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Cat No. | Product Name | Synonyms | Targets |
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T60762 | PCAF-IN-1 | ||
PCAF-IN-1 is a antitumor agents used in tumor treatment research. PCAF-IN-1 is a highly selective inhibitor of PCAF [1]. | |||
T60452 | PCAF-IN-2 | ||
PCAF-IN-2 (compound 17) is a potent inhibitor of PCAF with an IC50 of 5.31 µM. PCAF-IN-2 exhibits anti-tumor activity. CAF-IN-2 induces cell apoptosis and arrest the cell cycle at the G2/M phase[1]. | |||
T60558 | NSC 694623 | Histone Acetyltransferase | |
NSC 694623 is a potent histone acetyltransferase (HAT) inhibitor with IC50 of 15.9 μM against recombinant HAT p300/CBP associated factor (PCAF). NSC 694623 shows anti-proliferative activity against some cancer cells, whi... | |||
T5468 | YF-2 | Others , Epigenetic Reader Domain , Histone Acetyltransferase | |
YF-2 is blood-brain-barrier permeable histone acetyltransferase activator, acetylates H3 in the hippocampus, CBP, PCAF, and GCN5 with EC50s of 2.75 μM, 29.04 μM and 49.31 μM , respectively | |||
T28471 | PU139 | PU 139,PU-139 | Histone Acetyltransferase |
PU139 is a novel inhibitor of histone acetyltransferase (HAT). | |||
T11495L | GSK 4027 | Others | |
GSK 4027 is a PCAF/GCN5 bromodomain chemical probe. In a time-resolved fluorescence resonance energy transfer (TR-FRET) assay, it has a pIC50 of 7.4±0.11 for PCAF. | |||
T10604 | BRD-IN-3 | Others | |
BRD-IN-3 is a highly potent PCAF bromodomain (BRD) inhibitor (IC50: 7 nM). It also exhibits activity against GCN5 and FALZ. | |||
T11495 | GSK4028 | Others | |
GSK4028 is the enantiomeric negative control of GSK4027, which is a PCAF/GCN5 bromodomain chemical probe. The pIC50 of GSK4028 is 4.9 in a TR-FRET assay. | |||
T71724 | F2276-0099 | ||
F2276-0099 is a PCAF/GCN5 BRD inhibitor | |||
T71721 | F2276-0106 | ||
F2276-0106 is a PCAF/GCN5 BRD inhibitor | |||
T71720 | F2276-0104 | ||
F2276-0104 is a PCAF/GCN5 BRD inhibitor | |||
T23745 | APA-APA-MPO | APA APA MPO,APAAPAMPO | |
APA-APA-MPO is a PCAF bromodomain/Tat-AcK50 association inhibitor. | |||
T23746 | APA-H-MPO | APAHMPO | |
APA-H-MPO is a PCAF bromodomain/Tat-AcK50 association inhibitor. | |||
T25215 | CCT077791 | CCT 077791,CCT-077791 | Epigenetic Reader Domain , Histone Acetyltransferase |
CCT077791 is a potent inhibitor of p300 and PCAF histone acetyltransferase activity for cancer research. | |||
T11807 | L002 | Others , Histone Acetyltransferase , STAT | |
L002, a potent, cell-permeable, reversible, and specific acetyltransferase p300 (KAT3B) inhibitor with an IC50 of 1.98 μM, directly binds the acetyl-CoA pocket and competitively inhibits the FATp300 catalytic domain. By ... | |||
T71723 | F2276-0008 | ||
F2276-0008 is a PCAF/GCN5 BRD inhibitor. | |||
T32010 | GSK699 | GSK-699,GSK 699 | |
GSK699 is a potent, cell penetrant PCAF/GCN5 PROTAC. | |||
T38711 | YF-2 hydrochloride | ||
YF-2 hydrochloride is a potent histone acetyltransferase activator that exhibits high selectivity and can pass through the blood-brain barrier. It specifically acetylates H3 in the hippocampus, with EC50 values of 2.75 μ... | |||
T60018 | NSC 694621 | ||
NSC 694621 is a potent PCAF inhibitor with an IC 50 of 5.71 μM ( PCAF/H3 1-21 ). NSC 694621 exhibits good activity of inhibiting the proliferation of cancer cells that has the potential to be the new anticancer agent[1]. | |||
T11796L | L-Moses | L-45 | Others |
L-45 is the first potent and cell-active bromodomain (Brd) inhibitor of p300/CBP-associated factor (PCAF) (Kd: 126±15 nM). | |||
