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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T23602 | ABC99 | ABC 99,ABC-99 | Wnt/beta-catenin |
ABC99 is a selective irreversible inhibitor of the wnt-deacylating enzyme. ABC99 inhibited NOTUM (IC50: 13 nM). It also showed excellent selectivity across the serine hydrolase family. | |||
T23601 | ABC1183 | ABC 1183,ABC-1183 | GSK-3 , CDK |
ABC1183 is a novel diaminothiazole that inhibits GSK3α, GSK3β and CDK9. ABC1183 inhibits the growth of a numerous cancer cell lines by decreasing cell survival by inducing G2/M arrest and through altering GSK3, glycogen ... | |||
T6367 | Abacavir sulfate | Abacavir Hemisulfate,1592U89,ABC sulfate,Ziagen | Apoptosis , HIV Protease , Reverse Transcriptase |
Abacavir sulfate (Ziagen) , a nucleoside analogue, effectively utilize its antiviral activity | |||
T6750 | Opaganib | ABC294640 | S1P Receptor |
Opaganib (ABC294640) is an orally active and specific sphingosine kinase-2 (SphK2) inhibitor (IC50: 60 μM). | |||
T33648 | Nestifylline | ABC 99,ABC99,ABC-99 | |
Nestifylline is a biochemical. | |||
T80903 | Ulviprubart | ABC-008 | |
Ulviprubart, an anti-KLRG1 monoclonal antibody (mAb), is utilized in various disease research [1]. | |||
T25611 | Lanatoside | Lantoside,ABC lanatoside complex | |
Lanatoside is an FDA-approved cardiac glycoside that has been identified as a candidate anti-dengue compound. It has also been found to promote atherosclerosis. It also has anti-tumor activity, inhibiting the growth of c... | |||
T68352 | ABC294735 | ||
ABC294735 is a dual SK1/SK2 inhibitor with potential anticancer activity. | |||
T38316 | ABC34 | ||
ABC34 is an inactive control probe for JJH260 , the inhibitor of androgen-induced gene 1 (AIG1), an enzyme that hydrolyzes fatty acid esters of hydroxy fatty acids (FAHFAs). ABC34 demonstrates an IC50 value greater than ... | |||
T16040 | Mepazine | Pecazine | Apoptosis , MALT |
Mepazine (Pecazine) is a potent and selective inhibitor of MALT1. Mepazine inhibits GSTMALT1 full length and GSTMALT1 325-760 with IC50s of 0.83 μM and 0.42 μM. Mepazine enhances apoptosis and affects the cell viability. | |||
T8596 | Ceefourin 1 | MRP | |
Ceefourin 1 is a highly selective multidrug resistance protein 4 (MRP4) inhibitor. | |||
T71299 | M-25 | ||
M-25 is a Smoothened antagonist and inhibitor of the Hedgehog pathway. | |||
T5354 | IRAK4-IN-7 | CA-4948 | IRAK |
IRAK4-IN-7 (CA-4948) is a selective and potent IRAK4 kinase inhibitor with in vivo activity in a TLR4-induced cytokine release model. | |||
T8491 | Vorolanib | CM082,X-82 | VEGFR , PDGFR |
Vorolanib (X-82) is an orally active VEGFR/PDGFR dual inhibitor. | |||
T68135L | (Rac)-Sabcomeline HCl | sabcomeline HCl(149156-36-5 Free base) | AChR |
Sabcomeline HCl is an M1 receptor agonist that can be used to study Alzheimer's disease. | |||
T18962 | Dabcyl acid, SE | Dabcyl, SE | Others |
Dabcyl acid, SE (Dabcyl, SE) is the amino-reactive form of Dabcyl acid and used to prepare a variety of FRET-based probes that contain Dabcyl acid. | |||
T76844 | Abciximab | C7E3 | Integrin |
Abciximab (C7E3) is a mouse/human chimeric monoclonal antibody that is a potent glycoprotein IIb/IIIa inhibitor. Abciximab has anti-platelet aggregation and leukocyte adhesion, acting by binding to glycoproteins IIb/IIIa... | |||
T40303 | 5-A-RU-PABC-Val-Cit-Fmoc | Others | |
