其他產(chǎn)品及廠家

b-Casomorphin (1-3) Acetate；化合物b-Casomorphin (1-3) Acetateb-Casomorphin (1-3) Acetate (72122-59-9 Fr
b-casomorphin (1-3) acetate is a tri-peptide with an opioid effect.
更新時(shí)間:2025-12-04
BIM 23042 Acetate；化合物BIM 23042 AcetateBIM 23042 Acetate (111857-96-6 Free base)；BIM 23042 Acetate (1
bim 23042 acetate [d-nal-cys-tyr- d-trp-lys-val-cys-nal-nh2] is a selective antagonist of neuromedin b.?
更新時(shí)間:2025-12-04
Cadherin Peptide, avian Acetate；化合物Cadherin Peptide, avian AcetateCadherin Peptide, avian Acetate (1
cadherin peptide, avian acetate is a peptide with the sequence leu-arg-ala-his-ala-val-asp-val-asn-gly-nh2. cadherins are a class of type-1 transmembrane proteins.
更新時(shí)間:2025-12-04
DL-α-Hydroxyglutaric acid disodium salt；DL-Α-羥基戊二酸二鈉disodium 2-hydroxypentanedioate；disodium 2-hydro
dl-α-hydroxyglutaric acid disodium salt (disodium 2-hydroxypentanedioate) is an α -hydroxyacid formed from the hydrolysis of (r) -5-oxy-2-tetrahydrofuran carboxylic acid, which is overproduced in human neurometabolic disease d-α -hydroxyglutaric uria. ?
更新時(shí)間:2025-12-04
Donitriptan hydrochloride；鹽酸多尼普曲坦Donitriptan HCl|||Donitriptan monohydrochloride；鹽酸多尼普曲坦|||Donitript
donitriptan hydrochloride (donitriptan monohydrochloride) is a potent, high efficacy agonist of 5-ht1b/1d receptors with pkis of 9.4 and 9.3, respectively
更新時(shí)間:2025-12-04
FAUC-365；化合物FAUC-365FAUC-365 Benzo[b]thiophene-2-carboxylic acid {4-[4-(2,3-dichloro-nphenyl)-piper
fauc-365 is a d3 dopamine receptor agonist.
更新時(shí)間:2025-12-04
Finasteride acetate；化合物 T21668Finasteride acetate
finasteride (mk-906) acetate is a potent and competitive 5α-reductase inhibitor, with an ic 50 of 4.2 nm for type ii 5α-reductase. the affinity of finasteride acetate for type ii 5α-reductase enzyme was approximately 100-fold higher than that for the type i enzyme. finasteride acetate can be used for the research of benign prostatic hyperplasia (bph) and androgenic alopecia [1] [2] [3].
更新時(shí)間:2025-12-04
Haloperidol hydrochloride；化合物 T21669Haloperidol hydrochloride
haloperidol hydrochloride is a potent dopamine d2 receptor antagonist which is a potent antipsychotic agent.
更新時(shí)間:2025-12-04
lutidinic acid；盧剔啶酸2,4-Pyridinedicarboxylic acid|||2,4-Dicarboxypyridine|||2, 4-PDCA|||2,4-PDCA；2,4-
lutidinic acid (2,4-dicarboxypyridine) is an in vitro and in cell inhibitor, as well as a known inhibitor of the histone lysine demethylases.
更新時(shí)間:2025-12-04
N-Isopropylnoratropine；N-異丙基去甲托品N-Isopropylnoratropine
n-isopropylnoratropine is a noratropine derivative and an intermediate in the production of ipratropium, an atropine-like bronchodilator drug via an anticholinergic pathway. n-isopropylnoratropine is used to examine the stability of ipratropium [1].
更新時(shí)間:2025-12-04
PKA inhibitor fragment (6-22) amide Acetate；化合物T21674LPKA inhibitor fragment (6-22) amide Acetate(12
pka inhibitor fragment (6-22) amide acetate is a synthetic peptide which selectively inhibits pka activity by binding to its substrate site (ic50 < 2 nm).
更新時(shí)間:2025-12-04
SB 203580 hydrochloride；化合物 T21675SB 203580 hydrochloride
adezmapimod (sb 203580) hydrochloride is a selective atp-competitive inhibitor of p38 mapk, displaying ic50 values of 50 nm for sapk2a/p38 and 500 nm for sapk2b/p38β2. this compound also inhibits lck, gsk3β, and pkbα, albeit with ic50 values 100-500 times higher than those for sapk2a/p38. additionally, adezmapimod hydrochloride acts as an activator of autophagy and mitophagy [1].
更新時(shí)間:2025-12-04
SCH 51344；化合物 T21676SCH 51344
sch 51344 inhibits ras induced malignant transformation. sch 51344 prevents anchorage-independent growth of oncogene transformed fibroblasts [1].
