ADB-FUBICA

ADB-FUBICA
	File:ADB-FUBICA structure.png
法律規範狀態
法律規範	加：Schedule II; 德：NpSG; 英：Class B;
識別資訊
	IUPAC命名法 (S)-N-(1-amino-3,3-dimethyl-1-oxobutan-2-yl)-1-(4-fluorobenzyl)-1H-indole-3-carboxamide; ;
CAS號	1801338-23-7 check
UNII	S3ABP24K72;
化學資訊
化學式	C22H24FN3O2
摩爾質量	381.45 g·mol−1
3D模型（JSmol）	交互式圖像;
	SMILES O=C(C1=CN(CC2=CC=C(F)C=C2)C3=C1C=CC=C3)N[C@@H](C(C)(C)C)C(N)=O;
	InChI InChI=1S/C22H24FN3O2/c1-22(2,3)19(20(24)27)25-21(28)17-13-26(18-7-5-4-6-16(17)18)12-14-8-10-15(23)11-9-14/h4-11,13,19H,12H2,1-3H3,(H2,24,27)(H,25,28)/t19-/m1/s1; Key:QIFOZYUACLDTAJ-LJQANCHMSA-N;

ADB-FUBICA是一種含氮有機氟化合物，分子式C
22H
24FN
3O
2，能作為大麻素受體的激動劑，其對CB₁和CB₂的EC₅₀分別為2.6 nM和3.0 nM^[1]^[2]。

另見[編輯]

↑ Banister SD, Moir M, Stuart J, Kevin RC, Wood KE, Longworth M, et al. Pharmacology of Indole and Indazole Synthetic Cannabinoid Designer Drugs AB-FUBINACA, ADB-FUBINACA, AB-PINACA, ADB-PINACA, 5F-AB-PINACA, 5F-ADB-PINACA, ADBICA, and 5F-ADBICA. ACS Chemical Neuroscience. September 2015, 6 (9): 1546–59. PMID 26134475. doi:10.1021/acschemneuro.5b00112.
↑ Qian Z, Hua Z, Liu C, Jia W. Four types of cannabimimetic indazole and indole derivatives, ADB-BINACA, AB-FUBICA, ADB-FUBICA, and AB-BICA, identified as new psychoactive substances. Forensic Toxicology. November 2015, 34: 133–143. PMC 4705129 可免費查閱. PMID 26793280. doi:10.1007/s11419-015-0297-2.

法律規範狀態
File:ADB-FUBICA structure.png
法律規範	加：Schedule II 德：NpSG 英：Class B
識別資訊
IUPAC命名法 (S)-N-(1-amino-3,3-dimethyl-1-oxobutan-2-yl)-1-(4-fluorobenzyl)-1H-indole-3-carboxamide
CAS號	1801338-23-7 ^checkY
UNII	S3ABP24K72
化學資訊
化學式	C₂₂H₂₄FN₃O₂
摩爾質量	381.45 g·mol⁻¹
3D模型（JSmol）	交互式圖像
SMILES O=C(C1=CN(CC2=CC=C(F)C=C2)C3=C1C=CC=C3)N[C@@H](C(C)(C)C)C(N)=O
InChI InChI=1S/C22H24FN3O2/c1-22(2,3)19(20(24)27)25-21(28)17-13-26(18-7-5-4-6-16(17)18)12-14-8-10-15(23)11-9-14/h4-11,13,19H,12H2,1-3H3,(H2,24,27)(H,25,28)/t19-/m1/s1 Key:QIFOZYUACLDTAJ-LJQANCHMSA-N