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Substance Name: Chlorpheniramine maleate mixture with codeine
RN: 76095-56-2
InChIKey: MBUQBCLLECNCAB-QJJJDLSBSA-N

Classification Code

  • Drug / Therapeutic Agent

Molecular Formula

  • C18-H21-N-O3.C16-H19-Cl-N2.C4-H4-O4

Molecular Weight

  • 690.2326
 
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Names and Synonyms

Results Name

  • Chlorpheniramine maleate mixture with codeine

Name of Substance

  • Codicaps

Synonyms

  • Chlorpheniramine maleate mixture with codeine
  • Codicaps

Systematic Names

  • Morphinan-6-ol, 7,8-didehydro-4,5-epoxy-3-methoxy-17-methyl-, (5-alpha,6-alpha)-, mixed with gamma-(4-chlorophenyl)-N,N-dimethyl-2-pyridinepropanamine (Z)-2-butenedioate (1:1)
  • Morphinan-6-ol, 7,8-didehydro-4,5-epoxy-3-methoxy-17-methyl-, (5alpha,6alpha)-, mixt. with gamma-(4-chlorophenyl)-N,N-dimethyl-2-pyridinepropanamine (Z)-2-butenedioate (1:1)

Registry Numbers

CAS Registry Number

  • 76095-56-2

System Generated Number

  • 0076095562

Molecular Formulas

Molecular Formula

  • C18-H21-N-O3.C16-H19-Cl-N2.C4-H4-O4

Molecular Formula Fragments

  • C16-H19-Cl-N2
  • C18-H21-N-O3
  • C4-H4-O4
  • COMPONENT

Structure Descriptors

InChI

1S/C18H21NO3.C16H19ClN2.C4H4O4/c1-19-8-7-18-11-4-5-13(20)17(18)22-16-14(21-2)6-3-10(15(16)18)9-12(11)19;1-19(2)12-10-15(16-5-3-4-11-18-16)13-6-8-14(17)9-7-13;5-3(6)1-2-4(7)8/h3-6,11-13,17,20H,7-9H2,1-2H3;3-9,11,15H,10,12H2,1-2H3;1-2H,(H,5,6)(H,7,8)/b;;2-1-/t11-,12+,13-,17-,18-;;/m0../s1

InChIKey

MBUQBCLLECNCAB-QJJJDLSBSA-N

Smiles

CN1CC[C@]23c4c5ccc(c4O[C@H]2[C@H](C=C[C@H]3[C@H]1C5)O)OC.CN(C)CCC(c1ccc(cc1)Cl)c2ccccn2.C(=C\C(=O)O)\C(=O)O

Toxicity

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD oral > 40mL/kg (40mL/kg) ENDOCRINE: OTHER CHANGES

BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

SKIN AND APPENDAGES (SKIN): HAIR: OTHER
Yakuri to Chiryo. Pharmacology and Therapeutics. Vol. 16, Pg. 797, 1988.
rat LD oral > 40mL/kg (40mL/kg) KIDNEY, URETER, AND BLADDER: HEMATURIA

BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

ENDOCRINE: OTHER CHANGES
Yakuri to Chiryo. Pharmacology and Therapeutics. Vol. 16, Pg. 797, 1988.