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66

抑制剂 & 化合物

12

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
TP1483L	Abl Cytosolic Substrate acetate Abl Cytosolic Substrate acetate(168202-46-8 free base)	Others	Others
	Abl Cytosolic Substrate acetate(168202-46-8 free base) 是 Abelson 酪氨酸激酶 (Abl) 的底物。
TP1483	Abl Cytosolic Substrate
	Abl Cytosolic Substrate is a substrate for Abelson tyrosine kinase (Abl ).
T22043	BCATc Inhibitor 2	Others	Others
	BCATc Inhibitor 2 是选择性分支链氨基转移酶抑制剂，可用于神经退行性疾病的研究。能够抑制 rBCATc (IC50:0.2 μM)，hBCATc (IC50:0.8 μM)、 rBCATm (IC50:3.0 μM)。其中BCATc 也称为 BCAT1，存在于细胞质基质中的亚型。
T6500	Ferrostatin-1 Ferrostatin 1,Ferrostatin-1 (Fer-1)	Ferroptosis; Antifungal	Apoptosis; Microbiology/Virology
	Ferrostatin-1 (Fer-1) 是一种铁死亡抑制剂，具有强效性和选择性。Ferrostatin-1 有效抑制 Erastin 诱导的 HT-1080 细胞铁死亡 (EC50=60 nM)。Ferrostatin-1 还具抗氧化和抗真菌活性。
T8356	FPL 62064	Lipoxygenase; COX	Immunology/Inflammation; Metabolism; Neuroscience
	FPL 62064 是 5-脂氧合酶和COX 双重抑制剂，具有抗炎活性，对 RBL-1 胞质 5-脂氧合酶和前列腺素合成酶 (环氧化酶) 的IC50值分别为 3.5 和 3.1 μM。
TQ0105	CAY10650	Phospholipase	Metabolism
	CAY10650 是高效的胞浆磷脂酶A2α抑制剂，IC50=12 nM，能够抑制脂滴形成和 PGE2 分泌。
T0380	Bicalutamide 比卡鲁胺,ICI-176334	Androgen Receptor; Autophagy	Autophagy; Endocrinology/Hormones
	Bicalutamide (ICI-176334) 是一种具有口服活性的非甾体雄激素受体拮抗剂，可研究前列腺癌。
T5481	TRi-1	Others	Others
	TRi-1 是不可逆的胞质硫氧还蛋白还原酶1 的特异性抑制剂(IC50:12 nM)。它有抗肿瘤作用，且线粒体毒性很小。
TP1545L1	FFAGLDD amine salt	Others	Others
	FFAGLDD amine salt 是MMP9选择性裂解肽，用于多柔比星（DOX）的胞浆递送，实现时间和空间可控的缓慢药物递送和释放。
T11149	Ecopladib PLA 725	Phospholipase	Metabolism
	Ecopladib (PLA 725) 是一种胞浆磷脂酶 A2α (phospholipase A2α) 抑制剂，在 GLU micelle 和大鼠全血细胞中，IC50 值分别为 0.15 μM 和 0.11 μM。
T13613	ChX710	STING	Immunology/Inflammation
	ChX710可以引发 I 型干扰素对细胞溶质 DNA 的反应，其特异性细胞干扰素刺激基因 (ISG) 诱导 ISRE 启动子序列和干扰素调节因子 (IRF) 3 的磷酸化。
T10927	Cyt-PTPε Inhibitor-1 Cyt-PTP\|A Inhibitor-1	Phosphatase; Src	Angiogenesis; Metabolism; Tyrosine Kinase/Adaptors
	Cyt-PTPε Inhibitor-1 (A Inhibitor-1) 是胞质蛋白酪氨酸磷酸酶 ε 的抑制剂。 Cyt-PTPε Inhibitor-1 阻断 c-Src 的去磷酸化并表现出抗破骨活性。
T13072	Taltirelin acetate TA-0910 acetate	Thyroid hormone receptor(THR)	Endocrinology/Hormones
	Taltirelin acetate (TA-0910 acetate) 是促甲状腺激素释放激素受体(TRH-R)超激动剂(IC50:910 nM)，能够刺激细胞溶质Ca2+浓度增加 (Ca2+释放) ，其EC50值为 36 nM。
T77616	VU533 Nape-Pld activator	Phospholipase	Metabolism
	VU533 (Nape-Pld activator) 是一种NAPE-PLD 激活剂，其 EC50 值为0.30 µM。VU533 可以提高 NAPE-PLD 活性，增加巨噬细胞的胞葬作用。VU533 可用于与心脏代谢相关的疾病。
T6040	Aloxistatin E64d,Loxistatin,阿洛司他丁,E64c ethyl ester	SARS-CoV; Cysteine Protease	Microbiology/Virology; Proteases/Proteasome
	Aloxistatin (E64d) 是一种不可逆的、可透过膜的溶酶体和细胞溶质半胱氨酸蛋白酶抑制剂，能够抑制完整血小板中的钙蛋白酶活性。它是一种半胱氨酸蛋白酶抑制剂，具有血小板聚集抑制活性。
T61338	MS023 dihydrochloride MS023 2HCl	Histone Methyltransferase	Chromatin/Epigenetic
	MS023 dihydrochloride (MS023 2HCl) 是一种具有选择性、细胞活性和高效性的人I 型蛋白精氨酸甲基转移酶 (PRMTs)抑制剂，具有抗肿瘤活性，抑制 PRMT1，PRMT3，PRMT4，PRMT6和PRMT8，增加离体培养的 MuSC 的增殖能力，可用于研究乳腺癌。
T35868	BCAT-IN-2	Others	Others
	BCAT-IN-2 是一种具有口服活性和选择性的线粒体支链氨基转移酶（BCATm）抑制剂，抑制 BCATm 和 BCATc，可用于肥胖症和血脂异常。
T24089	GK470 GK 470,GK-470
	GK470 is a group IVA cytosolic phospholipase A2 inhibitor.
T25546	Isoproterenol tartrate, (-)- L-Isoproterenol D-bitartrate,Isoproterenol D-bitartrate, L-,Isolevin
	Isoproterenol tartrate, (-)- is a beta-Adrenoceptor agonist agent that increases cytosolic cAMP.