5-A-RU-PABC-Val-Cit-Fmoc is one of the precursors of 5-A-RU, a small molecule mucosal-associated MAIT activator that is a precursor for bacterial synthesis of riboflavin. | |||
T18963 | Dabcyl acid | DABCYL,Para-methyl red | Others |
Dabcyl acid (DABCYL) is the original dark fluorescence quencher. | |||
T3503 | MC-Val-Cit-PABC-PNP | Maleimidocaproyl-L-valine-L-citrulline-p-aminobenzyl alcohol p-nitrophenyl carbonate | Others , AChR |
MC-Val-Cit-PABC-PNP, also known as Mc-Val-Cit-PABC-PNP, is a cathepsin cleavable ADC peptide linker. For example, FDA approved drug, brentuximab vedotin, adopts this linker. Protein- and peptide-drug conjugates hold a pr... | |||
T18721 | MAC-VC-PABC-ST7612AA1 | Others | |
MAC-VC-PABC-ST7612AA1 is a part of antibody drug conjugates (ADCs) charged with HDAC inhibitor by a linker, shows antitumor activity[1]. | |||
T64082 | ABC44 | ||
ABC44 is a potent inhibitor of serine hydrolase with IC50s of 0.1 μM and 6.5 μM for palmitoyl protein thioesterase 1 (PPT1) in situ and in vitro, respectively. ABC44 can be used to study late infantile neuron-like lipofu... | |||
T77848 | Vc-PABC-DM1 | ||
vc-PABC-DM1 is a chemical compound utilized for the synthesis of an antibody-drug conjugate (ADC) that incorporates a disulfide linker. This compound is instrumental in investigating serum stability [1]. | |||
T78763 | ABCB1-IN-1 | ||
ABCB1-IN-1 (compound 3) is a potent inhibitor of ABCB1 that promotes cell apoptosis. Featuring 1-benzylimidazole, it exhibits IC50 values of 1.26 μM for Colo205 cells and 2.21 μM for Colo320 cells, respectively [1]. | |||
T79877 | MTvkPABC-P5 | ||
MTvkPABC-P5d, functioning as a TLR7 agonist, serves as an immune stimulant and is utilized in the synthesis of immune-stimulating antibody conjugates (ISACs) [1]. | |||
T35615 | Dabcyl-YVADAPV-EDANS | ||
Dabcyl YVADAPV EDANS is a fluorescent IL-1β converting enzyme (ICE) substrate that can be used to detect ICE-like protease activity. Dabcyl YVADAPV EDANS detects fluorescence at λex=360 nm, λem=480 nm. | |||
T77822 | Mal-PEG8-Val-Ala-PABC | ||
Mal-PEG8-Val-Ala-PABC is a cleavable linker utilized in the synthesis of Tesirine, an agent-linker conjugate for Antibody-Drug Conjugates (ADC) [1]. | |||
T81714 | N3-PEG8-Phe-Lys-PABC-Gefitinib | ||
N3-PEG8-Phe-Lys-PABC-Gefitinib is an antibody-drug conjugate (ADC) agent-linker complex exhibiting potent antitumor activity. It incorporates the orally active EGFR tyrosine kinase inhibitor Gefitinib, tethered by the cl... | |||
T17816 | DBCO-Val-Cit-PABC-PNP | Others | |
DBCO-Val-Cit-PABC-PNP is a cleavable linker for antibody-drug conjugate (ADC) synthesis[1]. | |||
T79513 | ABCG2-IN-1 | BCRP | |
ABCG2-IN-1 (compound K2), an analog of Ko143, constitutes an orally active inhibitor targeting ABCG2 with an inhibitory concentration (IC50) of 0.13 μM. Demonstrating favorable oral pharmacokinetics in mice, ABCG2-IN-1 s... | |||
T40342 | MC-VC-PABC-amide-PEG1-CH2-CC-885 | MC-VC-PABC-amide-PEG1-CH2-CC-885 | |
MC-VC-PABC-amide-PEG1-CH2-CC-885 is an Antibody-Drug Conjugate (ADC) utilizing a protein-degrading agent (protac molecular glue, etc.). | |||
T18875 | (Ac)Phe-Lys(Alloc)-PABC-PNP | Others | |
'(Ac)Phe-Lys(Alloc)-PABC-PNP serves as a valuable cleavable linker in the development of antibody-drug conjugates.' | |||
T18331 | MC-VC-PABC-DNA31 | Others | |
