∆-9-Tetrahydrocannabinol 30μM R08 exp445

Agonist of CB1 and CB2 cannabinoid receptors

  • Class / Subclass 1: Environmental Stresses / Controlled Substance
  • Class / Subclass 2: Signal Transduction / GPCR Agonist

Compound References

  • PubChem Name: Dronabinol
  • Synonyms: N/A
  • CAS #: 1972-08-3
  • PubChem CID: 16078
  • IUPAC: (6aR,10aR)-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydrobenzo[c]chromen-1-ol
  • INCHI Name: InChI=1S/C21H30O2/c1-5-6-7-8-15-12-18(22)20-16-11-14(2)9-10-17(16)21(3,4)23-19(20)13-15/h11-13,16-17,22H,5-10H2,1-4H3/t16-,17-/m1/s1
  • INCHI Key: CYQFCXCEBYINGO-IAGOWNOFSA-N
  • Molecular Weight: 314.5
  • Canonical SMILES: CCCCCC1=CC(=C2C3C=C(CCC3C(OC2=C1)(C)C)C)O
  • Isomeric SMILES: CCCCCC1=CC(=C2[C@@H]3C=C(CC[C@H]3C(OC2=C1)(C)C)C)O
  • Molecular Formula: C21H30O2

Compound Supplier

  • Supplier Name: Toronto Research Chemicals
  • Catalog #: T293200
  • Lot #: 7-YEN-94-6

Compound Characterization

  • HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C21H30O2 315.23186; found 315.23143

Dose Response Curve

  • Platform ID: THC
  • Min: -16.2079; Max: 99.4826





IC Concentration (µM)
IC10 26.9000
IC20 32.2200
IC30 36.3200
IC40 40.0700
IC50 43.8500
IC60 47.9900
IC70 52.9400
IC80 59.6900
IC90 71.4800


  • Round: 08
  • Dose: 30µM
  • Days of incubation: 8
  • Doublings: 2.5
  • Numbers of reads: 15258071
Sensitive/Resistant hits (FDR<0.05)CRANKSScore PlotTop 30 GenesScreen SimilarityTop 30 Sensitive GO termsTop 30 Resistant GO terms
17/10ScoresViewViewViewViewView

  • Last modified: 2026/01/15 21:36
  • by 127.0.0.1