T26693	AVX-001 FP-025,AKH-217,AKH217,AVX001,FP025
	AVX-001, a cytosolic phospholipase A2 (cPLA2) inhibitor, is used potentially for the treatment of psoriasis.
T13606	cGAMP 3',3'-cGAMP,Cyclic GMP-AMP	Others	Others
	cGAMP is an endogenous second messenger in metazoans and triggers interferon production in response to cytosolic DNA. It also is a STING ligand.
T69046	AK-106
	AK-106, also known as AK106-001616, is a selective inhibitor of cytosolic phospholipase A2 (cPLA2) inhibitor. AK-106 has been shown to have analgesic activites similar to non-steroidal anti-inflammatory drugs (NSAIDs).
T82922	BAPTA-TMFM
	BAPTA-TMFM为研究胞质游离钙行为专用的荧光螯合指示剂。
T26523	Abroquinone A
	Abroquinone A, a natural isoflavanquinone, has been shown to block cytosolic phospholipase A(2) and 5-lipoxygenase activation in neutrophils, it may have pharmaceutical potential as an antiallergic agent.
T37502	sn-Glycerol 3-phosphate lithium
	sn-Glycerol 3-phosphate lithium is synthesized via the cytosolic glycerol 3-phosphate dehydrogenase pathway. This process involves the conversion of dihydroxyacetone phosphate to sn-Glycerol 3-phosphate using NADH, which is generated during glycolysis.
T61650	CXCR4 antagonist 9
	CXCR4 antagonist 9 (Compound 2) is a potent CXCR4 antagonist displaying an IC50 of 15 nM. It effectively inhibits the cytosolic calcium increase induced by CXCL12, with an IC50 value of 1.3 nM [1].
T35640	trans-carboxy Glimepiride
	trans-carboxy Glimepiride is a metabolite of the sulfonylurea glimepiride .1It is formed from glimepiride in a two-step process mediated by the cytochrome P450 (CYP) isoform CYP2C9 and cytosolic enzymes. 1.Noh, K., Kim, E., Jeong, T.C., et al.Simultaneous determination of glimepiride and its metabolites in human plasma by liquid chromatography coupled to a tandem mass spectrometryArch. Pharm. Res.34(12)2073-2078(2011)
T71913	Bourgeonal
	Bourgeonal is an agonist of human testicular olfactory receptor hOR17-4. It increases cytosolic calcium levels in human spermatozoa, acts as a chemoattractant, and increases swimming speed in sperm chemotaxis assays in a concentration-dependent manner.
T81894	Lys-Phe-Glu-Arg-Gln
	Lys-Phe-Glu-Arg-Gln 促进无血清培养条件下人二倍体成纤维细胞胞浆蛋白的降解作用。
T37556	CAY10502
	Phospholipase A2 (PLA2) catalyzes the hydrolysis of phospholipids at the sn-2 position leading to the production of lysophospholipids and free fatty acids. Calcium-dependent cytosolic PLA2 (cPLA2α) is a 85 kDa enzyme that plays a key role in the arachidonic cascade and the inflammatory response associated with this metabolic pathway. CAY10502 is a potent inhibitor of calcium-dependent cytosolic PLA2α (cPLA2α) with an IC50 value of 4.3 nM for the purified enzyme from human platelets. It inhibits ...
T40566	2′-O-(2-Methoxyethyl)guanosine 2′-O-(2-Methoxyethyl)guanosine,2'-O-MOE-rG
	2′-O-(2-Methoxyethyl)guanosine (2'-O-MOE-rG), a modified nucleoside, can be enzymatically converted from 2′-O-(2-methoxyethyl)-2,6-diaminopurine riboside by adenosine deaminase. However, this compound is not readily phosphorylated by cytosolic nucleoside kinases, and it cannot be incorporated into cellular DNA or RNA.
T7590	Taltirelin TA-0910,他替瑞林	Thyroid hormone receptor(THR)	Endocrinology/Hormones
