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16

抑制剂 & 化合物

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Cat. No. Product Name Target Signaling Pathways
TP1420 Microtubule-associated protein tau (26-44)

Microtubule-associated protein tau (26-44) is a synthetic peptide with an amino group conjugated to glutamine and a carboxyl group conjugated to lysine.
T9504 MAP4343

Microtubule Associated Cytoskeletal Signaling
MAP4343 是孕烯醇酮的 3-甲基醚衍生物。它在体外与微管相关蛋白 2 (MAP2) 结合并刺激微管蛋白聚合,从而增强神经突延伸和保护神经元免受神经毒剂的侵害。
T15612 JH-VIII-157-02

Microtubule Associated; ALK Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors
JH-VIII-157-02 是一种 ALK 抑制剂,可抑制棘皮动物微管相关蛋白样 4-ALK (EML4-ALK),对EML4-ALK G1202R、EML4-ALKwt、EML4-ALK C1156Y、EML4-ALK F1174L 和 EML4-ALK F1174L 的 IC50 均为 2 nM。
T76726 Zagotenemab

LY33003560

Microtubule Associated Cytoskeletal Signaling
Zagotenemab 是一种人源化抗微管相关蛋白 tau 抗体,能选择性地调节大脑中的 tau 沉积物。Zagotenemab 可用于研究阿尔兹海默症等神经系统疾病。
T11184 EML4-ALK kinase inhibitor 1

EML4 ALK kinase inhibitor 1,EML4-​ALK kinase inhibitor 1

ALK Angiogenesis; Tyrosine Kinase/Adaptors
EML4-ALK kinase inhibitor 1 (EML4 ALK kinase inhibitor 1) 是有效的、具有口服活性的类棘皮细胞微管相关蛋白4-间变性淋巴瘤激酶 (EML4-ALK) 的抑制剂,其 IC50 值为 1 nM。
T60688 MKI-1

MASTL Kinase Inhibitor-1

Others Others
MKI-1 (MASTL Kinase Inhibitor-1) 是微管相关丝氨酸/苏氨酸样激酶 (MASTL) 抑制剂 (IC50= 9.9 μM)。MKI-1 通过激活乳腺癌中的PP2A 发挥放射增敏和抗肿瘤活性。
T25043 Alestramustine

Alestramustine is a cytostatic antineoplastic agent. The drug, via its active metabolites, binds to microtubule-associated proteins and β-tubulin and interferes with microtubule function, thereby suppressing cell division. Due to its estrogen moiety, Ales
T80616 Posdinemab

Posdinemab为一种针对微管相关蛋白tau (MAPT)的人源化IgG1κ抗体。
T81850 MASTL-IN-2

MASTL-IN-2为MASTL(microtubule-associated Ser/Thr kinase-like)抑制剂,能够抑制人上皮MIA PaCa癌细胞的增殖,其IC50值为2.8 nM。
T68873 Cornigerine

Cornigerine is a natural product analog of colchicine produced by Colchicum cornigerum that inhibited tubulin polymerization both with and without microtubule-associated proteins, inhibited the binding of radiolabeled colchicine to tubulin, and stimulated tubulin-dependent GTP hydrolysis.
T81851 MASTL-IN-1

MASTL-IN-1是一款针对MASTL(微管相关丝氨酸/苏氨酸样激酶)的抑制剂,起到调控细胞增殖、迁移及侵袭的作用。它显示出在癌症研究中的应用潜力。
T78552 PB118

PB118是一种新型组蛋白去乙酰化酶 6(HDAC6)抑制剂,具备穿越血脑屏障的能力,可用于AD治疗。PB118 对 HDAC6 的 IC50 为 5.6 nM。
T70808 Cabazitaxel-d6