更新時(shí)間:2025-12-04
Temafloxacin (hydrochloride)；化合物 T21677Temafloxacin (hydrochloride)
temafloxacin (hydrochloride) is an antibiotic and antimycobacterial agent. it used to treat lower respiratory tract infections, genital and urinary infections like prostatitis, and skin infections.
更新時(shí)間:2025-12-04
3MB-PP1；化合物3MB-PP13MB-PP1
3mb-pp1 is a bulky purine analog and a polo-like kinase 1 (plk1) inhibitor. in cells expressing analog-sensitive plk1 alleles, 3mb-pp1 blocks mitotic progression and cell division arise by targeting plk1. 3mb-pp1 specifically inhibits analog-sensitive ssn3 (cdk8). 3mb-pp1 inhibits leu93 mutant zipper-interacting protein kinase with ic50 of 2 μm. 3mb-pp1 can be used for the research of cell division and hypha formation of candida albicans.
更新時(shí)間:2025-12-04
2-(1,8-naphthyridin-2-yl)phenol；化合物2-NP2-(1,8-naphthyridin-2-yl)phenol
2-np is a stat1 enhancer.
更新時(shí)間:2025-12-04
A 68930 hydrochloride；化合物 T21680A 68930 hydrochloride
a68930 hydrochloride is a dopamine d1 receptor agonist which can be used for the research of bronchiectasis [1].
更新時(shí)間:2025-12-04
AACOCF3；化合物AACOCF3Arachidonyl trifluoromethyl ketone|||Arachidonyltrifluoromethane；Arachidonyl trifl
aacocf3 (arachidonyl trifluoromethyl ketone) is a cell-permeable trifluoromethyl ketone analog of arachidonic acid. it is a potent and selective slow binding inhibitor of the 85-kda cytosolic phospholipase a2 (cpla2). by blocking the production of arachidonate and 12-hydroxyeicosatetraenoic acid in calcium ionophore-challenged platelets, aacocf3 hinders their synthesis. moreover, aacocf3 inhibits glucose-induced insulin secretion from isolated rat islets. given its diverse applications, aacocf3
更新時(shí)間:2025-12-04
Bufuralol (hydrochloride)；化合物 T21684Bufuralol (hydrochloride)
bufuralol hydrochloride (ro 3-4787 hydrochloride) is a potent non-selective, orally active β-adrenoreceptor antagonist with partial agonist activity, which is also a cyp2d6 probe substrate [1] [2].
更新時(shí)間:2025-12-04
CCT 031374 hydrobromide；化合物CCT 031374 hydrobromideCCT 031374 hydrobromide
cct 031374 hydrobromide is a tcf/β-catenin inhibitor with antitumor activities.
更新時(shí)間:2025-12-04
CD 1530；化合物 CD 1530CD-1530|||CD1530；CD-1530|||CD1530
cd 1530 is a selective and potent rarγ agonist (kd:150 nm) with potential anticancer activity, shows insecticidal activity against cryptobacterium hidradii nematodes, and can be used to study oral carcinogenesis.
更新時(shí)間:2025-12-04
Conoidin A；1,4-二氧代-2,3-二溴甲基喹啉Conoidin A
conoidin a is a cell permeable inhibitor of t. gondii enzyme peroxiredoxin ii (tgprxii) with nematicidal properties. it covalently binds to the peroxidatic cys47 of tgprxii, irreversibly inhibiting its hyperperoxidation activity with an ic50 of 23 μm. it also inhibits hyperoxidation of mammalian prxi and prxii (but not prxiii). conoidin a has antioxidant, neuroprotective effects and can be used for the research of ischaemic heart disease.
更新時(shí)間:2025-12-04
Cytochrome c - pigeon (88-104) Acetate；化合物T21688LCytochrome c - pigeon (88-104) Acetate (86579-06-8
cytochrome c - pigeon (88-104) acetate (cytochrome c - pigeon ) is specific for a peptide within the cooh-terminal sequence 88-1041.?
更新時(shí)間:2025-12-04
Zebularine化合物ZebularineNSC309132|||4-Deoxyuridine
zebularine (4-deoxyuridine) is a dna methylation inhibitor. acts as a transition state analog inhibitor of cytidine deaminase by binding to the active size as covalent hydrates. it also inhibits cytidine deaminase (ki: 2 μm, in a cell-free assay).
更新時(shí)間:2025-12-04
NVP DPP 728 dihydrochloride；化合物 T21691NVP DPP 728 dihydrochloride
nvp-dpp728 is a potent, reversible, nitrile-dependent inhibitor of dipeptidyl peptidase iv (dpp-iv), demonstrating an inhibition constant (k i) of 11 nm for human dpp-iv amidolytic activity. by inhibiting the degradation of glucagon-like peptide-1 (glp-1), nvp-dpp728 enhances insulin release following glucose intake, making it useful for diabetes research [1].
