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Search Results for " spleen "

66

抑制剂 & 化合物

8

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T36582	Glucocerebrosides (Gaucher's spleen)
	Glucocerebrosides are formed by the tethering of glucose to a ceramide by glucosylceramide synthase. They are present in neuronal and non-neuronal mammalian tissues and are found at low quantities in a large number of plant species. Glucocerebrosides are precursors in the synthesis of lactosylceramides and gangliosides. Increased levels of glucocerebrosides are associated with obesity-induced insulin resistance in mice and with neuronal deficits observed in neuronopathic Gaucher disease. This pr...
T39437	Cevidoplenib dimesylate	Syk	Angiogenesis; Tyrosine Kinase/Adaptors
	Cevidoplenib dimesylate 是一种脾酪氨酸激酶 (Syk) 抑制剂，具有抗炎和免疫调节特性。
T16776	RO9021	Syk	Angiogenesis; Tyrosine Kinase/Adaptors
	RO9021 是口服具有活力的，ATP 竞争性的 SYK 抑制剂，其 IC50=5.6 nM。
T6594	MNS	Syk; Src; p97	Angiogenesis; Tyrosine Kinase/Adaptors; Ubiquitination
	MNS 是一种酪氨酸激酶抑制剂和广谱抗血小板药物，是一种 β-硝基苯乙烯衍生物。它完全抑制 U46619 (IC50:2.1 μM)、ADP (IC50:4.1 μM)、花生四烯酸 (IC50:5.8 μM)、胶原 (IC50:7.0 μM)和凝血酶 (IC50:12.7 μM)诱导的血小板聚集，并抑制 Src (IC50:27.3 μM)、Syk (IC50:2.8 μM) 和 FAK (IC50:97.6 μM)。
T4209	TAK-659 hydrochloride TAK-659	VEGFR; FLT; Tyrosine Kinases; JAK; Syk	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors
	TAK-659 hydrochloride (TAK-659) 是可逆的、高效的、选择性的、口服有效的 SYK/FLT3 双抑制剂，对 SYK 和 FLT3 作用的IC50值分别为 3.2 nM、4.6 nM。它能诱导肿瘤细胞死亡，却不作用于非肿瘤细胞，对慢性淋巴细胞白血病具有潜在的研究价值。
T11824LL	Lanraplenib GS-9876	Syk	Angiogenesis; Tyrosine Kinase/Adaptors
	Lanraplenib (GS-9876) 是高效的、选择性的、口服具有活力的 SYK 抑制剂 (IC50=9.5 nM) ，能够用于炎症性疾病的研究。它通过糖蛋白 VI (GPVI) 受体抑制血小板中的 SYK 活性，而不会延长猴子或人类的出血时间 (BT)。
T6101	Entospletinib GS-9973	Syk	Angiogenesis; Tyrosine Kinase/Adaptors
	Entospletinib (GS-9973) 是选择性的Syk 抑制剂，其IC50=7.7 nM。
T14331	Gusacitinib ASN-002	JAK; Syk	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors
	Gusacitinib (ASN-002) 是一种有效的 SYK 激酶和JAK 激酶的双抑制剂，IC50值为 5 到 46 nM 之间，具有抗癌活性。
T4348	Syk Inhibitor II	5-HT Receptor; Syk	Angiogenesis; GPCR/G Protein; Neuroscience; Tyrosine Kinase/Adaptors
	Syk Inhibitor II 是一种可渗透细胞、具有 ATP 竞争性的嘧啶-甲酰胺化合物，可选择性且可逆地抑制 Syk，IC50为 41 nM。
T6115	Fostamatinib R788,福他替尼	FLT; Syk; Monoamine Transporter; Adenosine Receptor	Angiogenesis; GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience; Tyrosine Kinase/Adaptors
	Fostamatinib (R788) 是一种口服具有活力的 R406 前药。其中R406 是具有口服活性的，有效的，ATP 竞争性的Syk/FLT3抑制剂(Ki:30 nM，IC50:41 nM)，也能够抑制 Lyn (IC50:63 nM) 和 Lck (IC50:37 nM)。
T6957	PRT-060318 P142-76,PRT318,PRT-060318 2HCl	Syk	Angiogenesis; Tyrosine Kinase/Adaptors
	PRT-060318 (P142-76) 是一种新颖的、选择性的酪氨酸激酶 (Syk) 抑制剂，其IC50=4 nM。
