List of JWH cannabinoids

Short description: None

The John W. Huffman research group at Clemson University synthesized over 450 cannabinoids.[1][2][3][4] Some of those are:

Cannabinoids and their Ki values[lower-alpha 1] Name  | Class  | Ki / nM at CB1 | Ki / nM at CB2 | Selectivity  | Structure

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JWH-004 | Naphthoylindole | 48 ± 13 | 4 ± 1.5 | CB2 (12x) |
JWH-007[5] | Naphthoylindole | 9.5 ± 4.5 | 2.9 ± 2.6 | CB2 (3.3x) |
JWH-009 | Naphthoylindole | >10000 | 141 ± 14 | CB2 (>70x) |
JWH-011 | Naphthoylindole |  |  |  |
JWH-015[5] | Naphthoylindole | 164 ± 22 | 13.8 ± 4.6 | CB2 (12x) |
JWH-016 | Naphthoylindole | 22 ± 1.5 | 4.3 ± 1.6 | CB2 (5.1x) |
JWH-018[5] | Naphthoylindole | 9 ± 5 | 2.9 ± 2.6 | CB2 (3.1x) |
JWH-019 | Naphthoylindole | 9.8 ± 2 | 5.55 ± 2 | CB2 (1.77x) |
JWH-020 | Naphthoylindole | 128 ± 17 | 205 ± 20 | CB1 (1.6x) |
JWH-030 | Naphthoylpyrrole | 87 ± 3 | 320 ± 127 | CB1 (3.7x) |
JWH-031 | Naphthoylpyrrole | 399 ± 109 |  |  |
JWH-032 | Naphthoylpyrrole | >10000 | >10000 | — |
JWH-033 | Naphthoylpyrrole | 666 ± 77 |  |  |
JWH-036 | Naphthoylpyrrole | 309 ± 11 |  |  |
JWH-042[6] | Naphthoylindole | >10000 | 5050 ± 192 | CB2 |
JWH-043[6] | Naphthoylindole | 1180 ± 44 | 964 ± 242 | CB2 (1.2x) |
JWH-044 | Naphthoylpyrrole | >10000 | >10000 | — |
JWH-045 | Naphthoylpyrrole | >10000 | >10000 | — |
JWH-046[6] | Naphthoylindole | 343 ± 38 | 16.3 ± 4.9 | CB2 (21x) |
JWH-047[6] | Naphthoylindole | 59 ± 3 | 3.47 ± 1.80 | CB2 (17x) |
JWH-048[6] | Naphthoylindole | 10.7 ± 1.0 | 0.49 ± 0.13 | CB2 (22x) |
JWH-049[6] | Naphthoylindole | 55.1 ± 17.0 | 32.3 ± 2.4 | CB2 (1.7x) |
JWH-050[6] | Naphthoylindole | 342 ± 6 | 526 ± 133 | CB1 (1.5x) |
JWH-051 | Dibenzopyran | 1.20 | 0.03 | CB2 (40x) |
JWH-056[7] | Dibenzopyran | >10000 | 32 ± 9 | CB2 |
JWH-057[8] | Dibenzopyran | 23 ± 7 | 2.9 ± 1.6 | CB2 (8x) |
JWH-065[7] | Dibenzopyran | 399 ± 76 | 10 ± 2 | CB2 (40x) |
JWH-070[6] | Naphthoylindole | >10000 | >10000 |  |
JWH-071[6] | Naphthoylindole | 1340 ± 123 | 2940 ± 852 | CB1 (2.2x) |
JWH-072 | Naphthoylindole | 1050 ± 5.5 | 170 ± 54 | CB2 (6x) |
JWH-073 | Naphthoylindole | 8.9 ± 1.8 | 27 ± 12 | CB1 (3x) |
JWH-076[5] | Naphthoylindole | 214 ± 11 | 106 ± 46 | CB2 (2x) |
JWH-077[6] | Naphthoylindole | >10000 | >10000 |  |
JWH-078[6] | Naphthoylindole | 817 ± 60 | 633 ± 116 | CB2 (1.3x) |
