首页工具

登录

搜索结果

Search Results for " vegfr-2 "

119

抑制剂 & 化合物

5

天然产物

如果没找到您满意的产品或者您对产品有其他要求，可以联系我们专业顾问为您提供针对性的合理建议。 QQ咨询网站留言咨询

Cat. No.	Product Name	Target	Signaling Pathways
T37078	VEGFR-2-IN-6	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2-IN-6（WO 02/059110）是一种 VEGFR2 的强效抑制剂，这是一种在血管生成调控中起关键作用的受体[1]。
T10123	VEGFR-2-IN-9 KDR-in-4	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2-IN-9 (KDR-in-4) 是一种高效的 KDR/VEGFR2 抑制剂（IC50：7 nM）,可用于研究乳腺癌。
T9979	VEGFR-2-IN-29	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2-IN-29是一种 VEGFR2抑制剂。
T2056	VEGFR-2-IN-5 2, 4-Pyrimidinediamine with linker,UNC0064-12,2,4-Pyrimidinediamine with linker	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2-IN-5 (UNC0064-12) 是 VEGFR2 抑制剂。
T40581	TIE-2/VEGFR-2 kinase-IN-2
	TIE-2/VEGFR-2 kinase-IN-2 is a powerful inhibitor of both VEGFR2 and Tie-2 kinases, displaying noteworthy pIC 50 values of 8.61 and 8.56, respectively. This compound acts as an anti-angiogenic agent, making it highly relevant for cancer research.
T79860	TIE-2/VEGFR-2 kinase-IN-5	VEGFR; Tie-2	Angiogenesis; Tyrosine Kinase/Adaptors
	TIE-2/VEGFR-2 kinase-IN-5 是一种高效的 TIE-2 和 VEGFR-2 酪氨酸激酶受体抑制剂，具有的抗血管生成活性，常用于血管生成相关的生物医学研究领域。
T8817	TIE-2/VEGFR-2 kinase-IN-1
	TIE-2/VEGFR-2 kinase-IN-1 用于合成TIE-2或者VEGFR-2抑制剂，可用于研究不适当的血管生成的相关疾病。
TP1474	LXW7	Integrin	Cytoskeletal Signaling
	LXW7 是一种整合素αvβ3抑制剂，是含 Arg-Gly-Asp (RGD) 的环状肽，对αvβ3整联蛋白具有很高的结合亲和力，IC50为 0.68 μM。它可增强 VEGFR-2 磷酸化和 ERK1/2 活化，具有抗炎活性。
T9724	VEGFR2-IN-2	Others	Others
	VEGFR2-IN-2 具有抗炎和镇痛活性。
T22432	SU5208 3-[(Thien-2-yl)methylene]-2-indolinone	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	SU5208 (3-[(Thien-2-yl)methylene]-2-indolinone) 对血管内皮生长因子受体2具有抑制作用。
T22349	JNJ-38158471 CS-2660	VEGFR; c-RET; c-Kit	Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors
	JNJ-38158471 (CS-2660) 是一种耐受性好的，有口服活性的、高效的、选择性的 VEGFR-2抑制剂 (IC50:40 nM)，还能抑制 Ret (IC50:180 nM) 和 Kit (IC50:500 nM)。
T22431	SU5204 3-[(2-Ethoxyphenyl)methylidene]-1H-indol-2-one	EGFR; VEGFR; HER	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	SU5204 (3-[(2-Ethoxyphenyl)methylidene]-1H-indol-2-one) 是酪氨酸激酶抑制剂，是 SU5025 的类似物，对 FLK-1 (VEGFR-2) 和 HER2 的IC50分别为 4 和 51.5 μM。
T5349	SCR-1481B1 麦他替尼胺丁三醇,c-Met inhibitor 2	VEGFR; c-Met/HGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	SCR-1481B1 (c-Met inhibitor 2) 能够作用于依赖 Met 激活的癌症，对 VEGFR 具有抑制作用。
