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32

抑制剂 & 化合物

14

天然产物

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Cat. No. Product Name Target Signaling Pathways
T3116 Atorvastatin hemicalcium salt

Lipitor,Atorvastatin hemicalcium,Atorvastatin Calcium,CI-981,阿托伐他汀钙,Sortis

Ferroptosis; HMG-CoA Reductase; Autophagy Apoptosis; Autophagy; Metabolism
Atorvastatin hemicalcium salt (Atorvastatin Calcium) 是一种口服有效的 HMG-CoA 还原酶抑制剂 ,可用作降低胆固醇的药物。它抑制人 SV-SMC 增殖和侵袭,IC50分别为 0.39 μM 和 2.39 μM。
T29067 Upacicalcet

PLS-240,SK-1403,AJT-240

Calcium Channel Membrane transporter/Ion channel; Metabolism
Upacicalcet (AJT-240) 是一种静脉内拟钙剂,是一种可用于人血液透析的 SHPT, 通过直接作用于甲状旁腺细胞膜钙敏感受体来抑制过量的甲状旁腺激素 (PTH) 分泌,从而降低血液中的 PTH 水平。 3 Upacicalcet 是钙敏感受体的正变构调节剂,可预防大鼠腺嘌呤诱导的继发性甲状旁腺功能亢进模型中的血管钙化和骨骼疾病。
T69984 Ticalopride

5-HT Receptor GPCR/G Protein; Neuroscience
Ticalopride是一种5-HT3 receptor激动剂,可用于治疗消化系统疾病、口颌疾病、耳鼻咽喉疾病,可用于研究神经性贪食症、胃食管反流和肠易激综合征。
TQ0200 Paricalcitol

Paricalcitol 是一种 vitamin D receptor 激活剂,是一种 vitamin D 类似物,用于研究继发性甲状旁腺功能亢进,该疾病与慢性肾功能衰竭有关。
T4200 Sacubitril hemicalcium salt

AHU-377 (hemicalcium salt),LCZ696中间体,AHU377 calcium salt

Neprilysin Metabolism
Sacubitril hemicalcium salt (AHU377 calcium salt) 是一种有效的 NEP 抑制剂,IC50=5 nM。它是研究心力衰竭药物 LCZ696 的组分之一。
T29067L Upacicalcet HCl

Upacicalcet HCl(1333218-50-0 Free base)

CaSR GPCR/G Protein
Upacicalcet HCl 是一种静脉内拟钙剂,通过直接作用于甲状旁腺细胞膜钙敏感受体来抑制过量的甲状旁腺激素 (PTH) 分泌,从而降低血液中的 PTH 水平。Upacicalcet HCl 可用于治疗血液是一种新型继发性甲状旁腺功能亢进化合物,靶向钙敏感受体的氨基酸结合位点。
T0380 Bicalutamide

比卡鲁胺,ICI-176334

Androgen Receptor; Autophagy Autophagy; Endocrinology/Hormones
Bicalutamide (ICI-176334) 是一种具有口服活性的非甾体雄激素受体拮抗剂,可研究前列腺癌。
TP2048L α-helical CRF 9-41 acetate

肾上腺皮质素释放因子多肽α-helical CRF 9-41乙酸盐,α-helical CRF 9-41 acetate(90880-23-2 Free base)

CRFR GPCR/G Protein
α-helical CRF 9-41 acetate 是 CRF2 的竞争性拮抗剂 (KB = 100 nM) 和 CRF1 的部分激动剂 (EC50 = 140 nM)。
T62848 AMG 837 hemicalcium

AMG 837 hemicalcium 是一种有效的、口服具有活力的 GPR40/FFA1部分激动剂。AMG 837 hemicalcium 能够抑制 [3H]AMG 837 与人类 FFA1受体的特异性结合 (pIC50: 8.13)。AMG 837 hemicalcium 能够提高啮齿动物的胰岛素分泌,减少葡萄糖水平。
T82900 Bemfivastatin hemicalcium

PPD 10558 hemicalcium

Bemfivastatin (PPD 10558) hemicalcium 作为口服HMG-CoA还原酶抑制剂,具备有效的降脂作用并能增强肝脏提取活性。该化合物的未观察到不良反应水平(NOAEL)在大鼠发育毒性研究中超过320 mg/kg/d,在家兔母体毒性及发育毒性研究中分别超过12.5 mg/kg/d和25 mg/kg/d。Bemfivastatin hemicalcium 适用于对他汀类药物不耐受且患有他汀相关性高胆固醇血症性肌痛的研究。
T69385 Baicalein monohydrate

