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BCL

BCL

Bcl-2 (B-cell lymphoma 2), encoded in humans by the BCL2 gene, is the founding member of the Bcl-2 family of regulator proteins that regulate cell death (apoptosis), by either inhibiting (anti-apoptotic) or inducing (pro-apoptotic) apoptosis.
TargetMol
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Cat. No. Product Name CAS No. Purity Chemical Structure
TN3152 6-Acetonyldihydrochelerythrine
化合物 TN3152
22864-92-2 98%
TargetMol Chemical Structure 6-Acetonyldihydrochelerythrine
6-Acetonyldihydrochelerythrine exhibits significant antioxidant activities, it exhibits significant anti-HIV activity in H9 lymphocytes with EC50 and TI (Therape...
TN4490 Manassantin B
化合物 TN4490
88497-88-5 98%
TargetMol Chemical Structure Manassantin B
Manassantin B is a potent inhibitor of NF-κB activation by the suppression of transciptional activity of RelA/p65 subunit of NF-κB. It also possesses anti-EBV ...
T14499 Bax activator-1
化合物 T14499
1638526-94-9 98%
TargetMol Chemical Structure Bax activator-1
Bax activator-1 (compound 106) is a Bax activator. It induces Bax-dependent tumor cell apoptosis[1].
TN1139 Dehydrocavidine
岩黄连碱
83218-34-2 98%
TargetMol Chemical Structure Dehydrocavidine
Dehydrocavidine (Dehydrocorydaline) 具有抗肿瘤活性,它通过诱导调节 Bax/Bcl-2 介导的细胞凋亡、激活半胱天冬酶以及切割 PARP 来抑制 MCF-7 细胞增殖。
TN3931 Ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid
化合物 TN3931
57719-81-0 98%
TargetMol Chemical Structure ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid
Ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid has anti-cancer activity, it induces apoptosis of human malignant cancer cells, it also inhibits hepatocellular ...
TN3653 Cimidahurinine
化合物 TN3653
142542-89-0 98%
TargetMol Chemical Structure Cimidahurinine
Cimidahurinine can attenuate Doxorubicin (DOX)-induced cardiotoxicity in a dose-dependent manner with EC50 values of 45.79 uM; it protects against cardiotoxicity...
T10485 PROTAC Bcl2 degrader-1
化合物 T10485
2378801-85-3 98%
TargetMol Chemical Structure PROTAC Bcl2 degrader-1
PROTAC Bcl2 degrader-1 is a PROTAC, which potently and selectively induces the degradation of Mcl-1 (IC50: 11.81 μM) and Bcl-2 (IC50: 4.94 μM; DC50: 3.0 μM).
TN2040 Panaxynol
人参炔醇
81203-57-8 98%
TargetMol Chemical Structure Panaxynol
Panaxynol is the most potent antiplatelet agent in ginseng and its mechanism of action is chiefly due to the inhibition of thromboxane formation.
TN4307 Isolimonexic acid
化合物 TN4307
73904-93-5 98%
TargetMol Chemical Structure Isolimonexic acid
Isolimonexic acid exhibits cytotoxicity on MCF-7 cell lines, it also inhibits Panc-28 cancer cell growth.
T5526 Glycoborinine
化合物 T5526
233279-39-5 98%
TargetMol Chemical Structure Glycoborinine
Glycoborinine is a potential molecule against cancer cells, it can induce HepG2 apoptosis through the mitochondrial-dependent pathway. Glycoborinine has photo-ac...
T13337 WEHI-539 hydrochloride
化合物 T13337
2070018-33-4 98%
TargetMol Chemical Structure WEHI-539 hydrochloride
WEHI-539 hydrochloride is a selective Bcl-XL inhibitor (IC50: 1.1 nM).
T13337L WEHI-539
化合物WEHI-539
1431866-33-9 98%
TargetMol Chemical Structure WEHI-539
WEHI-539是一种选择性的 Bcl-XL 抑制剂(IC50:1.1 nM)。
TN4271 Isochamaejasmine
异狼毒素
93859-63-3 98%
TargetMol Chemical Structure Isochamaejasmine
Isochamaejasmine 分离自 S. chamaejasme L. 中分离出来,可抑制 NF-κB 活化。 Isochamaejasmine 通过抑制 Bcl-2 家族蛋白的活性诱导白血病细胞凋亡,可用于抗癌研究。
TN3614 Cearoin
化合物 TN3614
52811-37-7 98%
TargetMol Chemical Structure Cearoin
Cearoin has anti-inflammatory, and antiallergic activities, it can markedly inhibit inflammatory responses including LPS-induced NO production by suppressing the...
TN2308 Wilfortrine
雷公藤春碱
37239-48-8 98%
TargetMol Chemical Structure Wilfortrine
Wilfortrine can induce liver cancer cell HepG2 apoptosis, but with no effect on the cell cycle, mainly by promoting Bax expression and inhibiting anti-apoptotic ...
TMA0153 Safflor Yellow A
化合物 TMA0153
85532-77-0 98%
TargetMol Chemical Structure Safflor Yellow A
Safflor Yellow A protects cultured rat cardiomyocytes against A/R injury, maybe via inhibiting cellular oxidative stress and apoptosis.
