
Common name
1-propylpiperidine
IUPAC name
1-propylpiperidine
SMILES
C(C)CN1CCCCC1
Common name
1-propylpiperidine
IUPAC name
1-propylpiperidine
SMILES
C(C)CN1CCCCC1
INCHI
InChI=1S/C8H17N/c1-2-6-9-7-4-3-5-8-9/h2-8H2,1H3
FORMULA
C8H17N

Common name
1-propylpiperidine
IUPAC name
1-propylpiperidine
Molecular weight
127.227
clogP
2.016
clogS
-1.760
Frequency
0.0041
HBond Acceptor
1
HBond Donor
0
Total PolarSurface Area
3.24
Number of Rings
1
Rotatable Bond
2
Drug ID | Common name | Structure CAS | Compound class | Therapeutic area |
---|---|---|---|---|
FDBD00183 | Ropivacaine |
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Anesthetics, Local; Anesthetics; Nervous System; Amides; Cytochrome P-450 CYP1A2 Inhibitors; Cytochrome P-450 CYP1A2 Inducers; Cytochrome P-450 CYP2B6 Inducers; Cytochrome P-450 CYP2B6 Inhibitors; CYP2B6 Inhibitors (strong); CYP2D6 Inducers; CYP2D6 Inducers (strong); CYP3A4 Inhibitors; | Used in obstetric anesthesia and regional anesthesia for surgery. |
FDBD00469 | Cisapride |
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Gastrointestinal Agents; Anti-Ulcer Agents; Serotonin Receptor Agonists; Prokinetic Agents; Alimentary Tract and Metabolism; Drugs for Functional Gastrointestinal Disorders; Propulsives; Cytochrome P-450 CYP1A2 Inhibitors; Cytochrome P-450 CYP2C9 Inhibitors; Cytochrome P-450 CYP1A2 Inducers; Cytochrome P-450 CYP2C8 Inhibitors; Cytochrome P-450 CYP2C9 Inducers; Cytochrome P-450 CYP2C19 Inducers; Cytochrome P-450 CYP2C8 Inducers; Cytochrome P-450 CYP2B6 Inducers; Cytochrome P-450 CYP2B6 Inhibitors; CYP2A6 Inhibitors; CYP2A6 Inhibitors (strong); CYP2A6 Inhibitors (moderate); CYP2A6 Inducers; CYP2A6 Inducers (strong); CYP2B6 Inhibitors (strong); CYP2D6 Inducers; CYP2D6 Inducers (strong); CYP3A4 Inhibitors; | For the symptomatic treatment of adult patients with nocturnal heartburn due to gastroesophageal reflux disease. |
FDBD00950 | Pimozide |
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Antipsychotic Agents; Dopamine Antagonists; Anti-Dyskinesia Agents; Nervous System; Psycholeptics; Diphenylbutylpiperidine Derivatives; Cytochrome P-450 CYP1A2 Inhibitors; Cytochrome P-450 CYP1A2 Inducers; Cytochrome P-450 CYP2C19 Inducers; CYP2D6 Inducers; CYP2D6 Inducers (strong); CYP2E1 Inhibitors; CYP2E1 Inducers; CYP2E1 Inducers (strong); CYP3A4 Inhibitors; Combined Inhibitors of CYP3A4 and P-glycoprotein; | Used for the suppression of motor and phonic tics in patients with Tourette's Disorder who have failed to respond satisfactorily to standard treatment. |
FDBD01030 | Domperidone |
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Antiprotozoal Agents; Antiemetics; Dopamine Antagonists; Alimentary Tract and Metabolism; Antiparasitic Products, Insecticides and Repellents; Agents Against Protozoal Diseases; Drugs for Functional Gastrointestinal Disorders; Propulsives; Cytochrome P-450 CYP1A2 Inhibitors; Cytochrome P-450 CYP1A2 Inducers; Cytochrome P-450 CYP2C8 Inhibitors; Cytochrome P-450 CYP2C8 Inducers; Cytochrome P-450 CYP2B6 Inducers; Cytochrome P-450 CYP2B6 Inhibitors; CYP2B6 Inhibitors (strong); CYP2D6 Inducers; CYP2D6 Inducers (strong); CYP3A4 Inhibitors; | For management of dyspepsia, heartburn, epigastric pain, nausea, and vomiting. |
FDBD01270 | Pipotiazine |
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Antipsychotic Agents; Phenothiazines; Nervous System; Psycholeptics; Phenothiazines With Piperidine Structure; Cytochrome P-450 CYP1A2 Inhibitors; Cytochrome P-450 CYP1A2 Inducers; Cytochrome P-450 CYP2C19 Inducers; CYP2D6 Inducers; CYP2D6 Inducers (strong); CYP3A4 Inhibitors; | For the maintenance treatment of chronic non-agitated schizophrenic patients. |
FDBD01352 | Iloperidone |
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Antipsychotic Agents; Adrenergic alpha-1 Receptor Antagonists; Nervous System; Psycholeptics; Cytochrome P-450 CYP1A2 Inhibitors; Cytochrome P-450 CYP1A2 Inducers; CYP2D6 Inducers; CYP2D6 Inducers (strong); CYP2E1 Inhibitors; CYP2E1 Inducers; CYP2E1 Inducers (strong); CYP3A4 Inhibitors; | Treatment of acute schizophrenia. |
FDBD01418 | Prucalopride |
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Alimentary Tract and Metabolism; Drugs for Constipation; | Investigated for use/treatment in constipation, ileus, and pediatric indications. |
FDBD01537 | Lomitapide |
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Hypolipidemic Agents; Lipid Modifying Agents, Plain; Lipid Modifying Agents; Cardiovascular System; CYP3A4 Inhibitors; | Used in homozygous familial hypercholesterolemia (HoFH) patients to reduce low-density lipoprotein cholesterol (LDL-C), total cholesterol (TC), apolipoprotein B (apo B), and non-high-density lipoprotein cholesterol (non-HDL-C). |
FDBD01612 | Eperisone |
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Musculo-Skeletal System; Muscle Relaxants, Centrally Acting Agents; Muscle Relaxants; | |
FDBD01620 | Clocapramine |
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12 ,
2
FRAGNAME | PDBID | SIMILIRITY | XSCORE | SMILE | HAC |
---|---|---|---|---|---|
4djh_ligand_3_16.mol2 | 4djh | 1 | -7.55 | C(C(C)C)C[N@H+]1C[C@@H]([C@H](CC1)C)C | 13 |
4djh_ligand_2_12.mol2 | 4djh | 1 | -6.73 | CC[N@H+]1C[C@@H]([C@H](CC1)C)C | 10 |
3i6m_ligand_3_9.mol2 | 3i6m | 1 | -6.59 | C(C)C[NH+]1CCCCC1 | 9 |
4djh_ligand_1_4.mol2 | 4djh | 1 | -6.45 | C[N@H+]1C[C@@H]([C@H](CC1)C)C | 9 |
4djh_ligand_frag_5.mol2 | 4djh | 1 | -6.40 | [NH2+]1C[C@@H]([C@H](CC1)C)C | 8 |
2rcw_ligand_2_5.mol2 | 2rcw | 1 | -6.23 | C(C)C[NH+]1CCCCC1 | 9 |
4gfd_ligand_3_34.mol2 | 4gfd | 1 | -6.20 | C1CCC[NH+](C1)CCC(C)(C)C | 12 |
2igy_ligand_3_266.mol2 | 2igy | 1 | -6.19 | C(C)(C)CC[NH+]1CCCCC1 | 11 |
113 ,
12