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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T16367 |
NVS-PAK1-1
|
PAK | Cytoskeletal Signaling |
NVS-PAK1-1 是一种有效的选择性变构 PAK1 抑制剂,IC50值为5 nM。 | |||
T30708 |
PAK 4437
|
Others | Others |
Carbamic acid, (3-(hexyloxy)phenyl)-, 1-butyl-4-piperidinyl ester, monohydrochloride (9CI) is a bioactive chemical. | |||
T27164 |
DHP-218
PAK-9,PAK9,PAK 9,DHP218 |
Others | Others |
DHP-218 is a calcium channel antagonist. DHP-218 inhibits Calcium-induced contraction of the rat aorta in high K+ solution with the pA2 value of 9.11. The IC50 value for the inhibitory effects of DHP-218 in high K+-induced and phenylephrine-induced contra | |||
T41166 |
NVS PAK1 C
|
Others | Others |
NVS PAK1 C is a negative control of NVS PAK1 1, a potent and selective PAK1 inhibitor. | |||
T35928 |
NVS-PAK1-C
NVS-PAK1-C |
Others | Others |
NVS-PAK1-C 是一种有效的、ATP 竞争的特异性变构 PAK1抑制剂探针。NVS-PAK1-C 可抑制去磷酸化的 PAK1(IC50= 5 nM) 和磷酸化的 PAK1(IC50= 6 nM)。NVS-PAK1-C 也可以抑制去磷酸化的 PAK2 (IC50=270 nM) 和磷酸化的 PAK2 (IC50=720 nM)。 | |||
T6840 |
FRAX486
|
PAK | Cytoskeletal Signaling |
FRAX486 是一种有效的 p21 活化激酶 (PAK) 抑制剂,对 PAK1、PAK2、PAK3 和 PAK4 的 IC50 值分别为 14、33、39 和 575 nM。 | |||
T16429 |
GNE 2861
|
PAK | Cytoskeletal Signaling |
GNE 2861 是一种 PAK 抑制剂,具有 II 组的选择性。它抑制 PAK4、PAK5 和 PAK6 的IC50值分别为7.5、36和126 nM。 | |||
T6839 |
FRAX1036
|
PAK | Cytoskeletal Signaling |
FRAX1036 是一种有效的选择性 PAK1 抑制剂,对 PAK1、PAK2 和 PAK4 的 Ki 值分别为 23.3 nM、72.4 nM 和 2.4 μM。 | |||
T11342L |
G-5555
|
PAK | Cytoskeletal Signaling |
G-5555 是 PAK1有效抑制剂,对 PAK1 和 PAK2 的Ki 值分别为 3.7 nM 和 11 nM。 | |||
T6546 |
IPA-3
IPA3,IPA 3 |
PAK | Cytoskeletal Signaling |
IPA-3 是一种选择性的非 ATP 竞争性 Pak1 抑制剂,IC50 为 2.5 μM。 | |||
T6014 |
FRAX597
|
PAK | Cytoskeletal Signaling |
FRAX597 是一种有效的 ATP 竞争性 I 组 PAK 抑制剂,作用于PAK1、2和3,IC50分别为 8、13 和 19 nM。 | |||
T11826 |
LCH-7749944
GNF-PF-2356 |
Apoptosis; PAK | Apoptosis; Cytoskeletal Signaling |
LCH-7749944 (GNF-PF-2356) 是一种 PAK4抑制剂,IC50为 14.93 μM。它通过下调 PAK4/c-Src/EGFR/cyclin D1 途径有效抑制人胃癌细胞的增殖,并诱导凋亡。 | |||
T2539 |
Fingolimod hydrochloride
Fingolimod (FTY720) HCl,FTY720,盐酸芬戈莫德 |
TRP/TRPV Channel; S1P Receptor; PAK; LPL Receptor | Cytoskeletal Signaling; GPCR/G Protein; Membrane transporter/Ion channel |
Fingolimod hydrochloride (FTY720) 是一种新型免疫调节剂,是一种 1-磷酸鞘氨醇(S1P) 拮抗剂,作用于 K562 和 NK 细胞,IC50为 0.033 nM。它诱导 S1P1 的内化,从而抑制 S1P 活性。它被鞘氨醇激酶磷酸化,尤其是被 SK2 磷酸化,从而可与 S1PR1、3、4 和 5 结合 | |||
T4230 |
PF-3758309 hydrochloride
PF-03758309 hydrochloride |
Apoptosis; PAK | Apoptosis; Cytoskeletal Signaling |
PF-3758309 hydrochloride (PF-03758309 hydrochloride) 是一种口服的、可逆的 ATP 竞争性PAK4抑制剂,Kd 为 2.7 nM,Ki 为 18.7 nM。它抑制锚定独立生长、诱导凋亡、细胞骨架重塑和抑制增殖,具有 PAK4 抑制剂的预期细胞功能。 | |||
T63031 |
PAK1-IN-1
|
Others | Others |
PAK1-IN-1 是一种选择性的、有效的 PAK1 抑制剂 (IC50: 9.8 nM)。PAK1-IN-1 通过剂量依赖性方式抑制 PAK1 相关肿瘤细胞的迁移和侵袭。 | |||
T63934 |
PAK4-IN-1
|
Others | Others |
