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Search Results for " regression "

Targets Recommended: Ras

49

抑制剂 & 化合物

1

天然产物

9

重组蛋白

1

同位素标记化合物

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Cat. No.	Product Name	Target	Signaling Pathways
T8684	Sotorasib AMG-510	Ras	GPCR/G Protein; MAPK
	Sotorasib (AMG-510) 是一种 KRAS G12C 共价抑制剂，具有口服活性和选择性。Sotorasib 与 KRAS G12C 非活性构象的 GDP 状态结合，抑制 KRAS 及其下游信号的传导。Sotorasib 对 KRAS G12C 突变肿瘤具有抑制活性。
T60021	ecMetAP-IN-1	Others	Others
	ecMetAP-IN-1 可用作 QSAR 模型，以使用多元线性回归研究蛋氨酸氨基肽酶抑制剂作为抗癌剂。
T70388	(S)-Enitociclib VIP152	CDK	Cell Cycle/Checkpoint
	(S)-Enitociclib (VIP152) 是一种选择性 CDK9 抑制剂，通过抑制 RNA 聚合酶 II 介导的转录来诱导 MYC+ 淋巴瘤的完全消退，抑制抗凋亡和促生存蛋白的转录。
T15249	Estrogen receptor modulator 1	Estrogen Receptor/ERR	Endocrinology/Hormones
	Estrogen receptor modulator 1 是一种有效的、具有口服活性的、选择性雌激素受体(estrogen receptor)调节剂 (SERM)，其 pIC50为 0.46。它能够诱导 Tamoxifen 耐药、激素非依赖性异种移植瘤的消退。
T36287	Pirtobrutinib	BTK	Angiogenesis; Tyrosine Kinase/Adaptors
	Pirtobrutinib (LOXO-305) is an advanced BTK inhibitor that displays high selectivity and operates through a non-covalent mechanism. This compound effectively inhibits various BTK C481 substitution mutations, leading to tumor regression in BTK-dependent lymphoma tumors in mouse xenograft models. Furthermore, Pirtobrutinib exhibits remarkable selectivity for BTK, with more than a 300-fold difference compared to 370 other kinases tested. Notably, at a concentration of 1 μM, Pirtobrutinib demonstrat...
T3678	Entrectinib RXDX-101,恩曲替尼,NMS-E628	Trk receptor; ROS; ALK; Autophagy; ROS Kinase	Angiogenesis; Autophagy; Immunology/Inflammation; Tyrosine Kinase/Adaptors
	Entrectinib (RXDX-101) 是一种可口服的 Trk、ROS1和 ALK 抑制剂，具有抗肿瘤和中枢神经活性，抑制 TrkA、TrkB、TrkC、ROS1 和 ALK 的 IC50值分别为 1、3、5、12 和 7 nM。
T6248	XL888	HSP	Cytoskeletal Signaling; Metabolism
	XL888 是一种 ATP 竞争性的 Hsp90 抑制剂，IC50值为 24 nM。
T2576	Brivanib (alaninate) 丙氨酸布立尼布,BMS-582664,Brivanib Alaninate	VEGFR; FGFR; Autophagy	Angiogenesis; Autophagy; Tyrosine Kinase/Adaptors
	Brivanib Alaninate (BMS-582664) 是一种血管内皮生长因子受体 2 (VEGFR2) 抑制剂的丙氨酸盐，IC50值为 25 nM，具有潜在的抗肿瘤活性。它对 VEGFR1 和 FGFR1 适度抑制，对 VEGFR2 的选择性是对 PDGFRβ 的 240 倍。
T39584	MI-3454	Histone Methyltransferase	Chromatin/Epigenetic
	MI-3454 是一种具有口服活性，选择性和高效性的 Menin-MLL1 相互作用抑制剂，可抑制具有 MLL1 易位或 NPM1 突变的急性白血病细胞增殖并诱导分化。MI-3454 通过下调参与白血病发生的关键基因，诱导MLL1重排或NPM1突变白血病小鼠模型中白血病的完全缓解或消退。
T11396	GGTI-2418	Transferase	Metabolism
	GGTI-2418 inhibits GGTase I and FTase activities with IC50s of 9.5 nM and 53 μM, respectively. GGTI-2418 also increases p27(Kip1) and induces significant regression of breast tumors. GGTI-2418 is a highly potent, competitive, and selective geranylgeranyltransferase I (GGTase I) inhibitor.
T39938	M-1211	Others	Others
	M 1121 is a covalent and orally active inhibitor of the menin-MLL interaction capable of achieving complete and persistent tumor regression.
T69479	CGC 11093	Others	Others
	CGC 11093 is a polyamine analog; inhibits growth of human prostate tumor xenografts in nude mice. It may prove useful in promoting regression of choroidal neovascularization.
