计算溶液所需的质量、体积或浓度。
| 活性类型 | 活性值-log(M) | 作用机制 | 期刊 | 参考文献(PubMed IDs) |
|---|
有货
为什么选择此级别
Moligand™ 级 提供 ≥98% 纯度，适用于对基线干扰要求严格的色谱和分析工作流程。
储存与运输
-20°C储存。超低温运输 。请查阅批次 COA 获取详细规格。
质量文档
SDS、COA、产品数据表及规格说明书均可下载。可通过批号查询获取批次 COA。
文献证明
在色谱分析、有机合成和交叉偶联反应领域已被 23 篇同行评审文献引用。
概述
Probenecid 是一种经典的有机阴离子运输竞争性抑制剂,同时也是一种瞬时感受器电位香草素受体亚家族2(TRPV2)的激动剂和人苦味觉感受器TAS2R16的抑制剂。An inhibitor of several ABC-transporters of the subfamily ABCC or MRP.
Probenecid is a classical competitive inhibitor of organic anion transport, which is also a TRPV2 agonist and an inhibitor of TAS2R16.
An inhibitor of several ABC-transporters of the subfamily ABCC or MRP.
规格
英文别名
PROBENECID (USP IMPURITY) | Benemid; Benecid; Benuryl | Benzoic acid, 4-((dipropylamino)sulfonyl)- | PROBENECID [WHO-IP] | Spectrum3_000554 | PROBAMPACIN COMPONENT PROBENECID | PROBENECID COMPONENT OF PROBAMPACIN | Probenecide | DTXCID901188 | Probexin |
规格或纯度
Moligand™, ≥98%
英文名称
Probenecid
生化机理
ABC转运蛋白抑制剂。竞争性MRP1阻滞剂。Pannexin通道阻滞剂（IC 50 = 150μM）。可用于阻断细胞内染料和指示剂的流出。
应用
An inhibitor of several ABC-transporters of the subfamily ABCC or MRP.
储存条件
-20°C储存
运输条件
超低温运输
作用类型
抑制剂
作用机制
溶质运载家族 22 成员 11 抑制剂
备注
如果有可能，您尽量在使用的当天配置溶液，并在当天使用完它。但是，如果您需要预先配制储备溶液，我们建议您将溶液等份保存在-20°C的密封小瓶中。通常，它们最多可以使用一个月。在使用前和打开样品瓶之前，我们建议您让您的产品在室温下平衡至少1小时。需要更多关于溶解度，用法和处理的建议吗？请访问我们的常见问题（FAQ）页面以获取更多详细信息。
纯度
≥98%
名称和识别符
PubChem SID
EC号
200-344-3
分子类型
小分子
IUPAC Name
4-(dipropylsulfamoyl)benzoic acid
INCHI
1S/C13H19NO4S/c1-3-9-14(10-4-2)19(17,18)12-7-5-11(6-8-12)13(15)16/h5-8H,3-4,9-10H2,1-2H3,(H,15,16)
InChi Key
DBABZHXKTCFAPX-UHFFFAOYSA-N
Smiles
CCCN(CCC)S(=O)(=O)C1=CC=C(C=C1)C(=O)O
Isomeric SMILES
CCCN(CCC)S(=O)(=O)C1=CC=C(C=C1)C(=O)O
UN Number
Packing Group
II
分子量
285.36
Reaxy-Rn
2815775
Reaxys-RN link address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2815775&ln=
技术文档
高级数据
系统学分类
分类树（Taxonomy Tree）
| 界（kingdom) | 有机化合物 |
|---|---|
| 超类（Superclass) | 苯类化合物 |
| 类（Class) | 苯及其取代衍生物 |
| 亚类（Subclass） | 苯磺酰胺类 |
| 中间层级节点（Intermediate Tree Nodes） | 暂无 |
| 直接上位类(Direct Parent) | 苯磺酰胺类 |
| 其他上位类（Alternative Parents） | 苯甲酸 苯磺酰基化合物 苯甲酰衍生物 有机磺酰胺 氨基磺酰基化合物 一元羧酸及其衍生物 羧酸 有机光子化合物 有机氧化合物 有机氮化合物 有机氧化物 碳氢化合物衍生物 |
| 分子骨架（Molecular Framework) | 芳香族同单环化合物 |
| 取代基（Substituents） | 氨基磺酰基化合物 - 芳香族同单环化合物 - 苯磺酰胺 - 苯磺酰基 - 苯甲酸 - 苯甲酸或衍生物 - 苯甲酰 - 羧酰胺基 - 羧酸衍生物 - 烃衍生物 - 单羧酸或其衍生物 - 有机硝基化合物 - 有机氧化物 - 有机氧化合物 - 有机磺酸或其衍生物 - 有机氮化合物 - 有机氧化合物 - 有机氮化合物 - 有机硫酰胺 - 有机磺酸或其衍生物 - 有机硫化合物 - 磺酰基 |
| 描述（Description） | 该化合物属于苯磺酰胺类有机化合物。这类化合物含有通过S键连接至苯环的磺酰胺基团。 |
| 外部描述符（External Descriptors） | sulfonamide - benzoic acids |
三维结构
交互式化学结构模型
产品属性
| ALogP | 3.2 |
|---|
关联靶点（人）
SLC22A6
Tclin
溶质载体家族 22 成员 6(Solute carrier family 22 member 6)