T13238	Tyrphostin AG1433 SU1433,AG1433	VEGFR; PDGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	Tyrphostin AG1433 (AG1433) 是选择性的PDGFRβ和VEGFR-2 (Flk-1/KDR)抑制剂，IC50分别为 5.0 μM 和 9.3 μM。Tyrphostin AG1433有防止血管形成的活性。
T6137	KRN-633 KRN633,N-[2-氯-4-[(6,7-二甲氧基-4-喹唑啉基)氧基]苯基]-N'-丙基脲	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	KRN-633 是一种 VEGFR 抑制剂，能够一种 VEGFR1 (IC50:170 nM)、VEGFR2 (IC50:160 nM)、VEGFR3 (IC50:125 nM)。
T61229	VEGFR-2/DHFR-IN-2
	VEGFR-2/DHFR-IN-2 (compound 5b) is a dual inhibitor targeting VEGFR-2 and DHFR, with respective IC50 values of 0.623 μM and 9.085 μM. It demonstrates potent cytotoxicity against C26, HepG2, and MCF7 cancer cell lines, with IC50 values ranging from 3.59 μM to 8.38 μM. VEGFR-2/DHFR-IN-2 holds promise for cancer research [1].
T72608	VEGFR-2/BRAF-IN-2
	VEGFR-2/BRAF-IN-2 是一种 VEGFR-2和 BRAF 双重抑制剂，对 VEGFR-2、BRAFV600E、BRAFWT 的 IC50分别为 0.111、0.089 和 0.071 µM。VEGFR-2/BRAF-IN-2 诱导细胞凋亡，在 G1 期阻滞细胞周期。
T74518	PROTAC VEGFR-2 degrader-2
	PROTACVEGFR-2降解剂-2（PROTAC-4），作为一种PROTACVEGFR-2降解剂，在VEGFR-2上的抑制作用微乎其微（IC50> 1 μM），但对EA.hy926细胞表现出抗增殖能力（IC50为133.248 μM）。
T7493	AG-13958 AG-013958,N-[2-氟-5-[[3-[(1E)-2-(2-吡啶基)乙烯基]-1H-吲唑-6-基]氨基]苯基]-1,3-二甲基-1H-吡唑-5-甲酰胺	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	AG-13958 (AG-013958) 是 VEGFR 酪氨酸激酶抑制剂，可用于年龄相关性黄斑变性 (AMD) 的脉络膜新生血管形成的研究。
T0263	Chloropyramine hydrochloride Nilfan,盐酸氯吡胺,Alergosan,Halopyramine hydrochloride	FAK; VEGFR; Histamine Receptor	Angiogenesis; Cytoskeletal Signaling; GPCR/G Protein; Immunology/Inflammation; Neuroscience; Tyrosine Kinase/Adaptors
	Chloropyramine hydrochloride (Alergosan) 是一种组胺受体 H1 拮抗剂，可抑制VEGFR-3和FAK 的生化功能。
T72607	VEGFR-2/BRAF-IN-1
	VEGFR-2/BRAF-IN-1 是一种 VEGFR-2和 BRAF 双重抑制剂，对 VEGFR-2、BRAFV600E 和BRAFWT 的IC50分别为 0.049、0.063 和 0.005 µM。VEGFR-2/BRAF-IN-1 诱导细胞凋亡，在 G1/S 期阻滞细胞周期。
T61489	VEGFR-2/DHFR-IN-1
	VEGFR-2/DHFR-IN-1 (compound 8b) 是 VEGFR-2和DHFR 的抑制剂，其IC50值分别为 0.384 和 7.881 μM。VEGFR-2/DHFR-IN-1 对大肠埃希菌，粪链球菌，肠沙门氏菌，金黄色酿脓葡萄球菌，MSSA 和MRSA 显示了良好的抗菌活性，MIC 值分别为 16，16，16，8 和 16 μg/mL。VEGFR-2/DHFR-IN-1 对 C26，HepG2 和 CF7 癌细胞系具有良好的细胞毒性，IC50值为 2.97-7.12 μM。VEGFR-2/DHFR-IN-1 可用于癌症的研究。
T74517	PROTAC VEGFR-2 degrader-1
	PROTACVEGFR-2 degrader-1（PROTAC-1），一种 PROTACVEGFR-2降解剂，对 VEGFR-2 的抑制作用很小（IC50> 1 μM），对 EA.hy926 细胞的抗增殖活性也很低（IC50> 100μM)。
T12574	PTC299 Emvododstat,(4-chlorophenyl) (1S)-6-chloro-1-(4-methoxyphenyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-2-carboxylate	VEGFR; Dehydrogenase	Angiogenesis; Metabolism; Tyrosine Kinase/Adaptors