T3185	R112 (E)-Elafibranor	Syk	Angiogenesis; Tyrosine Kinase/Adaptors
	R112 ((E)-Elafibranor) 是ATP 竞争性的 Syk 激酶抑制剂，它能够抑制Syk 激酶活性，Ki=6 nM，IC50=226 nM。
T2467	R406 free base R406 (free base)	Apoptosis; FLT; Syk	Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors
	R406 free base (R406(free base)) 是一种具有口服活性的，ATP 竞争性的Syk/FLT3抑制剂，Ki 为 30 nM。它有效抑制 Syk 激酶活性，IC50为 41 nM，可减轻免疫复合物介导的炎症。它还抑制 Lyn 和 Lck，IC50分别为 63 nM 和 37 nM。
T2487	Cerdulatinib PRT2070,赛度替尼,PRT062070	Tyrosine Kinases; JAK; Syk	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors
	Cerdulatinib (PRT2070) 是一种选择性 Tyk2抑制剂，IC50为 0.5 nM。它是 JAK 和 SYK 的双抑制剂，抑制JAK1、2、3 和SYK 的IC50分别为12、6、8 和 32。
T6174	R406 R-406 besylate	Apoptosis; FLT; Syk	Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors
	R406 (R-406 besylate) 是一种具有口服活性的 ATP 竞争性 Syk/FLT3抑制剂，Ki 为 30 nM。它有效抑制 Syk 激酶活性，IC50为 41 nM。它还抑制 Lyn 和 Lck，IC50值分别为 63 nM 和 37 nM。它可减轻免疫复合物介导的炎症。
T6776	BAY 61-3606 dihydrochloride BAY 61-3606,BAY-61-3606 dihydrochloride	Apoptosis; Syk	Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors
	BAY 61-3606 dihydrochloride (BAY 61-3606) 是一种口服有效的，ATP 竞争性的，可逆的选择性Syk 抑制剂。它降低神经母细胞瘤细胞中的 ERK1/2 和 Akt 磷酸化，也降低 K-rn 细胞裂解物中 Syk 磷酸化。它作用于乳腺癌细胞，通过下调 Mcl-1 促进 TRAIL 诱导的细胞凋亡。
T2696	PRT062607 hydrochloride PRT062607 (P505-15, BIIB057) HCl,P505-15 Hydrochloride	MLK; Syk; Src	Angiogenesis; MAPK; Tyrosine Kinase/Adaptors
	PRT062607 hydrochloride (P505-15 Hydrochloride) 是纯化的 Syk 抑制剂，IC50=1-2 nM。
T4263	BAY 61-3606 2-[[7-(3,4-二甲氧基苯基)咪唑并[1,2-C]嘧啶-5-基]氨基]-3-吡啶甲酰胺,Syk inhibitor IV	Apoptosis; Syk	Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors
	BAY 61-3606 (Syk inhibitor IV) 是一种具有口服活性的，ATP 竞争性的可逆选择性Syk 抑制剂。它作用于乳腺癌细胞，通过下调 Mcl-1 促进 TRAIL 诱导的细胞凋亡。它降低神经母细胞瘤细胞中的 ERK1/2 和 Akt 磷酸化，也降低 K-rn 细胞裂解物中 Syk 磷酸化。
T2605	Fostamatinib Disodium Tamatinib Fosdium,福他替尼二钠盐,R788(Disodium),R788 Disodium,R788 (Fostamatinib) Disodium	FLT; Syk	Angiogenesis; Tyrosine Kinase/Adaptors
	Fostamatinib Disodium (R788 Disodium) 是一种口服具有活力的 R406 前药。其中R406 是具有口服活性的，有效的，ATP 竞争性的Syk/FLT3抑制剂(Ki:30 nM，IC50:41 nM)，也能够抑制 Lyn (IC50:63 nM) 和 Lck (IC50:37 nM)。
T6104	Cerdulatinib hydrochloride Cerdulatinib,PRT2070,PRT062070 hydrochloride,PRT062070,PRT2070 hydrochloride	MLK; c-Fms; Tyrosine Kinases; Hippo pathway; JAK; Syk	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; MAPK; Stem Cells; Tyrosine Kinase/Adaptors
	Cerdulatinib hydrochloride (PRT2070 hydrochloride) 是一种选择性可逆，具有口服活性、 ATP 竞争性的 SYK 和 JAK 的双重抑制剂，抑制 JAK1、2、3、SYK 和 Tyk2的 IC50值分别为12、6、8、32 和 0.5 nM。它可用于研究自身免疫性疾病和B 细胞恶性肿瘤。
T28281	OXSI-2 OXSI 2,Syk Inhibitor	Syk	Angiogenesis; Tyrosine Kinase/Adaptors
	OXSI-2 (Syk Inhibitor) 是 Syk 的抑制剂，EC50 为 313 nM，IC50 为 14 nM。 OXSI-2 完全抑制适配器蛋白 LAT Y191 磷酸化和 Syk 介导的血小板聚集。