MC-VC-PABC-DNA31 is a drug-linker conjugate designed for Antibody-Drug Conjugates (ADC) that demonstrates potent antitumor activity. It employs DNA31, an effective inhibitor of RNA polymerase, connected through the MC-VC... | |||
T17351 | Acetylene-linker-Val-Cit-PABC-MMAE | LCB14-0602 | Others |
Acetylene-linker-Val-Cit-PABC-MMAE (LCB14-0602) is a drug-linker conjugate for antibody-drug conjugates (ADCs) that combines the ADC linker (Acetylene-linker-Val-Cit-PABC) with the potent tubulin inhibitor MMAE. | |||
T18332 | MC-VC-PABC-Aur0101 | Others | |
MC-VC-PABC-Aur0101 is a potent anticancer drug-linker conjugate designed for Antibody-Drug Conjugates (ADCs), comprising Aur0101, an auristatin microtubule inhibitor, connected through the MC-VC-PABC linker to enhance an... | |||
T17357 | AcLys-PABC-VC-Aur0101 | Others | |
AcLys-PABC-VC-Aur0101 is a drug-linker conjugate for anti-CXCR4 ADC with potent antitumor activity, comprising the auristatin microtubule inhibitor Aur0101, connected through the cleavable linker AcLys-PABC-VC[1]. | |||
T80128 | RE(EDANS)EVNLDAEFK(DABCYL)R | Beta-Secretase | |
RE (EDANS) EVNLDAEFK (DABCYL) R is a double-labeled peptide with EDANS and DABCYL, functioning as a fluorescent substrate for BACE1 with an emission wavelength of 360 nm and an excitation wavelength of 528 nm. Its utilit... | |||
T68135 | Sabcomeline | SB-202026,SB-202026 ; Memric,Memric | |
Sabcomeline, a potent and functionally selective partial agonist at muscarinic M1 receptors, enhances cognition and is utilized in Alzheimer's disease research [1] [2]. | |||
T75369 | DABCYL-Glu-Arg-Nle-Phe-Leu-Ser-Phe-Pro-EDANS | ||
DABCYL-Glu-Arg-Nle-Phe-Leu-Ser-Phe-Pro-EDANS is a fluorescent dye utilized as a fluorogenic substrate for aspartyl proteinase from the human malaria parasite [1]. It requires protection from light during storage. | |||
T77849 | Val-Ala-PABC-Exatecan | ||
Val-Ala-PABC-Exatecan is a Drug-Linker Conjugate for Antibody-Drug Conjugate (ADC) synthesis, comprising a cleavable Tesirine linker (Val-Ala-PABC) and the topoisomerase I inhibitor Exatecan. It is utilized in the constr... | |||
T18754 | TCO-PEG1-Val-Cit-PABC-OH | Others | |
TCO-PEG1-Val-Cit-PABC-OH, a cleavable 1-unit PEG ADC linker, is employed in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T28654 | Sabcomeline hydrochloride | BCI224,BRL-55473,BCI-224,CEB-2424,SB-202026A,Sabcomeline HCl | |
Sabcomeline is a selective M1 receptor partial agonist. | |||
T17528 | BCN-PEG1-Val-Cit-PABC-OH | Others | |
BCN-PEG1-Val-Cit-PABC-OH is a cleavable 1-unit PEG linker specifically utilized in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T17945 | Fmoc-Ala-Ala-Asn-PABC-PNP | Others | |
Fmoc-Ala-Ala-Asn-PABC-PNP is a peptide cleavable ADC linker[1]. | |||
T81832 | MC-VC-PABC-C6-alpha-Amanitin | ||
MC-VC-PABC-C6-alpha-Amanitin is an antibody-drug conjugate that combines the anticancer toxin alpha-Amanitin with the monoclonal antibody MC-VC-PABC-C6. Alpha-Amanitin acts as a potent inhibitor of RNA polymerase IIα, en... | |||
T68135L1 | (Rac)-Sabcomeline | ||
T18268 | Mal-PEG1-Val-Cit-PABC-OH | Others | |
Mal-PEG1-Val-Cit-PABC-OH is a 1 unit polyethylene glycol (PEG) ADC linker that possesses cleavable properties. This linker, commonly utilized in the synthesis of antibody-drug conjugates (ADCs), serves as a critical comp... | |||
T81753 | Mp-dLAE-PABC-MMAE | ||