T22290	CFT-743	Others	Others
	CFT-0743 could inhibits tumor growth (81% regression) potently with PDC50 value of 0.18 nM.
T38050	CP-609754	Transferase	Metabolism
	CP-609754 是高效的、可逆的法尼基转移酶抑制剂，对重组人 H-Ras 和重组 K-Ras 法尼基化的 IC50分别为 0.57 ng/mL 和 46 ng/mL。CP-609754有潜在的抗癌作用。
T35273	YPC-22026 YPC22026,YPC 22026	Others	Others
	YPC-22026 is a novel tumor regression inducer that inhibits the znf143 regulatory gene in the mouse xenotransplantation model.
T40223	EEDi-5273	Others	Others
	EEDi-5273 is a highly potent and orally efficacious inhibitor of EED, with an approximate IC50 value of 0.2 nM. This compound exhibits exceptional activity, capable of achieving complete and persistent regression of tumors.
T41205	3',3'-cGAMP sodium salt	Others	Others
	3',3'-cGAMP sodium salt is a STING agonist. Reduces B cell proliferation and induces apoptosis of malignant B cellsin vitro. Suppresses 5TGM1 multiple myeloma xenograft growth in immunodeficient mice, and induces leukemic regression in Eμ-TCL1 mice.
T79461	YK-029A	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	YK-029A为口服活性的EGFR突变抑制剂，特异性针对EGFRT790M及EGFRex20ins。该化合物在PDX模型上对肿瘤展现良好的抑制效果，显示出明显的抗肿瘤活性。
T63328	AMXI-5001 hydrochloride	Others	Others
	AMXI-5001 hydrochloride 是口服具有活力的、有效的 parp1/2 和微管聚合抑制剂，且IC50 值明显低于现有的临床 PARP1/2 抑制剂。MXI-5001 hydrochloride 对多种人类癌细胞表现出选择性抗肿瘤细胞毒性，能够诱导已建立的肿瘤，包括较大的肿瘤完全消退。
T71023	MI-888 free base	Others	Others
	MI-888 is a potent MDM2 inhibitor (Ki = 0.44 nM) with a superior pharmacokinetic profile and enhanced in vivo efficacy. MI-888 is capable of achieving rapid, complete, and durable tumor regression in two types of xenograft models of human cancer with oral administration and represents the most potent and efficacious MDM2 inhibitor reported to date.
T10252L2	ADU-S100 ammonium salt ML RR-S2 CDA ammonium salt,MIW815 ammonium salt	STING	Immunology/Inflammation
	ADU-S100 ammonium salt (ML RR-S2 CDA ammonium salt) 是干扰素基因刺激物的激活剂。 ADU-S100 ammonium salt 可导致有效的全身性肿瘤消退和免疫。
T70552	Ipatasertib tosylate	Others	Others
	Ipatasertib, also known as GDC0068, is an orally active, potent and selective Akt inhibitor. GDC-0068 blocked Akt signaling both in cultured human cancer cell lines and in tumor xenograft models. Inhibition of Akt activity by GDC-0068 resulted in blockade of cell-cycle progression and reduced viability of cancer cell lines. Markers of Akt activation, including high-basal phospho-Akt levels, PTEN loss, and PIK3CA kinase domain mutations, correlate with sensitivity to GDC-0068. In multiple tumor...
T70356	F-1394	Others	Others
	F-1394 is an acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor. F-1394 both prevents the formation of atherosclerosis and accelerates its regression without affecting the serum TC level, indicating that F-1394 acts directly on the arterial wall. F-1394 significantly reduced neointimal thickening and the extent of macrophages in lesions without affecting serum cholesterol levels. In vitro, F-1394 attenuated foam cell formation in mouse peritoneal macrophages.