PAK4-IN-1 是一个选择性的、有效的、口服具有活力的 PAK4 抑制剂,在酸性和中性条件下都很稳定。PAK4-IN-1 在体内表现出良好的抗肿瘤作用。 | |||
T6626 |
PF-3758309
PF-309,PF-03758309,PF 3758309 |
Apoptosis; PAK | Apoptosis; Cytoskeletal Signaling |
PF-3758309 (PF-03758309) 是一种可口服的、可逆的 ATP 竞争性 PAK4抑制剂。它是一种 PAK4 抑制剂,可抑制锚定独立生长、诱导凋亡、细胞骨架重塑和抑制增殖。 | |||
T81569 |
PAK4-IN-3
|
PAK | Cytoskeletal Signaling |
PAK4-IN-3 (compound 27e) 作为PAK4抑制剂,展现了10 nM的IC50。此化合物针对A549细胞表现出0.61 μM的IC50抗增殖效果,并能以浓度依赖的方式诱导A549细胞发生凋亡 (apoptosis),同时使细胞周期停滞在G0/G1期。 | |||
T61299 |
PAK4-IN-2
|
Others | Others |
PAK4-IN-2 is an exceptionally effective inhibitor of PAK4, exhibiting an IC 50 value of 2.7 nM. This compound is capable of arresting MV4-11 cells at the G0/G1 phase and inducing cell apoptosis. It holds significant potential in cancer research [1]. | |||
T6840L |
FRAX486 HCL(1232030-35-1 free base)
|
PAK | Cytoskeletal Signaling |
FRAX486 HCL(1232030-35-1 free base) 是一种有效的 p21 活化激酶 (PAK) 抑制剂,对 PAK1、PAK2、PAK3 和 PAK4 的 IC50 值分别为 14、33、39 和 575 nM。 | |||
T24078 |
G-9791
G9791 |
Others | Others |
G-9791 is an effective and selective inhibitor of group-I PAK. | |||
T82385 |
FMF-06-098-1
|
PROTACs | PROTAC |
FMF-06-098-1是一种多靶点蛋白降解剂。通过专一性降解作用,FMF-06-098-1针对多种激酶,能够有效降解AAK1, ABL2, AURKA, AURKB, BUB1B, CDC7, CDK1, CDK12, CDK13, CDK2, CDK4, CDK6, CDK7, CDK9, CHEK1, CSNK1D, EPHA1, PER, FGFR1, GAK, IRAK4, ITK, LIMK2, MAP4K2, MAP4K3, MAPK6, MAPK7, MARK4, MELK, PKN3, PLK4, PRKAA1, PTK2, PTK6, RPS6KA4, S1K2, STK35, TNK2, UHMK1, ULK1及WEE1等关键蛋白。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7939 |
Fingolimod
2-氨基-2-[2-(4-辛基苯基)乙基]-1,3-丙二醇,FTY-720A,FTY-720,芬戈莫德 |
S1P Receptor; PAK; LPL Receptor | Cytoskeletal Signaling; GPCR/G Protein |
Fingolimod (FTY-720A) 是一种 1-磷酸鞘氨醇 (S1P) 拮抗剂,作用于 K562 和 NK 细胞,IC50为 0.033 nM。它还是pak1激活剂和免疫抑制剂。 | |||
T0646 |
5-Aminosalicylic Acid
Mesalazine,5-ASA,5-氨基水杨酸,Mesalamine |
NF-κB; Lipoxygenase; COX; Glutathione Peroxidase; Endogenous Metabolite; PAK; PPAR | Cytoskeletal Signaling; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Neuroscience; NF-κB |
5-Aminosalicylic Acid (5-ASA) 是一种特异性的PPARγ激动剂,还抑制 p21-激活激酶1(PAK1) 和NF-κB,具有抗炎活性。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-02091 |
PAK1 Protein, Human, Recombinant (His & SUMO)
Serine/threonine-protein kinase PAK 1,p21-activated... |
Human | E. coli |
PAK1 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli. | |||
TMPY-04397 |
PAK-3 Protein, Human, Recombinant (His)
PAK3β,hPAK3,bPAK,PAK3bet... |
Human | Baculovirus Insect Cells |
PAK3 is a member of PAK proteins, a family of serine/threonine p21-activating kinases, serve as effectors of small Rho GTPases Cdc42 and RAC and have been implicated in a wide range of biological activities. There are six mammalian PAKs which can be divided into two groups: group I PAKs (PAK1-3) and group II PAKs (PAK4-6). Although the two PAK groups are architecturally similar there are differences in their mode of regulation suggesting their cellular functions are likely to be different. Group... | |||
