Periciazine

C₂₁H₂₃N₃OS — CID 4747

About Periciazine

Periciazine (PubChem CID 4747) has the molecular formula C₂₁H₂₃N₃OS and a molecular weight of 365.50 g/mol. Its IUPAC name is 10-[3-(4-hydroxypiperidin-1-yl)propyl]phenothiazine-2-carbonitrile.

Molecular Properties

• Compound Name: Periciazine
• PubChem CID: 4747
• Molecular Formula: C₂₁H₂₃N₃OS
• Molecular Weight: 365.50 g/mol
• Exact Mass: 365.16
• IUPAC Name: 10-[3-(4-hydroxypiperidin-1-yl)propyl]phenothiazine-2-carbonitrile
• SMILES: N#Cc1ccc2c(c1)N(CCCN1CCC(O)CC1)c1ccccc1S2
• InChI: InChI=1S/C21H23N3OS/c22-15-16-6-7-21-19(14-16)24(18-4-1-2-5-20(18)26-21)11-3-10-23-12-8-17(25)9-13-23/h1-2,4-7,14,17,25H,3,8-13H2
• InChIKey: LUALIOATIOESLM-UHFFFAOYSA-N
• XLogP: 4.01
• TPSA: 50.50 Ų
• H-Bond Donors: 1
• H-Bond Acceptors: 5
• Rotatable Bonds: 4
• Heavy Atoms: 26
• Complexity: —

Lipinski Rule of Five

Passes Rule of Five

Rule	Value
MW ≤ 500	365.50
LogP ≤ 5	4.01
H-Bond Donors ≤ 5	1
H-Bond Acceptors ≤ 10	5

Frequently Asked Questions

What is the IUPAC name of Periciazine?

The IUPAC name of Periciazine (CID 4747) is 10-[3-(4-hydroxypiperidin-1-yl)propyl]phenothiazine-2-carbonitrile.

What is the SMILES notation for Periciazine?

The canonical SMILES for Periciazine is N#Cc1ccc2c(c1)N(CCCN1CCC(O)CC1)c1ccccc1S2.

What is the InChIKey of Periciazine?

The InChIKey is LUALIOATIOESLM-UHFFFAOYSA-N. The full InChI is InChI=1S/C21H23N3OS/c22-15-16-6-7-21-19(14-16)24(18-4-1-2-5-20(18)26-21)11-3-10-23-12-8-17(25)9-13-23/h1-2,4-7,14,17,25H,3,8-13H2.

What are the key properties of Periciazine?

Periciazine has a molecular weight of 365.50 g/mol, XLogP of 4.01, 4 rotatable bonds, 1 hydrogen bond donors, and 5 hydrogen bond acceptors.

Where does this data come from?

All data for Periciazine is sourced from PubChem (CID 4747), the world's largest open chemistry database maintained by the National Library of Medicine (NIH).

Sources

• PubChem CID 4747 — identifiers, structure, computed properties (public domain)
• DrugCentral drug card 2107 — approved-drug record (CC BY-SA 4.0)

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