35
14
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2649 |
Menin-MLL inhibitor MI-2
Menin-MLL Inhibitor,MI2,MI-2,Menin-MLL inhibitor 2,MI 2 |
Apoptosis; Epigenetic Reader Domain; Histone Methyltransferase | Apoptosis; Chromatin/Epigenetic |
Menin-MLL inhibitor MI-2 (MI2) 抑制Menin-MLL 相互作用,IC50为 446±28 nM。 | |||
T9399 |
Menin-MLL inhibitor 20
|
Epigenetic Reader Domain; Histone Methyltransferase | Chromatin/Epigenetic |
Menin-MLL inhibitor 20 是一种不可逆的menin-MLL 相互作用抑制剂,具有抗肿瘤活性。 | |||
T2643 |
MI-3
Menin-MLL Inhibitor,Menin-MLL inhibitor 3,MI 3 |
Apoptosis; Epigenetic Reader Domain; Histone Methyltransferase | Apoptosis; Chromatin/Epigenetic |
MI-3 (Menin-MLL Inhibitor)是一种有高亲和力的 menin-MLL 抑制剂,IC50值为 648 nM,Kd 值为 201 nM。 | |||
T12002 |
Menin-MLL inhibitor 4
|
Others | Others |
Menin-MLL inhibitor 4 has antitumor activity.Menin-MLL inhibitor 4 is an inhibitor of Menin- MLL (mixed-lineage leukemia protein) interaction . | |||
T78151 |
Bleximenib oxalate
Menin-MLL inhibitor 24 oxalate |
Epigenetic Reader Domain | Chromatin/Epigenetic |
Bleximenib (Menin-MLL inhibitor 24) oxalate 是一种用于癌症研究的menin-mixed-lineage leukemia 1(menin-MLL)抑制剂。 | |||
T72360 |
Menin-MLL inhibitor 26
|
||
Menin-MLL inhibitor 26 是一种 Menin-MLL 抑制剂。Menin-MLL inhibitor 26 也是一个活性参照物。 Menin-MLL inhibitor 26 可以抑制细胞生长。Menin-MLL inhibitor 26 可用于白血病的研究。 | |||
T79117 |
Menin-MLL inhibitor 27
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
Menin-MLL inhibitor 27 是一种化合物,它能有效抑制Menin-MLL之间的相互作用,对于研究癌症具有潜在价值,尤其是在急性骨髓性白血病方面。 | |||
T79737 |
Menin-MLL inhibitor 29
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
Menin-MLL inhibitor 29(Compound C1)是一种选择性Menin-MLLPPI抑制剂。该化合物与Menin紧密结合,具有138 nM的KD值,并以46 nM的IC50值明显抑制Menin与MBM1(Menin结合motif 1)的相互作用。在体外条件下,Menin-MLL inhibitor 29对HepG2和Hep3B肝癌细胞系表现出抑制增殖的作用(IC50s分别为0.31 μM和0.71 μM),也能有效抑制肿瘤生长。 | |||
T12943 |
SNDX-5613
|
Epigenetic Reader Domain; Histone Methyltransferase | Chromatin/Epigenetic |
SNDX-5613 是一种 Menin-MLL 特异性抑制剂,Ki 为 0.149 nM,IC50 为 10 在 20 nM 之间,可用于 MLL 基因重排的急性白血病研究。 | |||
T72135 |
(1s,4s)-Menin-MLL inhibitor-23
|
||
(1s,4s)-Menin-MLL inhibitor-23 是Menin-MLL inhibitor-23 的对应异构体。Menin-MLL inhibitor-23 (Example 99A) 是一种menin-MLL 相互作用抑制剂。 | |||
T13336 |
VTP50469
|
Apoptosis; Epigenetic Reader Domain; Histone Methyltransferase | Apoptosis; Chromatin/Epigenetic |
VTP50469 是一种高选择性和口服活性的Menin-MLL 相互作用抑制剂,具有有效的抗白血病活性,Ki 为 104 pM。 | |||
T28036 |
MI-2-2
MI22,MI 2 2 |
Histone Methyltransferase | Chromatin/Epigenetic |
MI-2-2 是一种抑制 menin 和 MLL 之间二价蛋白质-蛋白质相互作用的抑制剂,IC50 为 46 nM。 MI-2-2 与 menin 结合,Kd 为 22 nM。 | |||
T69628 |
Iptacopan hydrochloride hydrate
|
||
Iptacopan hydrochloride hydrate is a highly potent and highly selective factor B inhibitor. | |||
T20705 |
Desmeninol
|
||
Desmeninol 是一种活性内源性代谢物,主要在尿液中检测到,在细胞内主要位于细胞质和脂肪体中。在有机合成中可作催化剂、氯化剂、固化剂和稳定剂;在染料工业中可作为生产分散红343的原料;在医药方面可用于生产奥沙拉秦等;可作为彩色照片的发色调节剂;也可作杀菌剂等。 | |||
T124064 |
Chamaejasmenin D
|
||
Chamaejasmenin D 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T124064。 | |||
T124063 |
Isochamaejasmenin B
|
||
Isochamaejasmenin B 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T124063。 | |||
TQ0069 |
MI-503
|
Epigenetic Reader Domain; Histone Methyltransferase | Chromatin/Epigenetic |
