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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1962 |
ASP3026
ASP 3026 |
Apoptosis; ALK | Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors |
ASP3026 是一种选择性的,具有口服活性的间变性淋巴瘤激酶抑制剂,可诱导肿瘤细胞凋亡,可研究非小细胞肺癌。 | |||
T6668 |
SGC-CBP30
|
Epigenetic Reader Domain; Histone Acetyltransferase | Chromatin/Epigenetic |
SGC-CBP30 是高选择性CBP/p300溴结构域的有效抑制剂,对CBP 和p300的Kd 值分别为 21 和 32 nM。它强烈减少 Th17 细胞中 IL-17A 的分泌,具有抗炎作用。 | |||
T77560 |
Histone acetyltransferase p300 Inhibitor 4c
|
Carbonic Anhydrase; AChE | Metabolism; Neuroscience |
Histone acetyltransferase p300 Inhibitor 4c 是2-氨基噻唑衍生物,Histone acetyltransferase p300 Inhibitor 4c 对 hCA I 、hCA II、AChE 和 BChE 具有抑制作用,Ki 值为 0.008 ± 0.001 、 0.124 ± 0.017、0.129 ± 0.030 和 0.083 ± 0.041 μM。 | |||
T7264 |
CBP/EP300-IN-1
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
CBP/EP300-IN-1是一种 CBP/EP300 溴结构域抑制剂。 | |||
T12345 |
CBP/p300-IN-3
P300/CBP-IN-3 |
Histone Acetyltransferase | Chromatin/Epigenetic |
CBP/p300-IN-3 (P300/CBP-IN-3) 是一种组蛋白乙酰转移酶抑制剂。 | |||
TNU0864 |
HUP30
|
Potassium Channel; Calcium Channel | Membrane transporter/Ion channel; Metabolism |
HUP30是一种强效的血管舒张剂。HUP30可以刺激可溶性鸟苷酸环化酶,激活 K+离子通道,阻断细胞外 Ca2+的内流。 | |||
T36682 |
USP30 inhibitor 18
|
DUB | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination |
USP30 inhibitor 18 是有效的USP30选择性抑制剂,IC50为 0.02 μM。它增加蛋白质泛素化并加速线粒体自噬。 | |||
T13267 |
USP30 inhibitor 11
USP30-IN-11 |
DUB | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination |
USP30 inhibitor 11 (USP30-IN-11) 是一个选择性的 USP30 抑制剂(IC50 : 0.01 µΜ),抑制 SVA,可用于研究癌症、线粒体功能障碍和帕金森。 | |||
T40143 |
PROTAC CBP/P300 Degrader-1
PROTAC CBP/P300 Degrader-1 |
||
PROTAC CBP/P300 Degrader-1 is an effective compound that degrades CBP/P300 in a potent manner. It significantly reduces cell viability in various cancer cell lines. | |||
T41181 | iP300v | ||
iP300v is a negative control for iP300w | |||
T10702 |
CBP/p300-IN-2
CBP/EP300-IN-2 |
Epigenetic Reader Domain; c-Myc | Cell Cycle/Checkpoint; Chromatin/Epigenetic |
CBP/EP300-IN-2 is an inhibitor of CBP/EP300 (IC50s: 1.07 nM and 5.96 nM for CBP/HTRF and Myc). | |||
T13191 |
TP3011
CH0793011 |
Others | Others |
TP3011 is a potent topoisomerase I inhibitor equipotent as SN38 and is an active metabolite of CH-0793076. | |||
T40144 |
CBP/p300 ligand 2
|
||
CBP/p300 ligand 2 is a selective ligand that binds to the target protein for PROTAC of dCBP-1, a potent and selective heterobifunctional degrader of p300/CBP. | |||
T63767 | P300 bromodomain-IN-1 | ||
P300 bromodomain-IN-1 是 p300 (EP300) bromodomain 的有效抑制剂 (IC50: 49 nM)。P300 bromodomain-IN-1 能够阻碍 c-Myc 的表达,并诱导 OPM-2 细胞的细胞周期阻滞在 G1/G0 期及诱导其凋亡 (apoptosis)。 | |||
T62415 | CBP/p300-IN-17 | ||
CBP/p300-IN-17 (compound 7) 是一种 EP300/CBP HAT 的有效抑制剂,能够作用于 HAT EP300 (IC50: 0.18 μM) 和 LK2 H3K27 (IC50: 0.69 μM)。 | |||