T9789	Cevidoplenib dimesylate hydrochloride	Syk	Angiogenesis; Tyrosine Kinase/Adaptors
	Cevidoplenib dimesylate hydrochloride 是一种脾酪氨酸激酶 (Syk) 抑制剂，具有潜在的免疫调节和抗炎特性。
T24584	P505-15 Acetate PRT 062607 Acetate,P505 15 Acetate,PRT-062607 Acetate,PRT062607 Acetate,P50515 Acetate	Tyrosinase	Proteases/Proteasome
	P505-15 Acetate 是脾脏酪氨酸激酶的选择性抑制剂，通过抑制白细胞免疫功能和炎症起作用，导致关节炎评分降低和组织学损伤减轻。
T78268	Anti-Mouse NK1.1 Antibody (PK136)
	Anti-Mouse NK1.1 Antibody (PK136) 是鼠源靶向 NK1.1的IgG2a类抗体，可消除外周血、脾脏和肺组织中的NK1.1和NK1.1NKT细胞，抑制 NK1.1 信号传导，可用于研究心肺衰竭。
TP1472	Tyroserleutide	Others	Others
	Tyroserleutide 是一种可从猪脾脏的降解产物中分离得到的小分子三肽，在体内外均对肿瘤生长具有抑制作用。
T9659	LCB 03-0110 3-(2-(3-(Morpholinomethyl)phenyl)thieno[3,2-b]pyridin-7-ylamino)phenol	Discoidin Domain Receptor (DDR)	Tyrosine Kinase/Adaptors
	LCB 03-0110 (3-(2-(3-(Morpholinomethyl)phenyl)thieno[3,2-b]pyridin-7-ylamino)phenol) 是一种盘状结构域受体家族酪氨酸激酶的强效抑制剂，可强烈抑制多种酪氨酸激酶，包括 c-Src 家族、脾酪氨酸激酶、布鲁顿酪氨酸激酶和血管内皮生长因子受体 2，它们对免疫很重要细胞信号传导和炎症反应。
T9543	Syk Inhibitor II hydrochloride	Others	Others
	Syk Inhibitor II hydrochloride 信号传导的影响在狼疮中可能很突出。
T4391	Syk Inhibitor II dihydrochloride Syk Inhibitor II (hydrochloride)	Others; Tyrosine Kinases; Syk; PKC; BTK	Angiogenesis; Chromatin/Epigenetic; Cytoskeletal Signaling; Others; Tyrosine Kinase/Adaptors
	Syk Inhibitor II (hydrochloride) 是一种非受体酪氨酸激酶，磷酸化后，它与 FcRγ 链的基于免疫受体酪氨酸的激活基序结合，并介导与血小板功能和炎症相关的下游信号传导。 Syk inhibitor II 是一种可渗透细胞的嘧啶-甲酰胺化合物，以 ATP 竞争性方式选择性和可逆地阻断 Syk (IC50 = 41 nM)。它对 PKCε、PKCβII、ZAP-70、Btk 和 Itk 的效力要低得多（IC50s 分别为5.1、11、11.2、15.5 和 22.6 μM）。
T70931	SYK-IN-II
	SYK-IN-II is an inhibitor of the spleen tyrosine kinase (STK).
T21062	TAK-659 TAK 659,TAK659
	TAK-659 is a spleen tyrosine kinase (SYK) inhibitor.
T27035	CL-184005 CL184005,CL 184005
	CL-184005 is a platelet activating factor (PAF) inhibitor. CL-184005 interferes with tumor necrosis factor synthesis. CL-184005 also dreases Spleen-associated tumor necrosis factor protein.
T37602	GSK 143
	Spleen tyrosine kinase (Syk) inhibitor (pIC50 = 7.5). Also inhibits phosphorylated Erk (pIC50 = 7.1). Decreases cell number and viability in chronic lymphocytic leukemia (CCL) cell lines. Liddle et al (2011) Discovery of GSK143, a highly potent, selective and orally efficacious spleen tyrosine kinase inhibitor. Bioorg.Med.Chem.Lett. 21 6188 PMID:21903390 \|Varghese et al (2018) Highly selective SYK inhibitor, GSK143, abrogates survival signals in chronic lymphocytic leukaemia. Br.J.Haematol 182 9...
T80912	Tyroserleutide TFA
	Tyroserleutide TFA，一种从猪脾脏的降解产物中分离得到的小分子三肽，可在体内外抑制肿瘤生长。
T78943	Syk-IN-7	Syk	Angiogenesis; Tyrosine Kinase/Adaptors
	Syk-IN-7（化合物17）是一类特定的酪氨酸激酶（SYK）抑制剂。
T70994	TAK-659 HCl
