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Cat No. | Product Name | Synonyms | Targets |
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T36466 | Chlorin E6 | Ce6,Chlorin e6,CE6 | Parasite |
Chlorin E6 (CE6) is a second-generation photosensitizer with antitumor activity when used in combination with irradiation. In a mouse model of implanted fibrosarcoma, Chlorin E6 (2.5-10 mg/kg, i.v., 50-200 J/cm2 irradiat... | |||
T40435 | Chlorin e6 trimethyl ester | ||
Chlorin e6 trimethyl ester, a derivative of methyl pheophorbide-a, is an effective photosensitizer for photodynamic therapy (PDT). | |||
T1254 | Chlorophyllin sodium copper salt | Chlorophyllin copper sodium complex,Chlorophyllin,Chlorophyllin coppered trisodium salt,Sodium-copper chlorin e6 | Others |
Chlorophyllin sodium copper salt (Chlorophyllin coppered trisodium salt) is a semi-synthetic mixture of water-soluble sodium copper salts derived from chlorophyll, primarily used as a food additive and alternative medici... | |||
T16978 | Talaporfin sodium | ME2906,NPe6,Mono-L-aspartyl chlorin e6 | Others |
Talaporfin is a photosensitizer used in photodynamic therapy. | |||
T60014 | SHEN26 | Antiviral | |
SHEN26 has antiviral activity and can be used in research on the treatment of viral infections. | |||
T0711 | Niclosamide | BAY2353,Niclocide | Antibiotic , STAT , Parasite |
Niclosamide (Niclocide)(BAY2353) is used to treat most tapeworm infections by inhibiting DNA replication. | |||
T1406 | Amantadine hydrochloride | 1-adamantanamine HCl,1-Adamantanamine hydrochloride,Symmetrel,CI-719,Amantadine HCl,1-Adamantylamine hydrochloride | Dopamine Receptor , Influenza Virus |
Amantadine hydrochloride (CI-719) is an antiviral that is used in the prophylactic or symptomatic treatment of influenza A and Parkinson disease. | |||
T4068 | E6446 dihydrochloride | TLR | |
E6446 dihydrochloride is a novel synthetic antagonist for nucleic acid-sensing TLRs; potently suppressed DNA stimulation of HEK:TLR9 cells with IC50 of 10 nM. | |||
T4206 | E6446 | TLR | |
E6446 inhibits Toll-like receptor (TLR)7 and 9 signaling. E6446 works in a variety of human and mouse cell types and inhibits DNA-TLR9 interaction in vitro. When administered to mice, this compound suppress responses to ... | |||
T11141 | E64FC26 | Others | |
E64FC26 is a potent protein disulfide isomerase (PDI) family pan-inhibitor with antitumor activity, inhibits PDIA1, PDIA3, PDIA4, TXNDC5 and PDIA6, and can be used in the study of multiple myeloma and pancreatic cancer. | |||
T31592 | E6801 | E 6801,E-6801 | 5-HT Receptor |
E6801 is a novel selective 5-HT6 receptor agonist with a wide range of biological activities.E6801 can be used in the study of dementia, Parkinson's disease, depression, obesity epilepsy, anxiety, and many other diseases... | |||
TP2103L | [D-p-Cl-Phe6,Leu17]-VIP acetate | Others | |
[D-p-Cl-Phe6,Leu17]-VIP acetate is a competitive and selective antagonist of vasoactive intestinal peptide (VIP) receptor (IC50 = 125.8 nM). | |||
TF0029 | Hexaethylene Glycol Monooctyl Ether (C8E6) | ||
Hexaethylene Glycol Monooctyl Ether (C8E6) is a useful organic compound for research related to life sciences. The catalog number is TF0029 and the CAS number is 4440-54-4. | |||
T10555 | BJE6-106 | B106 | PKC |
BJE6-106 (B106) is a potent, selective PKCδ inhibitor (IC50: 0.05 μM) and targets selectivity over classical PKCα (IC50: 50 μM). BJE6-106 induces caspase-dependent apoptosis with tumor-specific effect. | |||
T36651 | Anti-MERS-2E6 mAb | Anti-MERS-2E6 mAb | |
Anti-MERS-2E6 mAb (MERS-2E6), a human IgG1 neutralizing antibody, is expressed in CHO cells. It effectively competes with the virus Spike protein for binding to the CD26 receptor, consequently inhibiting viral invasion i... | |||