JWH-079[6] | Naphthoylindole | 63.0 ± 3.0 | 32.0 ± 6.0 | CB2 (2x) |
JWH-080[6] | Naphthoylindole | 8.9 ± 1.8 | 2.21 ± 1.30 | CB2 (4x) |
JWH-081[6] | Naphthoylindole | 1.2 ± 0.03 | 12.4 ± 2.2 | CB1 (10x) |
JWH-082[6] | Naphthoylindole | 5.3 ± 0.8 | 6.40 ± 0.94 | CB1 (1.2x) |
JWH-083[6] | Naphthoylindole | 106 ± 12 | 102 ± 50 | — |
JWH-091[9] (Δ8-THCP) | Dibenzopyran | 22.0 ± 3.9 |  |  |
JWH-093[6] | Naphthoylindole | 40.7 ± 2.8 | 59.1 ± 10.5 | CB1 (1.45x) |
JWH-094[6] | Naphthoylindole | 476 ± 67 | 97.3 ± 2.7 | CB2 (4.9x) |
JWH-095[6] | Naphthoylindole | 140 ± 4.3 | 312 ± 83 | CB1 (2.2x) |
JWH-096[6] | Naphthoylindole | 33.7 ± 2.9 | 13.3 ± 5.6 | CB2 (2.5x) |
JWH-097[6] | Naphthoylindole | 455 ± 28 | 121 ± 15 | CB2 (3.8x) |
JWH-098[6] | Naphthoylindole | 4.5 ± 0.1 | 1.9 ± 0.3 | CB2 (2.4x) |
JWH-099[6] | Naphthoylindole | 35.3 ± 9.0 | 17.8 ± 2.9 | CB2 (2x) |
JWH-100[6] | Naphthoylindole | 381 ± 102 | 155 ± 74 | CB2 (2.5x) |
JWH-102[7] | Dibenzopyran | 7.9 ± 0.9 | 5.2 ± 2.0 | CB2 (1.5x) |
JWH-103[7] | Dibenzopyran | 28 ± 3 | 23 ± 7 | CB2 (1.2x) |
JWH-116[10] | Naphthoylindole | 52 ± 5 |  |  |
JWH-120[5] | Naphthoylindole | 1054 ± 31 | 6.1 ± 0.7 | CB2 (173x) |
JWH-122[10] | Naphthoylindole | 0.69 ± 0.05 | 1.2 ± 1.2 | — |
JWH-124 (Δ8-Parahexyl) | Dibenzopyran | 41.0 ± 3.8 |  |  |
JWH-130 (Δ8-THCB) | Dibenzopyran | 65.0 ± 13 |  |  |
JWH-133[7] | Dibenzopyran | 677 ± 132 | 3.4 ± 1.0 | CB2 (200x) |
JWH-138[11] | Dibenzopyran | 8.5 ± 1.4 |  |  |
JWH-139[12] | Dibenzopyran | 2290 ± 505 | 14 ± 10 | CB2 (164x) |
JWH-142[7] | Dibenzopyran | 529 ± 49 | 35 ± 14 | CB2 (15x) |
JWH-143[7] | Dibenzopyran | 924 ± 104 | 65 ± 8 | CB2 (14x) |
JWH-145[13] | Naphthoylpyrrole | 14 ± 2 | 6.4 ± 0.4 | CB2 (2.2x) |
JWH-146[13] | Naphthoylpyrrole | 21 ± 2 | 62 ± 5 | CB2 (3.0x) |
JWH-147[13] | Naphthoylpyrrole | 11 ± 1 | 7.1 ± 0.2 | CB2 (1.5x) |
JWH-148[5] | Naphthoylindole | 123 ± 8 | 14.0 ± 1.0 | CB2 (8x) |
JWH-149[5] | Naphthoylindole | 5.0 ± 2.1 | 0.73 ± 0.03 | CB2 (6.8x) |
JWH-150[13] | Naphthoylpyrrole | 60 ± 1 | 15 ± 2 | CB2 (4x) |
JWH-151[5] | Naphthoylindole | >10000 | 30 ± 1.1 | CB2 (>333x) |
JWH-153[5] | Naphthoylindole | 250 ± 24 | 11 ± 0.5 | CB2 (23x) |
JWH-156[13] | Naphthoylpyrrole | 404 ± 18 | 104 ± 18 | CB2 (4x) |
JWH-159[5] | Naphthoylindole | 45 ± 1 | 10.4 ± 1.4 | CB2 (4.3x) |
JWH-160[5] | Naphthoylindole | 1568 ± 201 | 441 ± 110 | CB2 (3.6x) |
