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T15627(S)-JQ-35化合物 T15627TEN-010
(S)-JQ-35 (TEN-010) is an inhibitor of the Bromodomain and Extra-Terminal (BET) family bromodomain-containing proteins. It has a potential antineoplastic activity.
价 格:¥电议型 号:T15627产 地:中国大陆
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T15626JPM-OEt;化合物 T15626JPM-OEt
JPM-OEt is a broad spectrum cysteine cathepsin inhibitor with antitumor activity. JPM-OEt binds covalently in the active site and irreversibly inhibits the cysteine cathepsin family.
价 格:¥电议型 号:T15626产 地:中国大陆
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T15625JNJ4796;化合物 T15625JNJ4796
JNJ4796 is an oral active fusion inhibitor of the influenza virus, by inhibiting hemagglutinin (HA)-mediated fusion to neutralizing the influenza A group 1 virus. JNJ4796 mimics the functionality of the broadly neutralizing antibodies (bnAbs).
价 格:¥电议型 号:T15625产 地:中国大陆
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T15624JNJ-64619178;化合物JNJ-64619178JNJ-64619178
JNJ-64619178 is a selective, orally active, and pseudo-irreversible inhibitor of protein arginine methyltransferase 5 (IC50: 0.14 nM). It has effective activity In lung cancer.
价 格:¥电议型 号:T15624产 地:中国大陆
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T15623JNJ-61432059;化合物JNJ-61432059JNJ-61432059
JNJ-61432059 is an oral active and selective negative modulator of TARP γ?8 Selective AMPAR(pIC50: 9.7).
价 格:¥电议型 号:T15623产 地:中国大陆
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T15622JNJ-54175446;化合物 JNJ-54175446JNJ-5446;JNJ-5446
JNJ-54175446 (JNJ-5446) is a CNS-permeable and selective P2X7 receptor antagonist that attenuates the release of IL-1β/IL-18 from microglia, and may be used in the study of depression.
价 格:¥电议型 号:T15622产 地:中国大陆
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T15621Rilematovir;化合物RilematovirJNJ-53718678|||JNJ-678;JNJ-53718678|||JNJ-678
Rilematovir (JNJ-678) is an inhibitor of fusion protein with antiviral activity and low cytotoxicity. Rilematovir can be used in studies about respiratory syncytial virus treatment.
价 格:¥电议型 号:T15621产 地:中国大陆
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T1562Rebamipide;瑞巴派特Proamipide|||OPC12759;Proamipide|||OPC12759|||瑞巴派特
Rebamipide (OPC12759) is a quinolinone derivative with anti-ulcer and anti-inflammatory activities. Rebamipide induces cyclooxygenase 2 (COX2) synthesis which results in an increase in endogenous prostaglandin synthesis in the gastric mucosa. This agent also inhibits H. pylori-induced production of tumor necrosis factor (TNF) alpha and subsequent inflammation of the gastric mucosa. In addition, rebamipide scavenges oxygen-derived free radicals that potentially cause mucosal injury, and stimulate
价 格:¥电议型 号:T1562产 地:中国大陆
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T15619JNJ-46778212;化合物 JNJ-46778212VU 0409551;VU 0409551
JNJ-46778212 (VU 0409551) is a selective and potent mGlu5 allosteric modulator (EC50: 260 nM) for the study of neurodissection.
价 格:¥电议型 号:T15619产 地:中国大陆
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T15618JNJ-46281222;化合物 T15618JNJ-46281222
JNJ-46281222 is an metabotropic glutamate (mGlu) 2-selective, highly potent PAM (positive allosteric modulator). It has nanomolar affinity (Kd = 1.7 nM) and a high modulatory potency (pEC50 = 7.71).
价 格:¥电议型 号:T15618产 地:中国大陆
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T15617JNJ-38877618;化合物JNJ-38877618OMO-1;OMO-1
JNJ-38877618 (OMO-1) is an effective and highly selective inhibitor of Met kinase (IC50s: 2 and 3 nM for wild type and mutant Met, respectively).