T11973 Mcl1-IN-11
化合物 T11973
2042211-13-0 98%
TargetMol Chemical Structure Mcl1-IN-11
Mcl1-IN-11 (Compound G) is a selective Mcl-1 inhibitor, less potent at Bcl-2, with Kis of 0.06 and 4.2 μM, respectively.
T10577 BM 957
化合物 T10577
1391107-54-2 98%
TargetMol Chemical Structure BM 957
BM 957 is an effective Bcl-2 and Bcl-xL inhibitor (Kis: 1.2 and <1 nM; IC50s: 5.4 and 6.0 nM).
T16043 Metaproterenol
化合物 T16043
586-06-1 98%
TargetMol Chemical Structure Metaproterenol
Metaproterenol also has anti-inflammatory activity. Metaproterenol is a direct-acting sympathomimetic and a β2-adrenergic receptor (β2AR) agonist (IC50: 68 nM).
TN3486 Bakkenolide IIIa
化合物 TN3486
915289-60-0 98%
TargetMol Chemical Structure Bakkenolide IIIa
Bakkenolide IIIa has antioxidant, and neuroprotective effects, it protects against cerebral damage by inhibiting AKT and ERK1/2 activation and inactivated NF-κB...
6-Acetonyldihydrochelerythrine
TN3152
6-Acetonyldihydrochelerythrine exhibits significant antioxidant activities, it exhibits significant anti-HIV activity in H9 lymphocytes with EC50 and TI (Therape...
Manassantin B
TN4490
Manassantin B is a potent inhibitor of NF-κB activation by the suppression of transciptional activity of RelA/p65 subunit of NF-κB. It also possesses anti-EBV ...
Bax activator-1
T14499
Bax activator-1 (compound 106) is a Bax activator. It induces Bax-dependent tumor cell apoptosis[1].
Dehydrocavidine
TN1139
Dehydrocavidine (Dehydrocorydaline) 具有抗肿瘤活性,它通过诱导调节 Bax/Bcl-2 介导的细胞凋亡、激活半胱天冬酶以及切割 PARP 来抑制 MCF-7 细胞增殖。
ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid
TN3931
Ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid has anti-cancer activity, it induces apoptosis of human malignant cancer cells, it also inhibits hepatocellular ...
Cimidahurinine
TN3653
Cimidahurinine can attenuate Doxorubicin (DOX)-induced cardiotoxicity in a dose-dependent manner with EC50 values of 45.79 uM; it protects against cardiotoxicity...
PROTAC Bcl2 degrader-1
T10485
PROTAC Bcl2 degrader-1 is a PROTAC, which potently and selectively induces the degradation of Mcl-1 (IC50: 11.81 μM) and Bcl-2 (IC50: 4.94 μM; DC50: 3.0 μM).
Panaxynol
TN2040
Panaxynol is the most potent antiplatelet agent in ginseng and its mechanism of action is chiefly due to the inhibition of thromboxane formation.
Isolimonexic acid
TN4307
Isolimonexic acid exhibits cytotoxicity on MCF-7 cell lines, it also inhibits Panc-28 cancer cell growth.
Glycoborinine
T5526
Glycoborinine is a potential molecule against cancer cells, it can induce HepG2 apoptosis through the mitochondrial-dependent pathway. Glycoborinine has photo-ac...
WEHI-539 hydrochloride
T13337
WEHI-539 hydrochloride is a selective Bcl-XL inhibitor (IC50: 1.1 nM).
WEHI-539
T13337L
WEHI-539是一种选择性的 Bcl-XL 抑制剂(IC50:1.1 nM)。
Isochamaejasmine
TN4271
Isochamaejasmine 分离自 S. chamaejasme L. 中分离出来,可抑制 NF-κB 活化。 Isochamaejasmine 通过抑制 Bcl-2 家族蛋白的活性诱导白血病细胞凋亡,可用于抗癌研究。
Cearoin
TN3614
Cearoin has anti-inflammatory, and antiallergic activities, it can markedly inhibit inflammatory responses including LPS-induced NO production by suppressing the...
Wilfortrine
TN2308
Wilfortrine can induce liver cancer cell HepG2 apoptosis, but with no effect on the cell cycle, mainly by promoting Bax expression and inhibiting anti-apoptotic ...
Safflor Yellow A
TMA0153
Safflor Yellow A protects cultured rat cardiomyocytes against A/R injury, maybe via inhibiting cellular oxidative stress and apoptosis.
Mcl1-IN-11
T11973
Mcl1-IN-11 (Compound G) is a selective Mcl-1 inhibitor, less potent at Bcl-2, with Kis of 0.06 and 4.2 μM, respectively.
BM 957
T10577
BM 957 is an effective Bcl-2 and Bcl-xL inhibitor (Kis: 1.2 and <1 nM; IC50s: 5.4 and 6.0 nM).
Metaproterenol
T16043
Metaproterenol also has anti-inflammatory activity. Metaproterenol is a direct-acting sympathomimetic and a β2-adrenergic receptor (β2AR) agonist (IC50: 68 nM).
Bakkenolide IIIa
TN3486
Bakkenolide IIIa has antioxidant, and neuroprotective effects, it protects against cerebral damage by inhibiting AKT and ERK1/2 activation and inactivated NF-κB...
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