cangrelor
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cangrelor
Summary
cangrelor is a type of chemical entity[1]. cangrelor ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (89 views/month).[2]
Key Facts
- cangrelor's instance of is recorded as type of chemical entity[3].
- cangrelor's physically interacts with is recorded as G protein-coupled receptor 17[4].
- cangrelor's physically interacts with is recorded as Purinergic receptor P2Y12[5].
- cangrelor's physically interacts with is recorded as Purinergic receptor P2Y13[6].
- cangrelor's canonical SMILES is recorded as CSCCNC1=NC(=NC2=C1N=CN2C3C(C(C(O3)COP(=O)(O)OP(=O)(C(P(=O)(O)O)(Cl)Cl)O)O)O)SCCC(F)(F)F[7].
- cangrelor's chemical formula is recorded as C₁₇H₂₅Cl₂F₃N₅O₁₂P₃S₂[8].
- cangrelor is a type of chemical compound[9].
- cangrelor is used for medication[10].
- cangrelor's Commons category is recorded as Cangrelor[11].
- cangrelor's significant drug interaction is recorded as nabumetone[12].
- cangrelor's significant drug interaction is recorded as naproxen[13].
- cangrelor's significant drug interaction is recorded as celecoxib[14].
- cangrelor's significant drug interaction is recorded as Diclofenac[15].
- cangrelor's significant drug interaction is recorded as piroxicam[16].
- cangrelor's significant drug interaction is recorded as meloxicam[17].
- cangrelor's significant drug interaction is recorded as (RS)-fenoprofen[18].
- cangrelor's significant drug interaction is recorded as (±)-flurbiprofen[19].
- cangrelor's significant drug interaction is recorded as ibuprofen[20].
- cangrelor's significant drug interaction is recorded as indomethacin[21].
- cangrelor's significant drug interaction is recorded as (RS)-ketoprofen[22].
- cangrelor's significant drug interaction is recorded as (RS)-etodolac[23].
- cangrelor's significant drug interaction is recorded as sulindac[24].
- cangrelor's significant drug interaction is recorded as parecoxib[25].
- cangrelor's significant drug interaction is recorded as aceclofenac[26].
- cangrelor's significant drug interaction is recorded as tenoxicam[27].
Why It Matters
cangrelor ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (89 views/month).[2] cangrelor has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[28] cangrelor is known by 6 alternative names across languages and contexts.[29]