价 格:¥电议型 号:T15617产 地:中国大陆
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T15616JNJ-10198409;化合物JNJ-?10198409JNJ-?10198409;3-氟-N-(6,7-二甲氧基-2,4-二氢茚并[1,2-C〕吡唑-3-基苯基胺|||JNJ-?10198409
JNJ- 10198409 is a relatively selective and ATP competitive PDGF-RTK inhibitor (IC50=2 nM). JNJ-10198409 has good activity against PDGFR-β kinase (IC50=4.2 nM) and PDGFR-α kinase (IC50=45 nM). It is a dual-mechanism, antiangiogenic, and tumor cell antiproliferative agent.
价 格:¥电议型 号:T15616产 地:中国大陆
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T15615JND3229;化合物JND3229JND3229
JND3229 is a reversible EGFRC797S inhibitor with IC50 values of 5.8, 6.8 and 30.5 nM for EGFRL858R/T790M/C797S, EGFRWT and EGFRL858R/T790M, respectively. JND3229 has good anti-proliferative activity and can effectively inhibit tumour growth in vivo. JND3229 can be used in cancer research, especially in non-small cell carcinoma.
价 格:¥电议型 号:T15615产 地:中国大陆
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T15614JJKK 048;化合物JJKK 048JJKK 048
JJKK 048 is a potent and selective MAGL inhibitor.
价 格:¥电议型 号:T15614产 地:中国大陆
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T15613JHU-083;化合物 T15613JHU-083
JHU-083 is a selective glutaminase antagonist. JHU-083 blocks glutaminase activity in brain CD11b+ cells. JHU-083 also experimental cerebral malaria (ECM) resulting in a net decrease of glutamate levels in the animals.
价 格:¥电议型 号:T15613产 地:中国大陆
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T15612JH-VIII-157-02;化合物JH-VIII-157-02JH-VIII-157-02
JH-VIII-157-02 is an inhibitor of ALK and inhibits echinoderm microtubule-associated protein-like 4-ALK (EML4-ALK) with IC50s of 2 nM for EML4-ALK G1202R, EML4-ALKwt, EML4-ALK C1156Y, EML4-ALK F1174L, and EML4-ALK F1174L.
价 格:¥电议型 号:T15612产 地:中国大陆
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T15611JH-RE-06;化合物JH-RE-06JH-RE-06
JH-RE-06 disrupts mutagenic translesion synthesis (TLS) by preventing the recruitment of mutagenic POLζ. JH-RE-06 is an effective REV1-REV7 interface inhibitor (IC50=0.78 μM; Kd=0.42 μM), which targets REV1 that interacts with the REV7 subunit of POLζ. JH-RE-06 also improves chemotherapy.
价 格:¥电议型 号:T15611产 地:中国大陆
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T15610JFD00244化合物 T15610JFD 00244|||JFD-00244|||JFD00244
JFD00244 is an inhibitor of sirtuin 2 (SIRT2). It has an anti-tumor effect.
价 格:¥电议型 号:T15610产 地:中国大陆
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T1561Clobetasol propionate;丙酸氯倍他索Dermovate|||Clobetasol 17-propionate|||CGP9555|||Temovate|||CCl 4725;Der
Clobetasol propionate (CGP9555) exerts its effect by binding to cytoplasmic glucocorticoid receptors and subsequently activates glucocorticoid receptor-mediated gene expression. This results in the synthesis of certain anti-inflammatory proteins while inhibiting the synthesis of certain inflammatory mediators. Clobetasol Propionate is the propionate salt form of clobetasol, a topical synthetic corticosteroid with anti-inflammatory, antipruritic, and vasoconstrictive properties. Specifically, clo
价 格:¥电议型 号:T1561产 地:中国大陆
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T15609JC-1;化合物JC-1CBIC2;CBIC2
JC-1 (CBIC2) is a fluorescent lipophilic carbocyanine dye. It has been used to measure mitochondrial membrane potential. JC 1 can be used in a probe for measuring mitochondrial membrane potential by flow cytometry.
价 格:¥电议型 号:T15609产 地:中国大陆