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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T29472 | 6-Hexyl-m-cresol | ||
6-Hexyl-m-cresol is a bioactive chemical. | |||
T33232 | M-Cresol, 6-(methylthio)- | ||
m-Cresol, 6-(methylthio)- is a bioactive chemical. | |||
T33238 | M-Cresol, 6-propyl- | ||
m-Cresol, 6-propyl- is a bioactive chemical. | |||
T33236 | M-Cresol, 6-nonyl- | ||
m-Cresol, 6-nonyl- is a bioactive chemical. | |||
T33233 | M-Cresol, 6-butyl- | ||
m-Cresol, 6-butyl- is a bioactive chemical. | |||
T33235 | M-Cresol, 6-heptyl- | ||
m-Cresol, 6-heptyl- is a bioactive chemical. | |||
T33237 | M-Cresol, 6-octyl- | ||
m-Cresol, 6-octyl- is a bioactive chemical. | |||
T33234 | M-Cresol, 6-decyl- | ||
m-Cresol, 6-decyl- is a bioactive chemical. | |||
T15912 | M-PEG6-(CH2)6-Phosphonic acid | Others | |
m-PEG6-(CH2)6-Phosphonic acid serves as a PEG-based PROTAC linker for synthesizing PROTACs[1]. | |||
T15874 | M-PEG4-(CH2)6-Phosphonic acid | Others | |
m-PEG4-(CH2)6-Phosphonic acid is a polyethylene glycol-based linker compound, specifically designed for the synthesis of proteolysis targeting chimeras (PROTACs)[1]. | |||
T33190 | M-Anisidine, 4-((6-phenylhexyl)oxy)- | ||
m-Anisidine, 4-((6-phenylhexyl)oxy)- is a bioactive chemical. | |||
T29478 | 6-tert-Butyl-4-chloro-m-cresol | ||
6-tert-Butyl-4-chloro-m-cresol is a bioactive chemical. | |||
T33239 | M-Cresol, 6-tert-butyl-4-nitro- | ||
m-Cresol, 6-tert-butyl-4-nitro- is a bioactive chemical. | |||
T7402 | Meta-Topolin | m-Topolin | Others |
Meta-Topolin (m-Topolin) , a highly active aromatic cytokinin from poplar leaves | |||
T33153 | M-Acetotoluidide, 6'-chloro-2-(diethylamino)-, hydrochloride | ||
m-Acetotoluidide, 6'-chloro-2-(diethylamino)-, hydrochloride is a bioactive chemical. | |||
T10738 | Abemaciclib metabolite M20 | CDK4/6-IN-4,LSN3106726 | CDK |
Abemaciclib metabolite M20 (CDK4/6-IN-4) is an active metabolite of Abemaciclib. Abemaciclib metabolite M20 is a selective CDK4/6 inhibitor and can be used for researches on the treatment of cancer. | |||
T33152 | M-Acetotoluidide, 6'-chloro-2-(2-(diethylamino)ethyl)methylamino-, dihydrochloride | ||
m-Acetotoluidide, 6'-chloro-2-(2-(diethylamino)ethyl)methylamino-, dihydrochloride is a bioactive chemical. | |||
T33154 | M-Acetotoluidide, 6'-chloro-2-(diethylamino)-alpha,alpha,alpha-trifluoro-, hydrochloride | ||
m-Acetotoluidide, 6'-chloro-2-(diethylamino)-alpha,alpha,alpha-trifluoro-, hydrochloride is a bioactive chemical. | |||
T33240 | M-Cresol, alpha,alpha,alpha-trifluoro-6-nitro-, p-nitrobenzoate | ||
m-Cresol, alpha,alpha,alpha-trifluoro-6-nitro-, p-nitrobenzoate is a bioactive chemical. | |||
T25225 | Cephabacin M6 | Cephabacin M(sub 6) | |
Cephabacin M6 is a new cephem antibiotic isolated from bacterial. | |||
T18211 | M-PEG6-Hydrazide | Others | |
m-PEG6-Hydrazide is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system ... | |||
T15914 | M-PEG6-CH2CH2COOH | Others | |
m-PEG6-CH2CH2COOH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system... | |||
T15913 | M-PEG6-CH2CH2CHO | Others | |
m-PEG6-CH2CH2CHO is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | |||
T15918 | M-PEG6-Tos | Others | |
m-PEG6-Tos is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within... | |||
T15917 | M-PEG6-thiol | Others | |
m-PEG6-thiol is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system with... | |||
T15907 | M-PEG6-azide | Others | |
m-PEG6-azide is a six-unit polyethylene glycol linker functionalized with an azide moiety, serving as a non-cleavable linker for the synthesis of antibody-drug conjugates (ADCs). | |||
T15905 | M-PEG6-Amine | Others | |
m-PEG6-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T18212 | M-PEG6-Ms | Others | |
m-PEG6-Ms is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within ... | |||
T15909 | M-PEG6-Br | Others | |