JWH-161 | Dibenzopyran hybrid | 19.0 |  |  |
JWH-163[5] | Naphthoylindole | 2358 ± 215 | 138 ± 12 | CB2 (17x) |
JWH-164[5] | Naphthoylindole | 6.6 ± 0.7 | 6.9 ± 0.2 | — |
JWH-165[5] | Naphthoylindole | 204 ± 26 | 71 ± 8 | CB2 (2.9x) |
JWH-166[5] | Naphthoylindole | 44 ± 10 | 1.9 ± 0.08 | CB2 (23x) |
JWH-167 | Phenylacetylindole | 90 ± 17 | 159 ± 14 | CB1 (1.77x) |
JWH-171 | Hydrocarbon | 51 |  |  |
JWH-175[10] | Naphthylmethylindole | 22 ± 2 |  |  |
JWH-176[10] | Hydrocarbon | 26 ± 4 |  |  |
JWH-180[5] | Naphthoylindole | 26 ± 2 | 9.6 ± 2.0 | CB2 (2.7x) |
JWH-181[5] | Naphthoylindole | 1.3 ± 0.1 | 0.62 ± 0.04 | CB2 (2.1x) |
JWH-182[5] | Naphthoylindole | 0.65 ± 0.03 | 1.1 ± 0.1 | CB1 (1.7x) |
JWH-184[10] | Naphthylmethylindole | 23 ± 6 |  |  |
JWH-185[10] | Naphthylmethylindole | 17 ± 3 |  |  |
JWH-186[14] | Dibenzopyran | 187 ± 23 | 5.6 ± 1.7 | CB2 (33x) |
JWH-187[14] | Dibenzopyran | 84 ± 16 | 3.4 ± 0.5 | CB2 (25x) |
JWH-188[14] | Dibenzopyran | 270 ± 58 | 18 ± 2 | CB2 (15x) |
JWH-189[5] | Naphthoylindole | 52 ± 2 | 12 ± 0.8 | CB2 (4.3x) |
JWH-190[14] | Dibenzopyran | 8.8 ± 1.4 | 1.6 ± 0.03 | CB2 (5.5x) |
JWH-191[14] | Dibenzopyran | 1.8 ± 0.3 | 0.52 ± 0.03 | CB2 (3.5x) |
JWH-192[10] | Naphthylmethylindole | 41 ± 13 |  |  |
JWH-193[10] | Naphthoylindole | 6 ± 1 |  |  |
JWH-194[10] | Naphthylmethylindole | 127 ± 19 |  |  |
JWH-195[10] | Naphthylmethylindole | 113 ± 28 |  |  |
JWH-196[10] | Naphthylmethylindole | 151 ± 18 |  |  |
JWH-197[10] | Naphthylmethylindole | 323 ± 98 |  |  |
JWH-198[10] | Naphthoylindole | 10 ± 2 |  |  |
JWH-199[10] | Naphthylmethylindole | 20 ± 2 |  |  |
JWH-200[10] | Naphthoylindole | 42 ± 5 |  |  |
JWH-201[15] | Phenylacetylindole | 1064 ± 21 | 444 ± 14 | CB2 (2.4x) |
JWH-202[15] | Phenylacetylindole | 1678 ± 63 | 645 ± 6 | CB2 (2.6x) |
JWH-203[15] | Phenylacetylindole | 8.0 ± 0.9 | 7.0 ± 1.3 | — |
JWH-204[15] | Phenylacetylindole | 13 ± 1 | 25 ± 1 | CB1 (1.9x) |
JWH-205[15] | Phenylacetylindole | 124 ± 23 | 180 ± 9 | CB1 (1.45x) |
JWH-206[15] | Phenylacetylindole | 389 ± 25 | 498 ± 37 | CB1 (1.28x) |
JWH-207[15] | Phenylacetylindole | 1598 ± 134 | 3723 ± 10 | CB1 (2.33x) |
JWH-208[15] | Phenylacetylindole | 179 ± 7 | 570 ± 127 | CB1 (3.18x) |
JWH-209[15] | Phenylacetylindole | 746 ± 49 | 1353 ± 270 | CB1 (1.81x) |
JWH-210[5] | Naphthoylindole | 0.46 ± 0.03 | 0.69 ± 0.01 | CB1 (1.5x) |
JWH-211[5] | Naphthoylindole | 70 ± 0.8 | 12 ± 0.8 | CB2 (5.8x) |