更新時(shí)間:2025-12-04
PPM-18；化合物 T21693PPM-18
ppm-18 (nsc 73233) is a potent anti-inflammatory agent which inhibits nitric oxide synthase expression. ppm-18 is a potent inhibitor of inos expression by blocking the binding of nf-κb to promoter [1]. ppm-18 is an analog of vitamin k remarkably suppressed the proliferation and induced apoptosis in bladder cancer cells [2].
更新時(shí)間:2025-12-04
(R)-Lisofylline；化合物(R)-Lisofylline(R)-Lisophylline；(R)-Lisophylline
(r)-lisofylline ((r)-lisophylline) is an inhibitor of lysophosphatidic acid acyltransferase (ic50 = 0.6 ?m). (r)-lisofylline interrupts il-12 signaling-mediated stat4 activation and can be used in studies about the treatment of type 1 diabetes and autoimmune disorders.
更新時(shí)間:2025-12-04
VKGILS-NH2 Acetate；化合物VKGILS-NH2 AcetateVKGILS-NH2 Acetate (942413-05-0 Free base)；VKGILS-NH2 Acetat
vkgils-nh2 acetate is a reversed amino acid sequence control peptide for sligkv-nh2, a protease-activated receptor 2 (par2) agonist.
更新時(shí)間:2025-12-04
SKF-96365 hydrochloride；化合物SKF-96365 hydrochlorideSKF96365；1-[2-(4-甲氧基)-2-[3-(4-甲氧基苯基)丙氧基]乙基]咪唑|||SK
skf-96365 hydrochloride (skf96365) , a soce inhibitor, exhibits potent anti-neoplastic activity by inducing cell-cycle arrest and apoptosis in colorectal y cells. skf-96365 hydrochloride can induce cytoprotective autophagy to delay apoptosis by preventing the release of cytochrome c (cyt c) from the mitochondria into the cytoplasm. mechanistically, skf-96365 hydrochloride treatment inhibited the calcium/calmodulin-dependent protein kinase iiγ (camkiiγ)/akt signaling cascade in vitro and in vivo.
更新時(shí)間:2025-12-04
NOS-IN-1u00A0；化合物NOS-IN-1u00A02-Imino-4-methylpiperidine (acetate)；2-Imino-4-methylpiperidine (aceta
nos-in-1 (2-imino-4-methylpiperidine acetate) is a potent and orally active inhibitor of no synthase (nos) isoforms. nos-in-1 exhibits ic50s of 0.1 μm, 0.2 μm, and 1.1μm for human inos (hinos), hnnos and henos, respectively.
更新時(shí)間:2025-12-04
4-Chlorophenylguanidine hydrochloride；洗必泰二乙酸雜質(zhì)4-Chlorophenylguanidine hydrochloride
4-chlorophenylguanidine hydrochloride is a potent inhibitor of urokinase selectivity. ?
更新時(shí)間:2025-12-04
5-fluoro 203；化合物5-fluoro 2035F-203|||NSC-703786；5F-203|||NSC-703786
5-fluoro 203 (nsc-703786) is a cytotoxic molecule leading to cell death by forming dna adducts. 5-fluoro 203 induces aryl hydrocarbon receptor signaling, and elevates expression of cyp1a1. 5-fluoro 203 treatment of cells also leads to elevation of reactive oxygen species and activation of p38, jnk and erk.
更新時(shí)間:2025-12-04
8-CPT-Cyclic AMP (sodium salt)；化合物 T217058-CPT-Cyclic AMP (sodium salt)
8-cpt-cyclic amp (8-cpt-camp) sodium functions dually as a selective activator of cyclic amp-dependent protein kinase (pka) and as a potent inhibitor of the cyclic gmp-specific phosphodiesterase (pde va), demonstrating an inhibitory concentration (ic 50) of 0.9 μm. additionally, this compound inhibits pde iii and pde iv, while significantly activating epac, showcasing its diverse pharmacological activities [1] [2].
更新時(shí)間:2025-12-04
Angiotensin 1/2 + A (2 - 8) Acetate；化合物Angiotensin 1/2 + A (2 - 8) AcetateAngiotensin 1/2 + A (2 - 8
angiotensin 1/2 + a (2 - 8) acetate is a vasoconstrictor.
更新時(shí)間:2025-12-04
SEW?2871；化合物SEW2871SEW2871；SEW2871
sew 2871 is an orally available, highly selective s1p1 agonist with an ec50 of 13.8 nm.it reduces the number of lymphocytes in the blood and is used in studies related to diabetes, alzheimer´s disease, liver fibrosis, and inflammation. it activates erk, akt and rac signaling pathways and induces s1p1 internalization and recycling.