m-PEG6-Br is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within ... | |||
T15904 | M-PEG6-2-methylacrylate | Others | |
m-PEG6-2-methylacrylate is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome ... | |||
T15906 | M-PEG6-amino-Mal | Others | |
m-PEG6-amino-Mal is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system ... | |||
T15916 | M-PEG6-O-CH2COOH | Others | |
m-PEG6-O-CH2COOH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system ... | |||
T15915 | M-PEG6-NHS ester | Others | |
m-PEG6-NHS ester is a non-cleavable 5 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | |||
T18213 | M-PEG6-SS-PEG6-methyl | Others | |
m-PEG6-SS-PEG6-methyl is a cleavable 12-unit polyethylene glycol (PEG) linker employed for the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T15910 | M-PEG6-C6-phosphonic acid ethyl ester | Others | |
m-PEG6-C6-phosphonic acid ethyl ester serves as a PEG-based PROTAC linker for the synthesis of PROTACs[1]. | |||
T37645 | Dasatinib metabolite M6 | ||
Dasatinib metabolite M6 (Dasatinib carboxylic acid) is an oxidative metabolite of Dasatinib, a potent and orally active inhibitor of both Bcr-Abl and Src family tyrosine kinases[1]. | |||
T28020 | Mesendogen | TRP/TRPV Channel | |
Mesendogen is an inhibitor of TRPM6. Mesendogen alters magnesium homeostasis, promotes mesoderm and definitive endoderm differentiation. | |||
T10432L | AZD-8529 mesylate | GluR | |
AZD-8529 mesylate is a highly selective, and orally bioavailable positive allosteric modulator of mGluR2 (EC50: 285 nM). It shows no positive allosteric modulator responses at 20-25 M on the mGluR1, 3, 4, 5, 6, 7, and 8 ... | |||
T38034 | MAO-IN-M30 dihydrochloride | M 30 dihydrochloride | Monoamine Oxidase |
MAO-IN-M30 dihydrochloride (M 30 dihydrochloride) is a potent and brain selective monoamine oxidase (MAO) inhibitor (EC50 values are 37 and 57 nM for MAO-A and MAO-B, respectively). Also an iron chelator with antioxidant... | |||
T23543 | YIL 781 | GHSR | |
YIL 781 is a selective ghrelin receptor antagonist (GHS-R1a) (Ki = 17 nM), showing a weak affinity for kinesin receptors (K = 6 μM). YIL 781 improves glucose homeostasis in vivo and in vitro by blocking ghrelin secretion... | |||
TNU0523 | 1-(b-D-Xylofuranosyl)-N6-(m-methoxybenzyl) adenine | ||
1-(b-D-Xylofuranosyl)-N6-(m-methoxybenzyl) adenine is a Nucleoside Derivative - Xylo-nucleoside, 6-Modified purine nucleoside. | |||
TNU0537 | 3’-beta-C-Ethynyl-N6-(m-methoxybenzyl)adenosine | ||
3'-beta-C-Ethynyl-N6-(m-methoxybenzyl)adenosine is a Nucleoside Derivative - 3'-Modified nucleoside, 6-Modified purine nucleoside. | |||
TNU0530 | 3’-beta-C-Methyl-N6-(m-methoxybenzyl)adenosine | ||
3'-beta-C-Methyl-N6-(m-methoxybenzyl)adenosine is a Nucleoside Derivative - 3'-Modified nucleoside, 6-Modified purine nucleoside. | |||
TNU0527 | 3’-Deoxy-3’-fluoro-xylo-N6-(m-methoxybenzyl)adenosine | ||
3'-Deoxy-3'-fluoro-xylo-N6-(m-methoxybenzyl)adenosine is a Nucleoside Derivative - Xylo-nucleoside, 6-Modified purine nucleoside, Fluoro-modified nucleoside. | |||
TNU0539 | 3’-Deoxy-N6-(m-methoxy benzyl)adenosine | ||
3'-Deoxy-N6-(m-methoxy benzyl)adenosine is a Nucleoside Derivative - 3'-Modified nucleoside, 6-Modified purine nucleoside;3'-Deoxy nucleoside. | |||
TNU0524 | 1-(b-D-Xylofuranosyl)-N6-(m-trifluoromethyl benzyl) adenine | ||
1-(b-D-Xylofuranosyl)-N6-(m-trifluoromethyl benzyl) adenine is a Nucleoside Derivative - Xylo-nucleoside, 6-Modified purine nucleoside, Fluoro-modified nucleoside. | |||
T63816 | FGFR1 inhibitor-6 | ||
FGFR1 inhibitor-6 is a potent inhibitor of FGFR1 (IC50: 16.31 nM) with cytotoxic activity. fGFR1 inhibitor-6 is capable of blocking the cell cycle in pro-G1 and G2/M phases and inducing apoptosis. | |||
T61781 | MtTMPK-IN-6 | ||
MtTMPK-IN-6 (compound 1) is a highly effective inhibitor (IC 50 = 29 μM) of M. tuberculosis thymidylate kinase (Mtb TMPK). It is a valuable compound for tuberculosis research [1]. | |||
