Determine the necessary mass, volume, or concentration for preparing a solution.
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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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F134784-250mg
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250mg |
3
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$34.90
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F134784-1g
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1g |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
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$89.90
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F134784-5g
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5g |
1
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$289.90
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ROCK2 inhibitor
| Synonyms | KBio3_000841 | 5-[(Hexahydro-1H-1,4-diazepin-1-yl)sulfonyl]isoquinoline | 5-((HEXAHYDRO-1H-1,4-DIAZEPIN-1-YL)SULFONYL)ISOQUINOLINE | cid_163751 | HMS1990G13 | Tocris-0541 | AB00490076-08 | BDBM14027 | 1-(5-Isoquinolinylsulfonyl)homopiperazine | ISOQUINOLI |
|---|---|
| Specifications & Purity | Moligand™, ≥98%(HPLC) |
| Biochemical and Physiological Mechanisms | ROCK2 inhibitor (IC 50 = 1.9 µM). Also shown to inhibit PRK2 (IC 50 = 4 µM), MSK1 (IC 50 = 5 µM), Rsk2 (IC 50 = 15 µM), PKA, p70 S6 Kinase, CaM Kinase and MLCK. Calcium antagonist and vasodilator. |
| Storage Temp | Store at -20°C |
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
| Grade | Moligand™ |
| Action Type | INHIBITOR |
| Mechanism of action | Rho-associated protein kinase inhibitor |
| Note | Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Toxic, refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Isoquinolines and derivatives |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Isoquinolines and derivatives |
| Alternative Parents | 1,4-diazepanes Pyridines and derivatives Organosulfonamides Benzenoids Sulfonyls Heteroaromatic compounds Dialkylamines Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Isoquinoline - 1,4-diazepane - Diazepane - Pyridine - Organosulfonic acid amide - Benzenoid - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Heteroaromatic compound - Secondary amine - Secondary aliphatic amine - Azacycle - Amine - Organic nitrogen compound - Organic oxide - Organosulfur compound - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as isoquinolines and derivatives. These are aromatic polycyclic compounds containing an isoquinoline moiety, which consists of a benzene ring fused to a pyridine ring and forming benzo[c]pyridine. |
| External Descriptors | Not available |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| Pubchem Sid | 504750685 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504750685 |
| IUPAC Name | 5-(1,4-diazepan-1-ylsulfonyl)isoquinoline |
| INCHI | InChI=1S/C14H17N3O2S/c18-20(19,17-9-2-6-15-8-10-17)14-4-1-3-12-11-16-7-5-13(12)14/h1,3-5,7,11,15H,2,6,8-10H2 |
| InChIKey | NGOGFTYYXHNFQH-UHFFFAOYSA-N |
| Smiles | C1CNCCN(C1)S(=O)(=O)C2=CC=CC3=C2C=CN=C3 |
| Isomeric SMILES | C1CNCCN(C1)S(=O)(=O)C2=CC=CC3=C2C=CN=C3 |
| Molecular Weight | 291.37 |
| Reaxy-Rn | 5482739 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5482739&ln= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Nov 19, 2024 | F134784 | |
| Certificate of Analysis | Nov 19, 2024 | F134784 | |
| Certificate of Analysis | Nov 19, 2024 | F134784 | |
| Certificate of Analysis | Nov 19, 2024 | F134784 | |
| Certificate of Analysis | May 11, 2024 | F134784 | |
| Certificate of Analysis | Jun 15, 2022 | F134784 | |
| Certificate of Analysis | Jun 15, 2022 | F134784 | |
| Certificate of Analysis | Jun 15, 2022 | F134784 | |
| Certificate of Analysis | Jun 15, 2022 | F134784 | |
| Certificate of Analysis | Jun 15, 2022 | F134784 | |
| Certificate of Analysis | Jun 15, 2022 | F134784 |
| Solubility | Soluble in DMSO |
|---|---|
| Molecular Weight | 291.370 g/mol |
| XLogP3 | 1.000 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 2 |
| Exact Mass | 291.104 Da |
| Monoisotopic Mass | 291.104 Da |
| Topological Polar Surface Area | 70.700 Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 421.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Xueyan Li, Xiaojiao Yin, Jiazhuang Pang, Zhiwu Chen, Jiyue Wen. (2023) Hydrogen sulfide inhibits lipopolysaccharide-based neuroinflammation-induced astrocyte polarization after cerebral ischemia/reperfusion injury. EUROPEAN JOURNAL OF PHARMACOLOGY, 949 (175743). |
| 2. Zhou Yunlei, Wang Minghui, Yin Huanshun, Ai Shiyun. (2017) Amperometric determination of the activity of protein kinase a using a glassy carbon electrode modified with IgG functionalized gold nanoparticles conjugated to horseradish peroxidase. MICROCHIMICA ACTA, 184 (9): (3301-3308). |
| 3. Zhifeng Geng, Guoyi Deng, Ziyu Wang, Xin Xu, Xiaojiao Yin, Sen Zhang, Jiale Shao, Jiyue Wen. (2025) Distinct roles of A1/A2 astrocytes in blood-brain barrier injury following cerebral I/R via the ROCK/NF-κB and STAT3 pathways. INTERNATIONAL IMMUNOPHARMACOLOGY, 151 (114338). |