Baicalein monohydrate is an inhibitor of 12-lipoxygenase, leukotriene biosynthesis and release of lysosomal enzymes. It also inhibits cellular Ca2+ uptake and mobilization and adjuvant-induced arthritis.
T72101 Atorvastatin hemicalcium trihydrate

阿托伐他汀半钙三水合物,阿托他伐汀半钙三水合物

Atorvastatin hemicalcium trihydrate 是一种具有口服活性的 HMG-CoA 还原酶抑制剂,具有有效降低血脂的能力。Atorvastatin hemicalcium trihydrate 以 IC50值分别为 0.39 μM 和 2.39 μM 来抑制人 SV-SMC 细胞的增殖和侵袭。
T75891 α-Helical CRF(9-41) TFA

α-Helical CRF(9-41) TFA 是一种竞争性 CRF2受体拮抗剂,KB 约为 100 nM。α-Helical CRF(9-41) TFA 也是一种 CRF1受体的部分激动剂,EC50为 140 nM。
TP2048 α-Helical CRF(9-41)

α-helical CRF 9-41

Corticotropin-releasing factor receptor antagonist (Ki values are 17, 5 and 0.97 at human CRF1, rat CRF2α and mouse CRF2β receptors respectively).
T76360 a-Helical Corticotropin Releasing Factor (12-41)

a-Helical Corticotropin Releasing Factor (12-41),一种含有30个氨基酸的α螺旋促肾上腺皮质激素释放因子/激素类似物。作为下丘脑激素的促肾上腺皮质激素释放因子 (CRF) 能促进肾上腺皮质激素 (ACTH) 分泌,而a-Helical Corticotropin Releasing Factor (12-41) 则抑制该刺激效应。
T79916 4-Aminosalicylic acid hemicalcium

4-Aminosalicylic acid hemicalcium 是一种具有口服活性的抗结核药物,主要用于治疗肺结核。
T35817 Photoswitchable PAD Inhibitor (technical grade)

Photoswitchable PAD inhibitor is a photoactivated protein arginine deiminase (PAD) inhibitor and a derivative of BB-Cl-amidine that contains an azobenzene photoswitch allowing optical control of PAD activity.1 Without photoactivation, it is a weak inhibitor of PAD2 (IC50 = >100 μM) and is less potent than BB-Cl-amidine in inhibiting citrulline production in vitro (kinact/KIs = 2,300, 600, 1,000, and 10,510 M-1min-1 for PAD1-4, respectively) and does not inhibit histone H3 citrullination in HEK29...
T12283 O-Methyl Atorvastatin hemicalcium

Others Others
O-Methyl Atorvastatin is an impurity of Atorvastatin that is an orally active inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase, has the ability to effectively decrease blood lipids.
T62386 (R)-Bicalutamide

(R)-Bicalutamide 是一种 Bicalutamide 的 R 型对映体,是一种雄激素受体 (AR) 拮抗剂,表现出抗肿瘤效果。(R)-Bicalutamide 广泛的用于前列腺癌的研究。
T61232 (Rac)-Upacicalcet

(Rac)-Upacicalcet is a racemate of Upacicalcet, which serves as an intravenous calcimimetic agent. Upacicalcet acts by directly targeting calcium-sensing receptors on parathyroid cell membranes, effectively suppressing the release of excessive parathyroid hormone (PTH) and reducing blood PTH levels. This compound holds the potential for researching secondary hyperparathyroidism (SHPT) [1].
T12544 Proglumide hemicalcium

Others Others
Proglumide hemicalcium is a antagonist of nonpeptide and orally active cholecystokinin (CCK)-A/B receptors, has antiepileptic and antioxidant activities.
T76204 a-Helical Corticotropin Releasing Factor (9-41)

α-Helical Corticotropin Releasing Factor (9-41) 为corticotropin releasing factor (CRF)的拮抗剂,具有降低体内血浆生长激素(GH)水平的功能。
T36108 YW3-56 (hydrochloride) (technical grade)

YW3-56 (hydrochloride) (technical grade)

YW3-56 is an inhibitor of protein arginine deiminase 2 (PAD2) and PAD4 (IC50s = 0.5-1 and 1-5 μM, respectively).1It inhibits the growth of U2OS osteosarcoma cells (IC50= ~2.5 μM) in a p53-dependent mannerviainduction of SESN2 and subsequent inhibition of mTORC1. YW3-56 (10 mg/kg) reduces tumor growth in an S-180 murine sarcoma tumor model. It also inhibits tumor growth in the 1883 MDA-MB-231 breast cancer bone metastasis mouse xenograft model.2 1.Wang, Y., Li, P., Wang, S., et al.Anticancer pept...
T39444 Upacicalcet sodium

