其他產(chǎn)品及廠家

Caffeic Acid Phenethyl EsterCaffeic Acid Phenethyl Ester,CAPE,Phenylethyl Caffeate
caffeic acid phenethyl ester (cape) inhibits the activation of nuclear transcription factor nf-kappa b and may suppress p70s6k and akt-driven signaling pathways, with antineoplastic, cytoprotective and immunomodulating activities. cape is the phenethyl al
更新時(shí)間:2025-06-07
BV6BV6
bv6 is an antagonist of c-iap1 and xiap, members of the inhibitors of apoptosis (iap) family.
更新時(shí)間:2025-06-07
ButeinButein,2’,3,4,4’-tetrahydroxy Chalcone,
butein, a plant polyphenol, is isolated from rhus verniciflua. it can inhibit the activation of protein tyrosine kinase, nf-κb and stat3, and also can inhibit egfr.
更新時(shí)間:2025-06-07
Buclizine HClBuclizine HCl,UCB-4445,Longifene
buclizine hcl is the hydrochloride salt form of buclizine, a piperazine histamine h1 receptor antagonist with primarily antiemetic and antivertigo activities. buclizine binds to and blocks the histamine h1 receptor, thereby preventing the symptoms that ar
更新時(shí)間:2025-06-07
BTZ043 RacemateBTZ043 Racemate,Benzothiazinone 10526038,BTZ10526038
btz043 racemate is a decaprenylphosphoryl-β-d-ribose 2´-epimerase (dpre1) inhibitor, used as a new antimycobacterial agent.
更新時(shí)間:2025-06-07
Bromfenac SodiumBromfenac Sodium,AHR 10282R,Bronuck
bromfenac sodium is a nonsteroidal anti-inflammatory drug (nsaid), which has anti-inflammatory activity and may block prostaglandin synthesis by inhibiting cyclooxygenase 1 and 2.
更新時(shí)間:2025-06-07
BRL-15572BRL-15572,BRL15572,BRL 15572
brl-15572 is a 5-ht1d receptor antagonist with pki of 7.9, also shows a considerable affinity at 5-ht1a and 5-ht2b receptors, exhibiting 60-fold selectivity over 5-ht1b receptor.
更新時(shí)間:2025-06-07
Brimonidine TartrateBrimonidine Tartrate,AGN190342 (tartrate),UK 14304 (tartrate)
brimonidine tartrate is a quinoxaline derivative and adrenergic α-2 receptor agonist (ec50: 0.45 nm) that is used to manage intraocular pressure associated with open-angle glaucoma or ocular hypertension.
更新時(shí)間:2025-06-07
BRD73954BRD73954
brd73954, an effective and specific hdac inhibitor, which is with ic50 of 36 nm and 120 nm for hdac6 and hdac8, respectively.
更新時(shí)間:2025-06-07
BMS-707035BMS-707035,BMS707035,BMS 707035
bms-707035 is a specific hiv-i integrase (in) inhibitor with ic50 of 15 nm. phase 2.
更新時(shí)間:2025-06-07
BisacodylBisacodyl,Dulcolax,Brocalax
bisacodyl is a diphenylmethane stimulant laxative used for the treatment of constipation and for bowel evacuation.
更新時(shí)間:2025-06-07
CVT-12012CVT-12012
cvt-12012 is an orally bioavailable inhibitor of stearoyl-coa desaturase (scd; ic50 = 6.1 nm in hepg2 cells).
更新時(shí)間:2025-06-07
BiapenemBiapenem,L 627,LJC 10627
biapenem is a 1-beta-methylcarbapenem antibiotic with a wide range of antibacterial activity. biapenem has similar antibacterial activity to that of imipenem, but is more stable against human renal dehydropeptidase-i and with less neurotoxicity.
更新時(shí)間:2025-06-07
BexaroteneBexarotene,LGD1069,Targretin
bexarotene is a retinoid analogue that is used to treat the skin manifestations of cutaneous t cell lymphoma (ctcl).
更新時(shí)間:2025-06-07
SAR348830SAR348830
na
更新時(shí)間:2025-06-07
Beta-LapachoneBeta-Lapachone,NSC-26326,ARQ-501
beta-lapachone is a specific dna topoisomerase i inhibitor, and no inhibitory activities against dna topoisomerase ii or ligase.
