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Picrasidine N；化合物 T28415Picrasidine-N|||PicrasidineN；Picrasidine-N|||PicrasidineN (2024/9/4)
簡(jiǎn)介：picrasidine n is a naturally occurring dimeric alkaloid and a pparβ/δ agonist.
Piclozotan；化合物PiclozotanSUN-N-4057|||SUN4057|||SUNN-4057|||SUN-4057|||SUNN4057；SUN-N-4057|||SUN4057| (2024/9/4)
簡(jiǎn)介：piclozotan (anhydrous), a 5-ht1a receptor agonist, demonstrated significant neuroprotective activity in a transient middle cerebral artery occlusion (t-mcao) model, ameliorating motor complications in patients with advanced parkinson´s disease.
PI3KD/V-IN-01；化合物 T28413PI3KD/V IN 01|||PI3KD/VIN01；PI3KD/V IN 01|||PI3KD/VIN01 (2024/9/4)
簡(jiǎn)介：pi3kd/v-in-01 is a potent atp-competitive pi3kδ/vps34 dual inhibitor.
PI-091；化合物 T28412PI-091 (2024/9/4)
簡(jiǎn)介：pi-091 inhibits platelet aggregation.
EMS凍存條61067-13 (2024/9/4)
簡(jiǎn)介：美國(guó)ems授權(quán)經(jīng)銷(xiāo)商、原裝進(jìn)口、質(zhì)量保證、更多產(chǎn)品問(wèn)題請(qǐng)聯(lián)系我司銷(xiāo)售。
Physapubenolide；化合物 T28411NSC 368674|||NSC368674|||NSC-368674；NSC 368674|||NSC368674|||NSC-368674 (2024/9/4)
簡(jiǎn)介：physapubenolide is natural cytotoxic withanolide antitumor agent. physapubenolide induces apoptosis by decreasing mitochondrial membrane potential and elevating the bax/bcl-2 protein expression ratio.
PHPS1；化合物PHPS1PHPS-1|||PHPS 1；PHPS-1|||PHPS 1 (2024/9/4)
簡(jiǎn)介：phps1 is an inhibitor of shp2. phps1 efficiently inhibits activation of erk1/2 by the leukemia-associated shp2 mutant, shp2-e76k, and blocks the anchorage-independent growth of a variety of human tumor cell lines.
Plumbagin；白花丹素Plumbagone|||Plumbagine|||Plumbaein|||2-Methyljuglone；Plumbagone|||Plumbagine|||白花丹素|| (2024/9/4)
簡(jiǎn)介：plumbagin (plumbaein) is a yellow dye, formally derived from naphthoquinone. it is named after the plant genus plumbago, from which it was originally isolated. it is also commonly found in the carnivorous plant genera drosera and nepenthes. it is also a component of the black walnut drupe.
Photoregulin1；化合物 T28409Photoregulin1 (2024/9/4)
簡(jiǎn)介：photoregulin1 is a modulator of nr2e3. photoregulin1 slows the progression of photoreceptor degeneration in two common mouse models of autosomal dominant rp, the rhop23h and the pde6brd1 mutations.
EMS凍存條61067-03 (2024/9/4)
簡(jiǎn)介：美國(guó)ems授權(quán)經(jīng)銷(xiāo)商、原裝進(jìn)口、質(zhì)量保證、更多產(chǎn)品問(wèn)題請(qǐng)聯(lián)系我司銷(xiāo)售。
Phosphostim Sodium；化合物 T28408IPH1101|||Phosphostim|||IPH 1101|||IPH-1101；IPH1101|||Phosphostim|||IPH (2024/9/4)
簡(jiǎn)介：phosphostim, a gamma9deta2 t lymphocytes agonist, is used potentially for the treatment of renal cell carcinoma, hcv infection.
Phe-Pro-Arg-PABA-Resorufin；化合物 T28405Phe-Pro-Arg-PABA-Resorufin (2024/9/4)
簡(jiǎn)介：phe-pro-arg-paba-resorufin is a chromogenic and fluorogenic peptide substrate for the highly sensitive detection of proteases in biological matrices. the substrate is also applicable to the sensitive detection of the thrombin inhibitor dabigatran in human plasma and whole blood samples.
Phenyramidol Hydrochloride；化合物 T28404Vazalmin|||Analexin|||Firmalgil|||Phenyramidol HCl|||Betapirin； (2024/9/4)
簡(jiǎn)介：phenyramidol hydrochloride is an anticoagulant and analgesic.
全程高速;佛山到呂梁市興縣物流公司直達(dá)線(xiàn)-免費(fèi)提貨 (2024/9/4)
簡(jiǎn)介：
Phenoprolamine Hydrochloride；化合物 T28400phenoprolamine|||DDPH；phenoprolamine|||DDPH (2024/9/4)
簡(jiǎn)介：phenoprolamine hydrochloride is an adrenergic α1 receptor antagonist with potent antihypertensive, neuroprotective and cardioprotective effects. phenoprolamine hydrochloride inhibits cyp2d and cyp3a activities and down-regulates their mrna transcription and protein expression. phenoprolamine hydrochloride can efficiently penetrate through blood brain barrier and inhibit the contraction of vascular smooth muscle in the brain.