	PTC299 ((4-chlorophenyl) (1S)-6-chloro-1-(4-methoxyphenyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-2-carboxylate) 是一种口服活性的 VEGFA mRNA 翻译抑制剂，可选择性地抑制转录后水平的 VEGF 蛋白合成。它还是二氢乳酸脱氢酶 (DHODH) 的有效抑制剂，可研究血液系统恶性肿瘤。
T61631	VEGFR-2-IN-23
	VEGFR-2-IN-23 (compound 11b) is a highly potent and selective inhibitor of VEGFR-2, with an impressive IC 50 value of 0.34 nM. This compound exhibits notable antitumor activity, capable of inducing apoptosis and cell cycle arrest specifically at the G1 phase [1].
T4315	Ki20227 N-[4-[(6,7-二甲氧基-4-喹啉基)氧基]-2-甲氧基苯基]-N'-[1-(2-噻唑基)乙基]脲	c-Fms; VEGFR; CSF-1R; PDGFR; c-Kit	Angiogenesis; Tyrosine Kinase/Adaptors
	Ki20227 是一种高效的、口服具有活性的、选择性的CSF1R(c-Fms 酪氨酸激酶)抑制剂，对 CSF1R，VEGFR2，c-Kit 和PDGFRβ的IC50分别为 2 nM，12 nM，451 nM 和 217 nM。它可以阻止破骨细胞分化和溶骨性破坏。
T79859	TIE-2/VEGFR-2 kinase-IN-4
	TIE-2/VEGFR-2 kinase-IN-4，一种苯并咪唑衍生物，作为有效的TIE-2和VEGFR-2酪氨酸激酶受体抑制剂，其IC50值分别为5.2 nM和5.1 nM，适用于血管生成相关研究。
T79858	TIE-2/VEGFR-2 kinase-IN-3
	TIE-2/VEGFR-2 kinase-IN-3，为苯并咪唑衍生物，具备高效的抑制作用于TIE-2与VEGFR-2受体酪氨酸激酶，其IC50值分别达到6.9 nM和3.5 nM。本化合物主要用于血管生成相关研究。
T80874	VEGFR-2/c-Met-IN-1	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2/c-Met-IN-1为VEGFR-2及c-Met的双重抑制剂，IC50值为138 nM和74 nM，显示出抗肿瘤活性。
T63804	VEGFR-2-IN-28
	VEGFR-2-IN-28 是 VEGFR-2 的有效抑制剂 (IC50: 0.83 μM)。VEGFR-2-IN-28 能够诱导细胞凋亡 (apoptosis)，表现出抗肿瘤效果。
T64060	VEGFR-2-IN-21
	VEGFR-2-IN-21 是 VEGFR-2 的有效抑制剂 (IC50: 0.10 μM)，表现出抗癌作用。
T62796	VEGFR-2-IN-13
	VEGFR-2-IN-13 (Compound 19a) 是一种有效的 VEGFR-2 抑制剂 (IC50: 3.4 nM)。VEGFR-2-IN-13 能够将 HepG2 的细胞周期停滞在 G2/M 期，诱导细胞凋亡 (apoptosis)。
T62439	VEGFR-2-IN-14
	VEGFR-2-IN-14 (Compound 5) 是一种 VEGFR-2 的有效抑制剂。VEGFR-2-IN-14 对 HepG2 细胞在 Pre-G1 期的生长具有抑制作用，并能够诱导细胞凋亡 (apoptosis)。
T63900	VEGFR-2-IN-11
	VEGFR-2-IN-11 是 VEGFR-2 的有效抑制剂 (IC50: 60.27 nM)，其IC50值为 60.27 nM，能够诱导细胞凋亡 (apoptosis)，具有抗癌活性。
T79494	VEGFR-2-IN-31	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2-IN-31（compound 3i）是一款针对VEGFR-2的高效抑制剂（IC50=8.93 nM），具有抗前列腺癌的活性。该化合物能够导致细胞周期在S期停滞，并诱导细胞发生凋亡（apoptosis）。
T80872	VEGFR-2-IN-37	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2-IN-37（化合物12）是一种VEGFR-2抑制剂，其在200 μM浓度下的抑制率为56.9%。该化合物也是潜在的HUVEC增殖抑制剂。
T79587	hCA/VEGFR-2-IN-2	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	hCA/VEGFR-2-IN-2 (compound 8g) 是一种具有吲哚酮基苯磺酰胺结构的化合物，目标是癌症相关的hCA IX/XII 及VEGFR-2 的双重抑制剂。该化合物对VEGFR-2 表现出强效的抑制作用（IC50=204 nM），且对hCAs有高亲和力，Ki 值分别为 hCA IX 3.6 nM、hCA II 16.1 nM、hCA XII 16.7 nM 以及hCA I 75.3 nM。hCA/VEGFR-2-IN-2 还展现出针对过表达VEGFR-2 的乳腺癌细胞的抗增殖活性。
T62901	VEGFR-2-IN-27
