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产品数：86101
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T9078LY3405105anticancer,Cyclin dependent kinase,CDK,MCF7,SNU-16,Cyclin-dependent kinase,LY 3405105,LY340
LY3405105 is a novel CDK7 inhibitors.
价 格：￥电议型 号：T9078产 地：中国大陆
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T8819SU-9516SU 9516,SU9516
SU9516 is a selectively potent ATP-competitive inhibitor of CDKs.
价 格：￥电议型 号：T8819产 地：中国大陆
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TP1696LCGGRGD acetate(1260223-44-6 free base)CGGRGD acetate(1260223446 free base),CGGRGD acetate(1260223 44
CGGRGD acetate is a RGD derivative with cysteine as the n-terminal. CGGRGD was synthesized by solid phase peptide synthesis technology, and amino2-cyanobenzothiazole (2-cyanobenzothiazole) (2-cyanobenzothiazole (CBT) was added on the surface of PCL fiber for ammoniation.
价 格：￥电议型 号：TP1696L产 地：中国大陆
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T6816DASA-58DASA58,inhibit,Inhibitor,DASA 58,DASA-58,glycolysis,TXNIP,cancer metabolism,Pyruvate Kinase,p
DASA-58 is a specific and potent Pyruvate kinase M2 (PKM2) activator.
价 格：￥电议型 号：T6816产 地：中国大陆
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T16040Mepazinediffuse,B cell,inhibit,large,mucosa associated lymphoid tissue lymphoma translocation gene 1
Mepazine is a potent and selective inhibitor of MALT1. Mepazine inhibits GSTMALT1 full length and GSTMALT1 325-760 with IC50s of 0.83 μM and 0.42 μM. Mepazine enhances apoptosis and affects the cell viability.
价 格：￥电议型 号：T16040产 地：中国大陆
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T60160STX-0119STX0119
STX-0119 is a selective, orally active STAT3 dimerization inhibitor. STX-0119 inhibits STAT3 transcription with an IC50 of 74 μM.
价 格：￥电议型 号：T60160产 地：中国大陆
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TP1305LLEP(116-130)(mouse)TFA(258276-95-8 free base)LEP(116 130)(mouse)TFA(258276 95 8 free base),LEP(11613
LEP(116-130)(mouse) is a synthetic leptin peptide fragment.
价 格：￥电议型 号：TP1305L产 地：中国大陆
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T8929BC1618Ubiquitin activating enzyme,Mitochondrial Autophagy,fission,Mitophagy,inhibit,Inhibitor,mTORC,
BC1618 is an orally active Fbxo48 inhibitory compound, stimulates Ampk-dependent signaling. It promotes mitochondrial fission, facilitates autophagy and improves hepatic insulin sensitivity.
价 格：￥电议型 号：T8929产 地：中国大陆
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TN1661Ganoderic acid C2Ganoderic acid C-2,Inhibitor,Ganoderic acid C 2,Ganoderic acid C2,inhibit
Ganoderic acid C2 has anti-inflammatory,and anti-tumor-promoting activities. Ganoderic acid C2 can inhibit histamine release, it also has inhibitory effects on the induction of Epstein-Barr Virus early antigen. Ganoderic acid C2 exhibits high inhibitory activity against the rat lens aldose reductase (IC50 = 3.8 ?M).
价 格：￥电议型 号：TN1661产 地：中国大陆
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T16771RO-5963RO5963,RO 5963
RO-5963 is a dual inhibitor of p53-MDM2 and p53-MDMX (IC50s: ~17 nM and ~24 nM, respectively).
价 格：￥电议型 号：T16771产 地：中国大陆
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TP1627LPrepro VIP (111-122), human acetatePrepro VIP (111122), human acetate,Prepro VIP (111 122), human ac
Prepro VIP (111-122), human acetate is a prepro-vasoactive intestinal polypeptide (VIP)–derived peptide, corresponding to residues 111-122.
价 格：￥电议型 号：TP1627L产 地：中国大陆
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T61189E7016
E7016 is an orally available PARP inhibitor. E7016 inhibits of DNA repair. E7016 can enhance tumor cell radiosensitivity in vitro and in vivo.
价 格：￥电议型 号：T61189产 地：中国大陆
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TN1610Epimagnolin Afurfuran,Epimagnolin A,inhibit,Inhibitor,Parasite,lignan,antiplasmodial
Epimagnolin A is a lignan obtained from the flower buds of Magnolia fargesii, which is traditionally used in Asian medicine for treating headache and nasal congestion.
价 格：￥电议型 号：TN1610产 地：中国大陆
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T36851LPeptide5 acetatePeptide5 acetate,Peptide-5 aceate (916977-43-0 Free base)
Peptide5 acetate reduces animal swelling, astrogliosis, and neuronal cell death after spinal cord injury. Peptide5 acetate significantly reduces the degree of spinal cord injury (SCI) in a rodent ex vivo model.
价 格：￥电议型 号：T36851L产 地：中国大陆
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TP1236Etelcalcetide hydrochlorideEtelcalcetide hydrochloride,KAI-4169,AMG416,KAI4169,CaSR,KAI 4169,AMG 416
Etelcalcetide hydrochloride is a synthetic peptide as an allosteric modulator of the calcium (Ca)-sensing receptor (CaSR). Etelcalcetide hydrochloride is effective in lowering parathyroid hormone (PTH) concentrations in patients receiving dialysis with secondary hyperparathyroidism receiving hemodialysis.
价 格：￥电议型 号：TP1236产 地：中国大陆
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TN1658Ganoderenic acid DApoptosis,Inhibitor,inhibit,Ganoderenic acid D
Ganoderenic acid D is a natural product isolated from the effective compounds of Ganoderma lucidum extract (GLE). Ganoderenic acid D induces cell cycle arrest and apoptosis and inhibits the proliferation of cancer cells.
价 格：￥电议型 号：TN1658产 地：中国大陆
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T12164N6-(4-Hydroxybenzyl)adenosineinhibit,P2Y Receptor,Inhibitor
N6-(4-Hydroxybenzyl)adenosine is a platelet aggregation inhibitor.
价 格：￥电议型 号：T12164产 地：中国大陆
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TQ0219MK-8033bladder cancer,breast cancer,MK8033,EBC-1,H1993,MK 8033,MK-8033,anti-tumor,Inhibitor,GTL-16,r
MK-8033 is a new and selective dual ATP competitive c-Met/Ron inhibitor (IC50: 1 nM Wt c-Met).
价 格：￥电议型 号：TQ0219产 地：中国大陆
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T6S1652BenzoylpaeoniflorinApoptosis,inhibit,Inhibitor,Benzoylpaeoniflorin
1. Benzoylpaeoniflorin is active against cyclooxygenase-1 and cyclooxygenase-2 enzymes.
价 格：￥电议型 号：T6S1652产 地：中国大陆
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T6938PF-4989216Apoptosis,inhibit,Phosphoinositide 3-kinase,PF4989216,PF-4989216,PI3K,Inhibitor
PF-4989216 is a potent and selective PI3K inhibitor with IC50 of 2 nM, 142 nM, 65 nM, 1 nM, and 110 nM for p110α, p110β, p110γ, p110δ, and VPS34, respectively.
价 格：￥电议型 号：T6938产 地：中国大陆
