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T7086Tris(benzyltriazolylmethyl)aminechemical,tagging,Inhibitor,inhibit,proteins,Tris(benzyltriazolylmeth
TBTA is a tertiary amine with three 1, 2, 3-triazole groups. It complexes with, and stabilizes, copper(I) to accelerate azide-alkyne cycloadditions, as used in click chemistry.
价 格：￥电议型 号：T7086产 地：中国大陆
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T8751AZD8931 diFuMaric acidAZD8931 diFuMaric acid,AZD-8931 diFuMaric acid
AZD8931 is a reversible and ATP competitive inhibitor of EGFR, ErbB2 and ErbB3 (IC50 of 4 nM, 3 nM and 4 nM, respectively).
价 格：￥电议型 号：T8751产 地：中国大陆
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T7807Bendazaccataractogenic,Bendazac,antinecrotic,inhibit,choleretic,protein,inflammatory,antilipidaemic,
Bendazac is an anticataract drug. It may act by preventing protein denaturation.
价 格：￥电议型 号：T7807产 地：中国大陆
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T29522LN-[(1S)-5-tert-butyl-2,3-dihydro-1H-inden-1-yl]-N’-1H-indazol-4-ylurea(S)1(5(tertbutyl)2,3dihydro1Hi
N-[(1S)-5-tert-butyl-2,3-dihydro-1H-inden-1-yl]-N´-1H-indazol-4-ylurea is a potent TRPV1 antagonist, blocking activation of TRPV1 by capsaicin with the IC50 of 123 nM.
价 格：￥电议型 号：T29522L产 地：中国大陆
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T6633RanolazineNa+ channels,CVT-303,Ca2+ channels,inhibit,Sodium Channel,Ranolazine,Inhibitor,Calcium Cha
Ranolazine is a calcium uptake inhibitor via the sodium/calcium channel, used to treat chronic angina. It affects the sodium-dependent calcium channels during myocardial ischemia in rabbits by altering the intracellular sodium level.
价 格：￥电议型 号：T6633产 地：中国大陆
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TQ0128FurilazoleMON13900,Furilazole,Inhibitor,inhibit,MON-13900
Furilazole is a herbicide.
价 格：￥电议型 号：TQ0128产 地：中国大陆
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T10249Adoprazine
Adoprazine is a potential atypical antipsychotic bearing potent D2 receptor antagonist and 5-HT1A receptor agonist properties.
价 格：￥电议型 号：T10249产 地：中国大陆
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T8614[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]acetic acid[2(4Chlorophenyl)1,3thiazol4yl]acetic acid,[2 (4 Chl
[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]acetic acid is an anti-inflammatory thiazole
价 格：￥电议型 号：T8614产 地：中国大陆
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T6467Dexrazoxane hydrochlorideDexrazoxane,inhibit,ICRF 187,Inhibitor,NSC-169780,ADR 529,Dexrazoxane hydro
Dexrazoxane HCl is a cardio-protective drug.
价 格：￥电议型 号：T6467产 地：中国大陆
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T6992Sulfadiazine sodiumInhibitor,antimalarial,Sulfadiazine sodium,pig,Antibiotic,Sulfadiazine,veterinary
Sodium Sulfadiazine is a sodium salt form of sulfadiazine, an intermediate-acting bacteriostatic, synthetic sulfanilamide derivative.
价 格：￥电议型 号：T6992产 地：中国大陆
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T6401AzithromycinAntibiotic,CP-62993,inhibit,Azithromycin,Bacterial,CP62993,Autophagy,Inhibitor
Azithromycin is an antibiotic by inhibiting protein synthesis, used for the treatment of bacterial infections.
价 格：￥电议型 号：T6401产 地：中国大陆
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T8388VonoprazanTAK-438,TAK 438,GERD,TAK438,Bacterial,antisecretory,blocker,peptic,Proton Pump,secretion,i
Vonoprazan is an orally active potassium-competitive acid blocker.Vonoprazan can be used for the treatment of gastroduodenal ulcer and reflux esophagitis
价 格：￥电议型 号：T8388产 地：中国大陆
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T17576Biotin-PEG3-SS-azide
Biotin-PEG3-SS-azide is a cleavable ADC linker containing 3-unit PEG and can be used to synthesize antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T17576产 地：中国大陆
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T7116Sodium gualenateSodium gualenate,Inhibitor,inhibit,Guaiazulenesulfonate
Sodium gualenate (Guaiazulenesulfonate sodium), a hydrophilic derivative of guaiazulene (GA), is an unstable compound. It has anti-inflammatory and wound-healing effects.
价 格：￥电议型 号：T7116产 地：中国大陆
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T93342-Amino-6-(methylsulfonyl)benzothiazole2Amino6(methylsulfonyl)benzothiazole,2 Amino 6 (methylsulfony
2-Amino-6-(methylsulfonyl)benzothiazole is identified as a new development of improved pteridine reductase-1 (PTR1) inhibitors and anti-trypanosomatidic agents[1].
价 格：￥电议型 号：T9334产 地：中国大陆
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T91522-(2-Hydroxyphenyl)-1H-benzimidazole2 (2 Hydroxyphenyl) 1H benzimidazole,2(2Hydroxyphenyl)1Hbenzimid
2-(2-Hydroxyphenyl)-1H-benzimidazole is a chemical compound.
价 格：￥电议型 号：T9152产 地：中国大陆
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TN1786IsomerazinInhibitor,Isomerazin,Cholinesterase (ChE),inhibit
Isomeranzin has anti-inflammatory activity, it suppresses inflammation by inhibiting M1 macrophage polarization through the p65, NF-κB and ERK pathway.
价 格：￥电议型 号：TN1786产 地：中国大陆
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T30260AZD-5672
AZD-5672 is an antagonist of CCR5 with an IC50 of 0.32 nM. AZD-5672 inhibits hERG cardiac ion channel binding and P-gp-mediated digoxin transport with IC50s of 7.3 μM and 32 μM. AZD-5672 can be used in studies about rheumatoid arthritis.
价 格：￥电议型 号：T30260产 地：中国大陆
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T6399AZD1981Prostaglandin Receptor,AZD 1981,AZD1981,Inhibitor,AZD-1981,inhibit
AZD1981 is an effective and specific CRTh2 (DP2) receptor antagonist (IC50: 4 nM), showing >1000-fold selectivity over more than 340 other enzymes and receptors, including DP1. AZD1981 has been used in trials studying the treatment and basic science of Asthma, Postmenopausal, Pharmakokinetic, Asthma Patients, and Drug Interaction, among others.
价 格：￥电议型 号：T6399产 地：中国大陆
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T28475Pyrazoloacridinetumor,Inhibitor,leukemia,inhibit,solid,Apoptosis,NSC366140,carcinoma,Pyrazoloacridin
Pyrazoloacridine is a nucleic acid binding agent that inhibits the activity of topo I and II with an IC50 of 1.25 μM in K562 cells. Pyrazoloacridine shows anti-cancer activity.
价 格：￥电议型 号：T28475产 地：中国大陆