更新時(shí)間:2025-06-07
Besifloxacin HClBesifloxacin HCl,Besifloxacin Hydrochloride,Besivance hydrochloride
besifloxacin hcl is a fourth-generation fluoroquinolone antibiotic.
更新時(shí)間:2025-06-07
Bepotastine BesilateBepotastine Besilate,Bepotastine Beslilate,TAU 284
bepotastine is a non-sedating and selective h1 receptor antagonist (pic50: 5.7).
更新時(shí)間:2025-06-07
SiponimodSiponimod,BAF-312,
baf312 (siponimod), a next-generation s1p receptor modulator, is specific for s1p1 and s1p5 receptors with ec50 of 0.39 nm and 0.98 nm,respectively. the specificity of baf312 for s1p1 and s1p5 receptors exhibits >1000-fold over s1p2, s1p3 and s1p4 recepto
更新時(shí)間:2025-06-07
AzomycinAzomycin,Amicin,2-Nitroimidazole
azomycin is an antimicrobial antibiotic produced by a strain of nocardia mesenterica.
更新時(shí)間:2025-06-07
AzithromycinAzithromycin,CP 62993,XZ-450
azithromycin is an antibiotic by inhibiting protein synthesis, used for the treatment of bacterial infections.
更新時(shí)間:2025-06-07
AZD3514AZD3514
azd3514 is a potent and oral androgen receptor downregulator with ki of 2.2 μm and has ability of reducing ar protein expression.phase 1.
更新時(shí)間:2025-06-07
AZD1981AZD1981
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 as
更新時(shí)間:2025-06-07
AzaperoneAzaperone,R-1929,NSC 170976
azaperone is a pyridinylpiperazine and butyrophenone neuroleptic drug with sedative and antiemetic effects, which is used mainly as a tranquilizer in veterinary medicine.
更新時(shí)間:2025-06-07
Atracurium besylateAtracurium besylate,BW-33A,51W89
atracurium besylate is a non-depolarizing neuromuscular blocking agent with short duration of action. its lack of significant cardiovascular effects and its lack of dependence on good kidney function for elimination provide clinical advantage over alterna
更新時(shí)間:2025-06-07
AT101 acetateAT101 acetate,(-)-Gossypol acetic acid,(R)-Gossypol acetic acid
at101, the r-(-) enantiomer of gossypol acetic acid, binds with bcl-2, bcl-xl and mcl-1 with ki of 0.32 μm, 0.48 μm and 0.18 μm; does not inhibit bir3 domain and bid. phase 2.
更新時(shí)間:2025-06-07
Astragaloside AAstragaloside A,Astragalin A,Astramembrannin I
astragaloside a (astragaloside iv) is the primary pure saponin isolated from astragalus membranaceus, which has been widely used for the therapy of cardiovascular diseases.
更新時(shí)間:2025-06-07
AS-604850AS-604850,AS604850,AS 604850
as-604850 is a specific and atp-competitive pi3kγ inhibitor (ic50: 250 nm), 18-fold more selective for pi3kγ than pi3kα, and over 80-fold selectivity for pi3kγ than pi3kδ/β.
更新時(shí)間:2025-06-07
ARQ 621ARQ 621
arq 621 is an allosteric, and selective eg5 mitotic motor protein inhibitor. phase 1.
更新時(shí)間:2025-06-07
AR-42AR-42,AR42,AR 42
ar-42 is an hdac inhibitor (ic50: 30 nm).
更新時(shí)間:2025-06-07
AcetovanilloneAcetovanillone,Apocynin,Acetoguaiacone
apocynin is a specific nadph-oxidase inhibitor (ic50: 10 μm).
更新時(shí)間:2025-06-07
Anagrelide HClAnagrelide HCl,Anagrelide hydrochloride,BL4162A
anagrelide hydrochloride(bl4162a) is a drug used for the treatment of essential thrombocytosis.
更新時(shí)間:2025-06-07
Anacardic AcidAnacardic Acid,Hydroginkgolic acid,6-pentadecylsalicylic Acid
anacardic acid is an effective inhibitor of p300 and p300/cbp-associated factor histone acetyltranferases. it also has antimicrobial activity, antibacterial activity, and inhibits prostaglandin synthase, lipoxygenase, and tyrosinase.
