28
1
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T14116 |
ACP-105
|
Androgen Receptor | Endocrinology/Hormones |
ACP-105 是选择性的、可口服的雄激素受体调节剂 , 能够作用于野生型 AR (pEC50:9.0)和 T877A 突变型 AR (pEC50:9.3)。 | |||
T6946 |
Pimavanserin tartrate
ACP-103,ACP-103 tartrate,Nuplazid,Pimavanserin,匹莫范色林 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Pimavanserin tartrate (Nuplazid) 是一种有效的5-HT 2A 受体反向激动剂,pIC50和 pKi 值分别为8.73和9.3,用于治疗与帕金森病相关的精神病。 | |||
T29614 |
ACP-0052
SL052,SL 052,SL-052,ACP 0052 |
||
ACP-0052(SL-052, ACP-SL-052) is a photosensitizer based on hypoclintin that may be used in the treatment of prostate cancer. | |||
T2076 |
Pimavanserin
ACP-103,匹莫范色林 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Pimavanserin (ACP-103) 是特异性的 5-HT2A 受体反向激动剂,在基于细胞的功能测定中,平均 pIC50值为8.7。它是非典型抗精神病药,用于治疗帕金森病患者的幻觉和精神病。 | |||
T3626 |
Acalabrutinib
ACP-196,阿可替尼 |
BTK | Angiogenesis; Tyrosine Kinase/Adaptors |
Acalabrutinib (ACP-196) 是一种不可逆的、高效的、具有口服活性、选择性的第二代BTK 抑制剂。它与 BTK 的 ATP 结合口袋中的 Cys481 共价结合。它在慢性淋巴细胞性白血病 (CLL) 小鼠模型中显示出强大的靶向作用和功效。 | |||
T3484 |
trans-ACPD
Trans-(±)-ACP,1-amino-1,3-dicarboxycyclopentane,(±)-trans-ACPD |
GluR | Neuroscience |
trans-ACPD ((±)-trans-ACPD) 是代谢型受体激动剂,可促进钙离子活动及产生内向电流。 | |||
TP1837 |
Acyl Carrier Protein (ACP) (65-74)
Acyl Carrier Protein (ACP) 65-74 |
||
Acyl Carrier Protein (ACP) (65-74) is an active acyl carrier protein (ACP) fragment.Acyl Carrier Protein (ACP) is a component of plastid-located plant fatty acid synthetase. It binds acyl groups covalently via the prosthetic group, 4-phosphopantetheine, d | |||
T10240 | ACP-5862 | BTK | Angiogenesis; Tyrosine Kinase/Adaptors |
ACP-5862 is a major active and pyrrolidine ring-opened metabolite of Acalabrutinib (IC50: 5.0 nM for BTK). Acalabrutinib is an irreversible and highly selective BTK inhibitor (IC50: 3 nM; EC50: 8 nM). | |||
T34657 |
SL-017
ACPSL-017,S-017,ACP-SL-017,ACP-SL017 |
||
SL-017 (ACP-SL-017, ACPSL-017, ACP-SL-017) is a Hypocrellin-B (Hb) derivative and photosensitization agent that may be used to treat abnormal hair growth. SL017 targets the mitochondria and causes the mitochondrial membrane potential to collapse, producin | |||
T71732 |
Fmoc-ε-Acp-OH
|
||
Fmoc-ε-Acp-OH can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applications. Fmoc-ε-Acp-OH is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. | |||
T70840 |
Osemozotan Free Base
|
||
Osemozotan Free Base is a 5-HT(1A) receptor agonist. | |||
T70842 | ACP1b | ||
ACP1b is an activator of ClpP protease. | |||
TP1427L |
ReACp53 acetate
|
p53 | Apoptosis |
ReACp53 acetate 能够抑制 p53 amyloid 的形成, 挽救 p53 在癌细胞中的作用。 | |||
T75168 | Homo-BacPROTAC7 | ||
Homo-BacPROTAC7 是一个 ClpC1NTDBacPROTAC 降解剂,可以靶向 ClpC2。Homo-BacPROTAC7 能有效杀死 M. tuberculosis。 | |||
