| Weight | 100.165 g/mol |
|---|---|
| Formula | C5H12N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Homopiperazine (505-66-8)
1,4-diazepane
Score:
#51 in Medicinal chemistry
,
#6992 in Chemistry
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- The novel and specific Rho-kinase inhibitor (S)-(+)-2-methyl-1-[(4-methyl-5-isoquinoline)sulfonyl]-homopiperazine as a probing molecule for Rho-kinase-involved pathway (Pharmacology & Therapeutics, 2002)
- Discovery of a potent, CNS-penetrant orexin receptor antagonist based on an n,n-disubstituted-1,4-diazepane scaffold that promotes sleep in rats. (ChemMedChem, 2009)
- Identification and initial evaluation of 4-N-aryl-[1,4]diazepane ureas as potent CXCR3 antagonists (Bioorganic & Medicinal Chemistry Letters, 2006)
- 1,4-Diazepane-2-ones as novel inhibitors of LFA-1. (Bioorganic & Medicinal Chemistry Letters, 2003)
- Homopiperazine Pt(II) adducts with DNA bases and nucleosides: Crystal structure of [PtII(homopiperazine)(9-ethylguanine)2](NO3)2 (Polyhedron, 2006)
- A novel QSAR model for predicting the inhibition of CXCR3 receptor by 4-N-aryl-[1,4] diazepane ureas. (European Journal of Medicinal Chemistry, 2009)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1,4-diazepane
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SMILESC1CNCCNC1
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InChIKeyFQUYSHZXSKYCSY-UHFFFAOYSA-N
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Similar Compounds
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Homopiperazine
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