T76601 | (D-Phe6,Leu-NHEt13,des-Met14)-Bombesin (6-14) | ||
(D-Phe6,Leu-NHEt13,des-Met14)-Bombesin (6-14), a bombesin (BBN) antagonist, holds potential for cancer research applications [1]. | |||
T83945 | XIE62-1004 | ||
XIE62-1004 is a chemical compound that induces the interaction between p62 and LC3 by binding to the ZZ domain of p62. This interaction promotes p62 self-aggregation and its subsequent interaction with LC3 on autophagoso... | |||
TF0030 | Hexaethylene Glycol Monodecyl Ether (C10E6) | ||
Hexaethylene Glycol Monodecyl Ether (C10E6) is a useful organic compound for research related to life sciences. The catalog number is TF0030 and the CAS number is 5168-89-8. | |||
T61755 | E6201 | ||
E6201 (ER-806201) is a potent dual kinase inhibitor targeting MEK1 and FLT3, inhibiting their activities in an ATP-competitive manner. It effectively suppresses MEK1-induced ERK2 phosphorylation (IC50 = 5.2 nM), MKK4-ind... | |||
T62678 | YE6144 | ||
YE6144 is a typical inhibitor of interferon regulatory factor 5 (IRF5), which inhibits IRF5 phosphorylation and thus selectively inhibits IRF5 activity. | |||
T38774 | E67-2 | E67-2 | |
E67-2, a derivative of E67, is a low-toxicity, selective inhibitor of the KIAA1718 Jumonji domain. It has an IC 50 value of 3.4 μM. E67-2 specifically inhibits the Jumonji demethylase for histone H3 lysine 9 (H3K9) and h... | |||
T78003 | [D-p-Cl-Phe6,Leu17]-VIP TFA | ||
[D-p-Cl-Phe6,Leu17]-VIP TFA acts as a competitive and selective antagonist of the vasoactive intestinal peptide (VIP) receptor, exhibiting an IC50 of 125.8 nM. It shows no activity on glucagon, secretin, or growth hormon... | |||
TF0071 | Hexaethylene Glycol Monododecyl Ether (C12E6) | ||
Hexaethylene Glycol Monododecyl Ether (C12E6) is a useful organic compound for research related to life sciences. The catalog number is TF0071 and the CAS number is 3055-96-7. | |||
T11140 | E6130 | CXCR | |
E6130 may be effective in the treatment of inflammatory bowel disease and is a highly selective CX3CR1 regulator for oral administration. | |||
TP2103 | [D-p-Cl-Phe6,Leu17]-VIP | ||
Selective vasoactive intestinal peptide (VIP) receptor antagonist (IC50 = 125.8 nM). Displays no activity on glucagon, secretin or GRF receptors. | |||
T11442 | GNE684 | TNF | |
GNE684 is a potent inhibitor of potent receptor interacting protein 1 (RIP1) with average Ki app values of 21 nM, 189 nM and 691 nM for human mouse and rat RIP1, respectively [1]. | |||
T39812 | (E/Z)-E64FC26 | (E/Z)-E64FC26 | |
(E/Z)-E64FC26 is a mixture complex comprising E-E64FC26 and Z-E64FC26. E-E64FC26 is a highly potent pan-inhibitor of the protein disulfide isomerase (PDI) family, with IC50 values of 1.9, 20.9, 25.9, 16.3, and 25.4 μM ag... | |||
T33267 | Me6TREN 4HCl | Me6TREN Tetrahydrochloride,Me6-TREN Tetrahydrochloride,Me6 4HCl,Me 6 4HCl,Me-6 4HCl | |
Me6TREN 4HCl is a potent and efficacious mobilizing agent of hematopoietic stem and progenitor cells (HSPCs) that can act by activating MMP-9 expression and disrupting the SDF-1α/CXCR4 axis, exhibiting more significant m... | |||
T70900 | VT-ME6 | ||
VT-ME6 is a potent and selective sphingosine kinase 2 inhibitor. VT-ME6, contained a quaternary ammonium group as a warhead and established that a positively charged moiety is necessary for engaging key amino acid residu... | |||
T81254 | RPE65-IN-1 | ||
RPE65-IN-1 (Compound 16e) serves as a potent inhibitor of RPE65, applicable in studies related to retinopathy [1]. | |||
T17228 | Sabizabulin | ABI-231,VERU-111 | Microtubule Associated |