JWH-212[5] | Naphthoylindole | 33 ± 0.9 | 10 ± 1.2 | CB2 (3.3x) |
JWH-213[5] | Naphthoylindole | 1.5 ± 0.2 | 0.42 ± 0.05 | CB2 (3.6x) |
JWH-215[14] | Dibenzopyran | 1008 ± 117 | 85 ± 21 | CB2 (12x) |
JWH-216[14] | Dibenzopyran | 1856 ± 148 | 333 ± 104 | CB2 (5.6x) |
JWH-217[14] | Dibenzopyran | >10000 | 1404 ± 66 | CB2 (>7x) |
JWH-220 | Hydrocarbon | 19 |  |  |
JWH-224[14] | Dibenzopyran | 347 ± 34 | 28 ± 1 | CB2 (12.3x) |
JWH-225[14] | Dibenzopyran | >10000 | 325 ± 70 | CB2 (>31x) |
JWH-226[14] | Dibenzopyran | 4001 ± 282 | 43 ± 3 | CB2 (93x) |
JWH-227[14] | Dibenzopyran | 40 ± 6 | 4.4 ± 0.3 | CB2 (9x) |
JWH-229[16] | Dibenzopyran | 3134 ± 110 | 18 ± 2 | CB2 (174x) |
JWH-230[14] | Dibenzopyran | 15 ± 3 | 1.4 ± 0.12 | CB2 (10.7x) |
JWH-233[14] | Dibenzopyran | 14 ± 3 | 1.0 ± 0.3 | CB2 (14x) |
JWH-234[5] | Naphthoylindole | 8.4 ± 1.8 | 3.8 ± 0.6 | CB2 (2.2x) |
JWH-235[5] | Naphthoylindole | 338 ± 34 | 123 ± 34 | CB2 (2.7x) |
JWH-236[5] | Naphthoylindole | 1351 ± 204 | 240 ± 63 | CB2 (5.6x) |
JWH-237[15] | Phenylacetylindole | 38 ± 10 | 106 ± 2 | CB1 (2.8x) |
JWH-239[5] | Naphthoylindole | 342 ± 20 | 52 ± 6 | CB2 (6.6x) |
JWH-240[5] | Naphthoylindole | 14 ± 1 | 7.2 ± 1.3 | CB2 (1.9x) |
JWH-241[5] | Naphthoylindole | 147 ± 20 | 49 ± 7 | CB2 (3.0x) |
JWH-242[5] | Naphthoylindole | 42 ± 9 | 6.5 ± 0.3 | CB2 (6.5x) |
JWH-243[13] | Naphthoylpyrrole | 285 ± 40 | 41 ± 3 | CB2 (6.95x) |
JWH-244[13] | Naphthoylpyrrole | 130 ± 6 | 18 ± 1 | CB2 (7.22x) |
JWH-245[13] | Naphthoylpyrrole | 276 ± 4 | 25 ± 2 | CB2 (11x) |
JWH-246[13] | Naphthoylpyrrole | 70 ± 4 | 16 ± 1 | CB2 (4.38x) |
JWH-247[14] | Dibenzopyran | 427 ± 31 | 99 ± 4 | CB2 (4.3x) |
JWH-248[15] | Phenylacetylindole | 1028 ± 39 | 657 ± 19 | CB2 (1.56x) |
JWH-249[15] | Phenylacetylindole | 8.4 ± 1.8 | 20 ± 2 | CB1 (2.38x) |
JWH-250[15] | Phenylacetylindole | 11 ± 2 | 33 ± 2 | CB1 (3x) |
JWH-251[15] | Phenylacetylindole | 29 ± 3 | 146 ± 36 | CB2 (5x) |
JWH-252[15] | Phenylacetylindole | 23 ± 3 | 19 ± 1 | CB2 (1.2x) |
JWH-253[15] | Phenylacetylindole | 62 ± 10 | 84 ± 12 | CB1 (1.35x) |
JWH-254[14] | Dibenzopyran | 4724 ± 509 | 319 ± 16 | CB2 (14.8x) |
JWH-256[14] | Dibenzopyran | 4300 ± 888 | 97 ± 18 | CB2 (44x) |
JWH-258[5] | Naphthoylindole | 4.6 ± 0.6 | 10.5 ± 1.3 | CB1 (2.3x) |
JWH-259[5] | Naphthoylindole | 220 ± 29 | 74 ± 7 | CB2 (3.0x) |
JWH-260[5] | Naphthoylindole | 29 ± 0.4 | 25 ± 1.9 | CB2 (1.2x) |
