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T11478GSK1521498 free base (hydrochloride);化合物 T11478GSK1521498 free base (hydrochloride)
GSK1521498 free base (hydrochloride) is a selective antagonist of the μ-opioid receptor (MOR). It is being used for the treatment of disorders of compulsive consumption of food, alcohol, and drugs.
价 格:¥电议型 号:T11478产 地:中国大陆
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T11449L2Golotimod (TFA) (229305-39-9 free base);化合物 T11449L2SCV 07 (TFA)|||Gamma-D-glutamyl-L-tryptophan (TF
Golotimod TFA (SCV 07 TFA) is an immunomodulatory peptide with antibacterial properties that significantly increases the effectiveness of anti-tuberculosis studies, stimulates thymus and splenocyte proliferation and improves macrophage function. Golotimod TFA has the potential to be used in studies of recurrent genital herpes simplex virus type 2 (HSV-2).
价 格:¥电议型 号:T11449L2产 地:中国大陆
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T11449Golotimod hydrochloride (229305-39-9 free base);化合物 T11449Golotimod hydrochloride|||Gamma-D-glutamyl
Golotimod hydrochloride (SCV 07 hydrochloride) is an immunomodulating peptide with antimicrobial properties. It enhances antituberculosis therapy effectiveness, promotes thymic and splenic cell proliferation, and boosts macrophage functionality. Furthermore, it inhibits STAT3 signaling, thereby modifying the duration and intensity of oral mucositis in animal models subjected to radiation or a combination of radiation and Cisplatin. Additionally, Golotimod hydrochloride has shown potential as a t
价 格:¥电议型 号:T11449产 地:中国大陆
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T11432Glyoxalase I inhibitor free base;化合物 T11432Glyoxalase I inhibitor free base
Glyoxalase I inhibitor (free base), a candidate for anticancer agents, is a potent Glyoxalase I (GLO1) inhibitor.
价 格:¥电议型 号:T11432产 地:中国大陆
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T11406TT-OAD2 free base;化合物 T11406TT-OAD2 free base
TT-OAD2 free base has the potential for diabetes treatment. TT-OAD2 free base is a non-peptide glucagon-like peptide-1 (GLP-1) receptor agonist with an EC50 of 5 nM.
价 格:¥电议型 号:T11406产 地:中国大陆
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T11403LGln-AMS TFA (209543-57-7 free base);化合物 T11403LGln-AMS TFA;Gln-AMS TFA
Gln-AMS(TFA) inhibits glutaminyl-tRNA synthetase (GlnRS) with a Ki of 1.32 μM. Gln-AMS (TFA) is a type Ia aminoacyl-tRNA synthetase (AARS) inhibitor.
价 格:¥电议型 号:T11403L产 地:中国大陆
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T11402LGKI-1 HCl;GKI-1盐酸盐GKI-1 HCl( 2444764-03-6 Free base);GKI-1 HCl( 2444764-03-6 Free base)
GKI-1 HCl is a Greatwall (GWL) kinase inhibitor that inhibits hGWLFL and hGWL-KinDom.The inhibitory effect of GKI-1 HCl on ROCK1 is more significant.
价 格:¥电议型 号:T11402L产 地:中国大陆
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T11369LGB-110 hydrochloride (1252806-70-4 free base);化合物 T11369LGB-110 hydrochloride;GB-110 hydrochloride
GB-110 hydrochloride selectively induces PAR2-mediated intracellular Ca2+ release in HT29 cells with an EC50 of 0.28 μM. GB-110 hydrochloride is a potent, orally active, and nonpeptidic protease activated receptor 2 (PAR2) agonist.
价 格:¥电议型 号:T11369L产 地:中国大陆
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T11367Gastrofensin AN 5 free base;化合物 T11367Gastrofensin AN 5 free base
Gastrofensin AN 5 free base, is an antiulcer agent. a 4-phenyl-tetrahydroisoquinoline derivative.
价 格:¥电议型 号:T11367产 地:中国大陆
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T11346LG3-C12 acetate(848301-94-0 free base);化合物G3-C12 acetateG3-C12 acetate(848301-94-0 free base)
G3-C12 acetate shows anticancer activity.?is a galectin-3 binding peptide, with Kd of 88 nM.
价 格:¥电议型 号:T11346L产 地:中国大陆
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T11342G-5555 hydrochloride (1648863-90-4 free base);化合物 T11342G-5555 hydrochloride;G-5555 hydrochloride
G-5555 hydrochloride is a potent and selective p21-activated kinase 1 (PAK1) inhibitor with a Ki of 3.7 nM.
价 格:¥电议型 号:T11342产 地:中国大陆
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T11327LFR 167653 free base;化合物 T11327LFR 167653 free base
FR 167653 free base is an orally active p38 MAPK inhibitor and is effective in treating inflammation, relieving trauma, and ischemia-reperfusion injury in vivo. It also is a potent suppressor of TNF-α and IL-1β production via specific inhibition of p38 MAPK activity.
价 格:¥电议型 号:T11327L产 地:中国大陆
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T11323Frakefamide TFA (188196-22-7 free base);化合物 T11323Frakefamide TFA;Frakefamide TFA
Frakefamide is unable to penetrate the blood-brain-barrier and enter the central nervous system. Frakefamide TFA is a potent analgesic that acts as a peripheral active μ-selective receptor agonist.
价 格:¥电议型 号:T11323产 地:中国大陆
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T11321FR194738 free base;化合物FR194738 free baseFR194738 free base
FR194738 free base inhibits squalene epoxidase activity in HepG2 cell homogenates with an IC50 of 9.8 nM.?
价 格:¥电议型 号:T11321产 地:中国大陆
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T11319FR183998 free base;化合物FR183998FR183998 free base
FR183998 free base is an inhibitor of Na+/Ca2+ Exchanger.
价 格:¥电议型 号:T11319产 地:中国大陆
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T11316FOY 251 free base;化合物 T11316FOY 251 free base
FOY 251 free base acts as a proteinase inhibitor. FOY 251 free base is an anti-proteolytic active metabolite camostate.
价 格:¥电议型 号:T11316产 地:中国大陆
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T11290FK-448 Free base;化合物 T11290FK-448 Free base
FK-448 Free base is an effective and specific inhibitor of chymotrypsin, with an IC50 of 720 nM.
价 格:¥电议型 号:T11290产 地:中国大陆
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T11282LFGTI-2734 mesylate (1247018-19-4 free base);化合物 T11282LFGTI-2734 mesylate;FGTI-2734 mesylate
FGTI-2734 mesylate, a RAS C-terminal mimetic compound with dual farnesyl transferase (FT) and geranylgeranyl transferase-1 (GGT) inhibitory activities (IC50s of 250 nM and 520 nM for FT and GGT, respectively), mitigates KRAS resistance by preventing its membrane localization, effectively impeding mutant KRAS patient-derived pancreatic tumors.
价 格:¥电议型 号:T11282L产 地:中国大陆
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T11237LCamizestrant TFA;Camizestrant三氟乙酸盐Camizestrant TFA(2222844-89-3 Free base)|||AZD-9833 TFA;Camizestra
Camizestrant TFA (AZD-9833 TFA) is a potent and orally active antagonist of estrogen receptor (ER).
价 格:¥电议型 号:T11237L产 地:中国大陆
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T11220LUK 227786;化合物T11220Lhydrochloride(150452-18-9 Free base)|||1-[4-(1,3-Benzodioxol-5a-ylmethylamino)-6
UK 227786 is an inhibitor of phosphodiesterase 5 (PDE5), used for treatment of prostatic diseases.
价 格:¥电议型 号:T11220L产 地:中国大陆