Cabazitaxel-d6 is a deuterium labeled cabazitaxel. Cabazitaxel is a semi-synthetic derivative of the natural taxoid 10-deacetylbaccatin III with potential antineoplastic activity. Cabazitaxel binds to and stabilizes tubulin, resulting in the inhibition of microtubule depolymerization and cell division, cell cycle arrest in the G2/M phase, and the inhibition of tumor cell proliferation. Unlike other taxane compounds, this agent is a poor substrate for the membrane-associated, multidrug resistance...
T69305 Milataxel

Milataxel is an orally bioavailable taxane with potential antineoplastic activity. Upon oral administration, milataxel and its major active metabolite M-10 bind to and stabilize tubulin, resulting in the inhibition of microtubule depolymerization and cell division, cell cycle arrest in the G2/M phase, and the inhibition of tumor cell proliferation. Unlike other taxane compounds, milataxel appears to be a poor substrate for the multidrug resistance (MDR) membrane-associated P-glycoprotein (P-gp) ...
T71217 MPT0B214

MPT0B214 is a novel and potent microtubule inhibitor with potential anticancer activity. MPT0B214 inhibited tubulin polymerization through strongly binding to the tubulin's colchicine-binding site and had cytotoxic activity in a variety of human tumor cell lines. After treatment with MPT0B214, KB cells were arrested in the G2-M phase before cell death occurred, which were associated with upregulation of cyclin B1, dephosphorylation of Cdc2, phosphorylation of Cdc25C and elevated expression of th...
T68743 AZD4877 HCl

AZD4877 is a synthetic kinesin spindle protein (KSP) inhibitor with potential antineoplastic activity. KSP inhibitor AZD4877 selectively inhibits microtubule motor protein KSP (also called kinesin-5 or Eg5), which may result in the inhibition of mitotic spindle assembly; activation of the spindle assembly checkpoint; induction of cell cycle arrest during the mitotic phase; and cell death in tumor cells that are actively dividing. Because KSP is not involved in postmitotic processes, such as neur...

化合物

Microtubule-associated protein tau (26-44)
Cat.No: TP1420
Synonym:
Target:
MAP4343
Cat.No: T9504
Synonym:
Target: Microtubule Associated
JH-VIII-157-02
Cat.No: T15612
Synonym:
Target: Microtubule Associated, ALK
Zagotenemab
Cat.No: T76726
Synonym: LY33003560
Target: Microtubule Associated
EML4-ALK kinase inhibitor 1
Cat.No: T11184
Synonym: EML4 ALK kinase inhibitor 1,EML4-​ALK kinase inhibitor 1
Target: ALK
MKI-1
Cat.No: T60688
Synonym: MASTL Kinase Inhibitor-1
Target: Others
Alestramustine
Cat.No: T25043
Synonym:
Target:
Posdinemab
Cat.No: T80616
Synonym:
Target:
MASTL-IN-2
Cat.No: T81850
Synonym:
Target:
Cornigerine
Cat.No: T68873
Synonym:
Target:
MASTL-IN-1
Cat.No: T81851
Synonym:
Target:
PB118
Cat.No: T78552
Synonym:
Target:
Cabazitaxel-d6
Cat.No: T70808
Synonym:
Target:
Milataxel
Cat.No: T69305
Synonym:
Target:
MPT0B214
Cat.No: T71217
Synonym:
Target:
AZD4877 HCl
Cat.No: T68743
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T3S0209 Vincristine

ERK; p38 MAPK; NF-κB; Akt; JNK; mTOR Cytoskeletal Signaling; MAPK; NF-κB; PI3K/Akt/mTOR signaling
Vincristine 与微管蛋白结合并抑制微管的形成,从而抑制癌细胞的有丝分裂。 Vincristine 可用作微管去稳定剂,用于研究治疗血液系统癌症,如白血病和淋巴瘤以及儿童肉瘤的相关研究。

天然产物

Vincristine
Cat.No: T3S0209
Synonym:
Target: ERK, p38 MAPK, NF-κB, Akt, JNK, mTOR
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