Sabizabulin (ABI-231) is an effective and orally bioavailable inhibitor of α and β tubulin against panels of melanoma and prostate cancer cell lines. Sabizabulin inhibits tumor growth and metastatic phenotypes of cervica... | |||
T37173 | MPro Inhibitor 11a | ||
MProinhibitor 11a is an inhibitor of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) main protease (MPro; IC50= 0.053 μM in a TR-FRET assay).1It reduces viral yield in the culture supernatant of SARS-CoV-2-i... | |||
T1307 | Carmofur | HCFU | Nucleoside Antimetabolite/Analog , Virus Protease , SARS-CoV , DNA/RNA Synthesis |
Carmofur (HCFU) is a highly potent acid ceramidase inhibitor, used in the treatment of breast and colorectal cancer. Carmofur has been known to induce leukoencephalopathy. | |||
T15172 | DSHS00884 | SSYA10-001 | Others |
DSHS00884 is a potent inhibitor of human papillomavirus E6 (IC50: 10 μM). | |||
T28534 | RH02007 | CCG 40788,RH-02007,CCG40788,CCG-40788,RH 02007 | |
RH02007 is an inhibitor of the human papillomavirus (HPV) E6 oncoprotein. | |||
T71941 | Lig3 | ||
Lig3 is an inhibitor against high-risk strains of human papillomavirus (HPV) E6 oncoprotein. | |||
T40207 | SARS-CoV-2-IN-7 | ||
SARS-CoV-2-IN-7 demonstrates potent inhibition of viral replication in SARS-CoV-2-infected Vero E6 cells with an IC50 value of 844 nM. | |||
T79329 | SARS-CoV-2-IN-56 | SARS-CoV | |
SARS-CoV-2-IN-56 (Compound 63) is a SARS-CoV-2 inhibitor with antiviral activity, demonstrating inhibition of the virus in Vero E6 cells with an IC50 of 0.7 μM [1]. | |||
T79328 | SARS-CoV-2-IN-54 | SARS-CoV | |
SARS-CoV-2-IN-54 (Compound 2), a SARS-CoV-2 inhibitor, exhibits antiviral activity by impeding the virus in Vero E6 cells with an inhibitory concentration (IC50) of 21.4 μM [1]. | |||
T81209 | SARS-CoV-2-IN-62 | SARS-CoV | |
SARS-CoV-2-IN-62 (Compound R3b) effectively inhibits SARS-CoV-2 replication in Vero E6 and Calu-3 cells, demonstrating low cytotoxicity and EC50 values of 2.97 μM and 3.82 μM, respectively [1]. | |||
T72519 | Niclosamide sodium | BAY2353 sodium | |
Niclosamide sodium (BAY2353), an orally active antihelminthic agent employed in parasitic infection research, serves as a potent STAT3 inhibitor, demonstrating an IC50 of 0.25 μM in HeLa cells. Additionally, this compoun... | |||
T79462 | SARS-CoV-2 3CLpro-IN-14 | SARS-CoV | |
SARS-CoV-2 3CLpro-IN-14 (compound 11j) is an orally active inhibitor of SARS-CoV-2 3CLpro, demonstrating potent anti-SARS-CoV-2 properties with an EC50 of 0.18 μM and exhibits minimal cytotoxicity, having a CC50 greater ... | |||
T81208 | SARS-CoV-2-IN-63 | SARS-CoV | |
SARS-CoV-2-IN-63 (Compound R3e) serves as an inhibitor of SARS-CoV-2 replication, demonstrating low cytotoxicity. It effectively suppresses viral replication within Vero E6 cells and Calu-3 cells, yielding half-maximal e... | |||
T79661 | SARS-CoV-2 3CLpro-IN-18 | SARS-CoV | |
SARS-CoV-2 3CLpro-IN-18 (Compound 3C) is a covalent inhibitor of SARS-CoV-2 3CLpro with an IC50 of 0.478 μM. It demonstrates inhibition of SARS-CoV-2 in Vero E6 cells, with an EC50 of 2.499 μM, and exhibits low cytotoxic... | |||
T80686 | γ-AA peptide P6 | ||
γ-AA peptide P6 acts as a potent activator of E6 associated protein (E6AP), facilitating both its self-ubiquitination and the ubiquitination of E6AP substrates in vitro reconstituted reactions. Furthermore, γ-AA peptide ... | |||
T36435 | SP 10 | ||
Peptide originally derived from SARS-CoV Spike (S) protein; corresponds to amino acid residues 668 to 679. Highly potent inhibitor of SARS-CoV S protein and ACE2 interaction (IC50 = 1.88 nM in biochemical assay). Inhibit... | |||
T79455 | SARS-CoV-2 Mpro-IN-9 | SARS-CoV | |
