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T4457Pyridostatin Trihydrochloride；化合物Pyridostatin TrihydrochloridePyridostatin Trihydrochloride(free bas
Pyridostatin Trihydrochloride (RR-82 Trihydrochloride) 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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T4444A-674563 HCl (552325-73-2(free base))；化合物A-674563 HClA-674563 HCl (552325-73-2(free base))
A-674563 is an orally available, ATP-competitive, and reversible inhibitor of Akt (Ki: 11 nM for Akt1) [1]. It exhibits inhibitory activity against PKA and Cdk2 (IC50: 16/46 nM) but is 10- to >1, 800-fold selective for Akt1 versus additional kinases in the CMGC, CAMK, and TK families [1].
价 格：￥电议型 号：T4444产 地：中国大陆
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T4419UNC2025 2HCl (1429881-91-3(free base))；化合物UNC2025 2HClUNC2025 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))；化合物GSK2879552 2HClGSK2879552 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))；化合物LDC-4297 HClLDC-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))；化合物DAMGO TFADAMGO 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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T4393MS049 2HCl (1502816-23-0(free base))；化合物MS049 2HClMS049 2HCl (1502816-23-0(free base))
MS049 is a potent and selective inhibitor of PRMT4 (IC50 = 34 nM) and PRMT6 (IC50 = 43 nM). It is less active against additional type I PRMTs (IC50s = >130, >220, and 1.6 μM for PRMT1, PRMT3, and PRMT8, respectively) and displays no inhibition against type II or type III PRMTs nor any additional methyltransferases or nonepigenetic targets tested.
价 格：￥电议型 号：T4393产 地：中国大陆
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T4383GSK-J4 Hydrochloride；化合物GSK-J4 HydrochlorideGSK J4 HCl|||GSK J4 HCl (1373423-53-0 free base)；GSK J4
GSK-J4 Hydrochloride (GSK J4 HCl) is a cell permeable, potent and selective histone demethylase(JMJD3 )inhibitor. is an ethyl ester derivative of the GSK-J1 with an IC50 value greater than 50 μM in vitro.
价 格：￥电议型 号：T4383产 地：中国大陆
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T4334EPZ020411 2HCl (1700663-41-7(free base))；化合物EPZ020411 2HClEPZ020411 2HCl (1700663-41-7(free base))
EPZ020411 is an effective and specific small molecule PRMT6 inhibitor (IC50=10 nM).
价 格：￥电议型 号：T4334产 地：中国大陆
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T4324PQ401 hydrochloride (196868-63-0(free base))；化合物PQ401 hydrochloridePQ401 hydrochloride (196868-63-0(
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))；左旋氨氯地平|||(S)-Amlodipin
Levamlodipine besylate ((S)-Amlodipine Besylate (103129-82-4(free base))) , also known as S-amlodipine, is a pharmacologically active enantiomer of amlodipine, an antihypertensive and anti-anginal medication. Levamlodipine besylate belongs to the dihydropyridine group of calcium channel blockers. The names S-amlodipine and levamlodipine may be used interchangeably as both substances are the same, however, with differing nomenclature. As a racemic mixture, amlodipine contains (R) and (S)-amlodipi
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))；化合物BPR1J-097 hydrochlorideBPR1J-097 hydrochloride
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 InhibitorT.cruzi Inhibitor (1350920-22-7(free ba
T.cruzi Inhibitor is a Trypanosoma cruzi inhibitor.
价 格：￥电议型 号：T4248产 地：中国大陆
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T4233LCysteinylglycine acetate；半胱氨酸-甘氨酸醋酸盐Cys-Gly Acetate|||Cysteinylglycine acetate（19246-18-5 Free base）
Cysteinylglycine acetate (Cys-Gly Acetate) is an acetate salt of Cysteinylglycine. Cysteinylglycine is an endogenous metabolite. Cysteinylglycine is used in disease diagnosis.
价 格：￥电议型 号：T4233L产 地：中国大陆
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T4227SB1317 hydrochloride (1204918-72-8(free base))；化合物SB1317 hydrochlorideTG-02 hydrochloride；TG-02 hydr
SB1317 hydrochloride (1204918-72-8(free base)) (TG-02 hydrochloride) is an effective inhibitor of CDK2/JAK2/FLT3 (IC50: 13/73/56 nM).
价 格：￥电议型 号：T4227产 地：中国大陆
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T4211SAG hydrochloride (912545-86-9(free base))；化合物SAG hydrochlorideSmoothened Agonist HCl；Smoothened Ago
SAG hydrochloride (912545-86-9(free base)) (Smoothened Agonist HCl) acts as an SMO agonist.
价 格：￥电议型 号：T4211产 地：中国大陆
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T41369(S)-Butaprost free acid；化合物 (S)-Butaprost free acid(S)-Butaprost free acid
(S)-Butaprost (free acid) is a potent and highly selective EP2 receptor agonist[1].
价 格：￥电议型 号：T41369产 地：中国大陆
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T4122TAPI-1 trifluoroacetate (163847-77-6(free base))；化合物TAPI-1 trifluoroacetateTAPI-1 trifluoroacetate (
TAPI-1 is an ADAM17/TACE inhibitor, which blocks shedding of cytokine receptors.
价 格：￥电议型 号：T4122产 地：中国大陆
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T41151LK34c hydrochloride；K34c盐酸盐K34c hydrochloride(939769-93-4 Free base)；K34c hydrochloride(939769-93-4 F
K34c hydrochloride is an alpha5β1 integrin antagonist for glioblastoma study.
价 格：￥电议型 号：T41151L产 地：中国大陆
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T41060AnsofaxineAnsofaxineAnsofaxine|||LPM570065freebase|||Toludesvenlafaxine|||LY03005freebase
Ansofaxine, an SNRI compound, is commonly utilized in depression research as a serotonin-norepinephrine reuptake inhibitor.
价 格：￥电议型 号：T41060产 地：中国大陆