	VEGFR-2-IN-27 (compound 7a) 是一种 VEGFR-2 的高效抑制剂 (IC50: 14.8 nM)，能够用于抗癌研究。
T63168	VEGFR-2-IN-26
	VEGFR-2-IN-26 (compound 5h) 是一种 VEGFR-2 的高效抑制剂 (IC50: 15.5 nM)。VEGFR-2-IN-26 对白血病、中枢神经系统、非小肺、卵巢、肾、前列腺和乳腺癌细胞表现出良好的抗增殖作用。
T61561	VEGFR-2-IN-18
	VEGFR-2-IN-18 (Compound 15d) is a high-potency inhibitor of VEGFR-2, with an IC 50 value of 60 nM. This compound effectively initiates cell apoptosis and demonstrates significant antitumor properties [1].
T61137	VEGFR-2-IN-19
	VEGFR-2-IN-19 (Compound 15b) is a highly efficacious inhibitor of VEGFR2, a receptor involved in angiogenesis. Its mechanism of action involves the induction of cellular apoptosis and elevation of intracellular reactive oxygen species. Due to these properties, VEGFR-2-IN-19 holds promise as an effective anticancer agent [1].
T62314	VEGFR-2-IN-25
	VEGFR-2-IN-25 (compound 5d) 是一种 VEGFR-2 的高效抑制剂 (IC50: 12.1 nM)。VEGFR-2-IN-25 能够用于研究抗癌。
T63002	VEGFR-2-IN-15
	VEGFR-2-IN-15 (Compound 14b) 是一种 VEGFR-2 的有效抑制剂。VEGFR-2-IN-15 能够抑制 HepG2 细胞在 Pre-G1 期的生长，诱导细胞凋亡。
T79495	VEGFR-2-IN-32	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2-IN-32（Comp 3a）作为一种VEGFR-2的抑制剂，其IC50值为8.93 nM。该化合物对PC-3细胞表现出细胞毒性，IC50为1.22 μM，适用于前列腺癌研究。
T79403	VEGFR-2-IN-36	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2-IN-36（compound 15）是一种具有抗癌活性的VEGFR-2抑制剂（IC50：0.067 μM）和凋亡诱导剂。该化合物能够上调BAX水平和下调Bcl-2水平，对MCF-7（IC50=0.42 μM）和HepG2（IC50=0.22 μM）癌细胞展现出明显的毒性效果。
T37079	VEGFR2 Kinase Inhibitor II
	Vascular endothelial growth factor receptor 2 (VEGFR2, also known as KDR and FLK1) is a receptor tyrosine kinase that regulates angiogenesis, vascular development, and embryonic hematopoiesis in response to VEGF isoforms A, C, and D. VEGFR2 kinase inhibitor II is a reversible, cell-permeable inhibitor of VEGFR2's kinase activity (IC50 = 70 nM). It less potently inhibits the platelet-derived growth factor receptor β (PDGFRβ; IC50 = 920 nM) and related receptor and non-receptor tyrosine kinases. V...
T63822	VEGFR-2-IN-22
	VEGFR-2-IN-22 (Compound 25) 是 VEGFR-2 和 β-tubulin 聚合抑制剂，对 VEGFR-2 的 IC50=19.82 nM。VEGFR-2-IN-22 能够诱导细胞凋亡 (apoptosis)。
T62763	VEGFR-2-IN-12
	VEGFR-2-IN-12 (compound 6g) 是一种 2-oxoquinoxalinyl-1,2,4-triazole，是一种 VEGFR-2 的有效抑制剂 (IC50: 0.037 μM)。VEGFR-2-IN-12 能够高度抑制 MCF-7 细胞的生长 (GI50: 1.6 μM)。VEGFR-2-IN-12 具有抗肿瘤作用。
T63722	VEGFR-2-IN-24
	VEGFR-2-IN-24 是 VEGFR-2 的有效抑制剂 (IC50: 0.22 μM)，能够用于研究肿瘤。
T62071	VEGFR-2-IN-16
	VEGFR-2-IN-16 (Compound 15b) 是一种 VEGFR-2 的有效抑制剂 (IC50: 86.36 nM)，表现出抗肿瘤效果。

