9月
Carboxyamidotriazole；化合物 T14872CAI|||L-651582；CAI|||L-651582 (2024/9/1)
简介：carboxyamidotriazole is a cytostatic inhibitor of non-voltage-operated calcium channels and calcium channel-mediated signaling pathways. it shows anti-inflammatory, anti-tumor, and antiangiogenic effects.
Carboxyamidotriazole Orotate；化合物Carboxyamidotriazole OrotateL-651582 Orotate|||CAI Orotate；L-651582 (2024/9/1)
简介：carboxyamidotriazole orotate (l-651582 orotate) is a cytostatic inhibitor of non-voltage-operated calcium channels and calcium channel-mediated signaling pathways. carboxyamidotriazole orotate (l-651582 orotate) is the orotate salt form of carboxyamidotriazole (cai), an orally bioavailable signal transduction inhibitor that in vitro has been shown to possess antileukaemic activities. carboxyamidotriazole orotate shows anti-tumor, anti-inflammatory, and antiangiogenic effects.
Carboxy-PEG5-sulfonic acid；化合物 T14870Carboxy-PEG5-sulfonic acid (2024/9/1)
简介：carboxy-peg5-sulfonic acid, a peg-based protac linker, is utilized for the synthesis of protacs[1].
Fluvastatin sodium；氟伐他汀钠XU 62320 sodium|||XU-62-320|||Fluvastatin sodium salt；XU 62320 sodium|||XU-6 (2024/9/1)
简介：fluvastatin sodium (fluvastatin sodium salt), a competitive inhibitor of hydroxymethylglutaryl-coenzyme a reductase (hmgcr), is a commonly used cholesterol lowering agent.
Carboxy-PEG4-sulfonic acid；化合物 T14869Carboxy-PEG4-sulfonic acid (2024/9/1)
简介：carboxy-peg4-sulfonic acid is a peg-based linker commonly employed in protac synthesis [1].
Carboxy-PEG2-sulfonic acid；化合物 T14866Carboxy-PEG2-sulfonic acid (2024/9/1)
简介：carboxy-peg2-sulfonic acid is a polyethylene glycol (peg)-derived linker, specifically designed for the synthesis of proteolysis-targeting chimeras (protacs)[1].
Carboprost tromethamine；卡前列素氨基丁三醇Carboprost tromethamine (2024/9/1)
简介：carboprost tromethamine, a synthetic 15-methyl analogue of prostaglandin f2α, effectively promotes uterine contractions and significantly reduces bleeding during and post-delivery.
Caracemide；卡醋胺NSC-253272；NSC-253272|||卡醋胺 (2024/9/1)
简介：caracemide (nsc-253272) inhibits the enzyme ribonucleotide reductase of escherichia coli. caracemide can be used in anticancer studies.
Carabersat；卡拉博沙SB 204269；SB 204269 (2024/9/1)
简介：carabersat（sb 204269） is a novel and effective anticonvulsant and antiepileptic agent.
Caprylic/Capric Triglyceride；辛癸酸甘油酯Caprylic/Capric Triglyceride (2024/9/1)
简介：caprylic/capric triglyceride, a compound consisting of triglycerides and esters derived from fractionated vegetable oil, and fatty acids from coconut and palm kernel oils, serves as a food additive and is utilized in cosmetics. this substance demonstrates outstanding oxidation stability.
Camobucol；化合物 T14861AGIX 4207；AGIX 4207 (2024/9/1)
简介：camobucol is an orally active, anti-inflammatory compound. it also is a phenolic antioxidant with antirheumatic properties.
CaMKII-IN-1；化合物CaMKII-IN-1CaMKII-IN-1 (2024/9/1)
简介：camkii-in-1 is a potent and highly selective inhibitor of camkii (ic50 = 63 nm). camkii-in-1 exhibited more than 100-fold higher selectivity for camkii over camkiv, mlck, p38a, akt1, and pkc.
Oseltamivir phosphate；磷酸奥司他韦GS 4104；GS 4104|||磷酸奥司他韦 (2024/9/1)
简介：oseltamivir phosphate (gs 4104) is the phosphate salt of oseltamivir, a synthetic derivative prodrug of ethyl ester with antiviral activity. by blocking neuraminidases on the surfaces of influenza viruses, oseltamivir interferes with host cell release of complete viral particles.
Calyculin A；化合物 T14859(-)-Calyculin A；(-)-Calyculin A (2024/9/1)
简介：calyculin a is a potent and cell-permeable inhibitor of protein phosphatase 1 (pp1; ic50s: 2 nm). it also is a protein phosphatase 2a (pp2a) inhibitor (ic50s: 0.5-1 nm).
Calicheamicin；卡奇霉素Calicheamicin γ1；Calicheamicin γ1|||卡奇霉素 (2024/9/1)
简介：calicheamicin (calicheamicin γ1) is an antitumor antibiotic and is a dna synthesis inhibitor. it also is a cytotoxic agent that causes double-strand dna breaks.
Caldaret；化合物 T14857MCC-135；MCC-135 (2024/9/1)
简介：caldaret is an intracellular ca2+ handling modulator that acts through reverse mode na+/ca2+ exchanger inhibition.