T63565 |
CBP/p300-IN-19 hydrochloride
|
||
CBP/p300-IN-19 hydrochloride 是选择性的、有效的 p300/CBP HAT 抑制剂,能够作用于 p300-HAT (IC50: 1.4 μM)、CBP-HAT (IC50: 2.2 μM)、PCAF (IC50>100 μM)、Myst3 (IC50>100 μM)。CBP/p300-IN-19 hydrochloride 具有抗肿瘤作用。 | |||
T12346 |
CBP/p300-IN-5
P300/CBP-IN-5 |
Epigenetic Reader Domain | Chromatin/Epigenetic |
P300/CBP-IN-5 is a potent inhibitor of p300/CBP histone acetyltransferase (IC50 of 18.8 nM). | |||
T73921 |
Ep300/CREBBP-IN-2
|
||
Ep300/CREBBP-IN-2 (Example 73) 是一种有效的和具有口服活性的Ep300和CREBBP 抑制剂,IC50分别为 0.052 μM 和 0.148 μM。Ep300/CREBBP-IN-2 可用于癌症研究。 | |||
T73922 |
Ep300/CREBBP-IN-3
|
||
Ep300/CREBBP-IN-3 (Example 61) 是一种有效的Ep300和CREBBP 抑制剂,IC50分别为 0.056 μM 和 0.095 μM。Ep300/CREBBP-IN-3 可用于癌症研究。 | |||
T63110 |
CBP/p300-IN-15
|
||
CBP/p300-IN-15 (compound 13a) 是一种有效的 p300 (IC50: 2.5 nM) 和 CBP (IC50: 28.0 nM) 抑制剂。CBP/p300-IN-15 能够较好的抑制 OVCAR-3 细胞 (EC50: 0.865 μM) 和 A2780 细胞 (EC50: 2.71 μM)。 CBP/p300-IN-15 能够用于研究卵巢癌。 | |||
T73920 |
Ep300/CREBBP-IN-8
|
||
Ep300/CREBBP-IN-8 (Example 37) 是一种有效的和具有口服活性的 Ep300和CREBBP 抑制剂,IC50分别为 0.014 μM 和 0.018 μM。Ep300/CREBBP-IN-8 可用于癌症研究。 | |||
T72815 |
CBP/p300-IN-10
|
||
CBP/p300-IN-10 是一种高效的组蛋白乙酰转移酶 EP300和CREBBP 的抑制剂,IC50分别为 26 nM 和 39 nM。 | |||
T63122 | CBP/p300-IN-19 | ||
CBP/p300-IN-19 是一种 p300/CBP HAT 的有效抑制剂,能够作用于 p300-HAT (IC50: 1.4 μM)、CBP-HAT (IC50: 2.2 μM)、PCAF (IC50>100 μM)、Myst3 (IC50>100 μM)。CBP/p300-IN-19 具有抗肿瘤活性。 | |||
T40142 |
Thalidomide-NH-CBP/p300 ligand 2
Thalidomide-NH-CBP/p300 ligand 2 |
||
Thalidomide-NH-CBP/p300 ligand 2 (P-007) is a PROTAC-based compound designed to degrade CBP and p300, acting as a functional antagonist (WO2020173440). | |||
T62720 | CBP/p300-IN-18 | ||
CBP/p300-IN-18 (compound 8) 是一种 EP300/CBP HAT 的有效抑制剂,能够作用于 HAT EP300 (IC50: 0.056 μM) 和 LK2 H3K27 (IC50: 0.46 μM)。 | |||
T40344 |
CBP/p300-IN-14
CBP/p300-IN-14 |
||
CBP/p300-IN-14, efficiently inhibits CBP/EP300 (lysine acetyltransferase) with an IC50 value of 3.3 nM. | |||
T39826 |
CBP/p300-IN-8
CBP/p300-IN-8 |
||
CBP/p300-IN-8 is a potent inhibitor of the CBP/P300 family of bromodomains . CBP/p300-IN-8 inhibits CBP ( IC 50 =0.01-0.1 μΜ) and BRD4 ( IC 50 =1-1000 μΜ) activity. | |||
T73923 | Ep300/CREBBP-IN-4 | ||
Ep300/CREBBP-IN-4 (Example 56) 是一种有效的Ep300和CREBBP 抑制剂,IC50分别为 0.024 μM 和 0.064 μM。Ep300/CREBBP-IN-4 可用于癌症研究。 | |||
T79395 |
CBP/p300-IN-21
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
CBP/p300-IN-21 (Compound 5d) 作为一种选择性CBP/p300抑制剂,展现出对p300和CBP具有差异性的IC50值,分别为0.07 μM和1.755 μM。该化合物能有效降低H3K18Ac的水平,并抑制小鼠4T1肿瘤的生长。 | |||
T28439 |
PP30
PP 30,PP-30 |
||
PP30 is an inhibitor of mTORC1 and mTORC2. It is selective within the PI3K family, inhibiting other PI3Ks only at high concentrations. | |||
T62700 |
CBP/p300-IN-16
|
||
CBP/p300-IN-16 (compound 1) 是一种 EP300/CBP HAT 的有效抑制剂,作用于 HAT EP300 (IC50: 0.61 μM) 和 LK2 H3K27 (IC50: 2.24 μM)。 | |||