JWH-261[5] | Naphthoylindole | 767 ± 105 | 221 ± 14 | CB2 (3.5x) |
JWH-262[5] | Naphthoylindole | 28 ± 3 | 5.6 ± 0.7 | CB2 (5.0x) |
JWH-265[5] | Naphthoylindole | 3788 ± 323 | 80 ± 13 | CB2 (47x) |
JWH-266[5] | Naphthoylindole | >10000 | 455 ± 55 | CB2 (>22x) |
JWH-267[5] | Naphthoylindole | 381 ± 16 | 7.2 ± 0.14 | CB2 (53x) |
JWH-268[5] | Naphthoylindole | 1379 ± 193 | 40 ± 0.6 | CB2 (34x) |
JWH-277[14] | Dibenzopyran | 3905 ± 91 | 589 ± 65 | CB2 (6.6x) |
JWH-278[14] | Dibenzopyran | 906 ± 80 | 69 ± 6 | CB2 (13x) |
JWH-292[13] | Naphthoylpyrrole | 29 ± 1 | 20 ± 1 | CB2 (1.45x) |
JWH-293[13] | Naphthoylpyrrole | 100 ± 5 | 41 ± 4 | CB2 (2.44x) |
JWH-298[14] | Dibenzopyran | 812 ± 67 | 198 ± 23 | CB2 (4.1x) |
JWH-299[14] | Dibenzopyran | 415 ± 50 | 30 ± 2 | CB2 (13.8x) |
JWH-300[12] | Dibenzopyran | 118 ± 16 | 5.3 ± 0.1 | CB2 (22x) |
JWH-301[14] | Dibenzopyran | 295 ± 64 | 48 ± 4 | CB2 (6.1x) |
JWH-302[15] | Phenylacetylindole | 17 ± 2 | 89 ± 15 | CB1 (5.26x) |
JWH-303[15] | Phenylacetylindole | 117 ± 10 | 138 ± 12 | CB1 (1.18x) |
JWH-304[15] | Phenylacetylindole | 3363 ± 332 | 2679 ± 688 | CB2 (1.26x) |
JWH-305[15] | Phenylacetylindole | 15 ± 1.8 | 29 ± 5 | CB1 (1.93x) |
JWH-306[15] | Phenylacetylindole | 25 ± 1 | 82 ± 11 | CB1 (3.28x) |
JWH-307[13] | Naphthoylpyrrole | 7.7 ± 1.8 | 3.3 ± 0.2 | CB2 (2.33x) |
JWH-308[13] | Naphthoylpyrrole | 41 ± 1 | 33 ± 2 | CB2 (1.24x) |
JWH-309[13] | Naphthoylpyrrole | 41 ± 3 | 49 ± 7 | CB1 (1.20x) |
JWH-310[14] | Dibenzopyran | 1059 ± 51 | 36 ± 3 | CB2 (29x) |
JWH-311[15] | Phenylacetylindole | 23 ± 2 | 39 ± 3 | CB1 (1.70x) |
JWH-312[15] | Phenylacetylindole | 72 ± 7 | 91 ± 20 | CB1 (1.26x) |
JWH-313[15] | Phenylacetylindole | 422 ± 19 | 365 ± 92 | CB2 (1.16x) |
JWH-314[15] | Phenylacetylindole | 39 ± 2 | 76 ± 4 | CB1 (1.95x) |
JWH-315[15] | Phenylacetylindole | 430 ± 24 | 182 ± 23 | CB2 (3.36x) |
JWH-316[15] | Phenylacetylindole | 2862 ± 670 | 781 ± 105 | CB2 (3.66x) |
JWH-336[12] | Dibenzopyran | 4589 ± 367 | 153 ± 15 | CB2 (30x) |
JWH-338[14] | Dibenzopyran | >10000 | 111 ± 16 | CB2 (>90x) |
JWH-339[14] | Dibenzopyran | >10000 | 2317 ± 93 | CB2 (>4.3x) |
JWH-340[14] | Dibenzopyran | 135 ± 6 | 30 ± 1 | CB2 (4.5x) |
JWH-341[14] | Dibenzopyran | 100 ± 8 | 10 ± 0.1 | CB2 (10x) |
JWH-346[13] | Naphthoylpyrrole | 67 ± 6 | 39 ± 2 | CB2 (1.72x) |
