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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T17870 | cIAP1 ligand 1 | E3 ligase Ligand 12 | Others |
cIAP1 ligand 1 (E3 ligase Ligand 12) is an apoptotic protein ligand based on the LCL161 derivative that recruits IAP ubiquitin ligases to degrade target proteins, and can be used to couple with androgen receptor ligands ... | |||
T39609 | cIAP1 Ligand-Linker Conjugates 16 | cIAP1 Ligand-Linker Conjugates 16 | |
cIAP1 Ligand-Linker Conjugates 16 refers to a specific type of ligase ligand-linker conjugate, possessing the ability to engage with E3 ligases, which finds application in the synthesis of PROTACs. | |||
T69322 | cIAP1-IN-D19 | ||
cIAP1-IN-D19 is an inhibitor of E3 ligase activity of cIAP1. | |||
T17890 | cIAP1 Ligand-Linker Conjugates 2 Hydrochloride | E3 ligase Ligand-Linker Conjugates 37 Hydrochloride,cIAP1 Ligand-Linker Conjugates 2 Hydrochloride (1312302-14-9 free base) | Others |
cIAP1 Ligand-Linker Conjugates 2 Hydrochloride is a chemical compound that combines an IAP ligand, which targets the E3 ubiquitin ligase, with a PROTAC linker. It is utilized in the creation of SNIPERs[1]. | |||
T17869 | cIAP1 ligand 2 | E3 ligase Ligand 11 | Others |
cIAP1 ligand 2, a derivative of LCL161, is an IAP ligand that can be connected to the ABL ligand for protein via a linker, resulting in the formation of SNIPER. | |||
T17893 | cIAP1 Ligand-Linker Conjugates 5 | E3 ligase Ligand-Linker Conjugates 39 | Others |
cIAP1 Ligand-Linker Conjugates 5 is a chemical compound consisting of an IAP ligand that targets the E3 ubiquitin ligase, and a PROTAC linker. This compound, cIAP1 Ligand-Linker Conjugates 5, is specifically designed for... | |||
T17894 | cIAP1 Ligand-Linker Conjugates 3 | E3 ligase Ligand-Linker Conjugates 40 | Others |
cIAP1 Ligand-Linker Conjugates 3 are chemical compounds comprising an IAP ligand designed specifically for the E3 ubiquitin ligase and a PROTAC linker. These conjugates, denoted as cIAP1 Ligand-Linker Conjugates 3, find ... | |||
T17891 | cIAP1 Ligand-Linker Conjugates 2 | E3 ligase Ligand-Linker Conjugates 37 | Others |
cIAP1 Ligand-Linker Conjugates 2 is a chemical compound that combines an IAP ligand for the E3 ubiquitin ligase with a PROTAC linker. This compound is particularly useful in the design of SNIPERs [1]. | |||
T17889 | cIAP1 Ligand-Linker Conjugates 14 | E3 ligase Ligand-Linker Conjugates 36 | Others |
cIAP1 Ligand-Linker Conjugates 14 consist of an IAP ligand that targets the E3 ubiquitin ligase and a PROTAC linker. These conjugates, known as cIAP1 Ligand-Linker Conjugates 14, are used in the development of SNIPERs[1]... | |||
T17887 | cIAP1 Ligand-Linker Conjugates 15 | E3 ligase Ligand-Linker Conjugates 34 | Others |
cIAP1 Ligand-Linker Conjugates 15 consists of an IAP ligand that targets the E3 ubiquitin ligase, along with a PROTAC linker. This compound, cIAP1 Ligand-Linker Conjugates 15, is suitable for the development of SNIPERs[1... | |||
T17896 | cIAP1 Ligand-Linker Conjugates 4 | E3 ligase Ligand-Linker Conjugates 42 | Others |
cIAP1 Ligand-Linker Conjugates 4 is a chemical compound that comprises an IAP ligand specifically designed for the E3 ubiquitin ligase and a PROTAC linker. This compound, cIAP1 Ligand-Linker Conjugates 4, has the potenti... | |||