T22549 |
ACPT-I
|
Others | Others |
Agonist for group III mGlu receptors | |||
T22488 |
(1S,3R)-ACPD
|
Others | Others |
group I and II mGlu receptor agonist | |||
T22550 |
ACPT-II
|
Others | Others |
metabotropic receptor antagonist | |||
T19178 |
ACPK
|
Others | Others |
ACPK is a pyrrolysine analogue bearing an azide residue. | |||
T75171 | BacPROTAC-1 | ||
BacPROTAC-1 是一个 mSABacPROTAC 降解剂。BacPROTAC-1 对 mSA 和 ClpCNTD 具有高亲和力 (KD 分别为 3.9 μM 和 2.8 μM)。 | |||
TP1427 |
ReACp53
|
||
ReACp53 is a cell-penetrating peptide, designed to inhibit p53 amyloid formation, resues p53 function in cancer cell lines and in organoids derived from high-grade serous ovarian carcinomas (HGSOC). | |||
T75401 | D-galactosyl-β1-3-N-acetyl-D-hexosamine phosphorylase (BiGalHexNAcP) | ||
D-galactosyl-β1-3-N-acetyl-D-hexosamine phosphorylase (BiGalHexNAcP),属于CAZy糖苷水解酶GH112家族,主要应用于生化研究领域。该酶负责催化lacto-N-biose和lacto-N-neobiose的磷酸化反应,生成Gal-1-磷酸和相应的N-乙酰-D-己糖胺。 | |||
T75167 |
Homo-BacPROTAC6
|
||
Homo-BacPROTAC6 是一个 ClpC1NTDBacPROTAC 降解剂,可以靶向 ClpC2。Homo-BacPROTAC7 能有效杀死M. tuberculosis。 | |||
T23080 |
NPEC-caged-(1S,3R)-ACPD
|
Others | Others |
group I and II mGlu receptor agonist | |||
T61411 |
InhA-IN-4
|
Antibacterial | Microbiology/Virology |
InhA-IN-4 (TU14) 是一种有效的结核分枝杆菌InhA(烯酰 ACP 还原酶) 抑制剂,具有潜在的抗癌和抗增殖活性,可用于研究结核分枝杆菌感染。 | |||
T60866 |
InhA-IN-3
|
Antibacterial | Microbiology/Virology |
InhA-IN-3 (TU13) 是一种有效的结核分枝杆菌InhA(烯酰 ACP 还原酶) 抑制剂,具有潜在的抗癌和抗增殖活性,可用于研究结核分枝杆菌感染。 | |||
T4105L |
AFN-1252 tosylate
API-1252 tosylate |
||
AFN-1252 tosylate is an enoyl-ACP Reductase inhibitor. | |||
T70835 |
(4R,9S)-AG 205
|
||
AG-205 is a potent inhibitor of FabK, the enoyl-ACP reductase in Streptococcus pneumoniae. | |||
T38125 |
Platencin
|
||
Platencin is a natural, broad spectrum Gram-positive antibiotic isolated from S. platensis, which is also the source of platensimycin . Platencin inhibits two key enzymes in bacterial fatty acid synthesis, β-ketoacyl-ACP synthases II and III (FabF and FabH, respectively), unlike platensimycin which only targets FabF. The IC50 values for platencin against FabF and FabH are 1.95 and 3.91 μg/ml, respectively. It does not exhibit cross-resistance to antibiotic resistant bacterial strains, including ... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4852 |
Trimyristin
Trimyristoylglycerol,Tritetradecanoin,三肉豆蔻酸甘油酯,Glyceryl trimyristate,甘油三肉豆蔻酸酯,1,2,3-Tritetradecanoylglycerol |
Phosphatase; Endogenous Metabolite; AChE | Metabolism; Neuroscience |
Trimyristin (Tritetradecanoin) 是一种 Myristica fragransHoutt 的有效成分,能够显著抑制乙酰胆碱酯酶 (AChE),酸性和碱性磷酸酶 (ACP/ALP) 特性。它对 AChE,ACP 和 ALP 的 IC50分别为 0.11、0.16 和 0.18 mM。 |