Phloracetophenone；2,4,6-三羥基苯乙酮2,4,6-trihydroxyacetophenone|||1-(2,4,6-Trihydroxyphenyl)ethanone；2,4, (2024/9/4)
簡(jiǎn)介：phloracetophenone (1-(2,4,6-trihydroxyphenyl)ethanone) has antiobesity and hypolipidemic effects, may be partly mediated by delaying the intestinal absorption of dietary fat by inhibiting pancreatic lipase activity.
Phenanthriplatin；化合物 T28398cis-[Pt(NH3)2-(phenanthridine)Cl]NO3；cis-[Pt(NH3)2-(phenanthridine)Cl]NO3 (2024/9/4)
簡(jiǎn)介：phenanthriplatin, also known as cis-[pt(nh3)2-(phenanthridine)cl]no3, is a new drug candidate. it belongs to a family of platinum(ii)-based agents which includes cisplatin, oxaliplatin and carboplatin. phenanthriplatin acts as a covalent poison of topoisomerase ii cleavage complexes. phenanthriplatin exhibits significantly greater activity than cisplatin and oxaliplatin. the cellular uptake of phenanthriplatin is substantially greater than that of cisplatin and pyriplatin because of the hydropho
Phenaglycodol；化合物 T28397Atadiol|||Felixin|||Puasital|||Sedapsin|||Acalmid；Atadiol|||Felixin|||Puasit (2024/9/4)
簡(jiǎn)介：chlordimeform hydrochloride is an acaricide.
PGP-4008；化合物PGP-4008PGP 4008|||PGP4008；PGP 4008|||PGP4008 (2024/9/4)
簡(jiǎn)介：pgp-4008 is a selective and potent p-glycoprotein (pgp) inhibitor that inhibits tumor growth by co-administration with doxorubicin.
PG-116800；化合物PG-116800PG-530742|||PGE-7113313|||PGE 7113313|||PG 530742；PG-530742|||PGE-7113313|||PG (2024/9/4)
簡(jiǎn)介：pg-116800 (pg-530742) is a matrix metalloproteinase (mmp) inhibitor. pg-116800 can be used in studies about the treatment of osteoarthritis.
Pfn1-IN-C2；化合物 T28393Pfn1 inhibitor C2；Pfn1 inhibitor C2 (2024/9/4)
簡(jiǎn)介：pfn1-in-c2, an inhibitor of profilin1 (pfn1), has been shown to reduce the overall level of cellular filamentous (f)-actin, slow ec migration and proliferation, and inhibit the angiogenic ability of ec both in vitro and ex vivo.
Pfn1-IN-C1；化合物 T28392Pfn1INC1|||Pfn1 IN C1|||Pfn1 inhibitor C1；Pfn1INC1|||Pfn1 IN C1|||Pfn1 inhibito (2024/9/4)
簡(jiǎn)介：pfn1-in-c1, an inhibitor of profilin1 (pfn1), has been shown to reduce the overall level of cellular filamentous (f)-actin, slow ec migration and proliferation, and inhibit the angiogenic ability of ec both in vitro and ex vivo.
PF-9404C；化合物 T28391PF9404C；PF9404C (2024/9/4)
簡(jiǎn)介：pf-9404c is the s-s diesteroisomer of a beta adrenergic receptors blocker with vasodilatory properties. pf9404c increased the formation of cyclic gmp from 3 pmol mg?1 protein in basal conditions, to 53 pmol mg?1 protein in 10 μm in rat aorta smooth muscle cells.
低溫高壓樣本冷凍艙3750 (2024/9/4)
簡(jiǎn)介：美國(guó)ems授權(quán)經(jīng)銷(xiāo)商、原裝進(jìn)口、質(zhì)量保證、更多產(chǎn)品問(wèn)題請(qǐng)聯(lián)系我司銷(xiāo)售。
PF9238；化合物 T28390PF 9238|||PF-9238；PF 9238|||PF-9238 (2024/9/4)
簡(jiǎn)介：pf9238 is an inhibitor of beta-secretase i. pf9238 has a catd potency of 12 um in vivo.
零擔(dān)運(yùn)輸：佛山到臨汾市堯都物流公司-物流電話(huà) (2024/9/4)
簡(jiǎn)介：
Orsellinic acid；苷色酸Orsellinic acid (2024/9/4)
簡(jiǎn)介：orsellinic acid is a phenolic acid extracted from lichens.
PF-6422899；化合物 T28389PF6422899|||PF 6422899；PF6422899|||PF 6422899 (2024/9/4)
簡(jiǎn)介：pf-6422899 irreversibly inhibits egfr kinase activity by binding covalently to active-site cysteine residues in the atp binding pocket of egfr.
PF-5274857 mseylate (1373615-35-0 free base)；化合物 T28388PF5274857 HCl|||PF 5274857|||PF-5274857|||PF- (2024/9/4)
簡(jiǎn)介：pf-5274857 is a potent, orally active and selective inhibitor of hedgehog (hh) signaling pathway (ic50 = 5.8 nm, ki = 4.6 nm) . pf-5274857 effectively penetrates the blood-brain barrier and inhibits smo activity in the brain of primary medulloblastoma mice, resulting in improved animal survival rates.
PF-4950834；化合物 T28387PF 4950834|||PF4950834；PF 4950834|||PF4950834 (2024/9/4)
簡(jiǎn)介：pf-4950834, a atp-competitive, selective rho kinase inhibitor, provides therapeutic benefits in chronic inflammatory diseases.
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