其他產(chǎn)品及廠家

Lacidipine拉西地平；SN-305；GR-43659X；GX-1048
lacidipine is a lipophilic dihydropyridine calcium antagonist with an intrinsically slow onset of activity. due to its long duration of action, lacidipine does not lead to reflex tachycardia. it displays specificity in the vascular smooth muscle, where it
更新時間:2025-07-07
Azidamfenicol
azidamfenicol inhibits ribosomal peptidyltransferase (ki=22 μm)[1]. azidamfenicol is a broad-spectrum chloramphenicol-like antibiotic.
更新時間:2025-07-07
Ethacridine lactate monohydrate乳酸依沙吖啶一水物；利凡諾
ethacridine lactate hydrate is a topically applied anti-infective agent.
更新時間:2025-07-07
Capreomycin sulfate硫酸卷曲霉素；Capastat sulfate
capreomycin sulfate, a cyclic peptide antibiotic, binds to the 70s ribosomal unit leading to inhibition of protein synthesis.
更新時間:2025-07-07
Azido-PEG10-alcohol疊氮-十聚乙二醇
azido-peg10-alcohol is a peg-based protac linker that can be used in the synthesis of protacs[1].
更新時間:2025-07-07
Pizotifen苯噻啶；Pizotyline；BC-105
pizotifen is a strong serotonin and tryptamine antagonist, with weak anticholinergic, anti-histaminic and anti-kinin effects. it also possesses sedative and appetite-stimulating properties. pizotifen hydrochloride is an active ingredient in sandomigran, w
更新時間:2025-07-07
Memantine hydrochloride3,5-二甲基金剛胺鹽酸鹽；鹽酸美金剛；Memantine HCl；Namenda；D-145 (hydrochloride)
memantine hydrochloride is an amantadine derivative that has some dopaminergic effects. memantine hydrochloride has been proposed as an antiparkinson agent.
更新時間:2025-07-07
Lomefloxacin洛美沙星；SC47111A
lomefloxacin is a synthetic broad-spectrum fluoroquinolone with antibacterial activity.
更新時間:2025-07-07
Agomelatine阿戈美拉汀；S-20098；Thymanax；Valdoxan
agomelatine is structurally closely related to melatonin. agomelatine is a potent agonist at melatonin receptors and an antagonist at serotonin-2c (5-ht2c) receptors, tested in an animal model of depression.
更新時間:2025-07-07
Bambuterol hydrochloride鹽酸班部特羅；鹽酸班布特羅；(±)-Bambuterol hydrochloride；KWD-2183 hydrochloride；Bambuterol
bambuterol, a long-acting beta-adrenoceptor agonist, is utilized for the treating of asthma.
更新時間:2025-07-07
Fenclonine芬克洛寧；CP-10188；PCPA；4-Chloro-DL-phenylalanine；Fenchlonine；DL-4-Chlorophenylalanine
fenclonine is a selective and irreversible inhibitor of tryptophan hydroxylase, a rate-limiting enzyme in the biosynthesis of serotonin (5-hydroxytryptamine). fenclonine acts pharmacologically to deplete endogenous levels of serotonin.
更新時間:2025-07-07
Dasatinib達(dá)沙替尼；BMS-354825
dasatinib is a potent inhibitor of the bcr-abl and src family (ic50s: 0.6, 0.8, 79 and 37 nm for abl, src, c-kit, and c-kitd816v, respectively).
更新時間:2025-07-07
Azvudine4-氨基-1-(4-C-疊氮基-2-脫氧-2-氟-BETA-D-呋喃阿拉伯糖基)-2(1H)-嘧啶酮；RO-0622；FNC
azvudine is a potent nucleoside reverse transcriptase inhibitor (nrti), with antiviral activity on hiv, hbv and hcv. azvudine inhibits nrti-resistant viral strains. azvudine exerts highly potent inhibition on hiv-1 (ec50s ranging from 0.03 to 6.92 nm) and
更新時間:2025-07-07
Dasatinib monohydrateBMS-354825 Monohydrate；達(dá)沙替尼
dasatinib is an orally bioavailable synthetic small molecule-inhibitor of src-family protein-tyrosine kinases. dasatinib binds to and inhibits the growth-promoting activities of these kinases. apparently, because of its less stringent binding affinity for
更新時間:2025-07-07
Talipexole dihydrochloride鹽酸他利克索；Domnin；B-HT 920 dihydrochloride
talipexole dihydrochloride is a dopamine d2 receptor agonist, α2-adrenoceptor agonist, and 5-ht3 receptor antagonist in both rat cortical and intestinal membrane fractions with ki values of 0.35 μm and 0.22 μm, respectively. it displays antiparkinsonian a
更新時間:2025-07-07
BalovaptanRG7314
balovaptan is a highly potent and selective brain-penetrant vasopressin 1a (hv1a) receptor antagonist, with kis of 1 and 39 nm for human (hv1a) and mouse (mv1a) receptors. it is used for the research of autism.
