Bcl-2 Family
Bcl-2 Family(Bcl-2蛋白家族)
Bcl-2 family proteins are a group of proteins homologous to the Bcl-2 protein and characterized by containing at least one of four conserved Bcl-2 homology (BH) domains (BH1, BH2, BH3 and BH4). Bcl-2 family proteins, consisting of pro-apoptotic and anti-apoptotic molecules, can be classified into the following three subfamilies according to sequence homology within four BH domains: (1) a subfamily shares sequence homology within all four BH domains, such as Bcl-2, Bcl-XL and Bcl-w which are anti-apoptotic; (2) a subfamily shares sequence homology within BH1, BH2 and BH4, such as Bax and Bak which are pro-apoptotic; (3) a subfamily shares sequence homology only within BH3, such as Bik and Bid which are pro-apoptotic.
Bcl-2 Family 相关产品(120)
- GC32998Ginsenoside Rh4CAS: 174721-08-5纯度: >98.00%
Ginsenoside Rh4 is an important active ingredient of traditional Chinese medicine ginseng, which has been shown to inhibit Wnt/β-Catenin, JAK2/STAT3, TGF-β/Smad2/3 and other signaling pathways.
- GC33052VU0661013CAS: 2131184-57-9纯度: >98.50%
VU661013 is a novel, potent, selective MCL1 inhibitor with Ki of 97 ± 30 pM of human MCL-1 in a TR-FRET assay. However, VU661013 does not significantly inhibit BCL-xL or BCL-2 with Ki > 40 μM or = 0.73 μM. VU661013 de-stabilizes BIM/MCL-1 association, leads to apoptosis in AML.
- GC33239AZD-5991 S-enantiomerCAS: 2143061-82-7
AZD-5991S-enantiomer是AZD-5991的低活性S型对映体。AZD-5991S-enantiomer是一种Mcl-1抑制剂,FRET实验检测的IC50为6.3μM,SPR实验检测的Kd为0.98μM。
- GC33283AZD-5991 RacemateCAS: 2143010-83-5
AZD5991 is a macrocyclic MCL-1 inhibitor with sub-nanomolar affinity for MCL-1 (Ki = 0.13 nM). The binding affinity of AZD5991 is about 25-fold lower for mouse Mcl-1 vs. human Mcl-1 but only four-fold lower for rat Mcl-1.
- GC33401S55746 hydrochloride (BLC201 (hydrochloride))CAS: 1448525-91-4纯度: >98.50%
S55746 hydrochloride (BLC201 (hydrochloride)) (BCL201 hydrochloride) 是一种有效的,具有口服活性的选择性 BCL-2 抑制剂,Ki 为 1.3 nM,Kd 为 3.9 nM。 S55746 hydrochloride (BLC201 (hydrochloride)) (BCL201 hydrochloride) 具有低毒的抗肿瘤活性。
- GC34096(R)-(-)-Gossypol acetic acid (AT-101 (acetic acid))CAS: 866541-93-7纯度: >98.00%
(R)-(-)-Gossypol acetic acid (AT-101 (acetic acid))是一种新型的、具有口服活性的Bcl-2家族蛋白抑制剂,可抑制Bcl-2(K i =260±30nM),Mcl-1(K i =170±10nM)和Bcl-xL(K i =480±40nM)。
- GC34134Glycocholic acidCAS: 475-31-0纯度: >98.00% / >97.00%
Glycocholic acid是一种参与脂肪乳化的结晶胆汁酸,是胆酸与甘氨酸的结合物,它以钠盐的形式存在于哺乳动物的胆汁中。
- GC34980(E)-Ferulic acidCAS: 537-98-4纯度: >99.00%
Trans-ferulic acid is a potent activator of AMPKunder high glucose condition.
- GC35001(S)-Gossypol acetic acidCAS: 1189561-66-7纯度: >99.00%
(S)-Gossypol acetic acid 是天然产物 Gossypol 的异构体。(S)-Gossypol 以高亲和力结合到 Bcl-xL 和 Bcl-2 蛋白的 BH3 结合沟。
- GC36557Mcl1-IN-11CAS: 2042211-13-0
Mcl1-IN-11 (Compound G) 是一种选择性的 Mcl-1 抑制剂,对 Bcl-2 的作用较弱,Ki 值分别为 0.06 和 4.2 μM。
- GC36558Mcl1-IN-12CAS: 2042211-12-9
Mcl1-IN-12 (Compound F) 是一种选择性的 Mcl-1 抑制剂,对 Bcl-2 的作用较弱,Ki 值分别为 0.29 和 3.1 μM。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC32998 | Ginsenoside Rh4 | 174721-08-5 | >98.00% | |
Ginsenoside Rh4 is an important active ingredient of traditional Chinese medicine ginseng, which has been shown to inhibit Wnt/β-Catenin, JAK2/STAT3, TGF-β/Smad2/3 and other signaling pathways. | ||||
| GC33035 | Mcl1-IN-2 | 292057-76-2 | >98.00% | |
Mcl1-IN-2 是骨髓细胞因子 1 (Mcl-1) 的抑制剂。 Mcl1-IN-2 是一种非竞争性的德里 metallo-β-lactamase (NDM-1) 抑制剂。 | ||||