(1 活性数据)
SLCO1C1
Tbio
溶质载体有机阴离子转运蛋白家族成员1C1(Solute carrier organic anion transporter family member 1C1)
(0 活性数据)
TAS2R38
Tchem
2 型味觉受体成员 38(Taste receptor type 2 member 38)
(0 活性数据)
TRPV2
Tchem
瞬时受体电位阳离子通道亚家族V成员2(Transient receptor potential cation channel subfamily V member 2)
(1 活性数据)
CA2
Tclin
碳酸酐酶2(Carbonic anhydrase 2)
(3 活性数据)
CA9
Tclin
碳酸酐酶9(Carbonic anhydrase 9)
(3 活性数据)
TAS2R16
Tchem
型味觉受体成员 16(Taste receptor type 2 member 16)
(0 活性数据)
PDE5A
Tclin
Phosphodiesterase 5A
(5113 活性数据)
EGFR
Tclin
Epidermal growth factor receptor erbB1
(33727 活性数据)
CA2
Tclin
Carbonic anhydrase II
(17698 活性数据)
ESR1
Tclin
Estrogen receptor alpha
(17718 活性数据)
HMGCR
Tclin
HMG-CoA reductase
(2475 活性数据)
NR3C1
Tclin
Glucocorticoid receptor
(14987 活性数据)
INSR
Tclin
Insulin receptor
(5558 活性数据)
PGR
Tclin
Progesterone receptor
(8562 活性数据)
ADRB2
Tclin
Beta-2 adrenergic receptor
(11824 活性数据)
CHRM2
Tclin
Muscarinic acetylcholine receptor M2
(10671 活性数据)
ADRB1
Tclin
Beta-1 adrenergic receptor
(6630 活性数据)
HTR1A
Tclin
Serotonin 1a (5-HT1a) receptor
(14969 活性数据)
ADRA2A
Tclin
Alpha-2a adrenergic receptor
(9450 活性数据)
AR
Tclin
Androgen Receptor
(11781 活性数据)
CHRM1
Tclin
Muscarinic acetylcholine receptor M1
(12690 活性数据)
VDR
Tclin
Vitamin D receptor
(26531 活性数据)
ACE
Tclin
Angiotensin-converting enzyme
(1423 活性数据)
DRD2
Tclin
Dopamine D2 receptor
(23596 活性数据)
GABRA1
Tclin
GABA receptor alpha-1 subunit
(399 活性数据)
MAOA
Tclin
Monoamine oxidase A
(11911 活性数据)
CNR1
Tclin
Cannabinoid CB1 receptor
(20913 活性数据)
DRD1
Tclin
Dopamine D1 receptor
(9720 活性数据)
DRD4
Tchem
Dopamine D4 receptor
(7907 活性数据)
ACHE
Tclin
Acetylcholinesterase
(18204 活性数据)
PTGS1
Tclin
Cyclooxygenase-1
(9233 活性数据)
SLC6A2
Tclin
Norepinephrine transporter
(10102 活性数据)
HRH2
Tclin
Histamine H2 receptor
(5428 活性数据)
ADRA1D
Tclin
Alpha-1d adrenergic receptor
(4171 活性数据)
HTR1B
Tclin
Serotonin 1b (5-HT1b) receptor
(2801 活性数据)
HTR2A
Tclin
Serotonin 2a (5-HT2a) receptor
(14758 活性数据)
HTR2C
Tclin
Serotonin 2c (5-HT2c) receptor
(11471 活性数据)
AVPR2
Tclin
Vasopressin V2 receptor
(2912 活性数据)
ADORA1
Tclin
Adenosine A1 receptor
(17603 活性数据)
AGTR1
Tclin
Type-1 angiotensin II receptor
(5176 活性数据)
CALCR
Tclin
Calcitonin receptor
(2215 活性数据)
SLC6A4
Tclin
Serotonin transporter
(12625 活性数据)
ADRA1A
Tclin
Alpha-1a adrenergic receptor
(8359 活性数据)
PTGS2
Tclin
Cyclooxygenase-2
(13999 活性数据)
HRH1
Tclin
Histamine H1 receptor
(7573 活性数据)
ADRA1B
Tclin
Alpha-1b adrenergic receptor
(2912 活性数据)
OPRM1
Tclin
Mu opioid receptor
(19785 活性数据)
DRD3
Tclin
Dopamine D3 receptor
(14368 活性数据)
AVPR1A
Tclin
Vasopressin V1a receptor
(5412 活性数据)
OPRD1
Tclin
Delta opioid receptor