更新時間:2025-07-07
BaloxavirS-033447；Baloxavir acid；巴洛沙韋
baloxavir is a first-in-class cap-dependent endonuclease inhibitor of the influenza virus polymerase pa subunit.
更新時間:2025-07-07
BAMB-4ITPKA-IN-C14
bamb-4 is a highly membrane-permeable inhibitor of inositol-1,4,5-trisphosphate-3-kinase a (itpka). it acts by suppressing the metastasis-promoting effect of itpka in lung tumor cells(with ic50 of 37 μm in adp-glo assay).
更新時間:2025-07-07
BAM 15
bam 15 is an uncoupler of mitochondrial protonophore.
更新時間:2025-07-07
BAY-2402234
bay-2402234 is an inhibitor of dihydroorotate dehydrogenase (dhodh) for the treatment of myeloid malignancies.bay 2402234 is a selective low-nanomolar inhibitor of human dhodh enzymatic activity.
更新時間:2025-07-07
BAY-524BAY524
bay-524 is an inhibitor of bub1(ic50 = 450 nm.human bub1 in the presence of 2 mm atp).
更新時間:2025-07-07
Levofloxacin hydrate左氧氟沙星半水合物；Levofloxacin Hemihydrate；Tavanic hydrate；Cravit hydrate；Iquix hydrate；
levofloxacin is a broad-spectrum, third-generation fluoroquinolone antibiotic and optically active l-isomer of ofloxacin with antibacterial activity. levofloxacin diffuses through the bacterial cell wall and acts by inhibiting dna gyrase (bacterial topois
更新時間:2025-07-07
BAY1082439N-[8-[[(2R)-2-羥基-3-(嗎啉-4-基)丙基]氧基]-7-甲氧基-2,3-二氫咪唑并[1,2-C]喹唑啉-5-基]-2-甲基吡啶-3-甲酰胺
bay1082439 is highly effective in inhibiting pten-null prostate cancer growth[1][2] and it is an orally bioavailable, selective pi3kα/β/δ inhibitor. bay1082439 also inhibits mutated forms of pik3ca.
更新時間:2025-07-07
Axitinib阿昔替尼；阿西替尼；AG-013736
axitinib is an orally bioavailable tyrosine kinase inhibitor with ic50s of 0.1, 0.2, 0.1-0.3, 1.7, 1.6 nm for vegfr1, vegfr2, vegfr3, c-kit, and pdgfrβ, respectively.
更新時間:2025-07-07
Beaucage reagent
beaucage reagent, which is found to be effective in causing dna cleavage.
更新時間:2025-07-07
Phenformin hydrochloride鹽酸苯乙福明；Phenformin HCl；Phenethylbiguanide hydrochloride
phenformin is an agent belonging to the biguanide class of antidiabetics with antihyperglycemic activity.
更新時間:2025-07-07
Nialamide煙肼酰胺；Niamidal；Nialamid
nialamide is an mao inhibitor that is used as an antidepressive agent.
更新時間:2025-07-07
BI-1935
bi-1935 is an inhibitor of soluble epoxide hydrolase (seh). for diseases related to cardiovascular disease.
更新時間:2025-07-07
BI-3812
bi-3812 is an inhibitor of bcl6. which inhibiting the btb domain of bcl6 (ic50: 3 nm). bi-3812 also has antitumor activity.
更新時間:2025-07-07
BI-671800Cmpd A；AP-761
bi-671800 is a highly specific and potent antagonist of chemoattractant receptor-homologous molecule on th2 cells (dp2/crth2). with ic50 values of 4.5 nm and 3.7 nm for pgd2 binding to crth2 in hcrth2 and mcrth2 transfected cells, respectively. bi-671800
更新時間:2025-07-07
DeferasiroxCGP-72670；ICL 670；地拉羅司
deferasirox is an oral iron chelating agent used to treat chronic iron overload.
更新時間:2025-07-07
Bifenazate
bifenazate is a positive allosteric modulator of gaba receptor. bifenazate is an acaricide that controls 100% of mites at a concentration of 25 ppm.
更新時間:2025-07-07
Biotin-DADOOEZ-Link Amine-PEO2-Biotin；Biotinyl-3,6-dioxaoctanediamine
biotin-dadoo is a biotinylation reagent,which can be used to synthesize a biotin-estradiol conjugate (i.e., biotin-dadoo-estradiol) to develop a direct, broad range enzyme immunoassay to measure plasma estradiol concentrations.
