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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T23101 | O-3M3FBS | Others | |
Inactive analog of m-3M3FBS (PLC activator) | |||
T3188 | RE-640 | CCR , Parasite | |
NSC-5844 (RE-640) (RE640) is a bisquinoline compound with C-C chemokine receptor type 1 (CCR1)-agonistic activities. | |||
T9901A-006 | Vonlerolizumab | Pogalizumab,RG 7888,MOXR 0916 | Others |
Vonlerolizumab(MOXR 0916) is a humanized IgG agonistic OX40-specific monoclonal antibody with potential antitumor activity for the study of tumors and immune diseases. | |||
T8984 | FLTX1 | Estrogen Receptor/ERR , Estrogen/progestogen Receptor | |
FLTX1 is a fluorescent derivative of Tamoxifen, designed to efficiently target and label intracellular Tamoxifen-binding sites (estrogen receptors) both under permeabilized and non-permeabilized conditions. Additionally,... | |||
T60124 | 1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(7-(1-methyl-1H-pyrazol-4-yl)-2,3,4,9-tetrahydro-1H-carbazol-3-yl)urea | TNF | |
1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(7-(1-methyl-1H-pyrazol-4-yl)-2,3,4,9-tetrahydro-1H-carbazol-3-yl)urea, a TNF-α agonistic compound, could induce cells to secrete TNF- α. | |||
T61518 | TAK-653 | iGluR | |
TAK-653, a selective positive allosteric modulator (PAM) of AMPA receptors exhibiting minimal agonistic activity, elicits an antidepressant-like response while maintaining a favorable safety profile in rat models. | |||
T8779 | HBT1 | GluR | |
HBT1 is an AMPA receptor potentiator that induces production of brain-derived neurotrophic factor (BDNF) and exhibits little agonistic effect in primary neurons. HBT1 binds to ligand-binding domain of AMPA-R in glutamate... | |||
T0371 | Gliquidone | AR-DF 26,Glurenorm | Potassium Channel |
Gliquidone (AR-DF 26) is a potent, second-generation sulfonylurea with antihyperglycemic activity. Like other second-generation compounds, gliquidone exerts greater binding affinity to SUR1 and increased potency compared... | |||
T60325 | Viloxazine | Emovit,Viloxazin | 5-HT Receptor , Norepinephrine |
Viloxazine (Viloxazin) (Viloxazin) is a dual-action compound that functions as a norepinephrine reuptake inhibitor and exhibits potent agonistic activity towards 5-HT 2C receptors while acting as an antagonist for 5-HT 2... | |||
T0093L | Sorafenib | Bay 43-9006 | Apoptosis , Raf , VEGFR , FLT , Ferroptosis , PDGFR , c-Kit , Autophagy |
Sorafenib (Bay 43-9006) is a multikinase inhibitor that inhibits Raf-1, B-Raf, VEGFR2, VEGFR3, VEGFR4, PDGFRβ, FLT3, c-Kit, and others (IC50=6/22/90/15/20/20/57/58 nM) with oral activity. Sorafenib has antitumor activity... | |||
TP1541L | BDC2.5 mimotope 1040-31 acetate | BDC2.5 mimotope 1040-31 acetate(329696-49-3 free base) | Others |
BDC2.5 mimotope 1040-31 acetate is a effectively agonistic peptide (mimotope) for diabetogenic T cell clone BDC2.5. It can stimulate BDC2.5 cells with cells showing good response to this mimotope. 1040-31 peptide is spec... | |||
T6602 | Naratriptan hydrochloride | Naratriptan HCl,Amerge,Naramig,GR-85548A hydrochloride | 5-HT Receptor |
Naratriptan Hydrochloride is the hydrochloride salt form of naratriptan, a sulfonamide with selective serotonin (5-HT) 1 receptor agonistic activity and anti-migraine property. Naratriptan hydrochloride (GR-85548A hydroc... | |||
T69157 | H 160-51 | ||
H 160-51 is a calcium agonistic 1,4-dihydropyridine. | |||
T13461 | (+)-Cloprostenol | D-Cloprostenol | Others |
(+)-Cloprostenol is a analogue of prostaglandin F2α (PGF2α), and is selective prostaglandin receptor agonistic. | |||
T69116 | Agroclavine | ||
Agroclavine is a clavine type of ergot alkaloid with D1 dopamine and a-adrenoceptor agonistic properties. | |||
T17292 | ZK159222 | Others | |
ZK159222 is an effective 1α,25-(OH)2D3 receptor (VDR) agonist. ZK159222 has a partial agonistic character. | |||
T15256 | Etofylline clofibrate | Others | |
Etofylline clofibrate has a hypolipidemic and antithrombotic effect and it also has an agonistic interaction with intimal PGI2. | |||
TP1601 | BDC2.5 mimotope 1040-31 TFA(329696-49-3 free base) | BDC2.5 mimotope 1040-31 TFA | |
This is a strongly agonistic peptide (mimotope) for diabetogenic T cell clone BDC2.5. | |||
T35834 | (Sar1)-Angiotensin II | (Sar¹)-Angiotensin II | |
The substitution with Sar at position 1 of angiotensin II resulted in a partial agonistic activity. | |||
T14361 | Axomadol | EN3324 | Others |
Axomadol (EN3324) is a centrally active analgesic compound. It has opioid agonistic properties and inhibitory effects on the reuptake of monoamines. |