Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T39710 |
ARV-471
Vepdegestrant |
Estrogen Receptor/ERR | Endocrinology/Hormones |
ARV-471 (Vepdegestrant) 是一种高效的,口服有效的基于 Cereblon 配体的雌激素受体降解剂 PROTAC 。ARV-471 常用于研究乳腺癌。 | |||
T6798 |
Tretazicar
5-Aziridino-2,4-dinitrobenzamide,CB1954,NSC 115829 |
DNA Alkylator/Crosslinker; DNA Alkylation | DNA Damage/DNA Repair |
Tretazicar (NSC-115829) 是一种抗肿瘤前药,由 NAD(P)H 醌氧化还原酶 2 激活。它在酶促活化后生成细胞毒性双功能烷基剂,可以形成 DNA-DNA 链间交联。 | |||
T7750 |
N-[3,5-bis(trifluoroMethyl)phenyl]-N'-[(9R)-6'-Methoxycinchonan-9-yl]- Thiourea
N-[3,5-双(三氟甲基)苯基]-N′-[(9R)-6′-甲氧基-9-金鸡宁]硫脲 |
Others | Others |
N-[3,5-bis(trifluoroMethyl)phenyl]-N'-[(9R)-6'-Methoxycinchonan-9-yl]- Thiourea 是金鸡纳生物碱衍生的双功能催化剂。 | |||
T11938L |
Macropa-NH2
|
Others | Others |
Macropa-NH2 是 macropa 双功能类似物,是一种常与抗体偶联的载体分子,常作为螯合剂使用,参与癌症研究。 | |||
T17159 |
Treosulfan
NSC 39069,曲奥舒凡,Treosulphan |
DNA Alkylator/Crosslinker; DNA Alkylation | DNA Damage/DNA Repair |
Treosulfan (Treosulphan) 是一种双功能的烷化剂,对卵巢癌及其他的实体瘤都有抑制效果。 | |||
T15178 |
dTRIM24
|
Others | Others |
dTRIM24 是一种基于 PROTAC 技术的选择性双功能 TRIM24 降解剂,由von Hippel-Lindau 和TRIM24 两者配体构成。 | |||
T18728 |
Sulfo-SMCC sodium
|
Others | Others |
Sulfo-SMCC sodium 是一种异双功能、不可裂解的 ADC 交联剂,带有 N-羟基琥珀酰亚胺酯和马来酰亚胺基团,分别与伯胺和巯基反应。 | |||
T4382 |
Proguanil hydrochloride
Paludrine hydrochloride,盐酸氯胍,Chlorguanide hydrochloride,Chloroquanil |
Others; Dehydrogenase; DNA/RNA Synthesis; Antifolate; Parasite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology; Others |
Proguanil hydrochloride (Chloroquanil) 是一种双胍类抗疟疾剂,在体内代谢形成环胍。它还是一种二氢叶酸还原酶抑制剂。 | |||
T26803 |
Bibw 22
Bibw22,Bibw-22 |
||
Bibw 22 is a bifunctional modulator of P-glycoprotein and nucleoside transport. | |||
T19207 |
BFCAs-1
|
Others | Others |
BFCAs-1 is a polyamine polycarboxylic bifunctional chelating agent (BFCAs) with a broad range of applications in biology, chemistry, medicine and diagnostic imaging. | |||
T16181 |
N-(Azido-PEG2)-N-Boc-PEG4-Boc
|
Others | Others |
N-(Azido-PEG2)-N-Boc-PEG4-Boc is a PEG-based bifunctional linker employed for the synthesis of PROTACs. | |||
T18744 | t-Boc-Aminooxy-PEG7-bromide | Others | Others |
t-Boc-Aminooxy-PEG7-bromide is a polyethylene glycol (PEG)-based bifunctional linker utilized in the synthesis of proteolysis targeting chimeras (PROTACs)[1]. | |||
T19168 |
9-Azido-Neu5DAz
|
Others | Others |
9-Azido-Neu5DAz is a non-natural bifunctional carbohydrates as imaging agent. | |||
T28846 |
SR16835
AT-202,AT202,SR 16835,SR-16835 |
||
SR16835 is a NOP receptor agonist, with low-affinity bifunctional activity at the μ opioid receptor. | |||
T14267 |
Aminooxy-PEG3-C2-NH-Boc
|
Others | Others |
Aminooxy-PEG3-C2-NH-Boc is a PEGylated PROTAC linker utilized in the synthesis of PROTACs, an emerging class of bifunctional molecules for targeted protein degradation[1]. | |||
T25140 |
BCH 2763
BCH2763,BCH-2763 |
||
BCH 2763 is an effective, selective bifunctional thrombin inhibitor that blocks both the anion binding exosite and the active catalytic site. | |||
T17962 |
Fmoc-N-PEG36-acid
|
Others | Others |
Fmoc-N-amido-PEG36-acid is a polyethylene glycol (PEG)-based linker utilized in PROTAC synthesis. It has been designed specifically for constructing PROTACs, which are bifunctional molecules capable of recruiting target proteins to an E3 ubiquitin ligase for degradation[1]. | |||
T70925 |
GS-5759
|
||