(15096 活性数据)
OPRK1
Tclin
Kappa opioid receptor
(16155 活性数据)
HTR3A
Tclin
Serotonin 3a (5-HT3a) receptor
(3366 活性数据)
SLC6A3
Tclin
Dopamine transporter
(10535 活性数据)
GRIN1
Tclin
Glutamate (NMDA) receptor subunit zeta 1
(122 活性数据)
KCNH2
Tclin
HERG
(29587 活性数据)
HTR4
Tclin
Serotonin 4 (5-HT4) receptor
(2068 活性数据)
关联靶点（其它种属）
Agtr2
Angiotensin II type 2 (AT-2) receptor (803 活性数据)
Mc4r
Melanocortin receptor 4 (1205 活性数据)
Ltc4s
Leukotriene C4 synthase (1 活性数据)
Sigmar1
Sigma opioid receptor (160 活性数据)
Npy1r
Neuropeptide Y receptor type 1 (8 活性数据)
Cckar
Cholecystokinin A receptor (90 活性数据)
Pde4d
Phosphodiesterase 4D (4 活性数据)
Abcc1
Multidrug resistance-associated protein 1 (42 活性数据)
Abcb1b
P-glycoprotein 1 (174 活性数据)
Nos2
Nitric oxide synthase, inducible (3573 活性数据)
Mapk1
MAP kinase ERK2 (650 活性数据)
Hdac6
Histone deacetylase 6 (222 活性数据)
Mmp9
Matrix metalloproteinase 9 (38 活性数据)
Pseudomonas aeruginosa (123386 活性数据)
Klebsiella pneumoniae (43867 活性数据)
Staphylococcus aureus (210822 活性数据)
Acinetobacter baumannii (41033 活性数据)
Escherichia coli (133304 活性数据)
Plasmodium falciparum (966862 活性数据)
Cryptococcus neoformans (21258 活性数据)
Candida albicans (78123 活性数据)
Pan troglodytes (415 活性数据)
Rattus norvegicus (775804 活性数据)
Slc10a1
Bile acid transporter (65 活性数据)
rep
Replicase polyprotein 1ab (378 活性数据)
Trpa1
Transient receptor potential cation channel subfamily A member 1 (1003 活性数据)
Slc22a20
Solute carrier family 22 member 20 (86 活性数据)
| 活性类型 | Relation | Activity value | Units | Action Type | 期刊 | PubMed Id | doi | Assay Aladdin ID |
|---|
Slc22a6
Solute carrier family 22 member 6 (141 活性数据)
Plasma (328 活性数据)
Slc22a5
Solute carrier family 22 member 5 (44 活性数据)
fba
Putative fructose-1,6-bisphosphate aldolase (15559 活性数据)
Slco1a1
Solute carrier organic anion transporter family member 1A1 (265 活性数据)
Slco1a4
Solute carrier organic anion transporter family member 1A4 (114 活性数据)
Slc22a19
Putative organic anion transporter 5 (5 活性数据)
| 活性类型 | Relation | Activity value | Units | Action Type | 期刊 | PubMed Id | doi | Assay Aladdin ID |
|---|
Slco1c1
Solute carrier organic anion transporter family member 1C1 (11 活性数据)
Slco1a3
Solute carrier organic anion transporter family member 1A3 (65 活性数据)
Glra2
Glycine receptor (1745 活性数据)
SARS-CoV-2 (38078 活性数据)
作用机制
| 作用机制 | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | 参考文献 |
|---|
化学和物理性质
溶解性
Soluble in water (partly miscible), solutions of alkali hydroxides,, ethanol (100 mM), acetone, chloroform, sodium hydroxide (1 M), DMSO (100 mM), methanol, dilute acids (practically insoluble), dilute alkalies, and ether (slightly soluble).