T78442	TSPP tetrasodium
	TSPP tetrasodium 作为一种光敏剂, 在癌症与微生物感染治疗中展现出效用（Ex: 413 nm, Em: 640 nm）。
T32026	GYKI-13324 GYKI 13324,GYKI13324	Others	Others
	GYKI-13324 is bifunctional nitrosoureido derivative and alkylating agent. GYKI-13324 was studied on human colorectal tumor xenograft lines. Given orally in single or multiple daily doses, GYKI-13324 produced long-term or total regression of adenomatous, b
T77115	Plamotamab
	Plamotamab (XmAb-13676) 是一种人源双特异性抗体(bsAb)，目标是CD3和CD20，通过招募细胞毒性T细胞以消灭CD20+表达的肿瘤细胞。在体内，Plamotamab诱导了轻微的血液学反应(MR)并有效促进肿瘤消退。
T36201	AZD5582 dihydrochloride AZD 5582 dihydrochloride	Others	Others
	Dimeric Smac mimetic; potent inhibitor of X-linked (XIAP) and cellular (cIAP) inhibitor of apoptosis protein (IC50 values are 15, 15 and 21 nM for XIAP, cIAP1 and cIAP2 respectively). Binds to the BIR3 domain of XIAP to prevent interaction with caspase-9. Causes degradation of cIAP1 and cIAP2 and induces apoptosis in MDA-MB-231 breast cancer cells. Causes tumor regression in MDA-MB-231 xenograft-bearing mice. Hennessy et al (2013) Discovery of a novel class of dimeric Smac mimetics as potent IAP...
T74975	Zn-DPA-maytansinoid conjugate 1	Others	Others
	Zn-DPA-maytansinoid conjugate 1 为一种靶向小分子免疫检查点的类美坦素偶联物。其能持续诱导肿瘤生长消退，并激活肿瘤微环境（TME），转化为“炎热肿瘤”。
T9684	(Z)-Orantinib	Others	Others
	(Z)-Orantinib ((Z)-SU6668) 是一种有效，选择性，具有口服活性和 ATP 竞争性的 Flk‐1/KDR，PDGFRβ和 FGFR1抑制剂，IC50值分别为 2.1，0.008 和 1.2 μM。(Z)-Orantinib 是有效的抗血管生成和抗肿瘤剂，可诱导已形成的肿瘤消退。
T74749	AK-2292	PROTACs	PROTAC
	AK-2292 是一种有效和选择性STAT5PROTAC 降解剂，DC50值为 0.10 μM。AK-2292 在体外和体内诱导 STAT5A/B 蛋白的降解。AK-2292 可在急性髓性白血病和慢性髓性白血病异种移植小鼠模型中诱导肿瘤消退。
T64015	FGFR4-IN-6	Others	Others
	FGFR4-IN-6 是一种共价的、可逆的 FGFR4 抑制剂 (IC50: 5.4 nM)，表现出良好的口服药代动力学特性。在 Hep3B2.1-7 HCC 细胞系的异种移植小鼠模型中，FGFR4-IN-6 能够明显诱导肿瘤消退，且无明显的毒性。
T34278	Redaporfin F 2BMet,F2BMet,F-2BMet,LUZ11,LUZ 11,LUZ-11	Others	Others
	Redaporfin, also known as F-2BMet or LUZ-11, is a photosensitizer for Photodynamic Therapy (PDT) of cancer. Redaporfin showed a high efficacy in the treatment of male BALB/c mice with subcutaneously implanted colon (CT26) tumours. Vascular-PDT with 1.5 mg
T70588	Tazemetostat HCl	Others	Others
	Tazemetostat HCl is a potent, selective, and orally bioavailable small-molecule inhibitor of EZH2 enzymatic activity. EPZ-6438 induces apoptosis and differentiation specifically in SMARCB1-deleted MRT cells. Treatment of xenograft-bearing mice with EPZ-6438 leads to dose-dependent regression of MRTs with correlative diminution of intratumoral trimethylation levels of lysine 27 on histone H3, and prevention of tumor regrowth after dosing cessation. These data demonstrate the dependency of SMARCB1...
T9429	ZZW-115	Others	Others
	ZZW-115 是一种有效的 NUPR1抑制剂，Kd 为 2.1 μM。ZZW-115是三氟拉嗪(TFP)的衍生物。ZZW-115显示出剂量依赖性肿瘤消退，无神经系统副作用，主要通过坏死和凋亡诱导细胞死亡。
T78836	IHMT-PI3K-455	PI3K	PI3K/Akt/mTOR signaling