JWH-347[13] | Naphthoylpyrrole | 333 ± 17 | 169 ± 17 | CB2 (1.97x) |
JWH-348[13] | Naphthoylpyrrole | 218 ± 19 | 53 ± 1 | CB2 (4.11x) |
JWH-349[14] | Dibenzopyran | 376 ± 1 | 38 ± 4 | CB2 (9.9x) |
JWH-350[12] | Dibenzopyran | 395 ± 50 | 12 ± 1 | CB2 (33x) |
JWH-351[14] | Dibenzopyran | >10000 | 295 ± 3 | CB2 (>34x) |
JWH-352[14] | Dibenzopyran | >10000 | 47 ± 2 | CB2 (>213x) |
JWH-353[14] | Dibenzopyran | 1493 ± 10 | 31 ± 1 | CB2 (48x) |
JWH-354[14] | Dibenzopyran | 1961 ± 21 | 241 ± 14 | CB2 (8.1x) |
JWH-355[14] | Dibenzopyran | 2162 ± 220 | 108 ± 17 | CB2 (20x) |
JWH-356[14] | Dibenzopyran | 5837 ± 701 | 108 ± 17 | CB2 (54x) |
JWH-357[14] | Dibenzopyran | 647 ± 78 | 185 ± 4 | CB2 (3.5x) |
JWH-358[14] | Dibenzopyran | 1243 ± 266 | 52 ± 3 | CB2 (24x) |
JWH-359 | Dibenzopyran | 2918 ± 450 | 13.0 ± 0.2  | CB2 (220x) |
JWH-360[14] | Dibenzopyran | 2449 ± 606 | 160 ± 8 | CB2 (15x) |
JWH-361[14] | Dibenzopyran | 63 ± 3 | 2.7 ± 0.1 | CB2 (23x) |
JWH-362[14] | Dibenzopyran | 127 ± 8  | 34 ± 5 | CB2 (3.7x) |
JWH-363[13] | Naphthoylpyrrole | 245 ± 5 | 71 ± 1 | CB2 (3.45x) |
JWH-364[13] | Naphthoylpyrrole | 34 ± 3 | 29 ± 1 | CB2 (1.17x) |
JWH-365[13] | Naphthoylpyrrole | 17 ± 1 | 3.4 ± 0.2 | CB2 (5.0x) |
JWH-366[13] | Naphthoylpyrrole | 191 ± 12 | 24 ± 1 | CB2 (7.96x) |
JWH-367[13] | Naphthoylpyrrole | 53 ± 2 | 23 ± 1 | CB2 (2.30x) |
JWH-368[13] | Naphthoylpyrrole | 16 ± 1 | 9.1 ± 0.7 | CB2 (1.76x) | Error creating thumbnail: Unable to save thumbnail to destination
JWH-369[13] | Naphthoylpyrrole | 7.9 ± 0.4 | 5.2 ± 0.3 | CB2 (1.52x) |
JWH-370[13] | Naphthoylpyrrole | 5.6 ± 0.4 | 4.0 ± 0.5 | CB2 (1.40x) |
JWH-371[13] | Naphthoylpyrrole | 42 ± 1 | 64 ± 2 | CB1 (1.52x) |
JWH-372[13] | Naphthoylpyrrole | 77 ± 2 | 8.2 ± 0.2 | CB1 (9.39x) |
JWH-373[13] | Naphthoylpyrrole | 60 ± 3 | 69 ± 2 | CB1 (1.15x) |
JWH-387[17] | Naphthoylindole | 1.2 ± 0.1 | 1.1 ± 0.1 | — |
JWH-398[18] | Naphthoylindole | 2.3 ± 0.1 | 2.8 ± 0.2 | CB1 (1.22x) |
JWH-416[17] | Naphthoylindole | 73 ± 10 | 3.3 ± 0.1 | CB2 (22x) |
JWH-417[17] | Naphthoylindole | 522 ± 58 | 13 ± 0.2 | CB2 (40x) |
JWH-422[17] | Naphthoylindole | 501 ± 48 | 20 ± 0.4 | CB2 (25x) |
JWH-423[17] | Naphthoylindole | 140 ± 10 | 6.6 ± 0.2 | CB2 (21x) |
JWH-424[17] | Naphthoylindole | 21 ± 3.4 | 5.4 ± 0.2 | CB2 (3.9x) | Error creating thumbnail: Unable to save thumbnail to destination
JWH-425[17] | Naphthoylindole | 54 ± 11 | 10 ± 0.4 | CB2 (5.4x) |

