Apoptosis
Research Areas
Products Related to Apoptosis(675)
- GA20196(Gly¹⁴)-Humanin (human)CAS: 330936-70-4Purity: >98%
(Gly14)-Humanin (human) is a potent analogue of Humanin, with highly neuroprotective activity.
- GA20643Ac-Pro-Gly-Pro-OHCAS: 292171-04-1Purity: >98%
Ac-Pro-Gly-Pro-OH is an endogenous degradation product of extracellular collagen and acts as a CXCR2 agonist.
- GC10655DexrazoxaneCAS: 24584-09-6Purity: >99.50%
Dexrazoxane is a hydrophilic ring-closed analog of iron chelator ethylenediaminetetraacetic acid and also a strong inhibitor of topoisomerase II with IC 50 value of 10μM.
- GC10677AdemetionineCAS: 29908-03-0Purity: >98.00%
Ademetionine (S-Adenosyl methionine; AdoMet; SAMe) is an endogenous molecule generated from methionine and ATP by the action of methionine adenosyltransferase and plays an important role in cellular metabolism as the main methyl donor .
- GC11032Cl-Amidine (trifluoroacetate salt)CAS: 1043444-18-3Purity: >97.00%
Cl-Amidine (trifluoroacetate salt) is a multi-targeting peptidylarginine deminase (PAD) inhibitor with the functional group RC(NR)NR2 that inhibits PAD1 (IC 50 =0.8μM), PAD3 (IC 50 =6.2μM), and PAD4 (IC 50 =5.9μM) with 15min half-time.
- GC12604Fumonisin B1CAS: 116355-83-0Purity: >98.00%
Fumonisin B1 is a mycotoxin produced from F. moniliforme, a prevalent fungus of corn and other grains.
- GC131274-Nitroquinoline N-oxideCAS: 56-57-5Purity: >98.00%
4-Nitroquinoline N-oxide is a potent mutagenic and carcinogenic compound that induces DNA damage and oxidative stress, making 4-Nitroquinoline N-oxide an important tool for cancer research and the study of DNA repair mechanisms.
- GC132034-ethylphenyl sulfateCAS: 85734-98-1Purity: >97.00%
4-ethylphenyl sulfate is an orally active and blood-brain barrier-penetrating intestinal microbial metabolite.
- GC15892Cetrimonium Bromide (CTAB)CAS: 57-09-0Purity: >98.00%
Cetrimonium Bromide (CTAB), a common used surfactant, act as a drug solubilizer with intrinsic antibacterial properties.
- GC18346Cytochrome C (from pig)CAS: 9007-43-6Purity: >95.00%
Cytochrome c (from pig), a 'extreme multifunctional' protein that belongs to class 1 of the c-type cytochrome family, mediates electron-transfer in the respiratory chain and acts as a detoxifying agent to dispose of ROS and plays a role in cell apoptosis.
- GC18350Cytochrome C (from horse)CAS: 9007-43-6Purity: >95.00%
Cytochrome C (from horse) is an important mediator in the apoptotic pathway and has been used in various studies as an inducer of mitochondria-dependent apoptosis.
- GC19601Poly-L-lysine (M.W 70000~150000)CAS: 25988-63-0
Poly-L-lysine (M.W 70000~150000) is a polymer consists of numerous L-lysine with great biocompatibility.
- GC19602Poly-L-lysine hydrobromide (MW 150000-300000)CAS: 25988-63-0
Poly-L-lysine hydrobromide (MW 150000-300000) is a high-molecular-weight, positively charged synthetic polypeptide widely used to enhance cell adhesion to culture surfaces. Poly-L-lysine hydrobromide exhibits excellent water solubility and biocompatibility and serves as an essential reagent for the culture of primary neurons, epithelial cells, and stem cells.
- GC19603Poly-L-lysine (3~7W)CAS: 25988-63-0Purity: >98.00%
Poly-L-lysine (3~7W) is a positively charged synthetic polypeptide polymerized from L-lysine.
- GC19805UlinastatinCAS: 80449-31-6
Ulinastatin is a broad‑spectrum protease inhibitor that suppresses the activity of various hydrolases, including trypsin, chymotrypsin, and elastase.
- GC19824(±)-PinocembrinCAS: 68745-38-0Purity: >98.00%
(±)-Pinocembrin ((±)-5,7-Dihydroxyflavanone) is a GPR120 ligand able to promote wound healing in HaCaT cell line.
- GC19843NimbolideCAS: 25990-37-8Purity: >98.00%
Nimbolide is a triterpene derived from the leaves and flowers of Azadirachta indica L. Nimbolide inhibits NF- κ B induces tumor cell apoptosis. Nimbolide inhibited CDK4 / Cdk6 kinase activity. Nimbolide inhibits NF- κ B. Wnt, PI3K Akt, MAPK and JAK-STAT signaling pathways.