	IHMT-PI3K-455（Compound 15u）为一种高效、选择性且具口服活性的PI3Kγ/δ双重抑制剂，其针对PI3Kγ与PI3Kδ的IC50值分别为7.1 nM和0.57 nM。该化合物能够抑制AKT磷酸化，并通过促进CD8+杀伤性T细胞的招募与激活，抑制肿瘤生长，适用于肿瘤学研究领域。
T62847	AMXI-5001	Others	Others
	AMXI-5001 是一种有效的、口服具有活力的 parp1/2 和微管聚合抑制剂。MXI-5001 对多种人类癌细胞显示出选择性抗肿瘤细胞毒性，其 IC50s 远低于现有的临床 PARP1/2 抑制剂。AMXI-5001 能够诱导已建立的肿瘤（包括很大的肿瘤）完全消退。
T82517	DYSP-C34	Others	Others
	DYSP-C34是一种生物相容性强且有效的超声（US）激活多功能分子机器。它提升了亲脂性/亲水性平衡，增强了超声诱导的ROS产生，并改善了细胞渗透能力，进而显著提升了对肿瘤的靶向效果及声动力疗法（SDT）介导的肿瘤缩减能力。此外，DYSP-C34还通过激活APC展示出温和的免疫原性。
T68497	FI-700	Others	Others
	FI-700 is a novel and potent FLT3 inhibitor with promising antileukemia activity. FI-700 showed a potent IC(50) value against FLT3 kinase at 20 nmol/L in an in vitro kinase assay. FI-700 showed selective growth inhibition against mutant FLT3-expressing leukemia cell lines and primary acute myeloid leukemia cells, whereas it did not affect the FLT3 ligand (FL)-driven growth of Wt-FLT3-expressing cells. Oral administration of FI-700 induced the regression of tumors in a s.c. tumor xenograft model ...
T70779	BPR1J-340	Others	Others
	BPR1J-340 is a potent and selective FLT3 inhibitor with potential anticancer activity. BPR1J-340 was identified as a novel potent FLT3 inhibitor by biochemical kinase activity (IC50 approximately 25 nM) and cellular proliferation (GC50 approximately 5 nM) assays. BPR1J-340 inhibited the phosphorylation of FLT3 and STAT5 and triggered apoptosis in FLT3-ITD(+) AML cells. The pharmacokinetic parameters of BPR1J-340 in rats were determined. BPR1J-340 also demonstrated pronounced tumor growth inhibit...
T78804	PI3Kα-IN-12	PI3K	PI3K/Akt/mTOR signaling
	PI3Kα-IN-12（化合物13），作为一种高度选择性的PI3Kα抑制剂，展现出了1.2 nM的IC50值。在HCT-116和U87-MG细胞线上的抑制作用，IC50s分别为0.83 μM和1.25 μM。通过腹腔注射（IP）给予40 mg/kg的PI3Kα-IN-12，能够有效引起接受U87-MG细胞系异种移植的小鼠模型中的肿瘤退缩。
T36314	Wortmannin-Rapamycin Conjugate	Others	Others
	Phosphoinositide 3-kinase (PI3K) and mammalian target of rapamycin (mTOR) act synergistically in promoting cancer. Wortmannin is a potent inhibitor of PI3K enzymes, while rapamycin blocks mTOR Complex 1 TORC1. Wortmannin-rapamycin conjugate consists of analogs of 17-hydroxy wortmannin and rapamycin conjugated via a prodrug linker. Hydrolysis of the prodrug linker in vivo releases the inhibitors. The wortmannin-rapamycin conjugate inhibits the growth of HT-29 colon tumors and A498 renal tumors in...
T36404	PRLX-93936	Others	Others
	PRLX-93936 is an analog of erastin that has antitumor activity. It inhibits the hypoxia-inducible factor 1 (HIF-1) signaling pathway under hypoxic conditions (IC50 = 0.09 μM in a cell-based reporter assay). PRLX-93936 (1 μM) also inhibits hypoxia-induced increases in HIF-1α expression in ME-180 cervical cancer cells. It inhibits the growth of HT-1080 fibrosarcoma, OVCAR-5 ovarian cancer, BJELR tumorigenic primary fibroblast, and PANC-1 pancreatic cancer cells with IC50 values of less than 100 nM...
T64277	ODN 1585	Others	Others
	ODN 1585 是一种有效的 IFN 和 TNFα 产生诱导剂，也是一种 NK (natural killer) 的有效刺激剂，可用做疫苗佐剂。ODN 1585 能够增强 CD8+ T 细胞的功能，包括 CD8+ T 细胞介导的 IFN-γ 的产生。ODN 1585 可以诱导小鼠已建立的黑色素瘤消退，对小鼠的疟疾也表现出完全的保护作用。ODN 1585 能够用于研究急性骨髓性白血病 (AML) 和疟疾。