	Taltirelin (TA-0910) 是促甲状腺激素释放激素受体(TRH-R)超激动剂(IC50:910 nM)，能够刺激细胞溶质 Ca2+浓度增加 (Ca2+释放) (EC50:36 nM)。
TP1545	FFAGLDD	Others	Others
	FFAGLDD 是 MMP9 选择性切割肽，用于多柔比星 (DOX) 的胞浆递送，实现时间和空间控制的缓慢药物递送和释放。
T61363	CXCR4 antagonist 8
	CXCR4 antagonist 8 (Compound 3) is a potent inhibitor of CXCR4. It demonstrates an IC50 value of 57 nM in CXCR4 antagonism. In addition, it effectively inhibits the increase in cytosolic calcium induced by CXCL12 with an IC50 value of 0.24 nM. Furthermore, Compound 3 shows efficacy in the inhibition of CXCL12/CXCR4-mediated cell migration [1].
T61447	CXCR2 antagonist 4
	CXCR2 antagonist 4 (compound 7) is a highly potent antagonist that inhibits CXCR2 with an IC50 value of 0.13 μM. It also effectively inhibits the cytosolic calcium increase induced by CXCL8, with an IC50 value of 27 μM. CXCR2 antagonist 4 shows promising potential for anticancer research [1].
T37842	ASB 14780
	Potent and selective cytosolic phospholipase A2 alpha (cPLA2α) inhibitor (IC50 = 20 nM). Selective for cPLA2α over secreted PLA2α (sPLA2α; exhibits no inhibition at 10 μM). Inhibits cPLA2α-dependent inflammatory responses in vitro in guinea pig and human whole-blood assays. Improves diet-induced liver injury and CCl4-induced hepatic fibrosis in vivo. Orally bioavailable.
T40750	12,14-Dichlorodehydroabietic acid
	12,14-Dichlorodehydroabietic acid, a chlorinated resin acid, exhibits potent calcium-activated potassium (BK) channel opening activity. It effectively inhibits GABA-dependent chloride influx in the mammalian brain, functioning as a non-competitive antagonist of GABA A receptors. Moreover, 12,14-Dichlorodehydroabietic acid induces an elevation in cytosolic free calcium levels and promotes the release of neurotransmitters.
TP1296	Foxy-5 TFA(881188-51-8 free base) Foxy-5 (TFA)
	Foxy-5 is a peptide that mimics the WNT5A protein and is expected to reduce the mobility of the cancer cells. Foxy-5 triggers cytosolic free calcium signaling without affecting β-catenin activation and it impairs the migration and invasion of epithelial c
T37652	5(S),6(R)-DiHETE
	5(S),6(R)-DiHETE is a dihydroxy polyunsaturated fatty acid and a nonenzymatic hydrolysis product of leukotriene A4 (LTA4). Mouse liver cytosolic epoxide hydrolase catalyzes the conversion of LTA4 to 5(S),6(R)-DiHETE. It is a weak LTD4 receptor agonist in guinea pig lung membranes. It induces guinea pig ileum contraction with an ED50 value of 1.3 μM.
T37616	Leukotriene A4 methyl ester Leukotriene A4 methyl ester
	白三烯A4甲酯可在大鼠肝脏中主要碱性胞质谷胱甘肽转移酶的催化下转化为白三烯C4单甲酯，可用于代谢相关研究。
T61419	CXCR4 antagonist 5
	CXCR4 antagonist 5 (compound 23), a potent CXCR4 antagonist, exhibits high inhibition efficacy against CXCR4 with an IC50 value of 8.8 nM. It effectively suppresses CXCL12-induced cytosolic calcium increase (IC50 = 0.02 nM) and hinders CXCR4/CXCL12-mediated chemotaxis. Moreover, Compound 23 demonstrates favorable physicochemical properties and in vitro safety profiles, exhibiting only marginal to moderate inhibition of CYP isozymes and hERG [1].
T37824	MCT4-IN-1 MCT4-IN-1
