pempidine
chemical compound
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pempidine
Summary
pempidine is a type of chemical entity[1]. pempidine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (14 views/month).[2]
Key Facts
- pempidine's instance of is recorded as type of chemical entity[3].
- pempidine's chemical structure is recorded as Pempidine.svg[4].
- pempidine's CAS Registry Number is recorded as 79-55-0[5].
- pempidine's EC number is recorded as 201-211-2[6].
- pempidine's canonical SMILES is recorded as CC1(CCCC(N1C)(C)C)C[7].
- pempidine's InChI is recorded as InChI=1S/C10H21N/c1-9(2)7-6-8-10(3,4)11(9)5/h6-8H2,1-5H3[8].
- pempidine's InChIKey is recorded as XULIXFLCVXWHRF-UHFFFAOYSA-N[9].
- pempidine's chemical formula is recorded as C₁₀H₂₁N[10].
- pempidine's subclass of is recorded as chemical compound[11].
- pempidine's Commons category is recorded as Pempidine[12].
- pempidine's MeSH descriptor ID is recorded as D010393[13].
- pempidine's ChEMBL ID is recorded as CHEMBL1617409[14].
- pempidine's Freebase ID is recorded as /m/04g22sf[15].
- pempidine's UNII is recorded as N5I18JI9D6[16].
- pempidine's ChemSpider ID is recorded as 6353[17].
- pempidine's PubChem CID is recorded as 6603[18].
- pempidine's MeSH tree code is recorded as D03.383.621.610[19].
- pempidine's ChEBI ID is recorded as 94718[20].
- pempidine's Human Metabolome Database ID is recorded as HMDB0256215[21].
- pempidine's mass is recorded as {'unit': 'Q483261', 'amount': '+155.167'}[22].
- pempidine's ECHA Substance Infocard ID is recorded as 100.001.102[23].
- pempidine's NSC number is recorded as 758448[24].
- pempidine's subject has role is recorded as antihypertensive drug[25].
- pempidine's subject has role is recorded as ganglionic blockers[26].
- pempidine's subject has role is recorded as nicotinic antagonist[27].
Why It Matters
pempidine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (14 views/month).[2] pempidine has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28]