## See also

* List of AM cannabinoids
* List of CP cannabinoids
* List of HU cannabinoids
* List of miscellaneous designer cannabinoids

## Notes

1. ↑ Ki is the compound's binding affinity for the cannabinoid receptor type 1 (CB1) or cannabinoid receptor type 2 (CB2).

## References

1. ↑ "Indoles and related compounds as cannabinoid ligands". Mini Rev Med Chem 8 (4): 370–87. 2008. doi:10.2174/138955708783955935. PMID 18473928.
2. ↑ "Moving around the molecule: relationship between chemical structure and in vivo activity of synthetic cannabinoids". Life Sci 97 (1): 55–63. 2014. doi:10.1016/j.lfs.2013.09.011. PMID 24071522.
3. ↑ "Combination Chemistry: Structure-Activity Relationships of Novel Psychoactive Cannabinoids". Curr Top Behav Neurosci. Current Topics in Behavioral Neurosciences 32: 231–248. 2017. doi:10.1007/7854_2016_17. ISBN 978-3-319-52442-9. PMID 27753007.
4. ↑ "The Chemistry and Pharmacology of Synthetic Cannabinoid Receptor Agonists as New Psychoactive Substances: Origins". New Psychoactive Substances. Handbook of Experimental Pharmacology. 252. 2018. pp. 165–190. doi:10.1007/164_2018_143. ISBN 978-3-030-10560-0.
5. ↑ 5.00 5.01 5.02 5.03 5.04 5.05 5.06 5.07 5.08 5.09 5.10 5.11 5.12 5.13 5.14 5.15 5.16 5.17 5.18 5.19 5.20 5.21 5.22 5.23 5.24 5.25 5.26 5.27 5.28 5.29 5.30 5.31 5.32 5.33 5.34 5.35 5.36 5.37 5.38 "Structure-activity relationships for 1-alkyl-3-(1-naphthoyl)indoles at the cannabinoid CB(1) and CB(2) receptors: steric and electronic effects of naphthoyl substituents. New highly selective CB(2) receptor agonists". Bioorganic & Medicinal Chemistry 13 (1): 89–112. January 2005. doi:10.1016/j.bmc.2004.09.050. PMID 15582455.
6. ↑ 6.00 6.01 6.02 6.03 6.04 6.05 6.06 6.07 6.08 6.09 6.10 6.11 6.12 6.13 6.14 6.15 6.16 6.17 6.18 6.19 6.20 6.21 6.22 6.23 "Influence of the N-1 alkyl chain length of cannabimimetic indoles upon CB(1) and CB(2) receptor binding". Drug and Alcohol Dependence 60 (2): 133–40. August 2000. doi:10.1016/S0376-8716(99)00152-0. PMID 10940540.
7. ↑ 7.0 7.1 7.2 7.3 7.4 7.5 7.6 "3-(1',1'-Dimethylbutyl)-1-deoxy-delta8-THC and related compounds: synthesis of selective ligands for the CB2 receptor". Bioorganic & Medicinal Chemistry 7 (12): 2905–14. December 1999. doi:10.1016/s0968-0896(99)00219-9. PMID 10658595.
8. ↑ "Synthesis and pharmacology of a very potent cannabinoid lacking a phenolic hydroxyl with high affinity for the CB2 receptor". Journal of Medicinal Chemistry 39 (20): 3875–7. September 1996. doi:10.1021/JM960394Y. PMID 8831752.
9. ↑ Bow EW, Rimoldi JM. The Structure-Function Relationships of Classical Cannabinoids: CB1/CB2 Modulation. Perspect Medicin Chem. 2016 Jun 28;8:17-39. doi:10.4137/PMC.S32171 PMID 27398024
10. ↑ 10.00 10.01 10.02 10.03 10.04 10.05 10.06 10.07 10.08 10.09 10.10 10.11 10.12 10.13 10.14 "3-Indolyl-1-naphthylmethanes: new cannabimimetic indoles provide evidence for aromatic stacking interactions with the CB(1) cannabinoid receptor". Bioorganic & Medicinal Chemistry 11 (4): 539–49. February 2003. doi:10.1016/S0968-0896(02)00451-0. PMID 12538019.