化合物

Cat.No: T37078

Target: VEGFR

Cat.No: T10123

Synonym: KDR-in-4

Target: VEGFR

VEGFR-2-IN-29

Cat.No: T9979

Target: VEGFR

Cat.No: T2056

Synonym: 2, 4-Pyrimidinediamine with linker,UNC0064-12,2,4-Pyrimidinediamine with linker

Target: VEGFR

TIE-2/VEGFR-2 kinase-IN-2

Cat.No: T40581

TIE-2/VEGFR-2 kinase-IN-5

Cat.No: T79860

Target: VEGFR, Tie-2

TIE-2/VEGFR-2 kinase-IN-1

Cat.No: T8817

Cat.No: TP1474

Target: Integrin

Cat.No: T9724

Target: Others

Cat.No: T22432

Synonym: 3-[(Thien-2-yl)methylene]-2-indolinone

Target: VEGFR

Cat.No: T22349

Synonym: CS-2660

Target: VEGFR, c-RET, c-Kit

Cat.No: T22431

Synonym: 3-[(2-Ethoxyphenyl)methylidene]-1H-indol-2-one

Target: EGFR, VEGFR, HER

Cat.No: T5349

Synonym: 麦他替尼胺丁三醇,c-Met inhibitor 2

Target: VEGFR, c-Met/HGFR

Tyrphostin AG1433

Cat.No: T13238

Synonym: SU1433,AG1433

Target: VEGFR, PDGFR

Cat.No: T6137

Synonym: KRN633,N-[2-氯-4-[(6,7-二甲氧基-4-喹唑啉基)氧基]苯基]-N'-丙基脲

Target: VEGFR

VEGFR-2/DHFR-IN-2

Cat.No: T61229

VEGFR-2/BRAF-IN-2

Cat.No: T72608

PROTAC VEGFR-2 degrader-2

Cat.No: T74518

Cat.No: T7493

Synonym: AG-013958,N-[2-氟-5-[[3-[(1E)-2-(2-吡啶基)乙烯基]-1H-吲唑-6-基]氨基]苯基]-1,3-二甲基-1H-吡唑-5-甲酰胺

Target: VEGFR

Chloropyramine hydrochloride

Cat.No: T0263

Synonym: Nilfan,盐酸氯吡胺,Alergosan,Halopyramine hydrochloride

Target: FAK, VEGFR, Histamine Receptor

VEGFR-2/BRAF-IN-1

Cat.No: T72607

VEGFR-2/DHFR-IN-1

Cat.No: T61489

PROTAC VEGFR-2 degrader-1

Cat.No: T74517

Cat.No: T12574

Synonym: Emvododstat,(4-chlorophenyl) (1S)-6-chloro-1-(4-methoxyphenyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-2-carboxylate

