其他產品及廠家

Sodium butanoate丁酸鈉；Sodium Butyrate；Butanoic acid sodium salt
sodium butyrate is the sodium salt of butyrate with potential antineoplastic activity. butyrate, a short chain fatty acid, competitively binds to the zinc sites of class i and ii histone deacetylases (hdacs).
更新時間:2025-07-07
TLR1N-[(1S)-2-甲基-1-(1-吡咯烷羰基)丙基]-苯丙酰胺
tlr1 is a cell-penetrating toll/il-1 receptor/resistance (tir) domain/bb-loop mimic and inhibits il-1 receptor-mediated responses.
更新時間:2025-07-07
Ibuprofen(±)-Ibuprofe；Advil；Motrin；Brufen；布洛芬
ibuprofen is a propionic acid derivate and nonsteroidal anti-inflammatory drug (nsaid) with anti-inflammatory, analgesic, and antipyretic effects. ibuprofen inhibits the activity of cyclo-oxygenase i and ii, resulting in a decreased formation of precursor
更新時間:2025-07-07
Diatrizoic AcidDiatrizoate；Amidotrizoic acid；泛影酸
diatrizoic acid is an organic, iodinated radiopaque x-ray contrast medium used in diagnostic radiography.
更新時間:2025-07-07
UC-514321
uc-514321 directly targets stat3/5 and represses tet1 expression. uc-514321 has the potential to treat acute myeloid leukemia (aml) both in vitro and in vivo, with low toxicity.
更新時間:2025-07-07
UCB-9260
ucb-9260 inhibits tnf signaling by stabilizing an asymmetric form of the trimer.
更新時間: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
更新時間:2025-07-07
Tadalafil他達那非；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.
更新時間:2025-07-07
1A-116
1a-116 is a specific rac1 inhibitor.
更新時間: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
更新時間:2025-07-07
AZD7507
azd7507 is a csf-1r inhibitor with an ic50 of 32 nm. azd7507 has antitumor activity.
更新時間:2025-07-07
AZD7624AZD-7624
azd7624 is an p38 inhibitor. it has potent anti-inflammatory activity.
更新時間: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；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

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