mp-dLAE-PABC-MMAE is an agent-linker conjugate for antibody-drug conjugates (ADCs) that incorporates the potent tubulin inhibitor Monomethyl auristatin E (MMAE). This compound is utilized in the synthesis of ADCs to deli... | |||
T79514 | ABCG2-IN-2 | BCRP | |
ABCG2-IN-2 is a potent inhibitor of ABCG2, exhibiting favorable oral pharmacokinetic profiles in mice, and is applicable for investigating tumor multidrug resistance (MDR) and erythropoietic protoporphyria (EPP) [1]. | |||
T18737 | AcLysValCit-PABC-DMAE-SW-163D | Others | |
AcLysValCit-PABC-DMAE-SW-163D is a drug-linker conjugate for antibody-drug conjugates (ADCs), featuring a natural bis-intercalator, SW-163D, attached through an AcLysValCitPABC-DMAE linker[1]. |
Cat No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-01711 | ABCC1 Protein, Human, Recombinant (His) | Human | E. coli |
Mediates export of organic anions and drugs from the cytoplasm. Mediates ATP-dependent transport of glutathione and glutathione conjugates, leukotriene C4, estradiol-17-beta-o-glucuronide, methotrexate, antiviral drugs a... | |||
TMPH-00970 | ABCD1 Protein, Human, Recombinant (His) | Human | in vitro E. coli expression system |
ABCD1 Protein, Human, Recombinant (His) is expressed in in vitro E. coli expression system. | |||
TMPH-00981 | ABCB1 Protein, Human, Recombinant (His) | Human | E. coli |
ABCB1 Protein, Human, Recombinant (His) is expressed in E. coli. | |||
TMPJ-01145 | ABCB5 Protein, Human, Recombinant (Trx) | Human | E. coli |
ATP-binding cassette sub-family B member 5(ABCB5) is a plasma membrane-spanning protein. ABCB5 is principally expressed in physiological skin and human malignant melanoma. ABCB5 has been suggested to regulate skin progen... | |||
TMPH-03414 | RT0041 Protein, Rickettsia typhi, Recombinant (His & Myc) | Rickettsia typhi | E. coli |
Could be part of an ABC transporter complex. | |||
TMPH-03591 | PsaA Protein, S. pneumoniae, Recombinant (His & Myc) | Streptococcus pneumoniae | E. coli |
Part of an ABC transporter complex involved in manganese import. | |||
TMPH-00628 | GltI/YbeJ Protein, E. coli, Recombinant (His & SUMO) | E. coli | E. coli |
Part of the ABC transporter complex GltIJKL involved in glutamate and aspartate uptake. Binds to both glutamate and aspartate. | |||
TMPH-00652 | MMBP Protein, E. coli, Recombinant (His & Myc) | E. coli | E. coli |
Part of the ABC transporter complex MalEFGK involved in maltose/maltodextrin import. Binds maltose and higher maltodextrins such as maltotriose. | |||
TMPH-00786 | BtuD Protein, Halobacterium salinarum, Recombinant (His) | Halobacterium salinarum | E. coli |
Required for corrinoid utilization. Probably part of the ABC transporter complex BtuCDF involved in cobalamin (vitamin B12) import. Probably responsible for energy coupling to the transport system. | |||
TMPH-00787 | BtuD Protein, Halobacterium salinarum, Recombinant | Halobacterium salinarum | E. coli |
Required for corrinoid utilization. Probably part of the ABC transporter complex BtuCDF involved in cobalamin (vitamin B12) import. Probably responsible for energy coupling to the transport system. | |||
TMPY-02549 | GBP1 Protein, Human, Recombinant (His) | Human | HEK293 |
Guanylate-binding protein 1 (GBP-1) is a member of the GBP family whose members are GTPases induced in response to interferon-λ (IFN-λ), with seven highly homologous members in humans, termed HuGBP-1 to HuGBP-7. GBP-1 ex... |