T17885 | cIAP1 Ligand-Linker Conjugates 11 | E3 ligase Ligand-Linker Conjugates 33 | Others |
cIAP1 Ligand-Linker Conjugates 11 is a chemical compound that combines an IAP ligand specifically designed for the E3 ubiquitin ligase with a PROTAC linker. This compound, cIAP1 Ligand-Linker Conjugates 11, is useful in ... | |||
T17901 | cIAP1 Ligand-Linker Conjugates 10 | E3 ligase Ligand-Linker Conjugates 47 | Others |
cIAP1 Ligand-Linker Conjugates 10 comprise of an IAP ligand and a PROTAC linker, which facilitates the design of SNIPERs. These conjugates incorporate an IAP ligand that interacts with the E3 ubiquitin ligase, and a PROT... | |||
T17900 | cIAP1 Ligand-Linker Conjugates 8 | E3 ligase Ligand-Linker Conjugates 46 | Others |
cIAP1 Ligand-Linker Conjugates 8 comprises an IAP ligand for the E3 ubiquitin ligase and a PROTAC linker. This compound is specifically utilized for the purpose of SNIPER design[1]. | |||
T17884 | cIAP1 Ligand-Linker Conjugates 11 Hydrochloride | E3 ligase Ligand-Linker Conjugates 33 Hydrochloride | Others |
cIAP1 Ligand-Linker Conjugates 11 Hydrochloride is a chemical compound consisting of an IAP ligand that targets the E3 ubiquitin ligase, along with a PROTAC linker. It is primarily utilized in the development of SNIPERs,... | |||
T17895 | cIAP1 Ligand-Linker Conjugates 1 | E3 ligase Ligand-Linker Conjugates 41 | Others |
cIAP1 Ligand-Linker Conjugates 1 is composed of an IAP ligand for the E3 ubiquitin ligase and a PROTAC linker. This compound, cIAP1 Ligand-Linker Conjugates 1, is particularly useful in the development of SNIPERs[1]. | |||
T17892 | cIAP1 Ligand-Linker Conjugates 12 | E3 ligase Ligand-Linker Conjugates 38 | Others |
cIAP1 Ligand-Linker Conjugates 12 is a chemical compound that combines an IAP ligand, which targets the E3 ubiquitin ligase, with a PROTAC linker. This compound, cIAP1 Ligand-Linker Conjugates 12, is valuable for creatin... | |||
T17897 | cIAP1 Ligand-Linker Conjugates 13 | E3 ligase Ligand-Linker Conjugates 43 | Others |
cIAP1 Ligand-Linker Conjugates 13, containing an IAP ligand for the E3 ubiquitin ligase, and a PROTAC linker, are utilized in the development of SNIPERs[1]. | |||
T17899 | cIAP1 Ligand-Linker Conjugates 9 | E3 ligase Ligand-Linker Conjugates 45 | Others |
cIAP1 Ligand-Linker Conjugates 9 feature an IAP ligand specifically targeting the E3 ubiquitin ligase, along with a PROTAC linker. It is valuable tools for developing SNIPERs[1]. | |||
T17898 | cIAP1 Ligand-Linker Conjugates 7 | E3 ligase Ligand-Linker Conjugates 44 | Others |
cIAP1 Ligand-Linker Conjugates 7 is a chemical compound that combines an IAP ligand for the E3 ubiquitin ligase with a PROTAC linker. It is utilized in the design of SNIPERs[1]. | |||
T17888 | cIAP1 Ligand-Linker Conjugates 6 hydrochloride | E3 ligase Ligand-Linker Conjugates 35 hydrochloride | Others |
cIAP1 Ligand-Linker Conjugates 6 hydrochloride is a compound that combines an IAP ligand for the E3 ubiquitin ligase and a PROTAC linker. It is utilized for the purpose of designing SNIPERs[1]. | |||
T17886 | cIAP1 Ligand-Linker Conjugates 15 hydrochloride | E3 ligase Ligand-Linker Conjugates 34 hydrochloride | Others |
cIAP1 Ligand-Linker Conjugates 15 hydrochloride is a chemical compound that combines an IAP ligand for the E3 ubiquitin ligase and a PROTAC linker. This compound is useful in the development of SNIPERs[1]. | |||
