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32 results for "Apoptosis Inducer Compounds" in Products

Apoptosis Inducer Compounds

DNA cross-linking antitumor agent

Alternate Names:
NSC 241240,Paraplatin,JM 8
Chemical Name:
cis-Diammine(1,1-cyclobutanedicarboxylato)platinum(II)
Purity:
≥98%
DNA cross-linking antitumor agent

Potent pro-apoptotic anticancer agent; activates caspase-3

Alternate Names:
CDDP
Chemical Name:
cis-Diaminodichloroplatinum
Potent pro-apoptotic anticancer agent; activates caspase-3

Antitumor antibiotic agent. Inhibits DNA topoisomerase II

Alternate Names:
Adriamycin,NSC 123127
Chemical Name:
10-[(3-Amino-2,3,6-trideoxy-α-L-lyxohexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(hydroxyacetyl)-5,12-naphthacenedione hydrochloride
Purity:
≥98%
Doxorubicin treated cardiomyocytes secrete Troponin T
(3)

Inhibits RNA polymerase

Chemical Name:
2-Amino-(N,N)-1-bis(hexadecahydro-6,13-diisopropyl-2,5,9-trimethyl-1,4,7,11,14-pentaoxo-1H-pyrrolo[2,1]-[1,4,7,10,13] oxatetraazacyclohexadecin-10-yl)-4,6-dimethyl-3-oxo-3H-phenoxazine-1,9-dicarboxamide
Purity:
≥95%
Inhibits RNA polymerase

DNA cross-linking antitumor agent

Alternate Names:
Eloxatin
Chemical Name:
Oxalato[(1R-trans)-1,2-cyclohexanediamine]platinum(II)
Purity:
≥98%
DNA cross-linking antitumor agent

DNA-methylating antitumor agent

Alternate Names:
NSC 362856,CCRG 81045
Chemical Name:
3,4-Dihydro-3-methyl-4-oxoimidazo[5,1-d]-1,2,3,5-tetrazine-8-carboxamide
Purity:
≥98%
DNA-methylating antitumor agent

Purine analog; inhibits DNA synthesis

Chemical Name:
9-β-D-Arabinofuranosyl-2-fluoro-9H-purin-6-amine
Purity:
≥98%
Purine analog; inhibits DNA synthesis

DNA cross-linking antitumor agent

Alternate Names:
Ametycine
Chemical Name:
[1aS-(1aα,8β,8aα,8bα)]-6-Amino-8-[[(aminocarbonyl)oxy]methyl]-1,1a,2,8,8a,8b-hexahydro-8a-methoxy-5-methylazirino[2',3':3,4]pyrrolo[1,2-a]indole-4,7-dione
Purity:
≥98%
DNA cross-linking antitumor agent

DNA alkylator; antitumor and induces diabetes

Alternate Names:
Streptozotocin
Chemical Name:
2-Deoxy-2-[[(methylnitrosoamino)carbonyl]amino]-D-glucose
Purity:
≥95%
DNA alkylator; antitumor and induces diabetes

Inhibits RNAPII-mediated transcription; antitumor, anti-inflammatory and immunosuppressive

Chemical Name:
(3bS,4aS,5aS,6R,6aR,7aS,7bS,8aS,8bS)-3b,4,4a,6,6a,7a,7b,8b,9,10-Decahydro-6-hydroxy-8b-methyl-6a-(1-methylethyl)trisoxireno[4b,5:6,7:8a,9]phenanthro[1,2-c]furan-1(3H)-one
Purity:
≥98%
Inhibits RNAPII-mediated transcription; antitumor, anti-inflammatory and immunosuppressive

Antitumor and anti-HIV agent; activates NF-κB. Also TGR5 agonist

Chemical Name:
(+)-(3β)-3-Hydroxylup-20(29)-en-28-oic acid
Antitumor and anti-HIV agent; activates NF-κB. Also TGR5 agonist

Suppressor of MDK expression; inhibits PI 3-K signaling

Chemical Name:
3-[2-[(4-Fluorophenyl)methyl]imidazo[2,1-b]thiazol-6-yl]-2H-1-benzopyran-2-one
Purity:
≥98%
Suppressor of MDK expression; inhibits PI 3-K signaling

