
Common name
1-methylpiperidine
IUPAC name
1-methylpiperidine
SMILES
CN1CCCCC1
Common name
1-methylpiperidine
IUPAC name
1-methylpiperidine
SMILES
CN1CCCCC1
INCHI
InChI=1S/C6H13N/c1-7-5-3-2-4-6-7/h2-6H2,1H3
FORMULA
C6H13N

Common name
1-methylpiperidine
IUPAC name
1-methylpiperidine
Molecular weight
99.174
clogP
1.483
clogS
-0.911
Frequency
0.0172
HBond Acceptor
1
HBond Donor
0
Total PolarSurface Area
3.24
Number of Rings
1
Rotatable Bond
0
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. |
FDBD00184 | Bupivacaine |
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Anesthetics, Local; Anesthetics; Nervous System; Amides; Cytochrome P-450 CYP1A2 Inhibitors; Cytochrome P-450 CYP1A2 Inducers; Cytochrome P-450 CYP2C19 Inducers; CYP2D6 Inducers; CYP2D6 Inducers (strong); CYP3A4 Inhibitors; | For the production of local or regional anesthesia or analgesia for surgery, for oral surgery procedures, for diagnostic and therapeutic procedures, and for obstetrical procedures. |
FDBD00225 | Metixene |
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Nervous System; Anti-Parkinson Drugs; Anticholinergics; Tertiary Amines; | Used for the symptomatic treatment of parkinsonism. |
FDBD00258 | Trihexyphenidyl |
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Antiparkinson Agents; Muscarinic Antagonists; Antidyskinetics; Nervous System; Anti-Parkinson Drugs; Anticholinergics; Tertiary Amines; | Indicated for the treatment of parkinson's disease and extrapyramidal reactions caused by drugs. |
FDBD00329 | Pethidine |
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Analgesics; Analgesics, Opioid; Narcotics; Adjuvants, Anesthesia; Adjuvants; Nervous System; Opioids; Phenylpiperidine Derivatives; Cytochrome P-450 CYP2C19 Inducers; Cytochrome P-450 CYP2B6 Inducers; Cytochrome P-450 CYP2B6 Inhibitors; CYP2B6 Inhibitors (strong); CYP2D6 Inducers; CYP2D6 Inducers (strong); CYP3A4 Inhibitors; | Used to control moderate to severe pain. |
FDBD00354 | Raloxifene |
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Bone Density Conservation Agents; Estrogen Antagonists; Selective Estrogen Receptor Modulators; Antihypocalcemic Agents; Sex Hormones and Modulators of the Genital System; Genito Urinary System and Sex Hormones; Cytochrome P-450 CYP2C8 Inhibitors; Cytochrome P-450 CYP2C8 Inducers; Cytochrome P-450 CYP2B6 Inducers; Cytochrome P-450 CYP2B6 Inhibitors; CYP2B6 Inhibitors (strong); CYP3A4 Inhibitors; | For the prevention and treatment of osteoporosis in post-menopausal women, as well as prevention and treatment of corticosteroid-induced bone loss. Also for the reduction in the incidence of invasive breast cancer in postmenopausal women with osteoporosis or have a high risk for developing breast cancer. |
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. |
FDBD00502 | Astemizole |
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Anti-Allergic Agents; Histamine H1 Antagonists, Non-Sedating; Histamine Antagonists; Respiratory System; Antihistamines for Systemic Use; CYP2D6 Inducers; CYP2D6 Inducers (strong); CYP3A4 Inhibitors; Combined Inhibitors of CYP3A4 and P-glycoprotein; | Astemizole was indicated for use in the relieving allergy symptoms, particularly rhinitis and conjunctivitis. It has been withdrawn from the market however due to concerns of arrhythmias. |
FDBD00510 | Dyclonine |
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Anesthetics, Local; Anesthetics; Respiratory System; Throat Preparations; Nervous System; | Used to provide topical anesthesia of accessible mucous membranes prior to examination, endoscopy or instrumentation, or other procedures involving the esophagus, larynx, mouth, pharynx or throat, respiratory tract or trachea, urinary tract, or vagina. Also used to suppress the gag reflex and/or other laryngeal and esophageal reflexes to facilitate dental examination or procedures (including oral surgery), endoscopy, or intubation. Also used for relief of canker sores, cold sores or fever blister. |
FDBD00544 | Thioridazine |
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Antipsychotic Agents; Adrenergic alpha-1 Receptor Antagonists; Dopamine Antagonists; Phenothiazines; Nervous System; Psycholeptics; Phenothiazines With Piperidine Structure; 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; CYP2D6 Inducers; CYP2D6 Inducers (strong); CYP2E1 Inhibitors; CYP2E1 Inducers; CYP2E1 Inducers (strong); | For the treatment of schizophrenia and generalized anxiety disorder. |
50 ,
6
FRAGNAME | PDBID | SIMILIRITY | XSCORE | SMILE | HAC |
---|---|---|---|---|---|
2bys_ligand_frag_3.mol2 | 2bys | 1 | -6.50 | C1CCCC[NH+]1C | 7 |
2iog_ligand_1_10.mol2 | 2iog | 1 | -6.37 | [NH+]1(CCCCC1)C | 7 |
3m8q_ligand_1_4.mol2 | 3m8q | 1 | -6.30 | C[NH+]1CCCCC1 | 7 |
1o79_ligand_1_0.mol2 | 1o79 | 1 | -6.29 | C1CC[NH+](CC1)C | 7 |
1eve_ligand_1_4.mol2 | 1eve | 1 | -6.25 | C[NH+]1CCCCC1 | 7 |
3i6m_ligand_1_4.mol2 | 3i6m | 1 | -6.20 | [NH+]1(CCCCC1)C | 7 |
4li8_ligand_1_4.mol2 | 4li8 | 1 | -6.20 | [NH+]1(CCCCC1)C | 7 |
2y1w_ligand_1_2.mol2 | 2y1w | 1 | -6.18 | C[NH+]1CCCCC1 | 7 |
123 ,
13