MI-503 是一种高效且可口服的 menin-mLL 相互作用抑制剂。 | |||
T16072 |
MI-538
|
Epigenetic Reader Domain; Histone Methyltransferase | Chromatin/Epigenetic |
MI-538是一种menin 和MLL 融合蛋白相互作用的抑制剂,IC50值为 21 nM。 | |||
T11925 |
M‑89
|
Epigenetic Reader Domain; Histone Methyltransferase | Chromatin/Epigenetic |
M-89 可抑制 Menin-MLL 蛋白之间的相互作用,有研究混合谱系白血病的潜力。它是一种强特异性 menin 抑制剂,结合到 menin 的Kd 值为 1.4 nM。 | |||
T39584 |
MI-3454
|
||
MI-3454 is a highly potent, orally active, and selective inhibitor of the interaction between menin and MLL1, with an IC50 of 0.51 nM. This compound effectively inhibits the proliferation of leukemic cells and promotes their differentiation, leading to the regression or complete remission of leukemia in mouse models featuring MLL1 rearrangements or NPM1 mutations. This remarkable therapeutic effect is achieved through the downregulation of key genes involved in the development of leukemia. | |||
TQ0058 |
MI-463
|
Epigenetic Reader Domain; Histone Methyltransferase | Chromatin/Epigenetic |
MI-463 是一种有口服活性的menin-mLL 相互作用的高效小分子抑制剂,IC50为15.3 nM。 | |||
T6889 |
MI-136
|
Apoptosis; Epigenetic Reader Domain; Androgen Receptor | Apoptosis; Chromatin/Epigenetic; Endocrinology/Hormones |
MI136 是 menin-MLL(PPI) 蛋白互作的抑制剂,其 IC50值为31 nM,Kd 值为23.6 nM。它可抑制 DHT 诱导的雄激素受体 (AR) 靶基因的表达,有用于去势抵抗性肿瘤的潜能。 | |||
T24471 | MIV-6 | ||
MIV-6 is an inhibitor of the menin-mixed lineage leukemia interaction. | |||
T39938 |
M-1211
|
||
M 1121 is a covalent and orally active inhibitor of the menin-MLL interaction capable of achieving complete and persistent tumor regression. | |||
T13336L |
VTP50469 fumarate
|
Others | Others |
VTP50469 fumarate is a highly selective and orally active inhibitor of Menin-MLL interaction (Ki: 104 pM), and has potently anti-leukemia activity. | |||
T39937 |
M-808
|
||
M-808 is a potent and efficacious covalent inhibitor, targeting the interaction between Menin and MLL. It demonstrates a high binding affinity with an IC50 value of 2.6 nM. | |||
T61735 |
MI-1
|
||
MI-1 抑制 Menin-MLL 相互作用,IC50为 1.9 μM。 | |||
T15831 |
M-525
|
Others | Others |
M-525 binds to menin (IC50: 3 nM) and achieves low nanomolar potencies in cell growth inhibition and in the suppression of MLL regulated gene expression in MLL leukemia cells. M-525 is a first-in-class, highly potent, irreversible, and covalent menin-MLL | |||
T22978 | MI-2 (hydrochloride) | Others | Others |
MI-2 (Menin-MLL Inhibitor) is an effective menin-MLL interaction inhibitor (IC50: 446 ± 28 nM). | |||
T27134 |
DCYM21
DC YM 21,DC-YM21,DCYM-21,DC_YM21,DC YM21 |
||
DCYM21 is an inhibitor of menin-MLL interaction. DCYM21 demonstrates potent and selective blockage of proliferation and induces both cell cycle arrest and differentiation of leukemia cells harboring MLL translocations. | |||
T24472 |
MIV-6R
MIV6R,VU05163101,VU0516310-1,VU0516310 1,MIV 6R |
||
MIV-6R is an inhibitor of the menin- MLL interaction that acts by demonstrating strong and selective effects in MLL leukemia cells and validating specific mechanisms of action. | |||
T39585 |
Ziftomenib
KO-539 |
Histone Methyltransferase | Chromatin/Epigenetic |
Ziftomenib (KO-539) 是一种具有抗肿瘤活性的 menin-MLL 相互作用抑制剂,可以用于研究白血病。 | |||
T69629 | M‑89 MLL inhibitor | ||