	MCT4-IN-1 is an orally active and selective monocarboxylate transporter 4 (MCT4/SLC16A3) inhibitor with an IC50 of 77 nM and a Ki of 11 nM. MCT4-IN-1 targets to the cytosolic domain of MCT4. MCT4-IN-1 results in lactate efflux inhibition and reduction of cellular viability in MCT4 high expressing cells. MCT4-IN-1 has the potential for MCT4 transporter inhibition research[1].
T61420	CXCR4 antagonist 6
	CXCR4 antagonist 6 (compound 46) is a highly potent inhibitor of CXCR4 with an IC50 value of 79 nM. It effectively inhibits the cytosolic calcium flux induced by CXCL12, achieving an IC50 of 0.25 nM. Moreover, CXCR4 antagonist 6 demonstrates significant mitigation of cell migration mediated by the CXCL12/CXCR4 interaction. Notably, this compound exhibits remarkable efficacy in a mouse model of cancer metastasis [1].
T37303	5-OxoETE 5-KETE,5-OxoETE
	5-OxoETE is a polyunsaturated keto acid formed by the oxidation of 5-HETE in human neutrophils by a specific dehydrogenase.[1] It stimulates cytosolic calcium levels in neutrophils with an EC50 value of 2 nM.[2] 5-OxoETE selectively stimulates the migration and degranulation of eosinophils and activates the MAPK pathway in stimulated neutrophils via a specific G protein-coupled receptor.[3],[4],[5],[6]
T77131	Clervonafusp alfa
	Clervonafusp alfa (VAL-1221) 作为一种融合蛋白，针对胞浆及溶酶体糖原进行靶向。该化合物结合了穿透细胞的抗体Fab部分与重组人酸性葡萄糖苷酶 (rhGAA)，通过核苷转运体ENT-2进入细胞质，再利用甘露糖-6-磷酸受体(M6PRs)导向溶酶体。主要应用于晚发型庞贝病的研究领域。
T80771	WRR139
	WRR139为肽乙烯基砜类化合物，涉及诸如炎症与癌症等病症的生物学路径。该化合物同时作用于胞质酶N-聚糖酶1（NGLY1）与Nrf1，表现为抑制剂身份。WRR139可提升Carfilzomib对癌细胞的细胞毒效应。
T21681	AACOCF3 Arachidonyl trifluoromethyl ketone,Arachidonyltrifluoromethane	Phospholipase	Metabolism
	AACOCF3 (Arachidonyl trifluoromethyl ketone) is a cell-permeable trifluoromethyl ketone analog of arachidonic acid. It is a potent and selective slow binding inhibitor of the 85-kDa cytosolic phospholipase A2 (cPLA2). By blocking the production of arachidonate and 12-hydroxyeicosatetraenoic acid in calcium ionophore-challenged platelets, AACOCF3 hinders their synthesis. Moreover, AACOCF3 inhibits glucose-induced insulin secretion from isolated rat islets. Given its diverse applications, AACOCF3 ...
T36369	3,6-diacetoxy Phthalonitrile
	3,6-diacetoxy Phthalonitrile is a fluorescent probe for monitoring intracellular pH by flow cytometry in living cells. It rapidly crosses cell membranes and is cleaved by cytosolic esterases to form the fluorescent pH indicator 2,3-dicyano-hydroquinone (DCH), which is excited at UV wavelengths. DCH can be excited at 351 nm, with pH-dependent emission in the range of 450-476 nm (pH 5.0-10.0) using a potassium-based buffer.
TP1565L	Foxy-5 acetate Foxy-5 acetate(881188-51-8 free base)	Wnt/beta-catenin	Cytoskeletal Signaling; Stem Cells
	Foxy-5 acetate 是 Wnt 5A 的激动剂，Wnt 5A 是 Wnt 家族的非经典成员。 Foxy-5 acetate 损害上皮癌细胞的迁移和侵袭，触发细胞溶质游离钙信号传导，而不影响 β-连环蛋白活化。
T37182	AX 048
	The group IVA phospholipase A2 (PLA2), known as calcium-dependent cytosolic PLA2 (cPLA2), selectively releases arachidonic acid from membrane phospholipids, playing a central role in initiating the synthesis of prostaglandins and leukotrienes. AX 048 is a potent group IVA cPLA2 inhibitor that demonstrates 50% inhibition of the enzyme at a mole fraction (XI(50)) of 0.022. Pretreatment with AX 048 (ED50 = 1.2 mg/kg) dose-dependently reduces thermal hyperalgesia evoked by carrageenan injection of r...