TMPH-02092 |
PAK5 Protein, Human, Recombinant (His)
|
Human | Baculovirus Insect Cells |
N/A. PAK5 Protein, Human, Recombinant (His) is expressed in Baculovirus insect cells with N-6xHis tag. The predicted molecular weight is 34.9 kDa and the accession number is Q8TB93. | |||
TMPH-03701 |
Vespakinin-M Protein, Vespa mandarinia, Recombinant (His & KSI)
Vespakinin-M,Bradykinin-related peptide |
Vespa mandarinia | E. coli |
Bradykinins are a potent but short-lived agent of arteriolar dilation and increased capillary permeability. May target bradykinin receptors (BDKRB). May cause hypotension. Vespakinin-M Protein, Vespa mandarinia, Recombinant (His & KSI) is expressed in E. coli expression system with N-6xHis-KSI tag. The predicted molecular weight is 16.7 kDa and the accession number is Q7M3T3. | |||
TMPY-04559 |
CDC42BPB Protein, Human, Recombinant (His & GST)
CDC42 binding protein kinase beta (DMPK-like),MRCKB,CDC42 bi... |
Human | Baculovirus Insect Cells |
CDC42BPB is a member of the serine / threonine protein kinase family that contains a Cdc42 / Rsc-binding p21 binding domain similar to that of PAK kinase. The kinase domain of this protein is related to the myotonic dystrophy kinase related ROK and this kinase may have functions in downstream regulating of Cdc42 in cytoskeletal recognization. It has been reported that the CDC42BPB protein take part in regulating numerous cellular functions by binding to members of a serine / threonine protein ki... | |||
TMPY-01187 |
Rac1 Protein, Human, Recombinant (GST)
Rac-1,p21-Rac1,MIG5,ras-related C3 botulinum toxin substrate... |
Human | Baculovirus Insect Cells |
RAC1 is a GTPase that belongs to the RAS superfamily of small GTP-binding proteins. Members of this superfamily appear to regulate a diverse array of cellular events, including the control of cell growth, cytoskeletal reorganization, and the activation of protein kinases. Two transcript variants encoding different isoforms have been found for RAC1 gene. RAC1 is a plasma membrane-associated small GTPase which cycles between active GTP-bound and inactive GDP-bound states. In its active state, bind... | |||
TMPY-04460 |
OXSR1 Protein, Human, Recombinant (GST)
OSR1,oxidative stress responsive 1 |
Human | Baculovirus Insect Cells |
Oxidative stress-responsive 1 protein (OXSR1), also known as Serine/threonine-protein kinase OSR1, is a member of the Ser/Thr protein kinase family of proteins. OXSR1 regulates downstream kinases in response to environmental stress, and may play a role in regulating the actin cytoskeleton. OXSR1 is a 58 kDa protein of 527 amino acids that is widely expressed in mammalian tissues and cell lines. The amino acid (aa) sequence of the predicted OXSR1 protein is 39% identical to that of human SOK1. Of... |