Upacicalcet (sodium) is an intravenous calcimimetic agent that acts directly on parathyroid cell membrane calcium-sensing receptors to suppress excessive parathyroid hormone (PTH) secretion, thereby lowering blood PTH levels. It is indicated for the research of secondary hyperparathyroidism (SHPT).
T70899 Vidofludimus hemicalcium

4sc-101 hemicalcium,SC12267 hemicalcium,4sc-101 hemicalcium ; SC12267 hemicalcium

Vidofludimus (4sc-101 ; SC12267) hemicalcium 是一种口服有效的二氢乳清酸脱氢酶 (DHODH) 的抑制剂,也是法尼醇 X 受体 (FXR) 调节剂。Vidofludimus hemicalcium 作为一种免疫调节剂,可用于研究自身免疫性疾病,如炎症性肠病 (IBD)。Vidofludimus hemicalcium 还可通过靶向FXR 用于脂肪肝的研究。
T79848 Icalcaprant

Opioid Receptor Endocrinology/Hormones; GPCR/G Protein; Neuroscience
Icalcaprant为κ阿片受体拮抗剂。
T12363 Paricalcitol-D6

Others Others
Paricalcitol-D6 is the deuterated form of Paricalcitol, which is used for the prevention and treatment of secondary hyperparathyroidism (excessive secretion of parathyroid hormone) associated with chronic renal failure.
T82372 Free radical scavenger 1

Free radical scavenger 1 (compound 8) 显示出对DPPH自由基的清除能力,其半数抑制浓度(IC50)为43.39 μg/ml。
T83665 α-Helical CRF (9-41) TFA

α-Helical Corticotropin-Releasing Factor (9-41)

α-Helical CRF (9-41) 是一种合成的皮质酮释放因子(CRF)拮抗剂。它在0.5至5 µM浓度范围内,能抑制CRF诱导的大鼠前叶垂体细胞释放促肾上腺皮质激素(ACTH)。在体内研究中,α-Helical CRF (9-41) (0.02-0.6 µmol/kg) 能够抑制未经麻醉的完整大鼠体内CRF诱导的ACTH释放,并在0.6 µmol/kg剂量下抑制大鼠应激诱导的ACTH释放。此外,α-Helical CRF (9-41) 在尼古丁诱导的条件性焦虑大鼠模型中增加社交互动时间,并减少小鼠的类似暴饮暴食的乙醇消费。
T79817 S1P1 agonist 6 hemicalcium

LPL Receptor GPCR/G Protein
S1P1 agonist 6 hemicalcium (Compound I) 为一S1P1激动剂,其通过抑制淋巴细胞迁移而降低免疫反应,适用于自身免疫性疾病研究中的免疫抑制剂。
T60496 Ketorolac hemicalcium

Ketorolac (RS37619) hemicalcium 是一种非选择性的 COX 抑制剂,对 COX-1 的 IC50 为 20 nM,对 COX-2 的 IC50 为 120 nM。 Ketorolac hemicalcium 是一种非甾体类抗炎药 (NSAID),可用作 0.5% 滴眼液,用于研究过敏性结膜炎、黄斑囊样水肿、术中瞳孔缩小和术后眼部炎症和疼痛等。 Ketorolac hemicalcium 也是一种可用于癌症研究的 DDX3 抑制剂 [1] [4]。
T125615 Floricaline