T23489 |
UBP301
UBP 301 |
Others | Others |
UBP301 is a kainate receptor antagonist. |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-00033 |
ASFV (strain Ba71V) p30 Protein (His)
Ba71V-93,Phosphoprotein p30,p30,CP204L,Pho... |
ASFV | E. coli |
Modifies the subcellular distribution of heterogeneous nuclear ribonucleoprotein K (HNRNPK) and may contribute to modulate HNRNPK functions related to processing and export of mRNAs during ASFV infection. | |||
TMPY-02590 |
HMGB1 Protein, Mouse, Recombinant (hFc)
HMG-1,SBP-1,high mobility group box 1,p30,Hmg1,DEF,... |
Mouse | HEK293 Cells |
HMGB1 Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 53.3 kDa and the accession number is P63158. | |||
TMPJ-00083 |
NCR3 Protein, Human, Recombinant (hFc)
Activating Natural Killer Receptor p30,CD337,NK... |
Human | HEK293 Cells |
Natural Cytotoxicity Triggering Receptor 3 (NCR3) along with NKp44 and NKp46 constitute a group of receptors termed “Natural Cytotoxicity Receptors”. They play a major role in triggering NK-mediated killing of most tumor cells lines. NKp30 is a type I transmembrane protein having a single extracellular V-like immunoglobulin domain. NKp30 is selectively expressed both in resting and activated human NK cells. In addition, NKp30 is also involved in NK-mediated induction of dendritic cell (DC) matur... | |||
TMPH-03031 |
P30 adhesin Protein, Mycoplasma pneumoniae, Recombinant (GST & His)
|
Mycoplasma pneumoniae | E. coli |
Adhesin necessary for successful cytadherence and virulence. P30 adhesin Protein, Mycoplasma pneumoniae, Recombinant (GST & His) is expressed in E. coli expression system with N-6xHis-GST tag. The predicted molecular weight is 49.6 kDa and the accession number is P75330. | |||
TMPY-04616 |
NKp30/NCR3 Protein, Cynomolgus, Rhesus, Recombinant (His)
natural cytotoxicity triggering receptor 3 |
Cynomolgus,Rhesus | HEK293 Cells |
NKp30/NCR3 Protein, Cynomolgus, Rhesus, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 14.3 kDa and the accession number is XP_005553604.1. | |||
TMPY-01145 |
NKp30/NCR3 Protein, Human, Recombinant (His)
NCR3,natural cytotoxicity triggering receptor 3,CD337,1C7,DA... |
Human | HEK293 Cells |
NKp30/NCR3 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 14.4 kDa and the accession number is O14931-1. | |||
TMPK-00091 |
NKp30/NCR3 Protein, Human, Recombinant (His & Avi), Biotinylated
1C7,LY117,CD337,NKp30,MALS,NCR3 |
Human | HEK293 Cells |
NKp30, along with NKp44 and NKp46, constitute a group of receptors termed "Natural Cytotoxicity Receptors". These receptors play a major role in triggering NK-mediated killing of most tumor cells lines.NKp30 stimulates NK cells cytotoxicity toward neighboring cells producing these ligands. It controls, for instance, NK cells cytotoxicity against tumor cells. | |||