熔点
198-199°C
分子量
285.360 g/mol
XLogP3
3.200
氢键供体数Hydrogen Bond Donor Count
1
氢键受体数Hydrogen Bond Acceptor Count
5
可旋转键计数Rotatable Bond Count
7
精确质量Exact Mass
285.103 Da
单同位素质量Monoisotopic Mass
285.103 Da
拓扑极表面积Topological Polar Surface Area
83.100 Ų
重原子数Heavy Atom Count
19
形式电荷Formal Charge
0
复杂度Complexity
374.000
同位素原子数Isotope Atom Count
0
定义的原子立体中心计数Defined Atom Stereocenter Count
0
未定义的原子立体中心计数Undefined Atom Stereocenter Count
0
定义的键立体中心计数Defined Bond Stereocenter Count
0
未定义的键立体中心计数Undefined Bond Stereocenter Count
0
所有立体化学键的总数The total count of all stereochemical bonds
0
共价键合单元计数Covalently-Bonded Unit Count
1
安全和危险性（GHS）
象形图
信号词
警告
危险声明
H302: 吞食有害
预防措施声明
P264: 处理后要彻底洗手。
P270: 使用本产品时，请勿进食、饮水或吸烟。
P330: 漱口
P301+P312: 如误吞咽：如感觉不适，呼叫急救中心/医生。
P501: 将内容物/容器处理到。。。
WGK Germany
3
RTECS
DG9400000
Class
6.1
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
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分析证书 | P129440 |
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分析证书 | P129440 |
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分析证书 | P129440 |
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技术文档和文章
此产品的引用文献
引用文献
| 1. Xiao Fei, Jiang Haizhou, Li Zi, Jiang Xiaoxue, Chen Shanghai, Niu Yuguo, Yin Hanrui, Shu Yousheng, Peng Bo, Lu Wei, Li Xiaoying, Li Zhigang, Lan Shujue, Xu Xiaoyan, Guo Feifan. (2023) Reduced hepatic bradykinin degradation accounts for cold-induced BAT thermogenesis and WAT browning in male mice. Nature Communications, 14 (1): (1-17). [PMID:37130842] [10.1038/s41467-023-38141-0] |
| 2. Fan Wu, Ting Zhao, Yu Zhang, Yan Wang, Guoxin Liao, Baojing Zhang, Chao Wang, Xiangge Tian, Lei Feng, Bangjiang Fang, Xiaokui Huo, Xiaochi Ma. (2023) Beneficial herb-drug interaction of rhein in Jinhongtang and Imipenem/Cilastatin mediated by organic anion transporters. JOURNAL OF ETHNOPHARMACOLOGY, [PMID:37023835] [10.1016/j.jep.2023.116449] |
| 3. Chen Sun, Mingyu Zhang, Yanhong Zhao, Jianxin Pang, Ying Peng, Jiang Zheng. (2020) An LC-MS/MS- and hURAT1 cell-based approach for screening of uricosuric agents. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, [PMID:32905987] [10.1016/j.jchromb.2020.122336] |
| 4. Qingquan Zeng, Mengru Bai, Cui Li, Shuanghui Lu, Zhiyuan Ma, Yunchun Zhao, Hui Zhou, Huidi Jiang, Dongli Sun, Caihong Zheng. (2019) Multiple Drug Transporters Contribute to the Placental Transfer of Emtricitabine. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, [PMID:31160284] [10.1128/AAC.00199-19] |
| 5. Yufeng Chen, Fan Xue, Guobin Xia, Zhenlei Zhao, Chun Chen, Yunhong Li, Ying Zhang. (2019) Transepithelial transport mechanisms of 7,8-dihydroxyflavone, a small molecular TrkB receptor agonist, in human intestinal Caco-2 cells. Food & Function, 10 (8): (5215-5227). [PMID:31384856] [10.1039/C9FO01007F] |