M‑89 is a Highly Potent Inhibitor of the Menin-Mixed Lineage Leukemia (Menin-MLL) Protein−Protein Interaction (Kd = 1.4 nM; IC50 = 25nM). M-89 binds to menin with a Kd value of 1.4 nM and effectively engages cellular menin protein at low nanomolar concentrations. M-89 inhibits cell growth in the MV4;11 and MOLM-13 leukemia cell lines carrying MLL fusion with IC50 values of 25 and 55 nM, respectively, and demonstrates >100-fold selectivity over the HL-60 leukemia cell line lacking MLL fusion. | |||
T24484 |
ML399
VU-0516340,VU 0516340,ML-399,VU0516340,ML 399 |
||
ML399 is the menin-- MLL interaction inhibitor that acts by demonstrating strong and selective effects in MLL leukemia cells and validating specific mechanism of action. | |||
T24463 |
MI-1481
MI 1481 |
||
MI-1481 is an effective MML1 inhibitor (IC50: 3.6 nM). MI-1481 showed very potent inhibition of the menin-MLL1 interaction (IC50: 3.6 nM). MI-1481 also demonstrates pronounced activity in MLL leukemia cells and in vivo in MLL leukemia models. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2726 |
Sinomenine
Cucoline,Kukoline,青藤碱 |
Apoptosis; Others; NF-κB; Opioid Receptor; Autophagy | Apoptosis; Autophagy; Endocrinology/Hormones; GPCR/G Protein; Neuroscience; NF-κB; Others |
Sinomenine (Kukoline) 是来自汉防己的一种生物碱,是 μ 阿片受体激活剂,也是NF-κB 活化的阻断剂。 | |||
T2921 |
Sinomenine hydrochloride
盐酸青藤碱,Sabianine A hydrochloride,Cucoline hydrochloride,Kukoline hydrochloride |
Apoptosis; NF-κB; Opioid Receptor; Autophagy | Apoptosis; Autophagy; Endocrinology/Hormones; GPCR/G Protein; Neuroscience; NF-κB |
Sinomenine hydrochloride (Kukoline hydrochloride) 是来自汉防己的一种生物碱,是NF-κB 活化的阻断剂。Sinomenine 也是一种 μ 阿片受体激活剂。 | |||
TN3628 |
Chamaejasmenin B
|
Others | Others |
Chamaejasmenin B 是一种从 Stellera chamaejasme L 中分离得到的化合物。Chamaejasmenin B 具有抗癌和抗肿瘤活性,可抑制癌细胞迁移和侵袭,抑制肿瘤转移。Chamaejasmenin B 可用于研究如乳腺癌类的癌症。 | |||
TN7068 |
Sinomenine N-oxide
|
Others | Others |
Sinomenine N-oxide 是青藤碱循环代谢机制的主要代谢产物之一。 | |||
TN4547 |
Methyl isodrimeninol
|
Others | Others |
Methyl isodrimeninol是一种天然产物,属于蓼科蓼属,其产品编号为 TN4547,CAS号为 442851-27-6。Methyl isodrimeninol可用作对照参考。 | |||
TN5381 | 7-Ketoisodrimenin | ||
7-Ketoisodrimenin 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5381,CAS号为 73036-54-1。 | |||
TN4651 | Neuchromenin | Others | Others |
(-)-Neuchromenin is an inducer of neurite outgrowth of PC12 cells at concentration of 2.5-10 ug/ml. | |||
T83449 | 14-Episinomenine | ||
14-Episinomenine为Stephania cepharantha所含生物碱,具可提取性质。 | |||
TN4802 |
Plathymenin
|
Others | Others |
Plathymenin 是一种从 Spatholobus suberectus 中分离出来的天然产物。 | |||
TN2620 | 14,15-Didehydrovincamenine | Others | Others |
14,15-Didehydrovincamenine 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN2620,CAS号为 112219-48-4。 | |||
TN2599 | 12-Hydroxyisodrimenin | Others | Others |
12-Hydroxyisodrimenin 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN2599,CAS号为 218780-16-6。 | |||
TN3629 | Chamaejasmenin C | Others | Others |
Chamaejasmenin C 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3629,CAS号为 89595-70-0。 | |||
T83255 |
7(R)-7,8-Dihydrosinomenine
|
||
7(R)-7,8-Dihydrosinomenine是从青藤中分离出的异喹啉生物碱,具备抗破骨细胞活性。 | |||
T83481 |
1,1′-Disinomenine
|
||
1,1'-Disinomenine,一种从Sinomenium acutum茎部分离得到的生物碱,对A549和Hela细胞表现出较弱的抑制效果。 |