T70222	Ethonafide	Others	Others
	Ethonafide is an anthracene-containing derivative of amonafide that belongs to the azonafide series of anticancer agents. The lack of cross-resistance in multidrug-resistant cancer cell lines and the absence of a quinone and hydroquinone moiety make ethonafide a potentially less cardiotoxic replacement for existing anthracene-containing anticancer agents. Ethonafide was cytotoxic against three human prostate cancer cell lines at nanomolar concentrations. Ethonafide was found to be better tolerat...
T80750	YN14	PROTACs	PROTAC
	YN14是一种高效且选择性的KRASG12C蛋白水解靶向嵌合体(PROTAC)。其能够稳定诱导KRASG12C:YN14:VHL三元复合物，并展现出低结合自由能(ΔG)。YN14对KRASG12C突变型癌细胞的增殖具有抑制作用，显著抑制其生长，并能在MIA PaCa-2异种移植模型中促进肿瘤消退，实现超过100%的肿瘤生长抑制(TGI%)。
T68389	LY2457546	Others	Others
	LY2457546 is a potent and orally bioavailable inhibitor of multiple receptor tyrosine kinases involved in angiogenic and tumorigenic signalling. LY2457546 demonstrates potent activity against targets that include VEGFR2 (KDR), PDGFRβ, FLT-3, Tie-2 and members of the Eph family of receptors. In vivo, LY2457546 inhibited VEGF-driven autophosphorylation of lung KDR in the mouse and rat in a dose and concentration dependent manner. LY2457546 was well tolerated and exhibited efficacy in a 13762 synge...
T37130	MRTX1133 formic	Others	Others
	MRTX1133 is a highly selective, first-in-class inhibitor of KRAS G12D. MRTX1133 targets the KRAS G12D protein in both active and inactive states. MRTX1133 selectively inhibits KRAS G12D mutant, but not KRAS wild-type, tumor cells[1][2]. MRTX1133 demonstrates dose-dependent inhibition of the KRAS pathway tumor regression in G12D mutant tumor models[2]. [1]. Xiaolun Wang, et al.Kras g12d inhibitors.WO2021041671A1.[2]. KRAS G12D Inhibitor: MRTX1133. [(accessed on 22 April 2021)];2021 Available onli...
T36996	MSA-2 dimer	Others	Others
	MSA-2 dimer is a selective, orally active non-nucleotide STING agonist (Kd=145 μM) with long-term antitumor and immunogenic activity. MSA-2 dimer is bound to STING as a non-covalent dimer exhibiting higher permeability than cyclic dinucleotide[1]. MSA-2 dimer (60 mg/kg; p.o.; 50 days) inhibits tumor growth and prolongs overall survival[1]. MSA-2 dimer (40 mg/kg; s.c.; 25 days) induces complete tumor regression[1].MSA-2 dimer (60 mg/kg; p.o.; 4 hours) increases proinflammatory cytokine (IFN-β) le...
T37861	Talabostat	Others	Others
	Talabostat (PT100, Val-boroPro) is a potent, nonselective and orally available dipeptidyl peptidase IV (DPP-IV) inhibitor with a Ki of 0.18 nM. Talabostat is a nonselective DPP-IV inhibitor, inhibiting DPP8/9, FAP, DPP2 and some other DASH family enzymes essentially as potently as it inhibits DPP-IV[1]. Talabostat stimulates the immune system by triggering a proinflammatory form of cell death in monocytes and macrophages known as pyroptosis. The inhibition of two serine proteases, DPP8 and DPP9,...