TMPK-00090 |
NKp30/NCR3 Protein, Human, Recombinant (His & Avi)
NKp30,1C7,MALS,CD337,LY117,NCR3 |
Human | HEK293 Cells |
NKp30, along with NKp44 and NKp46, constitute a group of receptors termed "Natural Cytotoxicity Receptors". These receptors play a major role in triggering NK-mediated killing of most tumor cells lines.NKp30 stimulates NK cells cytotoxicity toward neighboring cells producing these ligands. It controls, for instance, NK cells cytotoxicity against tumor cells. Engagement of NCR3 by BAG6 also promotes myeloid dendritic cells (DC) maturation, both through killing DCs that did not acquire a mature ph... | |||
TMPH-03729 |
Zaire ebolavirus (strain Kikwit-95) VP30 Protein (His)
|
ZEBOV | E. coli |
Multifunctional protein that acts as a viral transcriptional activator. Promotes read-through of an RNA hairpin in the NP open reading frame to enhance viral transcription. Mechanistically, nonphosphorylated VP30 hexamers form a ternary complex with the viral leader RNA. Clamps the RNA template and the complex VP35-polymerase L together, thereby increasing the polymerase affinity for the RNA template to increase transcription initiation despite the presence of RNA secondary structures. Assists a... | |||
TMPY-00334 |
NKp30/NCR3 Protein, Rat, Recombinant (His)
natural cytotoxicity triggering receptor 3,1c7 |
Rat | HEK293 Cells |
NKp30/NCR3 Protein, Rat, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 15.2 kDa and the accession number is CAD23066.1. | |||
TMPH-02385 |
Lake Victoria marburgvirus (MARV) (strain Musoke-80) VP30 Protein (His & Myc)
|
MARV | E. coli |
Acts as a transcription anti-termination factor immediately after transcription initiation, but does not affect transcription elongation. This function has been found to be dependent on the formation of an RNA secondary structure at the transcription start site of the first gene. | |||
TMPY-05383 |
NKp30/NCR3 Protein, Human, Recombinant (hFc)
DAAP-90L16.3,natural cytotoxicity triggering receptor 3,NCR3... |
Human | HEK293 Cells |
NKp30/NCR3 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 39.6 kDa and the accession number is O14931-3. | |||
TMPY-03288 |
USP30 Protein, Human, Recombinant (SUMO)
ubiquitin specific peptidase 30 |
Human | Baculovirus Insect Cells |
Ubiquitin specific peptidase 30, also known as USP30, is a deubiquitinating enzyme that is embedded in the mitochondrial outer membrane. Depletion of USP30 expression by RNA interference induced elongated and interconnected mitochondria, depending on the activities of the mitochondrial fusion factors mitofusins, without changing the expression levels of the key regulators for mitochondrial dynamics. Mitochondria were rescued from this abnormal phenotype by ectopic expression of USP30 in a manner... |