T10432 | AZD-8529 | Others | |
AZD-8529 is a highly selective, and orally bioavailable positive allosteric modulator of mGluR2 (EC50: 285 nM). It shows no positive allosteric modulator responses at 20-25 M on the mGluR1, 3, 4, 5, 6, 7, and 8 subtypes. | |||
T72262 | Antituberculosis agent-6 | ||
Antituberculosis agent-6 is a potent antimycobacterial and antifungal compound with significant activity against M. tuberculosis (MIC of 3.49 μM) and A. niger (MIC of 62.50 μM), respectively. It also demonstrates high ga... |
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T8878 | Urolithin M6 | 3,8,9,10-tetrahydroxy urolithin | Others |
urolithin M6 (3,8,9,10-tetrahydroxy urolithin) (UM6) is an ellagitannin metabolite produced by gut microbiota, was identified as a putative galloflavin mimetic | |||
T36528 | Illudin M | Apoptosis , DNA Alkylator/Crosslinker | |
Illudin M is a cytotoxic sesquiterpene from the fungus O. illudens that alkylates DNA. It has a cytotoxicity of 6-100 nM against HL-60 human leukemia cells.Illudin M has anticancer activity and is a pre-drug for the synt... | |||
T8724 | 6-Methoxydihydrosanguinarine | Others | |
6-Methoxydihydrosanguinarine is a natural product. 6-Methoxydihydrosanguinarine shows strong cytotoxicity against MCF-7 and SF-268 cell lines with IC50 values of 0.61 μM and 0.54 μM, respectively.It has antibacterial act... | |||
T7472 | 7-Hydroxyflavone | P450 | |
7-Hydroxyflavone is a potent inhibitor of CYP1A1 with a Ki value of 0.015 μM and exhibits 6-fold greater selectivity for CYP1A1 over CYP1A2.with anti-inflammatory activity | |||
T3662 | Eleutheroside E | NF-κB | |
Eleutheroside E has anti-inflammatory effects by inhibiting NF-κB activities. Eleutheroside E significantly decreases the inflammatory cell infiltration, pannus formation, cartilage damage, bone erosion of CIA mice, the ... | |||
TN5341 | Pterosin Z | ||
Pterosin Z has smooth muscle relaxant activity, is approximately equipotent with that of the related fungal pterosin (EC50 of 2.9 +/- 1.6 x 10(-6) M). | |||
T81321 | Quercetin-3-O-b-D-galactopyranosyl-(1→6)-b-D-glucopyranoside | ||
Quercetin-3-O-β-D-galactopyranosyl-(1→6)-β-D-glucopyranoside (compound 1), a flavonoid glycoside, is extractable from M. delavayi leaves [1]. | |||
T38016 | Hirsutide | ||
Hirsutide is a cyclotetrapeptide fungal metabolite produced by the entomopathogenic fungus Hirsutella. It has antibacterial activity against C. pyogenes, S. aureus, P. aeruginosa, and K. pneumonia (MICs = 25, 13, 6, and ... | |||
T81991 | Kaempferol-3-O-[2″,6″-di-O-E-p-coumaroyl]-β-D-glucopyranoside | ||
Kaempferol-3-O-[2″,6″-di-O-E-p-coumaroyl]-β-D-glucopyranoside, an acylated kaempferol glucoside, can be extracted from the leaves of O. dentata and functions as a repellent to the fouling organism, the blue mussel M. edu... | |||
T37451 | Stachybotrysin B | ||
Stachybotrysin B is a fungal metabolite originally isolated from S. chartarum and has antiviral and anticancer activities.1,2 It has antiviral activity against HIV in SupT1 cells (IC50 = 19.2 μM).1 Stachybotrysin B is cy... | |||
T36563 | (E)-Guggulsterone | ||
Bile acids are essential for solubilization and transport of dietary lipids, are the major products of cholesterol catabolism, and are physiological ligands for farnesoid X receptor (FXR), a nuclear receptor that regulat... | |||
T35741 | Gliovirin | ||
Gliovirin is a fungal metabolite that has been found inT. harzianumand has fungicidal, antimicrobial and anti-inflammatory activities.1It is active against the plant pathogenic fungusP. ultimum(MIC = 60 ng/ml) and the pa... | |||
T35779 | Oosporein | ||
Oosporein is a mycotoxin that has been found inBeauveriaand has diverse biological activities.1,2It is cytotoxic to Sf9 and Sf21 insect cells with 50% cytotoxic concentration (CC50) values of 4.23 and 10.43 μM, respectiv... |