T64302 | XIAP/cIAP1 antagonist-1 | ||
XIAP/cIAP1 antagonist-1 is a potent, orally active XIAP/cIAP1 antagonist that acts on XIAP (EC50: 5.1 nM) and cIAP1 (EC50: 0.32 nM). xIAP/cIAP1 antagonist-1 dose-dependently inhibits tumour growth in vivo. | |||
T13410 | ZLDI-8 | Apoptosis , Phosphatase , Gamma-secretase , Immunology/Inflammation related | |
ZLDI-8 is an inhibitor of Notch activating/cleaving enzyme ADAM-17 and inhibits the cleavage of Notch protein. | |||
T8931L | ICCB-19 hydrochloride | ICCB-19 HCl(750621-52-4 free base) | Apoptosis , Others , Autophagy , RIP kinase |
ICCB-19 hydrochloride (ICCB-19 HCl) is an inhibitor of TRADD (TNFRSF1A Associated Via Death Domain). It binds to a pocket on the N-terminal TRAF2-binding domain of TRADD (TRADD-N), which interacts with the C-terminal dom... | |||
T14378L | AZD5582 acetate (1258392-53-8 free base) | IAP | |
AZD5582 acetate is an inhibitor of IAPs, which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. AZD5582 induces apoptosis. | |||
T36201L | AZD5582 TFA | AZD5582 TFA(1258392-53-8 free base) | Apoptosis , IAP |
AZD5582 TFA is a potent IAP antagonist that binds to the BIR3 domain of cIAP1, cIAP2, and XIAP with IC50 values of 15, 21, and 15 nM, respectively.AZD5582 TFA induces apoptosis. | |||
T6763 | Xevinapant | ARRY-334543,SM-406,AT406,Debio-1143 | IAP |
Xevinapant (Debio-1143) is a potent Smac mimetic and an antagonist of IAP (inhibitor of apoptosis protein via E3 ubiquitin ligase), binding to XIAP-BIR3, cIAP1-BIR3 and cIAP2-BIR3 with Ki of 66.4 nM, 1.9 nM, and 5.1 nM, ... | |||
T2080 | LCL161 | IAP | |
LCL161, a SMAC mimetic, effectivity binds to and inhibits multiple IAPs (i.e. XIAP, c-IAP). | |||
T6299 | GDC-0152 | GDC0152 | IAP |
GDC-0152 is a potent inhibitor of IAPs. | |||
T6007 | Birinapant | TL32711 | Apoptosis , IAP , HIV Protease |
Birinapant (TL32711) is a synthetic small molecule that is both a peptidomimetic of second mitochondrial-derived activator of caspases (SMAC) and inhibitor of IAP (Inhibitor of Apoptosis Protein) family proteins, with po... | |||
T12932L | SM-164 | Apoptosis , IAP | |
SM-164 binds to XIAP protein containing both the BIR2 and BIR3 domains (IC50: 1.39 nM). It acts as an extremely potent antagonist of XIAP. | |||
T36201 | AZD5582 dihydrochloride | AZD 5582 dihydrochloride | |
Dimeric Smac mimetic; potent inhibitor of X-linked (XIAP) and cellular (cIAP) inhibitor of apoptosis protein (IC50 values are 15, 15 and 21 nM for XIAP, cIAP1 and cIAP2 respectively). Binds to the BIR3 domain of XIAP to ... | |||
T14378 | AZD5582 | Apoptosis , IAP | |
AZD5582 is an inhibitor of IAPs, which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. It induces apoptosis. | |||
T23760 | AT-IAP | ||
AT-IAP is an effective dual antagonist of XIAP and cIAP1. | |||
T17545 | Biotin-BS | Others | |
Biotin-BS is a chemical compound composed of two distinct ligands: methyl-bestatin (MeBS) for cIAP1 and biotin. These ligands are interconnected through linkers. MeBS serves as a ligand specifically for the cellular inhi... | |||
T17706 | BzNH-BS | Others | |
BzNH-BS is a chemical compound comprising two distinct ligands: methyl-bestatin (MeBS) for cIAP1 and benzoyl-amide. The ligands are interconnected through linkers. MeBS functions as a ligand for cIAP1, a ubiquitin ligase... | |||
T69845 | MX107 | ||