更新時(shí)間:2025-12-04
BAY 41-8543；化合物BAY 41-8543BAY 41-8543
bay 41-8543 is a nitric oxide (no)-independent stimulator of soluble guanylyl cyclase (sgc).
更新時(shí)間:2025-12-04
BRD6688；化合物BRD6688BRD6688
brd6688 is a selective hdac2 inhibitor that acts by enhancing the learning and memory processes
更新時(shí)間:2025-12-04
SQ22536；化合物SQ 225369-(tetrahydrofuran-2-yl)-9h-purin-6-amine|||SQ 22536；9-(tetrahydrofuran-2-yl)-9h-
sq22536 (9-(tetrahydrofuran-2-yl)-9h-purin-6-amine) , the adenosine analogue 9-(tetrahydro-2-furyl)adenine, inhibited adenylate cyclase activity of crude membrane preparations from catfish (ictalurus melas) and rat isolated hepatocytes in a non-competitive manner.
更新時(shí)間:2025-12-04
GP-82996；化合物GP-82996Cdk4/6 Inhibitor IV|||CINK4；Cdk4/6 Inhibitor IV|||CINK4
gp-82996 (cink4) is a pharmacological inhibitor specifically targeting cdk4/6, exhibiting ic50 values of 1.5 μm for cdk4/cyclin d1, 5.6 μm for cdk6/cyclin d1, and 25 μm for cdk5/p35. it effectively induces apoptosis in u2os cancer cells, positioning it as a potential investigational tool in cancer research [1] [2].
更新時(shí)間:2025-12-04
Fas C-Terminal Tripeptide Acetate；化合物Fas C-Terminal Tripeptide AcetateFas C-Terminal Tripeptide Acet
fas c-terminal tripeptide acetate shows inhibitory activity of fas/fap-1 binding.
更新時(shí)間:2025-12-04
Ivermectin B1a；伊維菌素 B1aIvermectin B1a
ivermectin b1a is the major (80%) component of commercially available ivermectin and a derivative of avermectin b1a.
更新時(shí)間:2025-12-04
(±)-Lisofylline；利索茶堿(±)-Lisofylline
(±)-lisofylline is an enantiomer-specific, alkyl-substituted methylxanthine, which has specific and potent activity in down-regulating leukocyte activation. (±)-lisofylline is an anti-inflammatory agent.
更新時(shí)間:2025-12-04
Veratridine；藜蘆定Veratridine
veratridine is a benzoate-cevane found in veratrum and schoenocaulon. it activates sodium channels to stay open longer than normal.
更新時(shí)間:2025-12-04
NNGH；化合物 T21735NNGH
nngh functions as an inhibitor of stromelysin-1 (mmp-3), which is not only a direct transcriptional target but also a vital component of the wnt/β-catenin signaling pathway. additionally, matrix metalloproteinases (mmps) are established as playing a crucial role during the later stages of tumor progression [1].
更新時(shí)間:2025-12-04
PF-9184；化合物PF-9184PF-9184
pf-9184 is a potent and selective inhibitor of human microsomal prostaglandin e synthase-1 (mpges-1), ic50 =16.5 nm. pf-9184 inhibits il-1β-induced pge2 synthesis in vitro.
更新時(shí)間:2025-12-04
Quercetin；槲皮素Sophoretin；槲皮素|||Sophoretin
quercetin (sophoretin) is a natural flavonoid and is an agonist of sirt1. quercetin is also a pi3k inhibitor, inhibiting pi3kγ, pi3kδ, and pi3kβ (ic50=2.4/3.0/5.4 μm). quercetin can induce apoptosis and autophagy.
更新時(shí)間:2025-12-04
RD162；化合物RD162RD162
rd162 is a non-steroidal antiandrogen (nsaa) specifically binding to the androgen receptor (ar).
更新時(shí)間:2025-12-04
Beta-Lipotropin (1-10), porcine Acetate；化合物T21743LBeta-Lipotropin (1-10), porcine Acetate(77875-68-4
beta-lipotropin (1-10), porcine acetate (beta-lipotropin ) (beta-lph) was found to contain within its c-terminal sequence the primary structure of these peptides.
更新時(shí)間:2025-12-04
Terameprocol；化合物Terameprocoltetramethyl Nordihydroguaiaretic Acid|||EM-1421；tetramethyl Nordihydrogu
terameprocol (em-1421) is a synthetic tetra-methylated derivative of nordihydroguaiaretic acid (ndga) and transcriptional inhibitor with potential antiviral, antiangiogenic, and antineoplastic activities. terameprocol showed the strongest anti-hiv activity.
更新時(shí)間:2025-12-04
VU0483605；化合物VU0483605VU0483605
vu0483605 is an effective and selective positive allosteric modulator of mglur1 with ec50s of 390 and 356 nm for human and rat, respectively.
更新時(shí)間:2025-12-04

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