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T5129SRI-011381 hydrochlorideSRI-011381 hydrochloride [1629138-41-5(free base)]
SRI-011381, a new-type agonist of the TGF-beta signaling pathway, is utilized in the treatment of Alzheimer´s disease.
价 格：￥电议型 号：T5129产 地：中国大陆
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T5124SRT 1720 dihydrochloride[925434-55-5(free base)]
SRT 1720 is a selective activator of SIRT1 (EC1.5: 0.16 μM) and shows less potent activities on SIRT2 (EC1.5: 37 μM) and SIRT3 (EC1.5: 300 μM).
价 格：￥电议型 号：T5124产 地：中国大陆
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T5025LPralmorelin acetate 158861-67-7(free base）
Pralmorelin acetate stimulates growth hormone secretion.Pralmorelin acetate is an oral active synthetic peptide analogue of MEK. Pralmorelin acetate, an auxin releasing peptide/growth hormone secretory receptor agonist, can selectively stimulate ghrelin r
价 格：￥电议型 号：T5025L产 地：中国大陆
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T5021Leuprolide Acetate (53714-56-0 free base)Leuprolide Acetate；Leuprorelin acetate；醋酸亮脯利特
Leuprolide is an agonist at pituitary GnRH receptors. Leuprorelin is a gonadotropin-releasing hormone (GnRH) analog used to treat a wide range of sex hormone-related disorders including advanced prostatic cancer, endometriosis, and precocious puberty. Leu
价 格：￥电议型 号：T5021产 地：中国大陆
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T4696BMS202 hydrochloride (1675203-84-5(free base))PD-1/PD-L1 inhibitor 2 hydrochloride
PD-1/PD-L1 inhibitor 2 is a small-molecule PD-1/PD-L1 interaction inhibitor (IC50: 18 nM). Biophysical studies demonstrate that BMS202 binds directly to PD-L1. Binding of BMS202 promotes PD-L1 dimerisation and blocks the PD-L1/ PD1 interaction.
价 格：￥电议型 号：T4696产 地：中国大陆
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T4694AG-1557 hydrochloride (189290-58-2(free base))
AG-1557 is an inhibitor of the epidermal growth factor receptor (EGFR) tyrosine kinase (pIC50: 8.194).
价 格：￥电议型 号：T4694产 地：中国大陆
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T4690Betrixaban hydrochloride(330942-05-7(free base))盐酸贝曲西班；PRT054021 hydrochloride
Betrixaban is a potent, selective, and orally efficacious factor Xa (fXa) inhibitor (IC50: 1.5 nM).
价 格：￥电议型 号：T4690产 地：中国大陆
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T4689Palosuran hydrochloride 540769-28-6(free base）ACT-058362 hydrochloride
Palosuran is a new potent and specific antagonist of the human UT receptor with an IC50 of 3.6±0.2 nM.
价 格：￥电议型 号：T4689产 地：中国大陆
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T4657LWHI-P97 HCl 211555-05-4(free base)
WHI-P97 HCl is a potent and selective JAK-3 inhibitor. WHI-P97 had an estimated Ki value of 0.09 microM from modeling studies and a measured IC50 value of 2.5 microM in EGFR kinase inhibition assays. WHI-P97 effectively inhibited the in vitro invasiveness
价 格：￥电议型 号：T4657L产 地：中国大陆
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T4613Arg-Gly-Asp TFA (99896-85-2(free base))RGD；RGD Trifluoroacetate
RGD Trifluoroacetate is a tripeptide that effectively triggers cell adhesion, addresses certain cell lines and elicits specific cell responses; binds to integrins.
价 格：￥电议型 号：T4613产 地：中国大陆
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T4491LMPTP INHIBITOR 1 hydrochlorideLMPTP INHIBITOR 1 hydrochloride (1908414-82-3(free base))
LMPTP INHIBITOR 1 is a selective inhibitor of low molecular weight protein tyrosine phosphatase (LMPTP), with an IC50 of 0.8 μM LMPTP-A.
价 格：￥电议型 号：T4491产 地：中国大陆
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T4457Pyridostatin TrihydrochloridePyridostatin Trihydrochloride(free base 1085412-37-8 )；RR-82 Trihydroch
Pyridostatin hydrochloride is a G-quadruplexe stabilizer, with a Kd of 490 nM.
价 格：￥电议型 号：T4457产 地：中国大陆
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T4419UNC2025 2HCl (1429881-91-3(free base))
UNC2025 is a potent and orally bioavailable Mer/Flt3 dual inhibitor with IC50 of 0.8/0.74 nM for Mer/Flt3.
价 格：￥电议型 号：T4419产 地：中国大陆
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T4418GSK2879552 2HCl (1401966-69-5(free base))
GSK2879552 is an orally available, irreversible inhibitor of lysine specific demethylase 1 (LSD1), with potential antineoplastic activity.
价 格：￥电议型 号：T4418产 地：中国大陆
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T4417LDC-4297 HCl (1453834-21-3(free base))
LDC4297 is a potent and selective CDK7 inhibitor with an IC50 of 0.13 nM.
价 格：￥电议型 号：T4417产 地：中国大陆
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T4411DAMGO TFA (78123-71-4(Free base))
Potent, selective agonist of Mu-opioid receptor. Antinociceptive. Stimulates calcium-activated adenylyl cyclases related cAMP production. Expresses chemokines and chemokine receptors through TGF-beta1. Increases food intake of rats.
价 格：￥电议型 号：T4411产 地：中国大陆
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T4324PQ401 hydrochloride (196868-63-0(free base))
PQ401 inhibits autophosphorylation of IGF-1R domain with IC50 of <1 μM.
价 格：￥电议型 号：T4324产 地：中国大陆
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T4284Levamlodipine besylate左旋氨氯地平；(S)-Amlodipine Besylate (103129-82-4(free base))
Levamlodipine, also known as S-amlodipine, is a pharmacologically active enantiomer of amlodipine, an antihypertensive and anti-anginal medication. Levamlodipine belongs to the dihydropyridine group of calcium channel blockers. The names S-amlodipine and
价 格：￥电议型 号：T4284产 地：中国大陆
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T4261BPR1J-097 hydrochloride (1327167-19-0(free base))
BPR1J-097, a new-type small molecule FLT-3 inhibitor(IC50=11±7 nM), is with great anti-tumor activities in vivo.
价 格：￥电议型 号：T4261产 地：中国大陆
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T4248T.cruzi Inhibitor (1350920-22-7(free base))
T.cruzi Inhibitor is a Trypanosoma cruzi inhibitor.
价 格：￥电议型 号：T4248产 地：中国大陆