MX107 is a survivin inhibitor which induces degradation of XIAP and/or cIAP1, and suppresses genotoxic NF-kappaB activation. | |||
T18690 | SNIPER(ABL)-039 | Others | |
SNIPER(ABL)-039, conjugating Dasatinib (ABL inhibitor) to LCL161 derivative (IAP ligand) with a linker, induces the reduction of BCR-ABL protein with a DC50 of 10 nM. IC50s are 0.54 nM, 10 nM, 12 nM, and 50 nM for ABL, c... | |||
T18635 | PROTAC RAR Degrader-1 | Others | |
PROTAC RAR Degrader-1, an RAR degrader, consists of a cIAP1 ligand binding group, a linker, and an RAR ligand binding group. It achieves maximal RAR degradation at a concentration of 30 μM in HT1080 cells. Degradation in... | |||
T18596 | PROTAC AR Degrader-4 | Others | |
PROTAC AR Degrader-4 comprises a cIAP1 ligand binding group, a linker and an androgen receptor (AR) binding group. PROTAC AR Degrader-4 is an AR degrader. Degradation inducers based on cIAP1 are called specific and non-g... | |||
T16905 | SNIPER(BRD)-1 | Others | |
SNIPER(BRD)-1 is a chemical compound composed of a derivative of the IAP antagonist LCL-161 and the BET inhibitor (+)-JQ-1, linked together. It promotes the degradation of BRD4 through the ubiquitin-proteasome pathway an... | |||
T69840 | MX106 | ||
MX106 is a survivin inhibitor which induces degradation of XIAP and/or cIAP1, and suppresses genotoxic NF-kappaB activation. | |||
T78947 | CST626 | PROTACs | |
CST626 (Compound 9), a pan-IAP degrader PROTAC, effectively degrades XIAP, cIAP1, and cIAP2 in MM.1S cells with DC50 values of 0.7, 2.4, and 6.2 nM, respectively [1]. | |||
T18605 | PROTAC ERα Degrader-2 | Others | |
PROTAC ERα Degrader-2 is composed of a cIAP1 ligand binding group, a linker, and an estrogen receptor α (ERα) binding group, serving as an ERα degrader. It achieves maximal ERα degradation in human mammary tumor MCF7 cel... | |||
T3299 | Xevinapant hydrochloride | AT-406 HCl,SM-406 | Apoptosis , IAP |
Xevinapant hydrochloride (AT-406 HCl) , an orally active antagonist of multiple inhibitor of apoptosis proteins(IAP), inhibits progression of human ovarian Y binding to XIAP-BIR3, cIAP1-BIR3 and cIAP2-BIR3 with Ki of 66.... | |||
T13837 | PROTAC CRABP-II Degrader-2 | Others | |
PROTAC CRABP-II Degrader-2 is a potent degrader of cellular retinoic acid binding protein (CRABP-II) based on cIAp1. | |||
T13838 | PROTAC CRABP-II Degrader-3 | Others | |
PROTAC CRABP-II Degrader-3 is a potent degrader of cellular retinoic acid binding protein (CRABP-II) based on cIAp1. | |||
T13836 | PROTAC CRABP-II Degrader-1 | Others | |
PROTAC CRABP-II Degrader-1 is a potent degrader of cellular retinoic acid binding protein (CRABP-II) based on cIAp1. | |||
T14288 | Androstanolone acetate | Others | |
Androstanolone acetate is a compound that functions as an androgen ligand, specifically targeting the androgen receptor (AR). It binds to the cIAP1 ligand Bestatin through a linker, resulting in the formation of PROTACs[... |
Cat No. | Product Name | Species | Expression System |
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TMPY-01176 | cIAP1 Protein, Human, Recombinant (Avi) | Human | E. coli |
The cellular inhibitor of apoptosis protein-1 (cIAP1) is a member of the Inhibitor of Apoptosis family proteins are (IAP) whose members are characterized by a novel domain of about 70 amino acids termed baculoviral IAP r... |