Promotes apoptosome formation and activates caspase-9/caspase-3 pathway. Selectively induces tumor cell apoptosis

Chemical Name:
1-[(3,4-Dichlorophenyl)methyl]-1H-indole-2,3-dione
Purity:
≥98%
Promotes apoptosome formation and activates caspase-9/caspase-3 pathway. Selectively induces tumor cell apoptosis

Proapoptotic; downregulates PLK1 expression and activates mitochondrial Ca2+ uniporter

Alternate Names:
Kempferol
Chemical Name:
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
Purity:
≥98%
Proapoptotic; downregulates PLK1 expression and activates mitochondrial Ca2+ uniporter

High affinity and selective activator of Bax

Chemical Name:
2-[(2-Nitro-9H-fluorene-9-ylidene)methyl]phenol
Purity:
≥98%
High affinity and selective activator of Bax

Bcl-2 family inhibitor; mimics BH3 and induces apoptosis in cancer cell lines

Chemical Name:
4-[4-[(4'-Chloro[1,1'-biphenyl]-2-yl)methyl]-1-piperazinyl]-N-[[4-[[(1R)-3-(dimethylamino)-1-[(phenylthio)methyl]propyl]amino]-3-nitrophenyl]sulfonyl]benzamide
Purity:
≥97%
Bcl-2 family inhibitor; mimics BH3 and induces apoptosis in cancer cell lines

DNA synthesis inhibitor. Induces pulmonary inflammation and fibrosis

Alternate Names:
NSC125066
Purity:
≥90%
DNA synthesis inhibitor. Induces pulmonary inflammation and fibrosis

Hypoxia-activated DNA alkylating agent prodrug

Chemical Name:
(1-Methyl-2-nitro-1H-imidazol-5-yl)methyl N,N'-bis(2-bromoethyl)phosphorodiamidate
Purity:
≥98%
Hypoxia-activated DNA alkylating agent prodrug

Potent fatty acid synthase inhibitor; proapoptotic

Alternate Names:
trans-C 75
Chemical Name:
(2R*,3S*)-Tetrahydro-4-methylene-2-octyl-5-oxo-3-furancarboxylic acid
Purity:
≥94%
Potent fatty acid synthase inhibitor; proapoptotic

Stimulates RhoA activation; antiproliferative agent that slows cell cycle progression

Chemical Name:
(2S,3R,4S,4aR)-3,4,4a,5-Tetrahydro-2,3,4,7-tetrahydroxy-(1,3)dioxolo(4,5-j)phenanthridin-6(2H)-one
Purity:
≥98%
Stimulates RhoA activation; antiproliferative agent that slows cell cycle progression

Alkylating agent; chemotherapeutic

Chemical Name:
2-[bis(2-Chloroethyl)amino]tetrahydro-2H-1,3,2-oxazaphosphorine 2-oxide
Purity:
≥98%
Alkylating agent; chemotherapeutic

Potent and selective HDAC8 inhibitor

Chemical Name:
N-Hydroxy-1-[(4-methoxyphenyl)methyl]-1H-indole-6-carboxamide
Purity:
≥98%
Potent and selective HDAC8 inhibitor

ULK inhibitor

Chemical Name:
N-[3-[[5-Cyclopropyl-2-[(1,2,3,4-tetrahydro-2-methyl-6-isoquinolinyl)amino]-4-pyrimidinyl]amino]propyl]cyclobutanecarboxamide dihydrochloride
Purity:
≥98%
ULK inhibitor

Potent UNC-51-like kinase 1 (ULK1) agonist

Chemical Name:
2-[Bis(2-methylpropyl)amino]-1-[4-[2-(2,4-dichlorophenyl)-2-(2-naphthalenylmethoxy)ethyl]-1-piperazinyl]ethanone dihydrochloride
Purity:
≥98%
Potent UNC-51-like kinase 1 (ULK1) agonist

ULK inhibitor

Chemical Name:
N-[3-[[5-Cyclopropyl-2-[(1,2,3,4-tetrahydro-2-methyl-6-isoquinolinyl)amino]-4-pyrimidinyl]amino]propyl]cyclobutanecarboxamide dihydrochloride
Purity:
≥98%
ULK inhibitor
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