化合物

Cat.No: T8684

Synonym: AMG-510

Target: Ras

Cat.No: T60021

Target: Others

(S)-Enitociclib

Cat.No: T70388

Synonym: VIP152

Target: CDK

Estrogen receptor modulator 1

Cat.No: T15249

Target: Estrogen Receptor/ERR

Cat.No: T36287

Target: BTK

Cat.No: T3678

Synonym: RXDX-101,恩曲替尼,NMS-E628

Target: Trk receptor, ROS, ALK, Autophagy, ROS Kinase

Cat.No: T6248

Target: HSP

Brivanib (alaninate)

Cat.No: T2576

Synonym: 丙氨酸布立尼布,BMS-582664,Brivanib Alaninate

Target: VEGFR, FGFR, Autophagy

Cat.No: T39584

Target: Histone Methyltransferase

Cat.No: T11396

Target: Transferase

Cat.No: T39938

Target: Others

Cat.No: T69479

Target: Others

Cat.No: T22290

Target: Others

Cat.No: T38050

Target: Transferase

Cat.No: T35273

Synonym: YPC22026,YPC 22026

Target: Others

Cat.No: T40223

Target: Others

3',3'-cGAMP sodium salt

Cat.No: T41205

Target: Others

Cat.No: T79461

Target: EGFR

AMXI-5001 hydrochloride

Cat.No: T63328

Target: Others

MI-888 free base

Cat.No: T71023

Target: Others

ADU-S100 ammonium salt

Cat.No: T10252L2

Synonym: ML RR-S2 CDA ammonium salt,MIW815 ammonium salt

Target: STING

Ipatasertib tosylate

Cat.No: T70552

Target: Others

Cat.No: T70356

Target: Others

TSPP tetrasodium

Cat.No: T78442

Cat.No: T32026

Synonym: GYKI 13324,GYKI13324

Target: Others

Cat.No: T77115

AZD5582 dihydrochloride

Cat.No: T36201

Synonym: AZD 5582 dihydrochloride

Target: Others

Zn-DPA-maytansinoid conjugate 1

Cat.No: T74975

Target: Others

Cat.No: T9684

Target: Others

Cat.No: T74749

Target: PROTACs

Cat.No: T64015

Target: Others

Cat.No: T34278

Synonym: F 2BMet,F2BMet,F-2BMet,LUZ11,LUZ 11,LUZ-11

Target: Others

Tazemetostat HCl

Cat.No: T70588

Target: Others

Cat.No: T9429

Target: Others

Cat.No: T78836

Target: PI3K

Cat.No: T62847

Target: Others

Cat.No: T82517

Target: Others

Cat.No: T68497

Target: Others

Cat.No: T70779

Target: Others

Cat.No: T78804

Target: PI3K

Wortmannin-Rapamycin Conjugate

Cat.No: T36314

Target: Others

Cat.No: T36404

Target: Others

Cat.No: T64277

Target: Others

Cat.No: T70222

Target: Others

Cat.No: T80750

Target: PROTACs

Cat.No: T68389

Target: Others

MRTX1133 formic

Cat.No: T37130

Target: Others

Cat.No: T36996

Target: Others

Cat.No: T37861

Target: Others

Cat. No.	Product Name	Target	Signaling Pathways
T4867	Erucic acid Prifac 2990,芥酸,13(Z)-Docosenoic Acid,cis-13-docosenoic acid	PI3K; Endogenous Metabolite	Metabolism; PI3K/Akt/mTOR signaling
	Erucic acid (13(Z)-Docosenoic Acid) 是单不饱和脂肪酸，分离自萝卜的种子。Erucic acid 可以容易地穿过血脑屏障，使大脑中长链脂肪酸的积累正常化。Erucic acid 能够改善认知障碍并有效预防痴呆。