Cat No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-00685 | EMMPRIN/CD147 Protein, Human, Recombinant | Human | HEK293 Cells |
EMMPRIN/CD147 Protein, Human, Recombinant is expressed in HEK293 mammalian cells. The predicted molecular weight is 20.7 kDa and the accession number is P35613-2. | |||
TMPY-00684 | EMMPRIN/CD147 Protein, Human, Recombinant (hFc) | Human | HEK293 Cells |
EMMPRIN/CD147 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 46.8 kDa and the accession number is P35613-2. | |||
TMPK-01334 | EMMPRIN/CD147 Protein, Canine, Recombinant (His) | Canine | HEK293 Cells |
CD147, also known as extracellular matrix metalloproteinase inducer (EMMPRIN) or basigin, is expressed in a variety of cell types. It is involved in the regulation of extracellular matrix (ECM) remodeling during physiolo... | |||
TMPY-03521 | DcR3 Protein, Human, Recombinant (hFc) | Human | Baculovirus Insect Cells |
Tumor necrosis factor receptor superfamily member 6B (TNFRSF6B) also known as DcR3(Decoy Receptor 3) and M68 is the tumor necrosis factor receptor superfamily. DcR3/TNFRSF6B belongs to the tumor necrosis factor receptor ... | |||
TMPJ-01467 | Oncostatin M/OSM Protein, Human, Recombinant (E. coli, His) | Human | E. coli |
Oncostatin M (OSM) is a glycoprotein belonging to the interleukin-6 family of cytokines that includes leukemia-inhibitory factor, granulocyte colony-stimulating factor, and interleukin 6. OSM encodes a growth regulator, ... | |||
TMPK-00646 | Gp130/IL6ST Protein, Rhesus macaque, Recombinant (His) | Rhesus | HEK293 Cells |
gp130 is a common signal transducing component of the functional receptor complexes for the interleukin (IL)-6 family of cytokines, ie, IL-6, IL-11, leukemia inhibitory factor (LIF), oncostatin M, ciliary neurotrophic fa... | |||
TMPK-00412 | Gp130/IL6ST Protein, Human, Recombinant (His) | Human | HEK293 Cells |
gp130 is a common signal transducing component of the functional receptor complexes for the interleukin (IL)-6 family of cytokines, ie, IL-6, IL-11, leukemia inhibitory factor (LIF), oncostatin M, ciliary neurotrophic fa... | |||
TMPH-03345 | Oncostatin M/OSM Protein, Rat, Recombinant (His) | Rat | HEK293 Cells |
Growth regulator. Inhibits the proliferation of a number of tumor cell lines. It regulates cytokine production, including IL-6, G-CSF and GM-CSF from endothelial cells. Uses only type II OSM receptor (heterodimers compos... | |||
TMPK-01096 | IL-31RA Protein, Mouse, Recombinant (His) | Mouse | HEK293 Cells |
Interleukin-31 receptor A (IL-31RA) is a newly identified type I cytokine receptor, that is related to gp130, the common receptor of the interleukin (IL) -6 family cytokines. IL-31RA forms a functional receptor complex f... | |||
TMPK-01113 | IL-31RA Protein, Human, Recombinant (aa 20-519, hFc) | Human | HEK293 Cells |
Interleukin-31 receptor A (IL-31RA) is a newly identified type I cytokine receptor, that is related to gp130, the common receptor of the interleukin (IL) -6 family cytokines. IL-31RA forms a functional receptor complex f... | |||
TMPK-01114 | IL-31RA Protein, Human, Recombinant (aa 20-519, His) | Human | HEK293 Cells |
Interleukin-31 receptor A (IL-31RA) is a newly identified type I cytokine receptor, that is related to gp130, the common receptor of the interleukin (IL) -6 family cytokines. IL-31RA forms a functional receptor complex f... | |||
TMPJ-00047 | IL-31 Protein, Human, Recombinant | Human | E. coli |
Human Interleukin 31 (IL-31) is a cytokine containing a four-helix bundle structure. It shares several structural and functional characteristics with IL-6, Oncostatin M, LIF, and Cardiotrophin-1. Human IL-31 cDNA encodes... | |||
TMPH-00536 | Epstein-Barr virus (strain AG876) EBNA2 Protein (His & Myc) | EBV | P. pastoris (Yeast) |