	TAK-659 is an inhibitor of spleen tyrosine kinase (syk), with potential anti-inflammatory, immunomodulating, and antineoplastic activities. Spleen tyrosine kinase inhibitor TAK-659 may inhibit the activity of syk, which abrogates downstream B-cell receptor (BCR) signaling and leads to an inhibition of B-cell activation, chemotaxis, adhesion and proliferation. Note: TAK-659 free base is less stable. This product is supplied as dihydrochloride form.
T23898	Clocoumarol Clocoumarolum,BRN 1264788,DB 112
	Clocoumarol is an anticoagulant that prevents blood clotting. It also can inhibit the dilatation of the spleen and the congestion of lymph nodes.
T36357	Dimethyldioctadecylammonium (bromide)
	Dimethyldioctadecylammonium (DDA) is a cationic amphipathic lipid. DDA liposomes containing an Ag85B-ESAT-6 antigen induce antigen deposition at an intramuscular or subcutaneous injection site in mice, increasing immune cell exposure to the antigen. In a guinea pig model of M. tuberculosis infection, spleen bacterial load is reduced and lung and spleen lesion numbers are decreased when the mycobacterial lipid antigens Ac2SGL and PIM2 are administered in liposomes comprised of DDA and a synthetic...
T38278	9(Z),12(Z),15(Z),18(Z),21(Z)-Tetracosapentaenoic Acid
	9(Z),12(Z),15(Z),18(Z),21(Z)-Tetracosapentaenoic acid is an ω-3 very long-chain polyunsaturated fatty acid. It has been used to study the desaturation and elongation of ω-3 polyunsaturated fatty acids. It is elongated to form C26:5 or acted on by δ6 desaturase to form C24:6. 9(Z),12(Z),15(Z),18(Z),21(Z)-Tetracosapentaenoic acid is found at low levels in mouse brain and spleen and levels decrease in the brain and spleen of old and exceptionally old mice.
TP1598	Tyroserleutide hydrochloride
	Tyroserleutide hydrochloride is a small molecule tripeptide isolated from the degradation product of pig spleen, which can inhibit tumor growth in vivo and in vitro.
TP1558	Tyroserleutide TFA (138168-48-6 free base) Tyroserleutide TFA
	Tyroserleutide TFA, isolated from the degradation products of porcine spleen, is a small molecular tripeptide which inhibits tumor growth both in vitro and in vivo.
T70930	GSK SYK inhibitor
	The immunoregulator spleen tyrosine kinase (SYK) is upregulated in cutaneous lupus erythematosus (CLE). This double-blind, multicentre, Phase Ib study evaluated the safety, tolerability, pharmacokinetics, pharmacodynamics and clinical efficacy of the selective SYK inhibitor GSK2646264 in active CLE lesions
T63124	RORγt modulator 4
	RORγt modulator 4 是一种 RORγt 调节剂。RORγt modulator 4 能够调节源自小鼠脾脏的细胞中 IL-17A 产生的活性。
TP1764	Adrenomedullin (1-50), rat
	Adrenomedullin (1-50), rat is a 50 amino acid peptide, which induces a selective arterial vasodilation via activation of CGRP1 receptor. Adrenomedullin (1-50) is a peptide hormone with RNA expressed in rat adrenal glands, lung, kidney, heart, and spleen,