| 6. Peter Yaro, Jing Nie, Mingcheng Xu, Kui Zeng, Houhong He, Jianbiao Yao, Ruwei Wang, Su Zeng. (2019) Influence of organic anion transporter 1/3 on the pharmacokinetics and renal excretion of ginkgolides and bilobalide. JOURNAL OF ETHNOPHARMACOLOGY, [PMID:31325605] [10.1016/j.jep.2019.112098] |
| 7. Bin Lin, Libin Wan, Xiaojie Sun, Chuixiu Huang, Stig Pedersen-Bjergaard, Xiantao Shen. (2018) Electromembrane extraction of high level substances: A novel approach for selective recovery of templates in molecular imprinting. JOURNAL OF MEMBRANE SCIENCE, [10.1016/j.memsci.2018.09.056] |
| 8. Lili Wu, Yulian Chen, Han Liu, Zhikun Zhan, Zhi Liang, Tao Zhang, Zheng Cai, Ling Ye, Menghua Liu, Jie Zhao, Shuwen Liu, Lan Tang. (2018) Emodin-induced hepatotoxicity was exacerbated by probenecid through inhibiting UGTs and MRP2. TOXICOLOGY AND APPLIED PHARMACOLOGY, [PMID:30248416] [10.1016/j.taap.2018.09.029] |
| 9. Liu Yixian, Wang Yafeng, Peng Youmei, Liu Bingjie, Ma Fang, Jiang Jinhua, Wang Qingduan, Chang Junbiao. (2018) Effects of the antiretroviral drug 2'-deoxy-2'-β-fluoro-4'-azidocytidine (FNC) on P-gp, MRP2 and BCRP expressions and functions. PHARMAZIE, 73 (9): (503-507). [PMID:30223932] [10.1691/ph.2018.8555] |
| 10. Wei Li, Bi-De Liu, Kai Liao, Yong Liu, Zi-Jin Wan, Yu-Fen Dong, Qian-Qian Cao, Qian Zhu, Xiao Gu. (2018) Alteration of Androgen Receptor Protein Stability by Triptolide in LNCaP Cells. Medicina-Lithuania, 54 (3): (39). [PMID:30344270] [10.3390/medicina54030039] |
| 11. Yixian Liu, Bingjie Liu, Yan Zhang, Youmei Peng, Chenzheng Huang, Ning Wang, Jinhua Jiang, Qingduan Wang, Junbiao Chang. (2017) Intestinal absorption mechanisms of 2′-deoxy-2′-β-fluoro-4′-azidocytidine, a cytidine analog for AIDS treatment, and its interaction with P-glycoprotein, multidrug resistance-associated protein 2 and breast cancer resistance protein. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, [PMID:28487144] [10.1016/j.ejps.2017.05.009] |
| 12. Wen-Hao Yu, Na Zhang, Jin-Feng Qi, Chen Sun, Yong-Hui Wang, Mei Lin. (2015) Arsenic and Mercury Containing Traditional Chinese Medicine (Realgar and Cinnabar) Strongly Inhibit Organic Anion Transporters, Oat1 and Oat3, In Vivo in Mice. Biomed Research International, [PMID:26788513] [10.1155/2015/863971] |
| 13. Hongming Tang, Tao Hou, Han Zhou, Han Liao, Fangfang Xu, Xiaomin Xie, Wenjie Yuan, Zhixin Guo, Yanfang Liu, Jixia Wang, Weijia Zhou, Xinmiao Liang. (2024) Label-free cell phenotypic profiling of histamine H4R receptor and discovery of non-competitive H4R antagonist from natural products. BIOORGANIC CHEMISTRY, [PMID:38643561] [10.1016/j.bioorg.2024.107387] |
| 14. Yueyuan Wang, Bo Lv, Kai Fan, Cunjin Su, Delai Xu, Jie Pan. (2024) Metabolic Disturbances in a Mouse Model of MPTP/Probenecid-Induced Parkinson’s Disease: Evaluation Using Liquid Chromatography-Mass Spectrometry. Neuropsychiatric Disease and Treatment, [PMID:39220601] [10.2147/NDT.S471744] |
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