其他產(chǎn)品及廠家

UCB-9260
ucb-9260 inhibits tnf signaling by stabilizing an asymmetric form of the trimer.
更新時(shí)間:2025-07-07
UNC6852
unc6852 contains an eed ligand (ic50 = 247 nm) and a von hippel-lindau ligand and is a selective polycomb repressive complex 2 (prc2) degrader based on protac.
更新時(shí)間:2025-07-07
Bemegride貝美格；Bemegrid；3-Ethyl-3-methylglutarimide；Agipnon
bemegride is a central nervous system stimulant and antidote for barbiturate poisoning.
更新時(shí)間:2025-07-07
Watermelon ketone7-Methyl-2H-1,5-benzodioxepin-3(4H)-one；西瓜酮
watermelon ketone is a fragrance compound, with a special odorant. it has been widely used in the fragrance industry.
更新時(shí)間:2025-07-07
Xanthopterin (hydrate)
xanthopterin hydrate is isolated from butterfly wings and could replace folic acid in the nutrition of many animal species.
更新時(shí)間:2025-07-07
Sodium montmorillonite蒙脫石；Montmorillonite；Bentolite；Gelwhite L
sodium montmorillonite can catalyze reactions of the 5´-phosphorimidazolide of adenosine used as a model generated rna type oligomers.
更新時(shí)間:2025-07-07
ZL0580
zl0580 induces hiv suppression by inhibiting tat transactivation and transcription elongation as well as by inducing repressive chromatin structure at the hiv promoter.
更新時(shí)間:2025-07-07
(S)-3-Hydroxybutanoic acidL-β-Hydroxybutyric acid；(S)-β-Hydroxybutanoic acid；L-(+)-3-Hydroxybutyric
(s)-3-hydroxybutyric acid is a normal human metabolite that has been found elevated in geriatric patients remitting from depression. 3-hydroxybutyric acid is synthesized in the liver from acetyl-coa in humans, and can be used as an energy source by the br
更新時(shí)間:2025-07-07
Tadalafil他達(dá)那非；西力士；Cialis；IC-351
tadalafil is a carboline-based compound with vasodilatory activity. tadalafil selectively inhibits the cyclic guanosine monophosphate (cgmp)-specific type 5 phosphodiesterase- (pde-5)-mediated degradation of cgmp, which is found in the smooth muscle of th
更新時(shí)間:2025-07-07
Sucralose三氯蔗糖；E955；Trichlorosucrose
sucralose, an artificial sweetener, is not degraded by the body, so it is noncaloric.
更新時(shí)間:2025-07-07
1-Methyl-7-nitroisatoic anhydride1M7
1-methyl-7-nitroisatoic anhydride (1m7) is a reagent. it detects local nucleotide flexibility, for probing 2´-hydroxyl reactivity.
更新時(shí)間:2025-07-07
Demeclocycline hydrochlorideClortetrin；Detravis；Demeclocycline HCl；Declomycin；地美環(huán)素；鹽酸地美環(huán)素
demeclocycline hydrochloride is a tetracycline analog having a 7-chloro and a 6-methyl. because it is excreted more slowly than tetracycline, it maintains effective blood levels for longer periods of time.
更新時(shí)間:2025-07-07
11-Beta-hydroxyandrostenedione4-Androsten-11β-ol-3,17-dione；NSC-17102；4-雄烯-11β-醇-3,17-二酮
11-beta-hydroxyandrostenedione is a steroid mainly found in the adrenal origin (11β-hydroxylase is present in adrenal tissue, but absent in ovarian tissue), which is a 11β-hydroxysteroid dehydrogenase isozymes inhibitor. measuring plasma 11-beta-hydroxyan
更新時(shí)間:2025-07-07
12-Ketodeoxycholic acid
12-ketodeoxycholic acid is a metabolite from kidney as biomarkers for early detection of tubulo-interstitial nephropathy.
更新時(shí)間:2025-07-07
1A-116
1a-116 is a specific rac1 inhibitor.
更新時(shí)間:2025-07-07
2,2,5,7,8-Pentamethyl-6-ChromanolPMC
2,2,5,7,8-pentamethyl-6-chromanol is the anti-oxidant moiety of vitamin e (α-tocopherol), which has potent androgen receptor (ar) signaling modulation and anti-cancer activity against prostate cancer cell lines.
更新時(shí)間:2025-07-07
AY 9944
ay 9944 is a specific cholesterol biosynthesis inhibitor. ay 9944 inhibits the 7-dehydro cholesterol δ7-reductase (dhcr7) enzyme (ic50=13 nm). at high doses, ay 9944 inhibits also in cultured embryos sterol δ7-δ8 isomerase, which causes the accumulation o
更新時(shí)間:2025-07-07
AZ-Dyrk1B-333-(2-Methyl-4-pyrimidinyl)-1-(phenylmethyl)-1H-pyrrolo[2,3-c]pyridine
az-dyrk1b-33 is a potent and selective dyrk1b kinase inhibitor with an ic50 of 7 nm.