天然产物

Cat.No: T4867

Synonym: Prifac 2990,芥酸,13(Z)-Docosenoic Acid,cis-13-docosenoic acid

Target: PI3K, Endogenous Metabolite

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPY-05176	AMH Protein, Human, Recombinant (His) MIS,anti-Mullerian hormone,MIF	Human	HEK293 Cells
	Anti-Mullerian hormone (AMH), a member of the TGF-beta superfamily, is produced by granulosa cells (GCs) of preantral and small antral follicles and plays a role in regulating the recruitment of primordial follicles and the FSH-dependent development of follicles. BMP15 up-regulates the transcription of AMH and that the inhibition of p38 MAPK decreases the BMP15-induced expression of AMH and SOX9, suggesting that BMP15 up-regulates the expression of AMH via the p38 MAPK signaling pathway, and thi...
TMPH-01201	DRD2 Protein, Human, Recombinant (His & Myc) Dopamine D2 receptor,D(2) dopamine receptor,DRD2	Human	E. coli
	Dopamine receptor whose activity is mediated by G proteins which inhibit adenylyl cyclase. Positively regulates postnatal regression of retinal hyaloid vessels via suppression of VEGFR2/KDR activity, downstream of OPN5.
TMPH-03332	OPN4 Protein, Rat, Recombinant (His) Opn4,Melanopsin,Opsin-4	Rat	E. coli
	Photoreceptor that binds cis-retinaldehydes. Contributes to pupillar reflex, photoentrainment and other non-image forming responses to light. May be involved in the optokinetic visual tracking response. May be involved in the regulation of retinal hyaloid vessel growth and regression. OPN4 Protein, Rat, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 53.9 kDa and the accession number is Q8R456.
TMPH-01335	FGF-5 Protein, Human, Recombinant (GST & His & Myc) Smag-82,FGF5,Fibroblast growth factor 5,Heparin-binding grow...	Human	E. coli
	Plays an important role in the regulation of cell proliferation and cell differentiation. Required for normal regulation of the hair growth cycle. Functions as an inhibitor of hair elongation by promoting progression from anagen, the growth phase of the hair follicle, into catagen the apoptosis-induced regression phase. FGF-5 Protein, Human, Recombinant (GST & His & Myc) is expressed in E. coli expression system with N-10xHis-GST and C-Myc tag. The predicted molecular weight is 62.4 kDa and the ...
TMPH-02654	FGF-5 Protein, Mouse, Recombinant (His) Fgf5,Heparin-binding growth factor 5,Fibroblast growth facto...	Mouse	E. coli
	Plays an important role in the regulation of cell proliferation and cell differentiation. Required for normal regulation of the hair growth cycle. Functions as an inhibitor of hair elongation by promoting progression from anagen, the growth phase of the hair follicle, into catagen the apoptosis-induced regression phase. FGF-5 Protein, Mouse, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 32.8 kDa and the accession number is P15656.
TMPH-03400	SLC17A6 Protein, Rat, Recombinant (His) Slc17a6,Vesicular glutamate transporter 2,Solute carrier fam...	Rat	P. pastoris (Yeast)
	Mediates the uptake of glutamate into synaptic vesicles at presynaptic nerve terminals of excitatory neural cells. May also mediate the transport of inorganic phosphate. Involved in the regulation of retinal hyaloid vessel regression during postnatal development. May also play a role in the endocrine glutamatergic system of other tissues such as pineal gland and pancreas. SLC17A6 Protein, Rat, Recombinant (His) is expressed in yeast with C-6xHis tag. The predicted molecular weight is 11.1 kDa an...
TMPH-03241	Angiopoietin-2 Protein, Rat, Recombinant (E. coli, His) Angpt2,Angiopoietin-2,ANG-2	Rat	E. coli
	Binds to TEK/TIE2, competing for the ANGPT1 binding site, and modulating ANGPT1 signaling. Can induce tyrosine phosphorylation of TEK/TIE2 in the absence of ANGPT1. In the absence of angiogenic inducers, such as VEGF, ANGPT2-mediated loosening of cell-matrix contacts may induce endothelial cell apoptosis with consequent vascular regression. In concert with VEGF, it may facilitate endothelial cell migration and proliferation, thus serving as a permissive angiogenic signal. Angiopoietin-2 Protein,...
TMPJ-01114	GAMT Protein, Human, Recombinant (His) Guanidinoacetate N-methyltransferase,TP53I2,PIG2,GAMT	Human	E. coli
	GAMT is a methyltransferase which belongs to the class I-like SAM-binding methyltransferase superfamily. It contains one RMT2 (arginine N-methyltransferase 2-like) domain and is expressed in liver. GAMT converts guanidoacetate to creatine, using S-adenosylmethionine as the methyl donor. Defects in GAMT are the cause of guanidinoacetate methyltransferase deficiency, which is an autosomal recessive disorder characterized by developmental delay/regression, mental retardation, severe disturbance of ...
TMPH-03240	Angiopoietin-2 Protein, Rat, Recombinant (His) Angiopoietin-2,Angpt2,ANG-2	Rat	Baculovirus Insect Cells
	Binds to TEK/TIE2, competing for the ANGPT1 binding site, and modulating ANGPT1 signaling. Can induce tyrosine phosphorylation of TEK/TIE2 in the absence of ANGPT1. In the absence of angiogenic inducers, such as VEGF, ANGPT2-mediated loosening of cell-matrix contacts may induce endothelial cell apoptosis with consequent vascular regression. In concert with VEGF, it may facilitate endothelial cell migration and proliferation, thus serving as a permissive angiogenic signal. Angiopoietin-2 Protein,...

