes, vascular smooth muscle cells, renal epithelial cells, dorsal ganglia neuronal cells, and myocardial cells in patients with Fabry disease. C16 globotriaosylceramide is also upregulated in plasma of patients with ovarian carcinoma compared to those with benign ovarian tumors or uterine fibroids.
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C16 dihydro Ceramide (d18:0/16:0)
N-Palmitoyl Sphinganine, N-hexadecanoyl-D-erythro-Dihydrosphingosine, Ceramide (d18:0 16:0), Cer(d18:0 16:0), C16 dihydroceramide
T374545966-29-0
C16 dihydro Ceramide (d18:0 16:0) (Cer(d18:0 16:0)) is a precursor for the synthesis of ceramides, induces autophagy in the perinuclear region, and can be used to study cell membrane stability and neurological diseases.
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7-10 days
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3-hydroxy Palmitic Acid
T376792398-34-7
3-hydroxy Palmitic acid is a form of the 16:0 lipid palmitic acid . The lipid A part of lipopolysaccharides contain various 3-hydroxy fatty acids, making oxylipins such as 3-hydroxy palmitic acid useful as chemical markers of endotoxins. In R. solanacearum, 3-hydroxy palmitic acid is converted by an S-adenosyl methionine-dependent methyltransferase to 3-hydroxy palmitic acid methyl ester, which acts as a quorum sensing signal molecule for post-transcriptional modulation of genes involved in virulence. Long-chain 3-hydroxy fatty acids, such as 3-hydroxy palmitic acid, are also known to accumulate during long-chain 3-hydroxy-acyl-CoA dehydrogenase and mitochondrial trifunctional protein deficiencies. Such accumulation induces oxidative stress, leading to mitochondrial bioenergetics deregulation and eventual multi-organ dysfunction.
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C16 Galactosylceramide (d18:1/16:0)
C16 Galactosylceramide (d18:1 16:0)
T37872
C16 Galactosylceramide is a glycosphingolipid that contains a galactose moiety attached to a ceramide acylated with palmitic acid .
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C16 3'-sulfo Galactosylceramide (d18:1/16:0)
C16 3'-sulfo Galactosylceramide (d18:1 16:0)
T3817989771-78-8
C16 3'-sulfo Galactosylceramide (d18:1 16:0) is a sulfated glycolipid.C16 3'-sulfo Galactosylceramide (d18:1 16:0) is a relatively abundant sulfide found in porcine brain and plasma that decreases throughout development in mice.C16 3'-sulfo Galactosylceramide is a relatively abundant sulfide found in porcine brain and plasma that decreases throughout development in mice.C16 3'-sulfo Galactosylceramide is a relatively abundant sulfide found in porcine brain and plasma that decreases throughout development in mice. C16 3'-sulfo Galactosylceramide (d18:1 16:0) inhibits retinal ganglion cell growth in vitro.C16 3'-sulfo Galactosylceramide (d18:1 16:0) has been used as an internal standard for quantifying C16 3'-sulfo Galactosylceramide (d18:1 16:0) in rat cerebellum and white matter isolated from patients with multiple sclerosis. reference for sulphides.
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C16 Phytoceramide (t18:0/16:0)
T38180111149-09-8
C16 Phytoceramide (t18:0/16:0) is a phytoceramide, which is a family of sphingolipids found in the intestine, kidney, and extracellular spaces of the stratum corneum of the mammalian epidermis. C16 Phytoceramide (t18:0/16:0) is composed of a phytosphingosine backbone amine-linked to a C16 fatty acid chain. The levels of C16 phytoceramide (t18:0/16:0) increase following heat stress in S. cerevisiae. It has been used with other ceramides to create stratum corneum substitutes to study percutaneous penetration and psoriasis in vitro.
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N6-Benzyladenosine
T653464294-16-0
(2R,3R,4S,5R)-2-(6-(Benzylamino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol is a natural product for research related to life sciences. The catalog number is T65346 and the CAS number is 4294-16-0.
    7-10 days
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    16:0 TAP
    T74290139984-36-4
    16:0 TAP, a lipid compound, is utilized in the preparation of giant unilamellar vesicles for agent delivery [1].
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    16:0 EPC chloride
    T74315328250-18-6
    16:0 EPC chloride, a saturated cationic lipid and a P-O-ethyl derivative, functions as a DNA and RNA transfecting agent. It is also utilized as a co-adjuvant in vaccine preparation and to enhance drug delivery [1].
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    16:0-18:1 EPC chloride
    T74321328250-19-7
    16:0-18:1 EPC chloride, a cationic lipid, is utilized in the formation of liposomes for drug delivery applications [1].
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