更新時(shí)間:2025-07-07
AZ PFKFB3 26
az pfkfb3 26 is an effective and selective pfkfb3 inhibitor with an ic50 of 23 nm. the ic50s for pfkfb1 and pfkfb2 are 2.06 and 0.384 μm, respectively.
更新時(shí)間:2025-07-07
AZ10606120 dihydrochloride
az10606120 dihydrochloride has anti-depressant effects and reduces tumour growth[1]. az10606120 dihydrochloride is a selective, high affinity antagonist for p2x7 receptor (p2x7r) at human and rat with an ic50 of ~10 nm and it is little or no effect at oth
更新時(shí)間:2025-07-07
AZ1495
az1495 is an oral active inhibitor of interleukin-1 receptor associated kinase 4 (irak4), with ic50 values of 5 nm and 23 nm for irak4 and irak1, respectively. which shows activity in treatment of mutant myd88l265p diffuse large b-cell lymphoma (dlbcl).
更新時(shí)間:2025-07-07
AZD-0284
azd-0284 is an inverse agonist of the nuclear receptor rorγ. in development for the treatment of plaque psoriasis vulgaris and respiratory tract disorders[1].
更新時(shí)間:2025-07-07
D-PanthenolD-Pantothenyl alcohol；Ilopan；Dexpanthenol；Pantothenol；D-泛醇；D-泛醇（維生素原B5）
dexpanthenol is an alcoholic analogue of d-pantothenic acid and cholinergic agent. dexpanthenol acts as a precursor of coenzyme a necessary for acetylation reactions and is involved in the synthesis of acetylcholine. although the exact mechanism of the ac
更新時(shí)間:2025-07-07
AZD4320
azd4320 is an inhibitor of bh3-mimicking dual bcl2/bclxl. for kpum-ms3, kpum-uh1, and str-428 cells, the ic50s values are 26 nm, 17 nm, and 170 nm , respectively.
更新時(shí)間:2025-07-07
AZD5423
azd5423 is an inhaled, potent, selective, and non-steroidal modulator of glucocorticoid receptor (gr) and it effectively reduces allergen-induced responses in subjects with mild allergic asthma.
更新時(shí)間:2025-07-07
AZD5582 acetate (1258392-53-8 free base)
azd5582 acetate is an inhibitor of iaps, which binds to the bir3 domains ciap1, ciap2, and xiap with ic50s of 15, 21, and 15 nm, respectively. azd5582 induces apoptosis.
更新時(shí)間:2025-07-07
AZD5904
azd5904 is a potent and irreversible inhibitor of human myeloperoxidase (mpo, ic50: 140 nm) which has similar potency in mouse and rat.
更新時(shí)間:2025-07-07
Butoconazole nitrate硝酸布康唑；RS 35887
butoconazole nitrate is the nitrate salt form of butoconazole, a synthetic imidazole derivative with fungistatic properties. butoconazole nitrate interferes with steroid biosynthesis by inhibiting the conversion of lanosterol to ergosterol, thereby changi
更新時(shí)間:2025-07-07
AZD7507
azd7507 is a csf-1r inhibitor with an ic50 of 32 nm. azd7507 has antitumor activity.
更新時(shí)間:2025-07-07
AZD7624AZD-7624
azd7624 is an p38 inhibitor. it has potent anti-inflammatory activity.
更新時(shí)間:2025-07-07
AZD9056 hydrochloride
azd9056 hydrochloride is a p2x7 inhibitor，which plays a significant role in pain-causing diseases and inflammation.
更新時(shí)間:2025-07-07
AZD 4017
azd 4017 is an inhibitor of 11β-hydroxysteroid dehydrogenase type 1(11β-hsd1) (ic50: 7 nm).
更新時(shí)間:2025-07-07
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(shí)間:2025-07-07
Azidamfenicol
azidamfenicol inhibits ribosomal peptidyltransferase (ki=22 μm)[1]. azidamfenicol is a broad-spectrum chloramphenicol-like antibiotic.
更新時(shí)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(shí)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(shí)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(shí)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(shí)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(shí)間:2025-07-07
Lomefloxacin洛美沙星；SC47111A
lomefloxacin is a synthetic broad-spectrum fluoroquinolone with antibacterial activity.
更新時(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)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(shí)間:2025-07-07

最新產(chǎn)品

熱門儀器： 液相色譜儀 氣相色譜儀 原子熒光光譜儀 可見分光光度計(jì) 液質(zhì)聯(lián)用儀 壓力試驗(yàn)機(jī) 酸度計(jì)（PH計(jì)） 離心機(jī) 高速離心機(jī) 冷凍離心機(jī) 生物顯微鏡 金相顯微鏡 標(biāo)準(zhǔn)物質(zhì) 生物試劑