Stem Cell
Stem Cell(干细胞)
Stem Cell 相关产品(458)
- GC11775Nefopam HClCAS: 23327-57-3纯度: >99.50%
Nefopam HCl (Fenazoxine hydrochloride) 是一种中枢作用但非阿片类镇痛药,用于缓解中度至重度疼痛。
- GC13037CX-4945 (Silmitasertib)CAS: 1009820-21-6纯度: >99.50%
CX-4945 (Silmitasertib)是一种有效的具口服活性的酪蛋白激酶2(CK2)抑制剂,对CK2α的IC 50 值为1nM。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC11245 | XMU-MP-1 | 2061980-01-4 | >99.00% | |
XMU-MP-1是可逆的、选择性的MST1/2激酶的抑制剂,对MST1和MST2的IC 50 分别为71.1±12.9 nM和38.1±6.9 nM。 | ||||
| GC11275 | C34 | 40592-88-9 | >98.00% | |
C34是一种可口服的Toll样受体4(TLR4)选择性拮抗剂,C34通过抑制TLR4/MyD88/NF-κB信号通路,减少促炎细胞因子的产生,从而发挥抗炎作用。 | ||||
| GC11325 | CX-4945 sodium salt | 1309357-15-0 | >99.50% | |
A potent, orally bioavailable CK2 inhibitor | ||||
| GC11414 | GSK503 | 1346572-63-1 | >99.50% | |
A potent, selective EZH2 inhibitor | ||||
| GC11424 | Valproic acid | 99-66-1 | >98.00% | |
A class I HDAC inhibitor | ||||
| GC11454 | Neurodazine | 937807-66-4 | >98.00% | |
Neurodazine作为一种神经源性诱导剂,能够促进多能干细胞的神经发生。 | ||||
| GC11635 | TA 02 | 1784751-19-4 | >99.50% | |
An inducer of cardiomyocyte differentiation | ||||
| GC11674 | WIKI4 | 838818-26-1 | >99.50% | |
A potent TNKS1/2 inhibitor | ||||
| GC11775 | Nefopam HCl | 23327-57-3 | >99.50% | |
Nefopam HCl (Fenazoxine hydrochloride) 是一种中枢作用但非阿片类镇痛药,用于缓解中度至重度疼痛。 | ||||
| GC11987 | RSC-133 | 1418131-46-0 | - | |
Induces pluripotency in somatic cells | ||||
| GC12068 | SAG | 912545-86-9 | >99.50% | |
SAG(Smoothened Agonist)是一种有效的Smo受体激动剂。 | ||||
| GC12096 | Semagacestat (LY450139) | 425386-60-3 | >99.50% | |
A pan γ-secretase inhibitor | ||||
| GC12133 | Windorphen | 19881-70-0 | - | |
Wnt inhibitor | ||||
| GC12181 | TBB | 17374-26-4 | >99.00% / >99.50% / >98.00% | |
TBB是一种细胞可渗透的ATP竞争性CK2抑制剂,对大鼠肝脏CK2的IC 50 为0.15μM。 | ||||
| GC12191 | LY-411575 | 209984-57-6 | >98.00% | |
A γ-secretase inhibitor | ||||
| GC12192 | MRT 10 | 330829-30-6 | - | |
An antagonist of the Smo receptor | ||||
| GC12228 | SMANT hydrochloride | 1177600-74-6 | - | |
Smoothened (Smo) signaling inhibitor | ||||
| GC12392 | LGK-974 | 1243244-14-5 | >99.50% | |
LGK-974是一种高效且特异的Porcupine(PORCN)抑制剂。 | ||||
| GC12499 | O4I1 | 175135-47-4 | - | |
An inducer of Oct3/4 | ||||
| GC12653 | LY3039478 | 1421438-81-4 | >98.00% | |
A Notch inhibitor | ||||
| GC12741 | IMR-1 | 310456-65-6 | >98.50% | |
An inhibitor of Maml1 recruitment to chromatin | ||||
| GC12811 | BRD7116 | 329059-55-4 | >99.50% | |
A selective inhibitor of leukemia stem cells | ||||
| GC12951 | HhAntag | 496794-70-8 | >98.50% | |
A hedgehog pathway inhibitor | ||||
| GC13037 | CX-4945 (Silmitasertib) | 1009820-21-6 | >99.50% | |
CX-4945 (Silmitasertib)是一种有效的具口服活性的酪蛋白激酶2(CK2)抑制剂,对CK2α的IC 50 值为1nM。 | ||||
