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T94943-(IMIDAZOL-4-YL)PROPIONIC ACID3 (IMIDAZOL 4 YL)PROPIONIC ACID,3(IMIDAZOL4YL)PROPIONIC ACID
3-(IMIDAZOL-4-YL)PROPIONIC ACID is a product of histidine metabolism and may involve oxidation or transamination. 3-(IMIDAZOL-4-YL)PROPIONIC ACID is potent inhibitors of G. candidum histidinol dehydrogenase, showing IC50 values as low as 3.17 microM.
价 格：￥电议型 号：T9494产 地：中国大陆
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T10792LCHK1-IN-4 hydrochloride
CHK1-IN-4 hydrochloride is a potent inhibitor of checkpoint kinase 1 (chk1). CHK1-IN-4 hydrochloride potently inhibits chk1 phosphorylation in the tumor cells. CHK1-IN-4 hydrochloride has anti-tumor activity.
价 格：￥电议型 号：T10792L产 地：中国大陆
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T7197Fadrozole(Rac)-FAD286,inhibit,Fadrozole,CGS 16949A,Inhibitor,Aromatase
Fadrozole is a nonsteroidal aromatase inhibitor with potential antineoplastic activity(IC50 : 6.4 nM)
价 格：￥电议型 号：T7197产 地：中国大陆
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TP1031TetracosactideTetracosactide,adrenal gland,adrenocorticotrophic hormone,Inhibitor,corticosteroids,in
Tetracosactide (INN) is a synthetic peptide that is identical to the 24-amino acid segment (sequence: SYSMEHFRWGKPVGKKRRPVKVYP) at the N-terminal of adrenocorticotropic hormone.
价 格：￥电议型 号：TP1031产 地：中国大陆
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T35336Furosemide sodium
Furosemide sodium is a potent and orally active inhibitor of Na+/K+/2Cl- (NKCC) cotransporter, NKCC1 and NKCC2. Furosemide sodium is also a GABAA receptors antagonist and displays 100-fold selectivity for α6-containing receptors than α1-containing receptors. Furosemide sodium acts as a loop diuretic and used for the study of congestive heart failure, hypertension and edema.
价 格：￥电议型 号：T35336产 地：中国大陆
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T86486-AZATHYMINE6-Azathymine,6AZATHYMINE,antibacterial,nucleobase,Inhibitor,Influenza Virus,DNA,6-nitrog
6-azathymine is a potent inhibitors of D-3-aminoisobutyrate-pyruvate aminotransferase. 6-Azauracil acted as a competitive inhibitor with respect to beta-alanine, and was an uncompetitive inhibitor with respect to pyruvic acid with a Ki of approximately 8.9 mM.
价 格：￥电议型 号：T8648产 地：中国大陆
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T6836FIIN-2inhibit,FGFR,FIIN2,FIIN 2,Fibroblast growth factor receptor,Inhibitor,FIIN-2
FIIN-2, an irreversible, pan-FGFR inhibitor, inhibits FGFR1/2/3/4 with IC50 of 3.09 nM, 4.3 nM, 27 nM and 45.3 nM, respectively.
价 格：￥电议型 号：T6836产 地：中国大陆
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T12262L1NPS ALX Compound 4a hydrochloride(1:1)NPSALXCompound4ahydrochloride(299433106Freebase)
NPS ALX Compound 4a hydrochloride(1:1) is a potent and selective 5-hydroxytryptamine6 (5-HT6) receptor antagonist, with an IC50 of 7.2 nM and a Ki of 0.2 nM.
价 格：￥电议型 号：T12262L1产 地：中国大陆
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T9109SSAA09E2domain,SARS-CoV,receptor,SSAA09E2,inhibit,SARS coronavirus,Inhibitor,spike,ACE2,binding,SSAA
SSAA09E2 is a new SARS-CoV replication inhibitor, acting by blocking early interactions of SARS-S with the receptor for SARS-CoV, Angiotensin Converting Enzyme-2 (ACE2).
