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Bcl-2

Bcl-2

A family of proteins known as Bcl-2 have evolutionary connections. These proteins, which include Bcl-2 proper, Bcl-xL, and Bcl-w among a variety of others, control mitochondrial outer membrane permeabilization (MOMP). They can either be pro- or anti-apoptotic. The Bcl-2 family comprises a total of 25 known genes. These human genes include Bak1, Bax, Bal-2, Bok, and Mcl-1, which code for members of this family of proteins.

Bcl-2 related products

Structure Cat No. Product Name CAS No. Product Description
(R)-(-)-醋酸棉酚 V0006 AT101 866541-93-7 AT-101 [(R)-(-)-Gossypol acetic acid,the levorotatory isomer of a natural product Gossypol],is a novel, oral and potent inhibitor of Bcl-2, Bcl-xL and Mcl-1 with Ki of 0.32 μM, 0.48 μM and 0.18 μM in cell-free assays; it shows no inhibition against BIR3 and BID.
(Rac)-BDA-366 V85121 (Rac)-BDA-366 142645-19-0
(Rac)-HA14-1 V122018 (Rac)-HA14-1 927635-64-1 (Rac)-HA14-1 is the racemic form of HA14-1.
(Rac)-Lisaftoclax ((Rac)-APG-2575) V86177 (Rac)-Lisaftoclax ((Rac)-APG-2575) 2651980-10-6 (Rac)-Lisaftoclax ((Rac)-APG-2575) is a Bcl-2 inhibitor
(S)-Sabutoclax ((S)-BI-97C1) V85889 (S)-Sabutoclax ((S)-BI-97C1) 1228178-73-1
3-Tridecylphenol V111840 3-Tridecylphenol 72424-02-3 3-Tetrazylphenol is a cashew phenol compound that can be isolated from *K. hookeriana*.
4-(4-Fluorophenyl)benzoic acid V88439 4-(4-Fluorophenyl)benzoic acid 5731-10-2 4-(4-Fluorophenyl)benzoic acid (Compound 6) can bind to Bcl-2 with a KD value of 400 μM.
4-Hydroxyresveratrol V126419 4-Hydroxyresveratrol 331443-00-6 4-Hydroxyresveratrol is an analogue of resveratrol that can differentially induce the expression of the pro-apoptotic gene p53/Bax.
7-木糖甙-10-脱乙酰基紫杉醇 V28844 10-Deacetyl-7-xylosyl paclitaxel 90332-63-1 10-Deacetyl-7-xylosyl paclitaxel, a Paclitaxel analog, is ametabolite of Paclitaxel (TAXOL) which is a microtubule stabilizing agent/tubulin inhibitor and chemotherapeutic drug approved to treat various cancers.
A-1210477 V0010 A-1210477 1668553-26-1 A-1210477 is anovel, potent and specific MCL-1 (Myeloid cell leukemia-1) inhibitor with Ki and IC50 of 0.45 nM and 26.2 nM, respectively.
ABBV-467 V76047 ABBV-467 2287186-66-5 ABBV-467 is a selective MCL-1 inhibitor (Ki: <0.01 nM).
ABT-737 V0002 ABT-737 852808-04-9 ABT-737 is a novel, potent,selective and orally bioavailable BH3 mimetic inhibitor of Bcl-xL, Bcl-2 and Bcl-w with EC50 of 78.7 nM, 30.3 nM and 197.8 nM in enzymatic assays, respectively.
AF151 V128364 AF151 AF151 is a METTL3 PROTAC degrader with a DC50 of 0.43 μM in MOLM-13 cells.
AMG-176 V3448 AMG-176 1883727-34-1 AMG-176 (AMG176; tapotoclax) is a novel, potent, selective and orally bioavailable inhibitor of MCL-1 (myeloid cell leukemia-1) with aKiof 0.13 nM.
anti-TNBC agent-9 V129162 anti-TNBC agent-9 Anti-TNBC agent-9 is an anticancer drug used to treat triple-negative breast cancer (TNBC).
Anticancer agent 201 V88447 Anticancer agent 201 Anticancer agent 201 (Compound 2f) has IC50 values in the low micromolar range against a variety of tumor cell lines.
Anticancer agent 296 V128971 Anticancer agent 296 Anticancer agent 296 is a potent anticancer drug that induces endoplasmic reticulum stress by activating the PERK-eIF2α-CHOP signaling pathway, thereby regulating caspase and Bcl-2 family proteins and ultimately leading to apoptosis.
Anticancer agent 304 V128978 Anticancer agent 304 Anticancer agent 304 is an anticancer drug.
Antioxidant agent-22 V129136 Antioxidant agent-22 2996086-75-8 Antioxidant agent-22 is a tetracyclic spermidine cyclotriphosphazene compound, a p-hydroxybenzoic acid ester derivative.
Apoptosis inducer 19 V88440 Apoptosis inducer 19 Apoptosis inducer 19 (Compound 7g) is an apoptosis inducer.
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