更新時(shí)間:2025-06-07
AmprenavirAmprenavir,VX-478,141W94
amprenavir is a synthetic derivative of hydroxyethylamine sulfonamide that selectively binds to and inhibits human immunodeficiency virus (hiv) protease.
更新時(shí)間:2025-06-07
AmpiroxicamAmpiroxicam,CP 65703,Flucam
ampiroxicam is a nonselective cyclooxygenase inhibitor uesd as anti-inflammatory drug.
更新時(shí)間:2025-06-07
Ampicillin sodiumAmpicillin sodium,D-(-)-α-Aminobenzylpenicillin sodium salt,Domicillin
ampicillin sodium is the sodium salt form of ampicillin, a broad-spectrum semisynthetic derivative of aminopenicillin. ampicillin sodium inhibits bacterial cell wall synthesis by binding to penicillin binding proteins, thereby inhibiting peptidoglycan syn
更新時(shí)間:2025-06-07
Amoxicillin SodiumAmoxicillin Sodium,Clavulanate,
amoxicillin sodium is a moderate- spectrum, bacteriolytic, β-lactam antibiotic.
更新時(shí)間:2025-06-07
Ammonium GlycyrrhizinateAmmonium Glycyrrhizinate,AMGZ,Glycyram
ammonium glycyrrhizinate inhibits the cytopathology and growth of several unrelated dna/rna viruses.
更新時(shí)間:2025-06-07
Amikacin disulfateAmikacin disulfate,Amikacin sulfate,BAY-416651 sulfate
amikacin sulfate(bay416651 sulfate) is a semi-synthetic aminoglycoside antibiotic derived from kanamycin a.
更新時(shí)間:2025-06-07
Amifostine trihydrateAmifostine trihydrate,Amifostine,Ethyol trihydrate
amifostine is the first approved radioprotective drug, used to decrease the risk of kidney problems caused by treatment with cisplatin.
更新時(shí)間:2025-06-07
AMG-900AMG-900,AMG900,AMG 900
amg 900 is a potent and highly selective pan-aurora kinases inhibitor for aurora a/b/c with ic50 of 5 nm/4 nm /1 nm. it is >10-fold selective for aurora kinases than p38α, tyk2, jnk2, met and tie2. phase 1.
更新時(shí)間:2025-06-07
Enalaprilat DihydrateEnalaprilat Dihydrate,MK-422,MK-422 Dihydrate
enalaprilat（ic50=1.94 nm） is a potent angiotensin-converting enzyme (ace) inhibitor.
更新時(shí)間:2025-06-07
AG-14361AG-14361,AG14361,AG 14361
ag14361 is an effective inhibitor of parp1 (ki<5 nm).
更新時(shí)間:2025-06-07
RepSoxRepSox,SJN 2511,E-616452
repsox is a potent and selective of the tgfβr-1/alk5 inhibitor.
更新時(shí)間:2025-06-07
AmonafideAmonafide,AS1413,NSC308847,AS1413
amonafide(as1413) produces protein-associated dna-strand breaks through a topoisomerase ii-mediated reaction, but does not produce topoisomerase i-mediated dna cleavage.
更新時(shí)間:2025-06-07
Tie2 kinase inhibitorTie2 kinase inhibitor
tie2 kinase inhibitor， an optimized compound of sb-203580, is selective to tie2 with ic50 of 0.25 μm, which is 200-fold more effective than p38.
更新時(shí)間:2025-06-07
PevonedistatPevonedistat,MLN4924,
mln4924 is an effective and specific small molecule nedd8-activating enzyme (nae) inhibitor (ic50: 4.7 nm).
更新時(shí)間:2025-06-07
AST-1306 TsOHAST-1306 TsOH,Allitinib tosylate,AST-1306 (TsOH)
ast-1306 is a novel irreversible inhibitor of egfr and erbb2 with ic50 of 0.5 nm and 3 nm, respectively.
更新時(shí)間:2025-06-07
PI3Kδ-IN-2PI3Kδ-IN-2
pi3kδ-in-2 is a potent and selective inhibitor of pi3kδ
更新時(shí)間:2025-06-07
INO-1001INO-1001,INO1001,INO 1001
ino-1001 is an effective inhibitor of parp (ic50<50 nm in cho cells) and a mediator of oxidant-induced myocyte dysfunction during reperfusion.
更新時(shí)間:2025-06-07

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