Floricaline 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T125615。

化合物

Atorvastatin hemicalcium salt
Cat.No: T3116
Synonym: Lipitor,Atorvastatin hemicalcium,Atorvastatin Calcium,CI-981,阿托伐他汀钙,Sortis
Target: Ferroptosis, HMG-CoA Reductase, Autophagy
Upacicalcet
Cat.No: T29067
Synonym: PLS-240,SK-1403,AJT-240
Target: Calcium Channel
Ticalopride
Cat.No: T69984
Synonym:
Target: 5-HT Receptor
Paricalcitol
Cat.No: TQ0200
Synonym:
Target:
Sacubitril hemicalcium salt
Cat.No: T4200
Synonym: AHU-377 (hemicalcium salt),LCZ696中间体,AHU377 calcium salt
Target: Neprilysin
Upacicalcet HCl
Cat.No: T29067L
Synonym: Upacicalcet HCl(1333218-50-0 Free base)
Target: CaSR
Bicalutamide
Cat.No: T0380
Synonym: 比卡鲁胺,ICI-176334
Target: Androgen Receptor, Autophagy
α-helical CRF 9-41 acetate
Cat.No: TP2048L
Synonym: 肾上腺皮质素释放因子多肽α-helical CRF 9-41乙酸盐,α-helical CRF 9-41 acetate(90880-23-2 Free base)
Target: CRFR
AMG 837 hemicalcium
Cat.No: T62848
Synonym:
Target:
Bemfivastatin hemicalcium
Cat.No: T82900
Synonym: PPD 10558 hemicalcium
Target:
Baicalein monohydrate
Cat.No: T69385
Synonym:
Target:
Atorvastatin hemicalcium trihydrate
Cat.No: T72101
Synonym: 阿托伐他汀半钙三水合物,阿托他伐汀半钙三水合物
Target:
α-Helical CRF(9-41) TFA
Cat.No: T75891
Synonym:
Target:
α-Helical CRF(9-41)
Cat.No: TP2048
Synonym: α-helical CRF 9-41
Target:
a-Helical Corticotropin Releasing Factor (12-41)
Cat.No: T76360
Synonym:
Target:
4-Aminosalicylic acid hemicalcium
Cat.No: T79916
Synonym:
Target:
Photoswitchable PAD Inhibitor (technical grade)
Cat.No: T35817
Synonym:
Target:
O-Methyl Atorvastatin hemicalcium
Cat.No: T12283
Synonym:
Target: Others
(R)-Bicalutamide
Cat.No: T62386
Synonym:
Target:
(Rac)-Upacicalcet
Cat.No: T61232
Synonym:
Target:
Proglumide hemicalcium
Cat.No: T12544
Synonym:
Target: Others
a-Helical Corticotropin Releasing Factor (9-41)
Cat.No: T76204
Synonym:
Target:
YW3-56 (hydrochloride) (technical grade)
Cat.No: T36108
Synonym: YW3-56 (hydrochloride) (technical grade)
Target:
Upacicalcet sodium
Cat.No: T39444
Synonym:
Target:
Vidofludimus hemicalcium
Cat.No: T70899
Synonym: 4sc-101 hemicalcium,SC12267 hemicalcium,4sc-101 hemicalcium ; SC12267 hemicalcium
Target:
Icalcaprant
Cat.No: T79848
Synonym:
Target: Opioid Receptor
Paricalcitol-D6
Cat.No: T12363
Synonym:
Target: Others
Free radical scavenger 1
Cat.No: T82372
Synonym:
Target:
α-Helical CRF (9-41) TFA
Cat.No: T83665
Synonym: α-Helical Corticotropin-Releasing Factor (9-41)
Target:
S1P1 agonist 6 hemicalcium
Cat.No: T79817
Synonym:
Target: LPL Receptor
Ketorolac hemicalcium
Cat.No: T60496
Synonym:
Target:
Floricaline
Cat.No: T125615
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T8206 Cycleanine

Others Others
Cycleanine 是一种高效血管选择性Ca- 拮抗剂,具有缓解疼痛、肌肉松弛和抗炎作用。它还具有有效的抗菌、抗真菌、抗疟原虫和细胞毒活性。
T2775 Baicalin

黄芩苷,黄岑苷,Baicalein 7-O-β-D-glucuronide

NF-κB; HIV Protease; GABA Receptor; Autophagy Autophagy; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience; NF-κB; Proteases/Proteasome
Baicalin (Baicalein 7-O-β-D-glucuronide) 是一种从黄芩中分离出来的脯氨酰内肽酶抑制剂,具有抗氧化、抗肿瘤、抗 HIV 的特性。
T3921 Punicalagin

安石榴甙,安石榴苷

SARS-CoV; HBV Microbiology/Virology
Punicalagin 是一种在石榴中发现的主要鞣花单宁,是可逆且非竞争性的3CLpro 抑制剂,有抗氧化、抗炎和抗癌作用。它有潜力研究 COVID-19 。
T4S1718 Punicalin

HBV; HIV Protease Microbiology/Virology; Proteases/Proteasome
Punicalin 是从Punica granatumL. 或Terminalia catappaL. 的叶子中分离的,一种可水解的单宁,具有抗炎活性。它是一种抗乙型肝炎病毒药物。
TN1427 Baicalin methyl ester

Anti-infection Microbiology/Virology
Baicalin methyl ester 是黄芩苷根的一种成分。
T2858 Baicalein