重组蛋白

AMH Protein, Human, Recombinant (His)

Cat.No: TMPY-05176

Species: Human

Expression System: HEK293 Cells

DRD2 Protein, Human, Recombinant (His & Myc)

Cat.No: TMPH-01201

Species: Human

Expression System: E. coli

OPN4 Protein, Rat, Recombinant (His)

Cat.No: TMPH-03332

Species: Rat

Expression System: E. coli

FGF-5 Protein, Human, Recombinant (GST & His & Myc)

Cat.No: TMPH-01335

Species: Human

Expression System: E. coli

FGF-5 Protein, Mouse, Recombinant (His)

Cat.No: TMPH-02654

Species: Mouse

Expression System: E. coli

SLC17A6 Protein, Rat, Recombinant (His)

Cat.No: TMPH-03400

Species: Rat

Expression System: P. pastoris (Yeast)

Angiopoietin-2 Protein, Rat, Recombinant (E. coli, His)

Cat.No: TMPH-03241

Species: Rat

Expression System: E. coli

GAMT Protein, Human, Recombinant (His)

Cat.No: TMPJ-01114

Species: Human

Expression System: E. coli

Angiopoietin-2 Protein, Rat, Recombinant (His)

Cat.No: TMPH-03240

Species: Rat

Expression System: Baculovirus Insect Cells

Cat. No.	Product Name	Target	Signaling Pathways
TMIH-0124	Brivanib Alaninate-d4
	Brivanib Alaninate-d4 是 Brivanib Alaninate 的氘代化合物。Brivanib Alaninate 的 CAS 号为 649735-63-7。Brivanib alaninate 是一种血管内皮生长因子受体 2 (VEGFR2) 抑制剂的丙氨酸盐，IC50值为 25 nM，具有潜在的抗肿瘤活性。它对 VEGFR1 和 FGFR1 适度抑制，对 VEGFR2 的选择性是对 PDGFRβ 的 240 倍。

同位素标记化合物

Brivanib Alaninate-d4

Cat.No: TMIH-0124

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