价 格：￥电议型 号：T9109产 地：中国大陆
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T9541CTBHATs,Inhibitor,neurons,CTB,Apoptosis,MCF-7 cell,cancer,potent,HAT,autophagic flux,inhibit,Histone
CTB (Cholera Toxin B subunit) is an activator of p300 histone acetyltransferase and induces apoptosis in MCF-7 cells.
价 格：￥电议型 号：T9541产 地：中国大陆
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T8231Adrenocorticotropic Hormone (ACTH) (1-39), humaninhibit,Inhibitor,Adrenocorticotropic Hormone (ACTH)
Adrenocorticotropic Hormone (ACTH) (1-39), human is an agonist of melanocortin receptor.
价 格：￥电议型 号：T8231产 地：中国大陆
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T6561Laquinimodinhibit,multiple sclerosis,relapsing remitting,carboxamide,Nuclear factor-kappaB,Apoptosis
Laquinimod is an effective immunomodulator, which is currently under development in phase III trials for the treatment of multiple sclerosis as an oral therapy.
价 格：￥电议型 号：T6561产 地：中国大陆
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T75456-Aminonicotinamidereactions,DNA-crosslinking,Inhibitor,6Aminonicotinamide,ATP,redox,6-Aminonicotina
6-Aminonicotinamide (6-AN) is a well-established inhibitor of the NADP+-dependent enzyme.
价 格：￥电议型 号：T7545产 地：中国大陆
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T20094AdrenochromeAdrenochrome
Adrenochrome is a chemical compound produced by the oxidation of adrenaline.
价 格：￥电议型 号：T20094产 地：中国大陆
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T4065Fluorescein SodiumFluorescein Sodium,Fluorescein,inhibit,fluorescent probes,Inhibitor,tumor,Uranine,
Fluorescein Sodium is a phthalic indicator dye. It is used therapeutically as a diagnostic aid in corneal injuries and corneal trauma.
价 格：￥电议型 号：T4065产 地：中国大陆
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T6541Ibutilide FumarateIbutilide,antiarrhythmia agent,Potassium Channel,inhibit,Inhibitor,long QT syndrom
Ibutilide Fumarate is the fumarate salt form of ibutilide, a class III antiarrhythmic agent. Ibutilide exerts its effect by activating a slow, inward, predominately sodium current rather than by blocking outward potassium currents. This results in prolongation of atrial and ventricular action potential duration and refractory periods. Ibutilide slightly decreases the sinus rate and atrioventricular (AV) conduction and produces a dose-related prolongation of the QT interval.
价 格：￥电议型 号：T6541产 地：中国大陆
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T9623RORγt inverse agonist 13RORγt inverse agonist 13,ROR,RORγt inverse agonist-13,RAR-related orphan rec
RORγt inverse agonist 13 (Compound 3i) is a potent, orally active and selective RORγt inverse agonist (IC50=63.8 nM), with improved drug-like properties[1].
价 格：￥电议型 号：T9623产 地：中国大陆
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T8230PNU112455A hydrochlorideanticooperative,Cyclin dependent kinase,PNU112455A hydrochloride,Alzheimer’s
PNU 112455A is an ATP site competetive inhibitor of CDK2 and CDK5,binds to the ATP site of CDK2 and CDK5 with Kms of 3.6 and 3.2 μM, respectively.
价 格：￥电议型 号：T8230产 地：中国大陆
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T1636LParoxetine hydrochloride hemihydrate
Paroxetine hydrochloride hemihydrate is an effective and selective serotonin reuptake inhibitor (SSRI).
价 格：￥电议型 号：T1636L产 地：中国大陆
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T9011VU0155094VU0155094,Inhibitor,Metabotropic glutamate receptors,ML397,inhibit,mGluR
ML397 is a positive allosteric modulator with differential activity at the various group III mGluRs.
价 格：￥电议型 号：T9011产 地：中国大陆