GS-5759 is a bifunctional ß2-Adrenoceptor Agonist and Phosphodiesterase 4 Inhibitor for Chronic Obstructive Pulmonary Disease with a Unique Mode of Action. | |||
T82537 |
D-MoDE-A (1)
|
LYTACs | PROTAC |
D-MoDE-A(1)是一种双功能小分子,它通过ASGPR(去唾液酸糖蛋白受体)介导外源蛋白的降解。 | |||
T14163 |
Ald-Ph-amido-C2-PEG3-NH-Boc
|
Others | Others |
Ald-Ph-amido-C2-PEG3-NH-Boc is a polyethylene glycol (PEG)-based bifunctional linker utilized for the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1]. | |||
T68272 |
Batefenterol Succinate
|
||
Batefenterol Succinate is a first-in-class inhaled bifunctional bronchodilator possessing muscarinic receptor antagonist and β2-adrenoceptor agonist properties. | |||
T41024 |
FmocNH-PEG4-t-butyl acetate
FmocNH-PEG4-t-butyl acetate |
||
FmocNH-PEG4-t-butyl acetate is a polyethylene glycol (PEG)-derived PROTAC linker employed for the synthesis of PROTACs, bifunctional molecules designed to degrade target proteins. | |||
T40648 |
NOTA
|
||
NOTA, a bifunctional chelate, serves as a foundation for PET imaging tool construction, probe design, and signal amplification through the multivalent effect. | |||
T34173 |
p-SCN-Bn-HOPO
|
||
p-SCN-Bn-HOPO is an excellent bifunctional chelating agent for (89)Zr ImmunoPET, with low background, good tumor-organ contrast, and importantly, very low bone uptake for BT474 breast cancer imaging. | |||
T18834 | Thiol-PEG-CH2COOH (MW 5000) | Others | Others |
Thiol-PEG-CH2COOH (MW 5000) is a Polyethylene glycol (PEG) derived link molecule, commonly utilized in the construction of PROTACs, which are bifunctional compounds designed for targeted protein degradation [1]. | |||
T16234 |
N-Mal-N-bis(PEG4-NHS ester)
|
Others | Others |
N-Mal-N-bis(PEG4-NHS ester) is a polyethylene glycol (PEG)-based bifunctional linker utilized for synthesizing Proteolysis Targeting Chimeras (PROTACs)[1]. | |||
T14449 |
Azido-PEG4-hydrazide-Boc
|
Others | Others |
Azido-PEG4-hydrazide-Boc is a polyethylene glycol (PEG)-based bifunctional linker compound used in the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1]. | |||
T81433 |
p-NH2-CHX-A"-DTPA
|
||
p-NH2-CHX-A"-DTPA 是双功能螯合剂。 | |||
T18080 | m-PEG-acrylate (MW 30000) | Others | Others |
m-PEG-acrylate (MW 30000) is a polyethylene glycol (PEG)-based bifunctional linker commonly employed in the chemical synthesis of proteolysis targeting chimeras (PROTACs)[1]. | |||
T17469 |
Azide-PEG3-Sulfone-PEG3-azide
|
Others | Others |
Azide-PEG3-Sulfone-PEG3-azide is a polyethylene glycol (PEG)-based bifunctional molecule, specifically designed as a PROTAC linker for the synthesis of PROTACs[1]. | |||
T81384 |
PROTAC BRD9 Degrader-3
|
PROTACs | PROTAC |
PROTACBRD9 Degrader-3为BRD9靶向的双功能降解剂,用于癌症研究。 | |||
T31584 |
DST Crosslinker
DST Cross linker,DST Cross-linker |
||
DST crosslinker(disuccinimide tartarate) is an isotype bifunctional, cleavable crosslinker (cleavable by an oxidizer) for applications that require crosslinking cleavability and that do not interfere with protein disulfide bonds with reducing agents. | |||
T77936 |
PROTAC BRD9 Degrader-4
|
PROTACs | PROTAC |
PROTACBRD9 Degrader-4 是一种针对BRD9的双功能降解剂,用于癌症研究。 | |||
T18413 |
N-Desthiobiotin-N-bis(PEG4-t-butyl ester)
|
Others | Others |
N-Desthiobiotin-N-bis(PEG4-t-butyl ester) is a PEG-based linker compound employed for the synthesis of PROTACs, which are bifunctional molecules designed for targeted protein degradation[1]. | |||