T36109 | L Moses dihydrochloride | ||
High affinity and selective cell-permeable p300/CBP-associated factor (PCAF) inhibitor (Ki = 47 nM). Exhibits no significant activity against a panel of 48 other bromodomains except GCN5 (Kd = 600 nM). Exhibits >4500-fo... | |||
T60479 | NSC 698600 | ||
NSC 698600 is a potent inhibitor of PCAF(p300/CBP-associated factor) with IC 50 of 6.51 μM that shows good inhibition activity of cancer cell proliferation [1]. | |||
T62424 | L-Moses dihydrochloride | ||
L-Moses (L-45) dihydrochloride is the first, potent, selective p300/CBP-associated factor (PCAF) bromodomain (Brd) inhibitor (Kd: 126 nM). | |||
T73951 | Lys-CoA TFA | ||
Lys-CoA TFA, a selective p300 histone acetyltransferase (HAT) inhibitor (IC 50 =50-500 nM), exhibits a specificity that exceeds 100-fold over PCAF (IC 50 =200 μM). This compound effectively suppresses transcriptional act... | |||
T35818 | CAY10669 | ||
CAY10669 is an inhibitor of the histone acetyltransferase PCAF (p300/CREB-binding protein-associated factor; IC50 = 662 μM), displaying a 2-fold improvement in inhibitory potency over anacardic acid . At 30-60 μM, CAY106... | |||
T63565 | CBP/p300-IN-19 hydrochloride | ||
CBP/p300-IN-19 hydrochloride is a selective and potent inhibitor of p300/CBP HAT, capable of acting on p300-HAT (IC50: 1.4 μM), CBP-HAT (IC50: 2.2 μM), PCAF (IC50>100 μM), Myst3 (IC50>100 μM). CBP/p300-IN-19 hydrochlorid... | |||
T36626 | Lys-CoA | ||
Selective p300 histone acetyltransferase (HAT) inhibitor (IC50 = 50-500 nM). Exhibits approximately 100-fold selectivity for p300 over PCAF (IC50 = 200 μM). Inhibits p300-dependent transcription. Active in vivo. Lau et a... | |||
T63122 | CBP/p300-IN-19 | ||
CBP/p300-IN-19 is a potent inhibitor of p300/CBP HAT, which can act on P300-HAT (IC50: 1.4 μM), CBP-HAT (IC50: 1.4 μm), 2.2 μM), PCAF (IC50>100 μM), and Myst3 (IC50>100 μM). CBP/p300-IN-19 has anti-tumor activity. |
Cat No. | Product Name | Synonyms | Targets |
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T11366 | Garcinol | Apoptosis , Endogenous Metabolite , Histone Acetyltransferase , AChR , AChE | |
Garcinol also inhibits histone acetyltransferases (HATs, IC50= 7 μM) and p300/CPB-associated factor (PCAF, IC50 = 5 μM). Garcinol has anti-inflammatory and anti-cancer activity. Garcinol, a polyisoprenylated benzophenone... | |||
T6389 | Anacardic Acid | 6-pentadecylsalicylic Acid,Hydroginkgolic acid | Others , Epigenetic Reader Domain , Histone Acetyltransferase , Antibacterial |
Anacardic Acid (6-pentadecylsalicylic Acid) is an effective inhibitor of p300 and p300/CBP-associated factor histone acetyltranferases. It also has antimicrobial activity, antibacterial activity, and inhibits prostagland... |
Cat No. | Product Name | Species | Expression System |
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TMPH-02175 | TAF5L Protein, Human, Recombinant (GST) | Human | E. coli |
Functions as a component of the PCAF complex. The PCAF complex is capable of efficiently acetylating histones in a nucleosomal context. The PCAF complex could be considered as the human version of the yeast SAGA complex.... | |||
TMPY-01869 | SIRT1 Protein, Human, Recombinant (His) | Human | E. coli |
SIRT1 belongs to the sirtuin family. Members of the sirtuin family are characterized by a sirtuin core domain and grouped into four classes. SIRT1 is included in class I of the sirtuin family. It is a NAD-dependent prote... |