- GC19936Quisinostat dihydrochlorideCAS: 875320-31-3Purity: >98%
Quisinostat dihydrochloride (JNJ-26481585 dihydrochloride) is an orally available, potent pan-HDAC inhibitor with IC50s of 0.11 nM, 0.33 nM, 0.64 nM, 0.46 nM, and 0.37 nM for HDAC1, HDAC2, HDAC4, HDAC10 and HDAC11, respectively. Quisinostat dihydrochloride has a broad spectrum antitumoral activity.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GA20196 | (Gly¹⁴)-Humanin (human) | 330936-70-4 | >98% | |
(Gly14)-Humanin (human) is a potent analogue of Humanin, with highly neuroprotective activity. | ||||
| GA20643 | Ac-Pro-Gly-Pro-OH | 292171-04-1 | >98% | |
Ac-Pro-Gly-Pro-OH is an endogenous degradation product of extracellular collagen and acts as a CXCR2 agonist. | ||||
| GC10655 | Dexrazoxane | 24584-09-6 | >99.50% | |
Dexrazoxane is a hydrophilic ring-closed analog of iron chelator ethylenediaminetetraacetic acid and also a strong inhibitor of topoisomerase II with IC 50 value of 10μM. | ||||
| GC10677 | Ademetionine | 29908-03-0 | >98.00% | |
Ademetionine (S-Adenosyl methionine; AdoMet; SAMe) is an endogenous molecule generated from methionine and ATP by the action of methionine adenosyltransferase and plays an important role in cellular metabolism as the main methyl donor . | ||||
| GC11032 | Cl-Amidine (trifluoroacetate salt) | 1043444-18-3 | >97.00% | |
Cl-Amidine (trifluoroacetate salt) is a multi-targeting peptidylarginine deminase (PAD) inhibitor with the functional group RC(NR)NR2 that inhibits PAD1 (IC 50 =0.8μM), PAD3 (IC 50 =6.2μM), and PAD4 (IC 50 =5.9μM) with 15min half-time. | ||||
| GC12604 | Fumonisin B1 | 116355-83-0 | >98.00% | |
Fumonisin B1 is a mycotoxin produced from F. moniliforme, a prevalent fungus of corn and other grains. | ||||
| GC13127 | 4-Nitroquinoline N-oxide | 56-57-5 | >98.00% | |
4-Nitroquinoline N-oxide is a potent mutagenic and carcinogenic compound that induces DNA damage and oxidative stress, making 4-Nitroquinoline N-oxide an important tool for cancer research and the study of DNA repair mechanisms. | ||||
| GC13203 | 4-ethylphenyl sulfate | 85734-98-1 | >97.00% | |
4-ethylphenyl sulfate is an orally active and blood-brain barrier-penetrating intestinal microbial metabolite. | ||||
| GC13292 | EGTA | 67-42-5 | >99.00% | |
Calcium chelator | ||||
| GC14731 | MTT | 298-93-1 | >99.50% | |
MTT (MTT) is a colorimetric agent widely used to measure cell proliferation. | ||||
| GC15892 | Cetrimonium Bromide (CTAB) | 57-09-0 | >98.00% | |
Cetrimonium Bromide (CTAB), a common used surfactant, act as a drug solubilizer with intrinsic antibacterial properties. | ||||
| GC18346 | Cytochrome C (from pig) | 9007-43-6 | >95.00% | |
Cytochrome c (from pig), a 'extreme multifunctional' protein that belongs to class 1 of the c-type cytochrome family, mediates electron-transfer in the respiratory chain and acts as a detoxifying agent to dispose of ROS and plays a role in cell apoptosis. | ||||
| GC18350 | Cytochrome C (from horse) | 9007-43-6 | >95.00% | |
Cytochrome C (from horse) is an important mediator in the apoptotic pathway and has been used in various studies as an inducer of mitochondria-dependent apoptosis. | ||||
| GC19535 | Denosumab | 615258-40-7 | >99.50% | |
Denosumab is an IgG2 monoclonal antibody that targets the RANKL protein. | ||||
| GC19601 | Poly-L-lysine (M.W 70000~150000) | 25988-63-0 | - | |
Poly-L-lysine (M.W 70000~150000) is a polymer consists of numerous L-lysine with great biocompatibility. | ||||
| GC19602 | Poly-L-lysine hydrobromide (MW 150000-300000) | 25988-63-0 | - | |
Poly-L-lysine hydrobromide (MW 150000-300000) is a high-molecular-weight, positively charged synthetic polypeptide widely used to enhance cell adhesion to culture surfaces. Poly-L-lysine hydrobromide exhibits excellent water solubility and biocompatibility and serves as an essential reagent for the culture of primary neurons, epithelial cells, and stem cells. | ||||
| GC19603 | Poly-L-lysine (3~7W) | 25988-63-0 | >98.00% | |
Poly-L-lysine (3~7W) is a positively charged synthetic polypeptide polymerized from L-lysine. | ||||
| GC19805 | Ulinastatin | 80449-31-6 | - | |
Ulinastatin is a broad‑spectrum protease inhibitor that suppresses the activity of various hydrolases, including trypsin, chymotrypsin, and elastase. | ||||
| GC19824 | (±)-Pinocembrin | 68745-38-0 | >98.00% | |
(±)-Pinocembrin ((±)-5,7-Dihydroxyflavanone) is a GPR120 ligand able to promote wound healing in HaCaT cell line. | ||||
| GC19843 | Nimbolide | 25990-37-8 | >98.00% | |
Nimbolide is a triterpene derived from the leaves and flowers of Azadirachta indica L. Nimbolide inhibits NF- κ B induces tumor cell apoptosis. Nimbolide inhibited CDK4 / Cdk6 kinase activity. Nimbolide inhibits NF- κ B. Wnt, PI3K Akt, MAPK and JAK-STAT signaling pathways. | ||||
| GC19891 | CTB | 451491-47-7 | >99.00% | |
A potent p300 histone acetyltransferase activator | ||||
| GC19903 | HISPOLON(P) | 173933-40-9 | >95.00% | |
| GC19910 | 2,2',4,4'-Tetrabromodiphenyl Ether | 5436-43-1 | >95.00% | |
| GC19936 | Quisinostat dihydrochloride | 875320-31-3 | >98% | |
Quisinostat dihydrochloride (JNJ-26481585 dihydrochloride) is an orally available, potent pan-HDAC inhibitor with IC50s of 0.11 nM, 0.33 nM, 0.64 nM, 0.46 nM, and 0.37 nM for HDAC1, HDAC2, HDAC4, HDAC10 and HDAC11, respectively. Quisinostat dihydrochloride has a broad spectrum antitumoral activity. | ||||