化合物

Abl Cytosolic Substrate acetate

Cat.No: TP1483L

Synonym: Abl Cytosolic Substrate acetate(168202-46-8 free base)

Target: Others

Abl Cytosolic Substrate

Cat.No: TP1483

BCATc Inhibitor 2

Cat.No: T22043

Target: Others

Cat.No: T6500

Synonym: Ferrostatin 1,Ferrostatin-1 (Fer-1)

Target: Ferroptosis, Antifungal

Cat.No: T8356

Target: Lipoxygenase, COX

Cat.No: TQ0105

Target: Phospholipase

Cat.No: T0380

Synonym: 比卡鲁胺,ICI-176334

Target: Androgen Receptor, Autophagy

Cat.No: T5481

Target: Others

FFAGLDD amine salt

Cat.No: TP1545L1

Target: Others

Cat.No: T11149

Synonym: PLA 725

Target: Phospholipase

Cat.No: T13613

Target: STING

Cyt-PTPε Inhibitor-1

Cat.No: T10927

Synonym: Cyt-PTP|A Inhibitor-1

Target: Phosphatase, Src

Taltirelin acetate

Cat.No: T13072

Synonym: TA-0910 acetate

Target: Thyroid hormone receptor(THR)

Cat.No: T77616

Synonym: Nape-Pld activator

Target: Phospholipase

Cat.No: T6040

Synonym: E64d,Loxistatin,阿洛司他丁,E64c ethyl ester

Target: SARS-CoV, Cysteine Protease

MS023 dihydrochloride

Cat.No: T61338

Synonym: MS023 2HCl

Target: Histone Methyltransferase

Cat.No: T35868

Target: Others

Cat.No: T24089

Synonym: GK 470,GK-470

Isoproterenol tartrate, (-)-

Cat.No: T25546

Synonym: L-Isoproterenol D-bitartrate,Isoproterenol D-bitartrate, L-,Isolevin

Cat.No: T26693

Synonym: FP-025,AKH-217,AKH217,AVX001,FP025

Cat.No: T13606

Synonym: 3',3'-cGAMP,Cyclic GMP-AMP

Target: Others

Cat.No: T69046

Cat.No: T82922

Cat.No: T26523

sn-Glycerol 3-phosphate lithium

Cat.No: T37502

CXCR4 antagonist 9

Cat.No: T61650

trans-carboxy Glimepiride

Cat.No: T35640

Cat.No: T71913

Lys-Phe-Glu-Arg-Gln

Cat.No: T81894

Cat.No: T37556

2′-O-(2-Methoxyethyl)guanosine

Cat.No: T40566

Synonym: 2′-O-(2-Methoxyethyl)guanosine,2'-O-MOE-rG

Cat.No: T7590

Synonym: TA-0910,他替瑞林

Target: Thyroid hormone receptor(THR)

