An Analytical Reference Standard
Related Products
Isomer(s)
39730MDMB-PINACA
Parent Compound(s)
14293ADBICA
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ADBICA N-(4-hydroxypentyl) metabolite

Item No. 15240

Synonyms
Synonyms
  • ADB-PICA N-(4-hydroxypentyl) metabolite
Technical Information
Formal Name
N-[1-(aminocarbonyl)-2,2-dimethylpropyl]-1-(4-hydroxypentyl)-1H-indole-3-carboxamide
CAS Number
2460433-26-3
Molecular Formula
C20H29N3O3
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 12 mg/mlDMSO: 12 mg/mlDMSO:PBS (pH 7.2) (1:8): 0.1 mg/mlEthanol: 10 mg/ml
λmax
218, 290 nm
SMILES
CC(O)CCCN1C=C(C(NC(C(C)(C)C)C(N)=O)=O)C2=C1C=CC=C2
InChi Code
InChI=1S/C20H29N3O3/c1-13(24)8-7-11-23-12-15(14-9-5-6-10-16(14)23)19(26)22-17(18(21)25)20(2,3)4/h5-6,9-10,12-13,17,24H,7-8,11H2,1-4H3,(H2,21,25)(H,22,26)
InChi Key
IZMLODTWDCPVEI-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    ADBICA (Item No. 14293) is a synthetic cannabinoid (CB) that has recently been identified in herbal blends.1 Structurally, it is a modified aminoalkylindole like many cannabimimetics with pronounced activity at both CB receptors.2 ADBICA N-(4-hydroxypentyl) metabolite is a potential phase 1 metabolite of ADBICA, based on the known metabolism of other aminoalkylindoles.3,4 The physiological and toxicological properties of this compound have not been determined. This product is intended for forensic and research applications.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Uchiyama, N., Matsuda, S., Kawamura, M., et alTwo new-type cannabimimetic quinolinyl carboxylates, QUPIC and QUCHIC, two new cannabimimetic carboxamide derivatives, ADB-FUBINACA and ADBICA, and five synthetic cannabinoids detected with a thiophene derivative α-PVT and an opioid receptor agonist AH-7921 identified in illegal products. Forensic Toxicol. 31(2), 223-240 (2013).

    2. Aung, M.M., Griffin, G., Huffman, J.W., et alInfluence of the N-1 alkyl chain length of cannabimimetic indoles upon CB1 and CB2 receptor binding. Drug Alcohol Depend. 60(2), 133-140 (2000).

    3. Wintermeyer, A., Möller, I., Thevis, M., et alIn vitro phase I metabolism of the synthetic cannabimimetic JWH-018. Anal. Bioanal. Chem. 398(5), 2141-2153 (2010).

    4. Chimalakonda, K.C., Moran, C.L., Kennedy, P.D., et alSolid-phase extraction and quantitative measurement of omega and omega-1 metabolites of JWH-018 and JWH-073 in human urine. Anal. Chem. 83(16), 6381-6388 (2011).