T39874	GSK143 dihydrochloride
	GSK143 dihydrochloride is a highly selective, orally active inhibitor of spleen tyrosine kinase (SYK), exhibiting a pIC 50 value of 7.5. It effectively inhibits phosphorylated Erk (pErk) with a pIC 50 value of 7.1. The compound demonstrates anti-inflammatory properties and hinders the recruitment of immune cells in the intestinal muscularis of mice.
T61527	GSK2646264
	GSK2646264 (Compound 44) is a highly effective and specific inhibitor of spleen tyrosine kinase (SYK) with a pIC50 of 7.1. In addition to targeting SYK, GSK2646264 also inhibits several other kinases, including LCK, LRRK2, GSK3β, JAK2, VEGFR2, Aurora B, and Aurora A, with pIC50 values of 5.4, 5.4, 5.3, 5, 4.5, <4.6 and <4.3, respectively. Notably, GSK2646264 demonstrates skin penetrability, reaching both the epidermis and dermis [1].
T38626	GSK143
	GSK143 is a potent orally active and highly selective inhibitor of spleen tyrosine kinase (SYK) with a pIC 50 of 7.5. Furthermore, GSK143 effectively inhibits phosphorylated Erk (pErk) with a pIC 50 value of 7.1. In addition, GSK143 exhibits promising anti-inflammatory properties by reducing inflammation and impeding the recruitment of immune cells in the intestinal muscularis of mice.
T37302	PCTR3
	Protein conjugates in tissue regeneration 3 (PCTR3) is a specialized pro-resolving mediator (SPM) synthesized from docosahexaenoic acid . DHA is oxidized to 16S,17S-epoxy-protectin, which is converted to PCTR1 by glutathione S-transferase and to PCTR2 and PCTR3 via peptidases. PCTR3 is found in infected mouse spleens and resolving exudate as well as isolated human spleen and septic plasma. It is also found in both M1 and M2 macrophages differentiated from isolated human monocytes.
T78746	Mtb-IN-3
	Mtb-IN-3（化合物10c）是针对结核分枝杆菌（Mtb）的选择性抑制剂。该化合物具有有效的体外抗Mtb活性，并且不表现出细胞毒性。在小鼠结核病模型中，Mtb-IN-3可抑制脾脏的集落形成。
T37439	C18 Globotriaosylceramide (d18:1/18:0)
	C18 globotriaosylceramide is an endogenous sphingolipid found in mammalian cell membranes that is synthesized from lactosylceramide . It inhibits aggregation of human neutrophils induced by phorbol 12-myristate 13-acetate (PMA; 10008014) when used at a concentration of 1 μM. C18 globotriaosylceramide acts as a receptor for Shiga toxin in B cell-derived Raji cells and THP-1 monocytes. It accumulates in the brain, heart, kidney, liver, lung, and spleen in a mouse model of Fabry disease, a lysosoma...
T78641	ER-27319	Syk	Angiogenesis; Tyrosine Kinase/Adaptors
	ER-27319为吖啶酮衍生物，高效选择性抑制SYK，阻断其酪氨酸磷酸化和活性。本化合物阻止抗原刺激下人及大鼠肥大细胞释放过敏介质，IC50约为10 μM，适用于过敏性疾病研究。