更新時間:2025-07-07
Biotin Hydrazide
biotin hydrazide is a carbonyl-reactive biotinylation reagent, which is a carbonyl probe. biotin hydrazide is a great choice for labeling mouse monoclonal antibodies, lectins, sugars, unpaired cytosine residues in nucleic acids, and glycoprotiens.
更新時間:2025-07-07
Biotin NHSBiotin-NHS；NHS-Biotin；Biotin N-hydroxysuccinimide ester；(+)生物素-N-琥珀酰亞胺基酯
biotin nhs is an amino reactive biotin reagent used in the preparation of biotinylated surfaces or polypeptides.
更新時間:2025-07-07
Epalrestat依帕斯他；依帕司他；ONO2235
epalrestat, an aldose reductase inhibitor, is well tolerated in long-term therapy. it can effectually ameliorate the associated symptoms of diabetic neuropathy and delay the progression of the disease, particularly in patients with limited microangiopathy
更新時間:2025-07-07
Biotin-PEG3-acid18-[(3AS,4S,6AR)-六氫-2-氧代-1H-噻吩并[3,4-D]咪唑-4-基]-14-氧代-4,7,10-三氧雜-13-氮雜十八烷酸
biotin-peg3-acid is a biotin-labeled, peg-based protac linker that can be used in the synthesis of protacs.biotin-peg3-acid is a heterobiofunctional biotin peg derivative containing a carboxylic acid group. the hydrophilic peg spacer arm imparts water sol
更新時間:2025-07-07
Cisatracurium besylate51W89；順苯磺酸阿曲庫銨；順苯磺阿曲庫銨
cisatracurium besylate is a nondepolarizing skeletal muscle relaxant for intravenous administration.
更新時間:2025-07-07
Biotin-PEG3-azideN-[2-[2-[2-(2-疊氮乙氧基)乙氧基]乙氧基]乙基]生物素胺
biotin-peg3-azide is a peg-based protac linker can be used in the synthesis of protacs.
更新時間:2025-07-07
Biotin-PEG4-alkyne生物素-四聚乙二醇-丙炔基
biotin-peg4-alkyne is a biotin-labeled, peg-based protac linker that can be used in the synthesis of protacs.
更新時間:2025-07-07
Dicyclomine hydrochloride
dicyclomine hydrochloride is a muscarinic antagonist used as an antispasmodic and in urinary incontinence.
更新時間:2025-07-07
Candesartan坎地沙坦；CV 11974
candesartan is an angiotensin ii receptor blocker used widely in the therapy of hypertension and heart failure.
更新時間:2025-07-07
Captopril甲巰丙脯酸；卡托普利；SA333；SQ-14534；SQ 14225
captopril is a potent and specific inhibitor of peptidyl-dipeptidase a. it blocks the conversion of angiotensin i to angiotensin ii, a vasoconstrictor and important regulator of arterial blood pressure.
更新時間:2025-07-07
Ramelteon雷美替胺；TAK-375
ramelteon is a melatonin receptor agonist. the mechanism of action of ramelteon is as a melatonin receptor agonist.
更新時間:2025-07-07
Bis-PEG3-NHS ester
bis-peg3-nhs ester is a nonclaevable 3-unit peg linker for antibody-drug-conjugation (adc).
更新時間:2025-07-07
Toremifene citrate枸櫞酸托瑞米芬；NSC 613680；NK 622；FC 1157a
toremifene citrate is a selective estrogen receptor modulator (serm). it is an estrogen agonist for bone tissue and cholesterol metabolism but is antagonistic on the mammary and uterine tissue.
更新時間:2025-07-07
Mupirocin莫匹羅星；Pseudomonic acid；BRL-4910A
mupirocin is a rna synthetase inhibitor antibacterial. it has shown excellent activity against gram-positive staphylococci and streptococci.
更新時間:2025-07-07
NadifloxacinOPC7251；那氟沙星
nadifloxacin has been used in trials studying the treatment of acne vulgaris.
更新時間:2025-07-07
Motixafortide TFA(664334-36-5,Free)TF 14016 TFA；BKT140 TFA；T140 TFA；BL-8040 TFA
motixafortide is an antagonist of cxcr4 with ic50 of ～1 nm. it induces the apoptosis of aml blasts by down-regulating erk, bcl-2, mcl-1 and cyclin-d1 via altered mir-15a/16-1 expression.
更新時間:2025-07-07
BLT-1
blt-1 is a scavenger receptor bi (sr-bi)inhibitor.
更新時間:2025-07-07

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