T69149 |
L2-b
|
||
L2-b is a bifunctional Aβ-interacting, metal-chelating molecule that modulates ROS production in, and improves survival of neuroblastoma cells incubated in the presence of Aβ along with Copper or Zinc. In cell-free aggregation studies, L2-b inhibits metal-induced Aβ aggregation, and also promotes the dissociation of Ab aggregates in homogenates of human AD brain samples. | |||
T81385 |
PROTAC BRD9 Degrader-2
|
PROTACs | PROTAC |
PROTACBRD9 Degrader-2是针对癌症研究的BRD9双功能性降解剂。 | |||
T77155 | Dalutrafusp alfa | ||
Dalutrafusp alfa (AGEN-1423; GS-1423) 为针对CD73与TGF-β的特异性双功能抗体,涉及免疫抑制路径。 | |||
T26049 |
RB 6145
RB6145,RB-6145 |
||
RB 6145是一种双功能硝基咪唑,低氧细胞放射增敏剂RSU 1069的前药,它的毒性较RSU 1069降低。它具有缺氧细胞优先细胞毒性和抗肿瘤治疗活性。 | |||
T81779 |
M-MoDE-A (2)
|
LYTACs | PROTAC |
M-MoDE-A (2)为双功能小分子,其作用机理包括促进通过ASGPR (去唾液酸糖蛋白受体) 介导的细胞外蛋白质降解。 | |||
T32026 |
GYKI-13324
GYKI 13324,GYKI13324 |
||
GYKI-13324 is bifunctional nitrosoureido derivative and alkylating agent. GYKI-13324 was studied on human colorectal tumor xenograft lines. Given orally in single or multiple daily doses, GYKI-13324 produced long-term or total regression of adenomatous, b | |||
T31588 |
Dynasylan 1161
Y 9138 |
||
Dynasylan 1161 是一种双官能有机硅烷,可以与合适的聚合物反应。在水存在时,Dynasylan 1161可与各种无机基材结合。 | |||
T82560 |
di-Ellipticine-RIBOTAC
|
PROTACs | PROTAC |
Di-Ellipticine-RIBOTAC是一款双功能小分子,在体外和体内肌萎缩侧索硬化(ALS)模型中能够减少c9ALS/FTD r(G4C2)的重复扩增。 | |||
T81675 |
NICE-01
AP1867-PEG2-JQ1,AP-PEG2-JQ1 |
||
NICE-01 (AP1867-PEG2-JQ1; AP-PEG2-JQ1)是一款具有双功能的化合物,它通过特异性结合到细胞内特定亚细胞区室中的蛋白质,并以BRD4蛋白的核定位含溴结构域作为诱导,实现将胞浆中的货物输送至细胞核。 | |||
T68942 |
Caricotamide
|
||
Caricotamide is a synthetic co-substrate that activates the human endogenous enzyme NRH:quinone oxidoreductase 2 (NQO2) with potential chemoadjuvant activity. When caricotamide is administered simultaneously with the prodrug tretazicar, NQO2 converts tretazicar to the bifunctional alkylating agent dinitrobenzamide, which is capable of forming a high degree of DNA interstrand cross-links, resulting in the inhibition of DNA replication and the induction of apoptosis. NQO2 has been found to be over... | |||
T28464 |
p-SCN-Bn-TCMC HCl
p-SCN-Bn-TCMC |
||
p-SCN-Bn-TCMC is a bifunctional chelator, it contains a powerful chelator TCMC and reactive tioisocyante linker. TCMC is a powerful chelator with capability to strongly bind radio-isotopic heavy metal ion, which are widely used for radio-diagnostic/imagin | |||
T78879 |
CXCR4-IN-2
|
CXCR | Autophagy; GPCR/G Protein; Immunology/Inflammation |
CXCR4-IN-2(compound A1)是一款具有抗癌活性的双功能氟化小分子,是CXCR4的强效抑制剂。它对小鼠结直肠癌(CRC)细胞展现出显著的细胞毒性(IC50:60 μg/mL;72小时)和抗增殖能力,能够引导细胞在G2/M期发生阻滞并诱导细胞凋亡(apoptosis)。 | |||
T78352 |
N-acetylglucosamine-1-P uridyltransferase (AGX1)
GlcNAc1pUT |
||
N-acetylglucosamine-1-P uridyltransferase (AGX1) (GlcNAc1pUT) 是具有双功能乙酰转移酶/尿苷转移酶活性的原核生物专有酶。该酶能结合GlcNAc-1-P与UTP,催化合成UDP-GlcNAc的尿苷酰转移反应。 | |||
T82866 |
Biotin-PEG-Biotin (MW 20000)
|
||
Biotin-PEG-azide (MW 2000) 为含有生物素标记的聚乙二醇 (PEG) 衍生物。该生物素(Biotin)作为酶辅因子,在蛋白质标记应用中具有重要作用,而PEG是低毒性且具亲水性的水溶性聚合物。 | |||
T81035 |
TAT-NSF222 Fusion Peptide
|
||
TAT-NSF222 Fusion Peptide为包含TAT和NSF两个结构域的融合多肽,TAT负责通过巨胞饮促进细胞摄取,而NSF结构域则抑制N-乙基马来酰亚胺敏感因子(NSF)活性。该融合多肽是exocytosis的抑制剂。 | |||
T79618 |
M3/PDE4 modulator-1
|
||
M3/PDE4 modulator-1 (10f) 为多功能化合物,具备M3mAChR拮抗和PDE4抑制作用。于OVA大鼠模型中,M3/PDE4 modulator-1 (10-1000 nM/kg;iv) 能降低半胱氨酸嗜酸性粒细胞内流。 |