化合物

Glucocerebrosides (Gaucher's spleen)

Cat.No: T36582

Cevidoplenib dimesylate

Cat.No: T39437

Target: Syk

Cat.No: T16776

Target: Syk

Cat.No: T6594

Target: Syk, Src, p97

TAK-659 hydrochloride

Cat.No: T4209

Synonym: TAK-659

Target: VEGFR, FLT, Tyrosine Kinases, JAK, Syk

Cat.No: T11824LL

Synonym: GS-9876

Target: Syk

Cat.No: T6101

Synonym: GS-9973

Target: Syk

Cat.No: T14331

Synonym: ASN-002

Target: JAK, Syk

Syk Inhibitor II

Cat.No: T4348

Target: 5-HT Receptor, Syk

Cat.No: T6115

Synonym: R788,福他替尼

Target: FLT, Syk, Monoamine Transporter, Adenosine Receptor

Cat.No: T6957

Synonym: P142-76,PRT318,PRT-060318 2HCl

Target: Syk

Cat.No: T3185

Synonym: (E)-Elafibranor

Target: Syk

Cat.No: T2467

Synonym: R406 (free base)

Target: Apoptosis, FLT, Syk

Cat.No: T2487

Synonym: PRT2070,赛度替尼,PRT062070

Target: Tyrosine Kinases, JAK, Syk

Cat.No: T6174

Synonym: R-406 besylate

Target: Apoptosis, FLT, Syk

BAY 61-3606 dihydrochloride

Cat.No: T6776

Synonym: BAY 61-3606,BAY-61-3606 dihydrochloride

Target: Apoptosis, Syk

PRT062607 hydrochloride

Cat.No: T2696

Synonym: PRT062607 (P505-15, BIIB057) HCl,P505-15 Hydrochloride

Target: MLK, Syk, Src

Cat.No: T4263

Synonym: 2-[[7-(3,4-二甲氧基苯基)咪唑并[1,2-C]嘧啶-5-基]氨基]-3-吡啶甲酰胺,Syk inhibitor IV

Target: Apoptosis, Syk

Fostamatinib Disodium

Cat.No: T2605

Synonym: Tamatinib Fosdium,福他替尼二钠盐,R788(Disodium),R788 Disodium,R788 (Fostamatinib) Disodium

Target: FLT, Syk

Cerdulatinib hydrochloride

Cat.No: T6104

Synonym: Cerdulatinib,PRT2070,PRT062070 hydrochloride,PRT062070,PRT2070 hydrochloride

Target: MLK, c-Fms, Tyrosine Kinases, Hippo pathway, JAK, Syk

Cat.No: T28281

Synonym: OXSI 2,Syk Inhibitor

Target: Syk

Cevidoplenib dimesylate hydrochloride

Cat.No: T9789

Target: Syk

P505-15 Acetate

Cat.No: T24584

Synonym: PRT 062607 Acetate,P505 15 Acetate,PRT-062607 Acetate,PRT062607 Acetate,P50515 Acetate

Target: Tyrosinase

Anti-Mouse NK1.1 Antibody (PK136)

Cat.No: T78268

Cat.No: TP1472

Target: Others

Cat.No: T9659

Synonym: 3-(2-(3-(Morpholinomethyl)phenyl)thieno[3,2-b]pyridin-7-ylamino)phenol

Target: Discoidin Domain Receptor (DDR)

Syk Inhibitor II hydrochloride

Cat.No: T9543

Target: Others

Syk Inhibitor II dihydrochloride

Cat.No: T4391

Synonym: Syk Inhibitor II (hydrochloride)

Target: Others, Tyrosine Kinases, Syk, PKC, BTK

Cat.No: T70931

Cat.No: T21062

Synonym: TAK 659,TAK659

Cat.No: T27035

Synonym: CL184005,CL 184005

Cat.No: T37602

Tyroserleutide TFA

Cat.No: T80912

Cat.No: T78943

Target: Syk

Cat.No: T70994

Cat.No: T23898

Synonym: Clocoumarolum,BRN 1264788,DB 112

Dimethyldioctadecylammonium (bromide)

Cat.No: T36357

9(Z),12(Z),15(Z),18(Z),21(Z)-Tetracosapentaenoic Acid

Cat.No: T38278

Tyroserleutide hydrochloride

Cat.No: TP1598

Tyroserleutide TFA (138168-48-6 free base)

Cat.No: TP1558

Synonym: Tyroserleutide TFA

GSK SYK inhibitor

Cat.No: T70930

RORγt modulator 4

Cat.No: T63124

Adrenomedullin (1-50), rat

Cat.No: TP1764

GSK143 dihydrochloride

Cat.No: T39874

Cat.No: T61527

Cat.No: T38626

Cat.No: T37302

Cat.No: T78746

C18 Globotriaosylceramide (d18:1/18:0)