Calcipotriol；卡泊三醇MC 903|||Calcipotriene；MC 903|||卡泊三醇|||Calcipotriene (2024/9/1)
简介：calcipotriol (mc 903) is a synthetic vitd3 analogue. which has a high affinity for the vitamin d receptor.
Calcein；钙黄绿素Fluorexon；Fluorexon|||钙黄绿素 (2024/9/1)
简介：calcein (fluorexon) is a fluorescent dye and self-quenching probe that used as an indicator of lipid vesicle leakage, and a complexometric indicator for titration of calcium ions with edta, and for fluorometric determination of calcium.
Caerulomycin A；浅蓝霉素Cerulomycin|||Caerulomycin；浅蓝霉素|||Cerulomycin|||Caerulomycin (2024/9/1)
简介：caerulomycin a (caerulomycin) (cerulomycin; caerulomycin) is an antifungal compound. which induces generation of t cells, enhances tgf-β-smad3 protein signaling via suppressing interferon-γ-induced stat1 signaling. antifungal and antibiotic activity, and used in autoimmune diseases.
Cabergoline；卡麦角林FCE-21336；FCE-21336|||卡麦角林 (2024/9/1)
简介：cabergoline (fce-21336) is an ergot derived-dopamine d2-like receptor agonist. it has high affinity for d2, d3, and 5-ht2b receptors (ki=0.7, 1.5, and 1.2, respectively).cabergoline permits rapid and effective hormonal and tumor control by normalizing prolactin-producing pituitary adenomas levels.
C527；化合物C527C527 (2024/9/1)
简介：c527 is a is a pan dub enzyme inhibitor. which has a high potency for the usp1/uaf1 complex (ic50=0.88 μm).
C2-Bis-phosphoramidic acid diethyl ester；化合物 T14851C2-Bis-phosphoramidic acid diethyl ester (2024/9/1)
简介：c2-bis-phosphoramidic acid diethyl ester is an alkyl chain-derived protac linker utilized for the synthesis of protacs[1].
C-NH-Boc-C-Bis-(C1-PEG1-PFP)；化合物 T14850C-NH-Boc-C-Bis-(C1-PEG1-PFP) (2024/9/1)
简介：c-nh-boc-c-bis-(c1-peg1-pfp) is a polyethylene glycol (peg)-derived protac linker, which finds application in the synthesis of protacs[1].
Methotrexate；甲氨蝶呤NCI-C04671|||WR19039|||Amethopterin|||CL14377；NCI-C04671|||WR19039|||Amethopterin|| (2024/9/1)
简介：methotrexate (wr19039) is a folate analog, an inhibitor of the dihydrofolate reductase dhfr. methotrexate has antimetabolic, antitumor, and immunosuppressive activities, and is commonly used in rheumatoid arthritis and various tumors.
Perindopril erbumine；培哚普利叔丁胺S9490-3|||Perindopril tert-butylamine salt；培哚普利叔丁胺|||培哚普利叔丁胺盐|||S9490-3| (2024/9/1)
简介：perindopril erbumine (s9490-3) is the tert-butylamine salt of perindopril, the ethyl ester of a non-sulfhydryl angiotensin-converting enzyme (ace) inhibitor with antihypertensive activity. upon hydrolysis, perindopril erbumine (s9490-3) is converted to its active form perindoprilat, inhibiting ace and the conversion of angiotensin i to angiotensin ii; consequently, angiotensin ii-mediated vasoconstriction and angiotensin ii-stimulated aldosterone secretion from the adrenal cortex are inhibited a
C-NH-Boc-C-Bis-(C-PEG1-Boc)；化合物 T14849C-NH-Boc-C-Bis-(C-PEG1-Boc) (2024/9/1)
简介：c-nh-boc-c-bis-(c-peg1-boc) is a versatile alkyl/ether-based protac linker for synthesizing protacs[1].
C 87；化合物C 87C 87 (2024/9/1)
简介：c 87 is a small-molecule tnf-α inhibitor. c 87 directly binds to tnfα, potently inhibits tnf-α-induced cytotoxicity (ic50 = 8.73 μm), and effectively blocks tnf-α-triggered signaling activities.
B I09；化合物B I09B I09 (2024/9/1)
简介：b i09, an ire-1 rnase inhibitor with an ic50 of 1230 nm, inhibits splicing of xbp1 mrna in human wac3 cells and expression of xbp-1 in lps-stimulated b cells. b i09 can be used to simulate the defects of xbp-1 in cll cells., an ire-1 rnase inhibitor with an ic50 of 1230 nm, inhibits splicing of xbp1 mrna in human wac3 cells and expression of xbp-1 in lps-stimulated b cells. b i09 can be used to simulate the defects of xbp-1 in cll cells., an ire-1 rnase inhibitor with an ic50 of 1230 nm, inhibit
Bz 423化合物Bz 423BZ48 (2024/9/1)
简介：bz 423 is a potent immunomodulator that induces apoptosis by activating bax and bak to induce mitochondrial outer membrane permeabilization and cytochrome c release.bz 423 shows partial activity in a mouse model of lupus.
BX471 hydrochloride化合物 T14845ZK-811752 hydrochloride (2024/9/1)
简介：bx471 hydrochloride (zk-811752 hydrochloride) is a potent, selective non-peptide ccr1 antagonist (ki: 1 nm for human ccr1). it shows 250-fold selectivity for ccr1 over ccr2, ccr5, and cxcr4.
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