Target: VEGFR, Dehydrogenase

VEGFR-2-IN-23

Cat.No: T61631

Cat.No: T4315

Synonym: N-[4-[(6,7-二甲氧基-4-喹啉基)氧基]-2-甲氧基苯基]-N'-[1-(2-噻唑基)乙基]脲

Target: c-Fms, VEGFR, CSF-1R, PDGFR, c-Kit

TIE-2/VEGFR-2 kinase-IN-4

Cat.No: T79859

TIE-2/VEGFR-2 kinase-IN-3

Cat.No: T79858

VEGFR-2/c-Met-IN-1

Cat.No: T80874

Target: VEGFR

VEGFR-2-IN-28

Cat.No: T63804

VEGFR-2-IN-21

Cat.No: T64060

VEGFR-2-IN-13

Cat.No: T62796

VEGFR-2-IN-14

Cat.No: T62439

VEGFR-2-IN-11

Cat.No: T63900

VEGFR-2-IN-31

Cat.No: T79494

Target: VEGFR

VEGFR-2-IN-37

Cat.No: T80872

Target: VEGFR

hCA/VEGFR-2-IN-2

Cat.No: T79587

Target: VEGFR

VEGFR-2-IN-27

Cat.No: T62901

VEGFR-2-IN-26

Cat.No: T63168

VEGFR-2-IN-18

Cat.No: T61561

VEGFR-2-IN-19

Cat.No: T61137

VEGFR-2-IN-25

Cat.No: T62314

VEGFR-2-IN-15

Cat.No: T63002

VEGFR-2-IN-32

Cat.No: T79495

Target: VEGFR

VEGFR-2-IN-36

Cat.No: T79403

Target: VEGFR

VEGFR2 Kinase Inhibitor II

Cat.No: T37079

VEGFR-2-IN-22

Cat.No: T63822

VEGFR-2-IN-12

Cat.No: T62763

VEGFR-2-IN-24

Cat.No: T63722

VEGFR-2-IN-16

Cat.No: T62071

Cat. No.	Product Name	Target	Signaling Pathways
T8213	Isolinderalactone	NOS; STAT	Immunology/Inflammation; JAK/STAT signaling; Stem Cells
	Isolinderalactone 具有抗炎和抗癌能力，具有中等的 iNOS 抑制活性，IC50 值为 0.30 uM。
T13108	Pamufetinib H2OL3Q4XRD,4-(2-Fluoro-4-(3-(2-phenylacetyl)thioureido)phenoxy)-7-methoxy-N-methylquinoline-6-carboxamide,TAS-115	VEGFR; c-Met/HGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	Pamufetinib (TAS-115) 是VEGFR 和c-Met/HGFR 抑制剂，能够抑制 rVEGFR2 (IC50:30 nM)和 rMET (IC50:32 nM)的活性。
T14055	5Z-7-Oxozeaenol FR148083,L783279,LL-Z 1640-2	VEGFR; FLT; MEK; MAPK; PDGFR; Antibiotic; Src	Angiogenesis; MAPK; Microbiology/Virology; Tyrosine Kinase/Adaptors
	5Z-7-Oxozeaenol (FR148083) 是一种天然抗原生动物抑制剂，不可逆的选择性抑制 TAK1和 VEGF-R2，IC50值分别为 8 nM 和 52 nM。
TN1557	Decursinol angelate	ERK; VEGFR; PKC; JNK	Angiogenesis; Chromatin/Epigenetic; Cytoskeletal Signaling; MAPK; Tyrosine Kinase/Adaptors
	Decursinol angelate 是从朝鲜当归根部分离得到的一种天然产物，是 PKC 激酶的激活剂，有细胞毒性，抗肿瘤和抗炎活性。
T38250	L-Sepiapterin
	L-Sepiapterin, also known as Sepiapterin, is a precursor compound crucial for the production of tetrahydrobiopterin (BH4), which serves as a coenzyme for endothelial nitric oxide synthase (eNOS). This compound demonstrates its efficacy by improving endothelial dysfunction in small mesenteric arteries from db/db mice and promoting angiogenesis. Moreover, L-Sepiapterin exerts inhibitory effects on cellular proliferation and migration in ovarian cancer cells through the down-regulation of p70S6K-de...

天然产物

Isolinderalactone

Cat.No: T8213

Target: NOS, STAT

Cat.No: T13108

Synonym: H2OL3Q4XRD,4-(2-Fluoro-4-(3-(2-phenylacetyl)thioureido)phenoxy)-7-methoxy-N-methylquinoline-6-carboxamide,TAS-115

Target: VEGFR, c-Met/HGFR

5Z-7-Oxozeaenol

Cat.No: T14055

Synonym: FR148083,L783279,LL-Z 1640-2

Target: VEGFR, FLT, MEK, MAPK, PDGFR, Antibiotic, Src

Decursinol angelate

Cat.No: TN1557

Target: ERK, VEGFR, PKC, JNK

Cat.No: T38250

我们的所有产品和服务仅用于科学研究，不能被用于人体，我们也不向个人提供产品和服务。

Copyright © 2015-2024 TargetMol Chemicals Inc. All rights reserved. 沪ICP备20019793号-4

沪公网安备 31010602006700号

沪公网安备 31010602006700号

TargetMol Loading

联系我们

电话：

400-820-0310

邮箱：

service@tsbiochem.com

QQ：

2881945090（终端用户）

2885109491（经销商）

经销：

终端：

地址：

上海市静安区江场三路238号8楼