Plays a key role in the activation of the host resting B-cell and stimulation of B-cell proliferation. Acts by up-regulating the expression of viral EBNA1-6, LMP1, LMP2A and LMP2B genes, as well as several host genes inc... | |||
TMPY-04542 | CDK2 Protein, Human, Recombinant (His) | Human | Baculovirus Insect Cells |
CDK2 is a member of the Ser/Thr protein kinase family. This protein kinase is highly similar to the gene products of S. cerevisiae cdc28, and S. pombe cdc2. It is a catalytic subunit of the cyclin-dependent protein kinas... | |||
TMPY-03010 | NRG1 beta 1 Protein, Human, Recombinant | Human | HEK293 Cells |
NRG1 beta 1 Protein, Human, Recombinant is expressed in HEK293 mammalian cells. The predicted molecular weight is 26.8 kDa and the accession number is Q02297-6. | |||
TMPY-02705 | NRG1 beta 1 Protein, Human, Recombinant (hFc) | Human | HEK293 Cells |
NRG1 beta 1 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with Fc tag. The predicted molecular weight is 55.2 kDa and the accession number is Q02297-6. | |||
TMPY-04277 | CD45 Protein, Mouse, Recombinant (hFc) | Mouse | HEK293 Cells |
CD45 Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 71.7 kDa and the accession number is P06800-6. | |||
TMPJ-00827 | Tau-D Protein, Human, Recombinant (His) | Human | E. coli |
Microtubule-Associated Protein TAU is abundantly expressed in neurons of the central nervous system and less commonly expressed elsewhere, but is also expressed at very low levels in CNS astrocytes and oligodendrocytes. ... | |||
TMPK-00614 | NKp46/NCR1 Protein, Human, Recombinant (His) | Human | HEK293 Cells |
NKp46, along with NKp30 and NKp44, are activating receptors that have been collectively termed the natural cytotoxicity receptors (NCR).These receptors lack significant sequence homology to one another. They are expresse... | |||
TMPK-00615 | NKp46/NCR1 Protein (Primary Amine Labeling), Human, Recombinant (His), Biotinylated | Human | HEK293 Cells |
NKp46, along with NKp30 and NKp44, are activating receptors that have been collectively termed the natural cytotoxicity receptors (NCR).These receptors lack significant sequence homology to one another. They are expresse... | |||
TMPY-03128 | LAIR1 Protein, Mouse, Recombinant (hFc) | Mouse | HEK293 Cells |
LAIR1 Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 39.6 kDa and the accession number is Q8BG84-6. | |||
TMPY-02600 | NRG1 beta 1 Protein, Human, Recombinant (EGF Domain, hFc) | Human | HEK293 Cells |
NRG1 beta 1 Protein, Human, Recombinant (EGF Domain, hFc) is expressed in HEK293 mammalian cells with Fc tag. The predicted molecular weight is 36.7 kDa and the accession number is Q02297-6. | |||
TMPY-05798 | VEGF145 Protein, Human, Recombinant | Human | HEK293 Cells |
VEGF145 Protein, Human, Recombinant is expressed in HEK293 mammalian cells. The predicted molecular weight is 16.92 kDa and the accession number is P15692-6. | |||
TMPJ-00567 | NCR1 Protein, Human, Recombinant (hFc) | Human | HEK293 Cells |
Natural cytotoxicity triggering receptor 1(NCR1) is a single-pass type I membrane protein .It contains 2 Ig-like (immunoglobulin-like) domains and belongs to the natural cytotoxicity receptor (NCR) family. The protein is... | |||
TMPK-01364 | SIRP alpha V6 Protein, Human, Recombinant (His & Avi), Biotinylated | Human | HEK293 Cells |
Signal regulatory protein α (SIRPα) is a regulatory membrane glycoprotein from SIRP family expressed mainly by myeloid cells and also by stem cells or neurons.SIRPα acts as inhibitory receptor and interacts with a broadl... | |||
TMPK-01358 | SIRP alpha V6 Protein, Human, Recombinant (His & Avi) | Human | HEK293 Cells |
Signal regulatory protein α (SIRPα) is a regulatory membrane glycoprotein from SIRP family expressed mainly by myeloid cells and also by stem cells or neurons.SIRPα acts as inhibitory receptor and interacts with a broadl... |