5,6,7-Trihydroxyflavone,黄芩素,黄芩黄素

Ferroptosis; Influenza Virus; ROS; Xanthine Oxidase Apoptosis; Immunology/Inflammation; Metabolism; Microbiology/Virology
Baicalein (5,6,7-Trihydroxyflavone) 是一种黄嘌呤氧化酶抑制剂,其IC50值为 3.12 μM。
TN3848 Dihydrobaicalein

PLK Cell Cycle/Checkpoint
Dihydrobaicalein 是 一种来自黄芩的天然产物, 一种PLK1抑制剂(IC50:6.3μM)。Dihydrobaicalein 对VRK2和PLK2有抑制作用。
T3551 D-Pantothenic acid hemicalcium salt

泛酸钙,D-Pantothenic Acid Calcium,D-泛酸半钙,Calpanate,Calcium D-pantothenate,Vitamin B5 calcium salt,Calcium pantothenate,Calcium D-Panthotenate

Apoptosis; Endogenous Metabolite Apoptosis; Metabolism
D-Pantothenic acid hemicalcium salt (Calcium pantothenate) 是一种水溶性维生素,能够减少苹果汁中的棒曲霉素。
TN3480 Baicalein 7-O-beta-D-ethylglucuronide

Others Others
Baicalein 7-O-beta-D-ethylglucuronide is a natural product from Scutellaria baicalensis Georgi.
TN3268 8,8''-Bibaicalein

Others Others
8,8''-Bibaicalein is a natural product from Scutellaria baicalensis.
TN1426 Baicalein 6-O-glucoside

Others Others
Baicalein 6-O-glucoside is a natural product from Thymus serpyllum L.
T80862 Vitamin B15 hemicalcium

Pangamic Acid hemicalcium

Vitamin B15 (Pangamic Acid) hemicalcium 是一种自然存在于植物种子中的化合物,具有促进细胞呼吸的作用。它包含了D-葡萄糖基二甲基氨基乙酸,并可作为免疫校正剂。Vitamin B15 hemicalcium 在多种疾病研究中有应用。
T10662 Calcimycin hemicalcium salt

Antibiotic A-23187 hemicalcium salt,A-23187 hemicalcium salt

Others Others
Calcimycin (A-23187) hemicalcium salt is an antibiotic and a unique divalent cation ionophore (like calcium and magnesium). It induces Ca2+-dependent cell death by increasing intracellular calcium concentration.
T82558 Dihydrobaicalin

Dihydrobaicalin,一种从黄芩(Scutellaria lateriflora L.) 中分离出的黄酮苷。

天然产物

Cycleanine
Cat.No: T8206
Synonym:
Target: Others
Baicalin
Cat.No: T2775
Synonym: 黄芩苷,黄岑苷,Baicalein 7-O-β-D-glucuronide
Target: NF-κB, HIV Protease, GABA Receptor, Autophagy
Punicalagin
Cat.No: T3921
Synonym: 安石榴甙,安石榴苷
Target: SARS-CoV, HBV
Punicalin
Cat.No: T4S1718
Synonym:
Target: HBV, HIV Protease
Baicalin methyl ester
Cat.No: TN1427
Synonym:
Target: Anti-infection
Baicalein
Cat.No: T2858
Synonym: 5,6,7-Trihydroxyflavone,黄芩素,黄芩黄素
Target: Ferroptosis, Influenza Virus, ROS, Xanthine Oxidase
Dihydrobaicalein
Cat.No: TN3848
Synonym:
Target: PLK
D-Pantothenic acid hemicalcium salt
Cat.No: T3551
Synonym: 泛酸钙,D-Pantothenic Acid Calcium,D-泛酸半钙,Calpanate,Calcium D-pantothenate,Vitamin B5 calcium salt,Calcium pantothenate,Calcium D-Panthotenate
Target: Apoptosis, Endogenous Metabolite
Baicalein 7-O-beta-D-ethylglucuronide
Cat.No: TN3480
Synonym:
Target: Others
8,8''-Bibaicalein
Cat.No: TN3268
Synonym:
Target: Others
Baicalein 6-O-glucoside
Cat.No: TN1426
Synonym:
Target: Others
Vitamin B15 hemicalcium
Cat.No: T80862
Synonym: Pangamic Acid hemicalcium
Target:
Calcimycin hemicalcium salt
Cat.No: T10662
Synonym: Antibiotic A-23187 hemicalcium salt,A-23187 hemicalcium salt
Target: Others
Dihydrobaicalin
Cat.No: T82558
Synonym:
Target:
TargetMol Loading
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