SARS-CoV-2 Mpro-IN-9 (compound c7), a nonpeptidic, noncovalent inhibitor of SARS-CoV-2 main protease (Mpro), exhibits potent inhibitory action (IC50 = 0.085 μM) and improved physicochemical and drug metabolism and pharma... | |||
T37174 | SARS-CoV MPro-IN-1 | ||
MProinhibitor 11b is an inhibitor of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) main protease (MPro; IC50= 0.04 μM in a TR-FRET assay).1It reduces viral yield in the culture supernatant of SARS-CoV-2-in... | |||
T83947 | HDAC4 CHDI Degrader 11 | ||
HDAC4 CHDI Degrader 11 is a potent, selective degrader of HDAC4 (PROTAC) with DC_50 values of 4 nM and 6 nM in Jurkat E6-1 and Jurkat cells, respectively. This compound integrates the class IIa HDAC inhibitor trifluorome... |
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T7060 | Amantadine | 1-Aminoadamantane,1-Adamantanamine,1-Adamantylamine | Others |
Amantadine (1-Aminoadamantane) is an antiviral, is a weak antagonist of the NMDA-type glutamate receptor, increases dopamine release, and blocks dopamine reuptake. | |||
TN2149 | Reynosin | BCL , Others , TNF | |
Reynosin has hepatoprotective, and anti-inflammatory effects, it has protective effect against dopamine-induced neuronal cell death, which may be due to the reciprocal up-regulation of E6-associated protein and down-regu... | |||
T79941 | Antimycin A2c | Apoptosis | |
Anticancer Agent 141 (Compound AE), an antimycin alkaloid, exhibits inhibitory potential against HPV-infected cervical cancer. It impedes HeLa cell proliferation by arresting the cell cycle at the S phase and induces cas... |
Cat No. | Product Name | Species | Expression System |
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TMPK-01467 | HLA-A*02:01&B2M&HPV 16 E6 (KLPQLCTEL) Monomer Protein, Human, MHC (His & Avi) | Human | HEK293 Cells |
Human papillomavirus (HPV) 16 infection is a necessary condition for the pathogenesis and development of cervical cancer. The E6 protein is expressed by the HPV16 E6 gene and promotes malignant phenotype transformation, ... | |||
TMPK-01466 | HLA-A*02:01&B2M&HPV 16 E6 (KLPQLCTEL) Tetramer Protein, Human, MHC (His & Avi) | Human | HEK293 Cells |
Human papillomavirus (HPV) 16 infection is a necessary condition for the pathogenesis and development of cervical cancer. The E6 protein is expressed by the HPV16 E6 gene and promotes malignant phenotype transformation, ... | |||
TMPH-01833 | Human Papilloma Virus type 16 (HPV 16) Protein E6 (His) | HPV 16 | P. pastoris (Yeast) |
Human Papilloma Virus type 16 (HPV 16) Protein E6 (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 21.2 kDa and the accession number is P03126. | |||
TMPH-01832 | Human Papilloma Virus type 16 (HPV 16) Protein E6 (E. coli, His) | HPV 16 | E. coli |
Human Papilloma Virus type 16 (HPV 16) Protein E6 (E. coli, His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 23.2 kDa and the accession number is P03126. | |||
TMPJ-01258 | RNASE6 Protein, Human, Recombinant (His) | Human | HEK293 Cells |
Ribonuclease K6 (RNASE6) is a secreted protein that belongs to the pancreatic ribonuclease family. Human RNASE6 is synthesized as a 150 amino acid precursor that contains a 23 amino acid signal sequence, and a 127 amino ... | |||
TMPH-02033 | RPE65 Protein, Human, Recombinant (His & Myc) | Human | Baculovirus Insect Cells |
RPE65 Protein, Human, Recombinant (His & Myc) is expressed in Baculovirus. | |||
TMPY-02842 | UBE2L6 Protein, Human, Recombinant (His) | Human | E. coli |
UBCH8, also known as UBE2L6, belongs to the ubiquitin-conjugating enzyme family. The family of ubiquitin-conjugating (E2) enzymes is characterized by the presence of a highly conserved ubiquitin-conjugating (UBC) domain.... |