Cat.No: T37439

Cat.No: T78641

Target: Syk

Cat. No.	Product Name	Target	Signaling Pathways
T0610	Piceatannol 白皮杉醇,trans-Piceatannol,Astringenin	Apoptosis; Serine/threonin kinase; PKA; Syk; PKC; Autophagy	Angiogenesis; Apoptosis; Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; Metabolism; Tyrosine Kinase/Adaptors
	Piceatannol (Astringenin) 是一种Syk 抑制剂，可降低由 TNF 诱导的 iNOS 表达，可研究急性肺损伤。它是存在于各种水果和蔬菜中天然存在的多酚二苯乙烯，可诱导细胞自噬和凋亡，具有抗癌和抗炎特性。
T3829	Ginsenoside F3 人参皂苷F3	Others; IFNAR; Interleukin	Immunology/Inflammation; Others
	Ginsenoside F3 是一种皂苷，提取自Panax ginseng 叶片。它能够调节1 型 (IL-2, IFN-γ) 及 2 型细胞因子(IL-4 and IL-10) 的产生和表达，有免疫增强的作用。
TN2151	Rhamnocitrin	Others	Others
	Rhamnocitrin 是一种分离自黄芪(沙源子)中的类黄酮，具有抗氧化，抗炎和抗动脉粥样硬化活性。它是 DPPH 的清除剂(IC50:28.38 mM)。
T4A2462	Telocinobufagin Telobufotoxin,远华蟾蜍精,Telocinobufogenin	Others	Others
	Telocinobufagin (Telobufotoxin) 是一种从蟾酥中分离提取获得的组份。
T75502	Brazilein
	Brazilein为从Caesalpinia sappan L.中提取的关键免疫抑制成分，能够诱导小鼠脾淋巴细胞(apoptosis)。
T36791	Lysophosphatidylcholine 18:2
	1-Linoleoyl-2-hydroxy-sn-glycero-3-PC (LGPC) is a lysophospholipid containing linoleic acid at thesn-1 position that has been found in mouse heart, lung, liver, spleen, kidney, plasma, and serum.1Serum levels of LGPC decrease with increasing insulin resistance and dysglycemia in humans.2 1.Okudaira, M., Inoue, A., Shuto, A., et al.Separation and quantification of 2-acyl-1-lysophospholipids and 1-acyl-2-lysophospholipids in biological samples by LC-MS/MSJ. Lipid Res.55(10)2178-2192(2014) 2.Gall, ...
T37291	Lyso-Globotriaosylceramide (d18:1) Lyso-Globotriaosylceramide (d18:1)
	Lyso-globotriaosylceramide is a form of globotriaosylceramide that is lacking the fatty acyl group. It binds to Shiga toxin 1 (Stx1) in the presence of cholesterol and phosphatidylcholine but does not bind Stx2. It also reduces viability and aggregation of human neutrophils induced by phorbol 12-myristate 13-acetate when used at concentrations of 50 and 1 μM, respectively. Lyso-globotriaosylceramide accumulates in the brain, heart, kidney, liver, lung, and spleen in a mouse model of Fabry diseas...
T16791	Rottlerin Mallotoxin,NSC 56346,粗糠柴苦素,NSC 94525	CaMK; Apoptosis; Others; HIV Protease; PKA; PKC; Autophagy	Apoptosis; Autophagy; Chromatin/Epigenetic; Cytoskeletal Signaling; Microbiology/Virology; Neuroscience; Others; Proteases/Proteasome; Tyrosine Kinase/Adaptors
	Rottlerin (NSC-56346) 是一种从Mallotus Philippinensis 中得到的天然产物，是 PKC 的特异性抑制剂，抑制HIV-1整合和狂犬病病毒感染。它通过活化 caspase 3 诱导细胞凋亡.

天然产物

Cat.No: T0610

Synonym: 白皮杉醇,trans-Piceatannol,Astringenin

Target: Apoptosis, Serine/threonin kinase, PKA, Syk, PKC, Autophagy

Cat.No: T3829

Synonym: 人参皂苷F3

Target: Others, IFNAR, Interleukin

Cat.No: TN2151

Target: Others

Telocinobufagin

Cat.No: T4A2462

Synonym: Telobufotoxin,远华蟾蜍精,Telocinobufogenin

Target: Others

Cat.No: T75502

Lysophosphatidylcholine 18:2

Cat.No: T36791

Lyso-Globotriaosylceramide (d18:1)

Cat.No: T37291

Synonym: Lyso-Globotriaosylceramide (d18:1)

Cat.No: T16791

Synonym: Mallotoxin,NSC 56346,粗糠柴苦素,NSC 94525

Target: CaMK, Apoptosis, Others, HIV Protease, PKA, PKC, Autophagy

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