Cat.No: TP1545

Target: Others

CXCR4 antagonist 8

Cat.No: T61363

CXCR2 antagonist 4

Cat.No: T61447

Cat.No: T37842

12,14-Dichlorodehydroabietic acid

Cat.No: T40750

Foxy-5 TFA(881188-51-8 free base)

Cat.No: TP1296

Synonym: Foxy-5 (TFA)

5(S),6(R)-DiHETE

Cat.No: T37652

Leukotriene A4 methyl ester

Cat.No: T37616

Synonym: Leukotriene A4 methyl ester

CXCR4 antagonist 5

Cat.No: T61419

Cat.No: T37824

Synonym: MCT4-IN-1

CXCR4 antagonist 6

Cat.No: T61420

Cat.No: T37303

Synonym: 5-KETE,5-OxoETE

Clervonafusp alfa

Cat.No: T77131

Cat.No: T80771

Cat.No: T21681

Synonym: Arachidonyl trifluoromethyl ketone,Arachidonyltrifluoromethane

Target: Phospholipase

3,6-diacetoxy Phthalonitrile

Cat.No: T36369

Cat.No: TP1565L

Synonym: Foxy-5 acetate(881188-51-8 free base)

Target: Wnt/beta-catenin

Cat.No: T37182

Cat. No.	Product Name	Target	Signaling Pathways
T19343L	Glycerol 3-phosphate biscyclohexylammonium salt	Endogenous Metabolite	Metabolism
	Glycerol 3-phosphate biscyclohexylammonium salt 是胞质甘油 3-磷酸脱氢酶途径中产生的，即利用 NADH 还原二羟丙酮磷酸的过程。
TN2215	Taurochenodeoxycholic acid sodium 牛磺鹅去氧胆酸钠盐,Sodium taurochenodeoxycholate,牛磺鹅去氧胆酸钠	Apoptosis; Endogenous Metabolite	Apoptosis; Metabolism
	Taurochenodeoxycholic acid sodium (Sodium taurochenodeoxycholate) 是动物胆汁酸的主要生物活性物质之一。它可诱导细胞凋亡，具有抗炎和免疫调节作用。
TL0008	Gigantol	Wnt/beta-catenin; Glucosidase	Cytoskeletal Signaling; Metabolism; Stem Cells
	Gigantol 是一种联苄基化合物，从几种药用兰花中获得，是一种Wnt/β-catenin 通路抑制剂，具有抗肿瘤活性。
T37977	Succinyladenosine
	Succinyladenosine is a biochemical marker of adenylosuccinase (ASL) deficiency. It is formed through the dephosphorylation of intracellular adenylosuccinic acid (S-AMP) by cytosolic 5-nucleotidase [1].
T19253	Cyclic ADP-ribose cADPR	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Cyclic ADP-ribose (cADPR) is an effective calcium mobilization second messenger, which is synthesized from NAD + by ADP-ribosyl cyclase. Cyclic ADP-ribose mainly increases cytosolic calcium through Ryanodine receptor-mediated endoplasmic reticulum release
T37687	Cyclic ADP-ribose ammonium
	Cyclic ADP-ribose ammonium (cADPR ammonium) is a powerful calcium mobilization second messenger synthesized from NAD+ by an ADP-ribosyl cyclase. It primarily raises cytosolic calcium levels through Ryanodine receptor-mediated release from the endoplasmic reticulum, while also facilitating extracellular influx through the opening of TRPM2 channels [1][2][3].
TN6458	Acetylshikonin
	Acetylshikonin can effectively inhibit tumor cells, it can be used to treat hepatocellular carcinoma cells expressing hepatitis B virus X protein (HBX) by inducing ER stress , an oncoprotein from hepatitis B virus. Acetylshikonin inhibits the production of eicosanoid, is due to the attenuation of cytosolic phospholipase A(2) membrane recruitment via the decrease in [Ca(2+)](i) and to the blockade of cyclooxygenase and 5-lipoxygenase activity.
T35895	Ingenol 3,20-dibenzoate
