Drug

D0491 | clemastine

Molecular Formula C21H26ClNO
Molecular Weight 343.9
Structure
State solid
Route of elimination Urinary excretion is the major mode of elimination.
Absorption Rapidly absorbed from the gastrointestinal tract.

D

R

R06AA54 Clemastine, combinations


[R06AA] Aminoalkyl ethers


[R06A] ANTIHISTAMINES FOR SYSTEMIC USE


[R06] ANTIHISTAMINES FOR SYSTEMIC USE


[R] Respiratory system


R06AA04 Clemastine


[R06AA] Aminoalkyl ethers


[R06A] ANTIHISTAMINES FOR SYSTEMIC USE


[R06] ANTIHISTAMINES FOR SYSTEMIC USE


[R] Respiratory system


D04AA14 Clemastine


[D04AA] Antihistamines for topical use


[D04A] ANTIPRURITICS, INCL. ANTIHISTAMINES, ANESTHETICS, ETC.


[D04] ANTIPRURITICS, INCL. ANTIHISTAMINES, ANESTHETICS, ETC.


[D] Dermatological drugs


Toxicity Dose Time Species Model Method Action Positive criterion Reference
UNCOUPLING rat isolated liver mitochondria measurements of mitochondrial respiration; RST inhibition assay, RST uncoupling assay; IC 50ratio of glucose/galactose assay increase 53


  • (+)-(2R)-2-(2-(((R)-p-Chloro-alpha-methyl-alpha-phenylbenzyl)oxy)ethyl)-1-methylpyrrolidine (+)-(2R)-2-[2-[[(R)-p-Chloro-alpha-methyl-alpha-phenylbenzyl]oxy]ethyl]-1-methylpyrrolidine (2R)-2-(2-{[(1R)-1-(4-chlorophenyl)-1-phenylethyl]oxy}ethyl)-1-methylpyrrolidine
    (2R)-2-[2-[(1R)-1-(4-chlorophenyl)-1-phenyl-ethoxy]ethyl]-1-methyl-pyrrolidine (2R)-2-[2-[(1R)-1-(4-chlorophenyl)-1-phenyl-ethoxy]ethyl]-1-methyl-pyrrolidine;fumarate (2R)-2-[2-[(1R)-1-(4-chlorophenyl)-1-phenylethoxy]ethyl]-1-methylpyrrolidine
    (2R)-2-{2-[(1R)-1-(4-chlorophenyl)-1-phenylethoxy]ethyl}-1-methylpyrrolidine (E)-2-butenedioate;(2R)-2-[2-[(1R)-1-(4-chlorophenyl)-1-phenylethoxy]ethyl]-1-methylpyrrolidine (E)-but-2-enedioate;(2R)-2-[2-[(1R)-1-(4-chlorophenyl)-1-phenyl-ethoxy]ethyl]-1-methyl-pyrrolidine
    (E)-but-2-enedioate;(2R)-2-[2-[(1R)-1-(4-chlorophenyl)-1-phenylethoxy]ethyl]-1-methylpyrrolidine; (R)-2-(2-((R)-1-(4-chlorophenyl)-1-phenylethoxy)ethyl)-1-methylpyrrolidine (R)-2-[2-[(R)-1-(4-chlorophenyl)-1-phenylethoxy]ethyl]-1-methylpyrrolidine
    15686-51-8 2(R)-[2-[(1R)-(4-Chlorophenyl)-1-phenyl-ethoxy]ethyl-1-methylpyrrolidine 2-(2-(1-(4-Chlorophenyl)-1-phenylethoxy)ethyl)-1-methylpyrrolidine
    2-(2-(4-Chlor-alpha-methylbenzhydryloxy)ethyl)-1-methylpyrrolidin 686C518 95QN29S1ID
    AB00053766-06 AB00053766-07 AB00053766_08
    AB00053766_09 API0009140 BDBM50253157
    BDBM94606 BIDD:GT0391 BPBio1_000300
    BRD-K30240666-051-05-0 BRD-K30240666-051-08-4 BSPBio_000272
    BSPBio_002045 C-23710 C21H26ClNO
    CAS-14976-57-9 CC-25901 CHEBI:3738
    CHEMBL1626 Clemastina Clemastina [INN-Spanish]
    Clemastine [USAN:BAN] Clemastine [USAN:INN:BAN] Clemastinum
    Clemastinum [INN-Latin] DB00283 DL-247
    DTXSID2022832 DivK1c_000285 FT-0772929
    GTPL6063 HMS2089I22 HS 592
    HS-592 IDI1_000285 KBio1_000285
    KBio3_001265 KBioGR_001570 KSC-315-033-
    KUC112480N LS-137531 Lopac-C-8903
    M192 MLS002154260 Meclastin
    Meclastine Mecloprodin NCGC00015281-01
    NCGC00016710-01 NCGC00016710-02 NCGC00025168-01
    NINDS_000285 Prestwick0_000306 Prestwick1_000306
    Prestwick2_000306 Prestwick3_000306 Pyrrolidine, 2-(2-(1-(4-chlorophenyl)-1-phenylethoxy)ethyl)-1-methyl-, (R-(R*,R*))-
    Q418145 SBI-0052796.P003 SCHEMBL4178
    SMR001233520 SPBio_000817 SPBio_002491
    Spectrum2_000689 Spectrum3_000353 Spectrum4_000955
    Spectrum5_001520 Tavist (*Fumarate*) Tocris-1453
    UNII-95QN29S1ID YNNUSGIPVFPVBX-NHCUHLMSSA-N ZINC402830
    cid_45479735 clemastine

    DrugBank Name clemastine
    DrugBank DB00283
    CAS Number 14976-57-9, 15686-51-8, 63813-90-1
    PubChem Compound 26987
    KEGG Compound ID C06913
    KEGG Drug D03535
    ChEBI 3738