| GC33052 | VU0661013 | 2131184-57-9 | >98.50% | |
VU661013 is a novel, potent, selective MCL1 inhibitor with Ki of 97 ± 30 pM of human MCL-1 in a TR-FRET assay. However, VU661013 does not significantly inhibit BCL-xL or BCL-2 with Ki > 40 μM or = 0.73 μM. VU661013 de-stabilizes BIM/MCL-1 association, leads to apoptosis in AML. | ||||
| GC33239 | AZD-5991 S-enantiomer | 2143061-82-7 | - | |
AZD-5991S-enantiomer是AZD-5991的低活性S型对映体。AZD-5991S-enantiomer是一种Mcl-1抑制剂,FRET实验检测的IC50为6.3μM,SPR实验检测的Kd为0.98μM。 | ||||
| GC33247 | AZD-5991 | 2143061-81-6 | >98.50% | |
An Mcl-1 inhibitor | ||||
| GC33255 | AZD4320 | 1357576-48-7 | >99.00% | |
AZD4320是BH-3的新型类似物,有效的BCL2/BCLxL的双重抑制剂。AZD4320对于KPUM-MS3,KPUM-UH1,和STR-428细胞系的IC50分别为26nM,17nM,和170nM。 | ||||
| GC33283 | AZD-5991 Racemate | 2143010-83-5 | - | |
AZD5991 is a macrocyclic MCL-1 inhibitor with sub-nanomolar affinity for MCL-1 (Ki = 0.13 nM). The binding affinity of AZD5991 is about 25-fold lower for mouse Mcl-1 vs. human Mcl-1 but only four-fold lower for rat Mcl-1. | ||||
| GC33295 | MIK665 (S-64315) | 1799631-75-6 | >98.50% | |
An Mcl-1 inhibitor | ||||
| GC33312 | ML311 | 315698-17-0 | >98.00% | |
An Mcl-1 inhibitor | ||||
| GC33347 | Mcl1-IN-3 | 1814891-79-6 | - | |
Mcl1-IN-3是Mcl1的抑制剂,来自专利专利WO2015153959A2,化合物实例57;IC50和Ki值分别为0.67和0.13μM。 | ||||
| GC33364 | Mcl1-IN-4 | 1580484-04-3 | - | |
Mcl1-IN-4是Mcl1的抑制剂,IC50值为0.2μM。 | ||||
| GC33401 | S55746 hydrochloride (BLC201 (hydrochloride)) | 1448525-91-4 | >98.50% | |
S55746 hydrochloride (BLC201 (hydrochloride)) (BCL201 hydrochloride) 是一种有效的,具有口服活性的选择性 BCL-2 抑制剂,Ki 为 1.3 nM,Kd 为 3.9 nM。 S55746 hydrochloride (BLC201 (hydrochloride)) (BCL201 hydrochloride) 具有低毒的抗肿瘤活性。 | ||||
| GC33407 | BM 957 | 1391107-54-2 | - | |
BM957是Bcl-2和Bcl-xL的有效抑制剂,其Ki值分别为1.2,<1nM,IC50值分别为5.4,6.0nM。 | ||||
| GC34096 | (R)-(-)-Gossypol acetic acid (AT-101 (acetic acid)) | 866541-93-7 | >98.00% | |
(R)-(-)-Gossypol acetic acid (AT-101 (acetic acid))是一种新型的、具有口服活性的Bcl-2家族蛋白抑制剂,可抑制Bcl-2(K i =260±30nM),Mcl-1(K i =170±10nM)和Bcl-xL(K i =480±40nM)。 | ||||
| GC34134 | Glycocholic acid | 475-31-0 | >98.00% / >97.00% | |
Glycocholic acid是一种参与脂肪乳化的结晶胆汁酸,是胆酸与甘氨酸的结合物,它以钠盐的形式存在于哺乳动物的胆汁中。 | ||||
| GC34263 | Bak BH3 | - | - | |
BakBH3是一种多肽,源于Bak蛋白的BH3结构域,在细胞中,能够抑制Bcl-xL的活性。 | ||||
| GC34389 | PUMA BH3 | - | - | |
PUMABH3是一种p53正向凋亡调控因子(PUMA)BH3结构域多肽,作为Bak的直接激活剂,Kd值为26nM。 | ||||
| GC34980 | (E)-Ferulic acid | 537-98-4 | >99.00% | |
Trans-ferulic acid is a potent activator of AMPKunder high glucose condition. | ||||
| GC35001 | (S)-Gossypol acetic acid | 1189561-66-7 | >99.00% | |
(S)-Gossypol acetic acid 是天然产物 Gossypol 的异构体。(S)-Gossypol 以高亲和力结合到 Bcl-xL 和 Bcl-2 蛋白的 BH3 结合沟。 | ||||
| GC35882 | dMCL1-2 | 2351218-88-5 | - | |
dMCL1-2 是一种基于 PROTAC 技术的,高效、选择性的 MCL1 降解剂,结合 MCL1 的 KD 值为 30 nM。dMCL1-2 通过降解 MCL1 激活细胞凋亡。 | ||||
| GC36556 | Mcl1-IN-1 | 713492-66-1 | >98.00% | |
Mcl1-IN-1 是一种骨髓细胞因子 1 (Mcl-1) 抑制剂,IC50 为 2.4 ?M。 | ||||
| GC36557 | Mcl1-IN-11 | 2042211-13-0 | - | |
Mcl1-IN-11 (Compound G) 是一种选择性的 Mcl-1 抑制剂,对 Bcl-2 的作用较弱,Ki 值分别为 0.06 和 4.2 μM。 | ||||
| GC36558 | Mcl1-IN-12 | 2042211-12-9 | - | |
Mcl1-IN-12 (Compound F) 是一种选择性的 Mcl-1 抑制剂,对 Bcl-2 的作用较弱,Ki 值分别为 0.29 和 3.1 μM。 | ||||
| GC36559 | Mcl1-IN-9 | 1810769-31-3 | - | |
Mcl1-IN-9 是一种有效的髓细胞白血病基因 1 (Mcl-1) 抑制剂,在重组的 BCR-ABL+ B-ALL 细胞中的 IC50 值为 446 nM,Ki 值为 0.03 nM。 | ||||