	Ingenol 3,20-dibenzoate is a powerful activator of protein kinase C (PKC) isoforms. It effectively induces the translocation of nPKC-delta, -epsilon, and -theta as well as PKC-mu from the cytosolic fraction to the particulate fraction. Through de novo synthesis of macromolecules, it triggers apoptosis with characteristic morphology. Moreover, Ingenol 3,20-dibenzoate enhances IFN-γ production and degranulation in NK cells, particularly when stimulated by NSCLC cells[1][2].
TN5221	(-)-Variabilin
	Variabilin, a novel inhibitor of human platelet aggregation, it is a potent RGD (Arg-Gly-Asp)-containing antagonist of the fibrinogen receptor glycoprotein IIb-IIIa (GPIIb-IIIa; αIIbβ3) and the vitronectin receptor αvβ3.Variabilin is also an antimicrobial furanosesterterpene. Variabilin is an inhibitor of human secretory and cytosolic phospholipase A2 (PLA2) activities that controls eicosanoid production in vitro and in vivo, inhibits neutrophil degranulation and superoxide generation in vitro a...
T73717	cGAMP diammonium
	cGAMP (Cyclic GMP-AMPP) diammonium 是一种内源性第二信使，通过触发干扰素的产生来响应胞浆 DNA。它通过激活干扰素基因刺激因子（STING），启动信号级联，进而导致I型干扰素及其他免疫介质的生成。
TN2511	Britannilactone diacetate 1,6-O,O-Diacetylbritannilactone	IL Receptor; PARP; ROS; MAPK; Caspase; JAK; JNK; STAT	Angiogenesis; Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Immunology/Inflammation; JAK/STAT signaling; MAPK; Proteases/Proteasome; Stem Cells
	1,6-O,O-Diacetylbritannilactone(OODBL) has anti-inflammatory activity, it has a potential therapeutic efficacy on inflammatory diseases especially allergic airway disease as a lead compound. OODBL has anti-asthmatic activity, it reduces leukotriene C4 pro
T36954	Nemorosone
	Nemorosone is a polycyclic polyprenylated acylphloroglucinol (PPAP) originally isolated from C. rosea that has antiproliferative properties.1 Nemorosone inhibits growth of NB69, Kelly, SK-N-AS, and LAN-1 neuroblastoma cells (IC50s = 3.1-6.3 μM), including several drug-resistant clones, but not MRC-5 human embryonic fibroblasts (IC50 = >40 μM).2 It increases DNA fragmentation in LAN-1 cells in a dose-dependent manner, and decreases N-Myc protein levels and phosphorylation of ERK1/2 by MEK1/2. Nem...

天然产物

Glycerol 3-phosphate biscyclohexylammonium salt

Cat.No: T19343L

Target: Endogenous Metabolite

Taurochenodeoxycholic acid sodium

Cat.No: TN2215

Synonym: 牛磺鹅去氧胆酸钠盐,Sodium taurochenodeoxycholate,牛磺鹅去氧胆酸钠

Target: Apoptosis, Endogenous Metabolite

Cat.No: TL0008

Target: Wnt/beta-catenin, Glucosidase

Succinyladenosine

Cat.No: T37977

Cyclic ADP-ribose

Cat.No: T19253

Synonym: cADPR

Target: Calcium Channel

Cyclic ADP-ribose ammonium

Cat.No: T37687

Cat.No: TN6458

Ingenol 3,20-dibenzoate

Cat.No: T35895

Cat.No: TN5221

cGAMP diammonium

Cat.No: T73717

Britannilactone diacetate

Cat.No: TN2511

Synonym: 1,6-O,O-Diacetylbritannilactone

Target: IL Receptor, PARP, ROS, MAPK, Caspase, JAK, JNK, STAT

Cat.No: T36954

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