11. ↑ Martin BR, Jefferson R, Winckler R, Wiley JL, Huffman JW, Crocker PJ, Saha B, Razdan RK. Manipulation of the tetrahydrocannabinol side chain delineates agonists, partial agonists, and antagonists. J Pharmacol Exp Ther. 1999 Sep;290(3):1065-79. PMID 10454479
12. ↑ 12.0 12.1 12.2 12.3 "International Union of Pharmacology. XXVII. Classification of cannabinoid receptors". Pharmacological Reviews 54 (2): 161–202. June 2002. doi:10.1124/pr.54.2.161. PMID 12037135.
13. ↑ 13.00 13.01 13.02 13.03 13.04 13.05 13.06 13.07 13.08 13.09 13.10 13.11 13.12 13.13 13.14 13.15 13.16 13.17 13.18 13.19 13.20 13.21 13.22 13.23 13.24 13.25 13.26 13.27 "1-Alkyl-2-aryl-4-(1-naphthoyl)pyrroles: new high affinity ligands for the cannabinoid CB1 and CB2 receptors". Bioorganic & Medicinal Chemistry Letters 16 (20): 5432–5. October 2006. doi:10.1016/j.bmcl.2006.07.051. PMID 16889960.
14. ↑ 14.00 14.01 14.02 14.03 14.04 14.05 14.06 14.07 14.08 14.09 14.10 14.11 14.12 14.13 14.14 14.15 14.16 14.17 14.18 14.19 14.20 14.21 14.22 14.23 14.24 14.25 14.26 14.27 14.28 14.29 14.30 14.31 14.32 14.33 14.34 14.35 14.36 14.37 14.38 "Recent advances in the development of selective ligands for the cannabinoid CB(2) receptor". Current Topics in Medicinal Chemistry 8 (3): 187–204. 2008. doi:10.2174/156802608783498014. PMID 18289088.
15. ↑ 15.00 15.01 15.02 15.03 15.04 15.05 15.06 15.07 15.08 15.09 15.10 15.11 15.12 15.13 15.14 15.15 15.16 15.17 15.18 15.19 15.20 15.21 15.22 15.23 15.24 15.25 15.26 "1-Pentyl-3-phenylacetylindoles, a new class of cannabimimetic indoles". Bioorganic & Medicinal Chemistry Letters 15 (18): 4110–3. September 2005. doi:10.1016/j.bmcl.2005.06.008. PMID 16005223.
16. ↑ "1-Methoxy-, 1-deoxy-11-hydroxy- and 11-hydroxy-1-methoxy-Delta(8)-tetrahydrocannabinols: new selective ligands for the CB2 receptor". Bioorganic & Medicinal Chemistry 10 (12): 4119–29. December 2002. doi:10.1016/s0968-0896(02)00331-0. PMID 12413866.
17. ↑ 17.0 17.1 17.2 17.3 17.4 17.5 17.6 "Synthesis and pharmacology of 1-alkyl-3-(1-naphthoyl)indoles: Steric and electronic effects of 4- and 8-halogenated naphthoyl substituents". Bioorganic & Medicinal Chemistry 20 (6): 2067–2081. 2012. doi:10.1016/j.bmc.2012.01.038. PMID 22341572.
18. ↑ The Cannabinoid Receptors. The Receptors. 2009. doi:10.1007/978-1-59745-503-9. ISBN 978-1-58829-712-9.

* v
* t
* e

Cannabinoids

Phytocannabinoids|

* Alkylamides
* Caryophyllene
* CBC
* CBCV
* CBD
* CBDV
* CBG
* CBGM
* CBGV
* CBL
* CBDL
* CBN
* CBV
* Epigallocatechin gallate
* Gallocatechol
* Perrottetinene
* Serinolamide A
* THC
* THC-C4
* THCA
* THCV
* Yangonin

* Active metabolites: 8,11-DiOH-THC
* 11-COOH-THC
* 11-OH-THC

Endocannabinoids|

* Arachidonoyl ethanolamide (AEA; anandamide)
* 2-Arachidonoylglycerol (2-AG)
* 2-Arachidonyl glyceryl ether (2-AGE; noladin ether)
* 2-Oleoylglycerol (2-OG)
* N-Arachidonoyl dopamine (NADA)
* N-Arachidonylglycine (NAGly)
* 2-Arachidonoyl lysophosphatidylinositol (2-ALPI)
* N-Arachidonoyl serotonin (AA-5-HT)
* Docosatetraenoylethanolamide (DEA)
* Lysophosphatidylinositol (LPI)
* Oleamide
* Oleoylethanolamide (OEA)
* Palmitoylethanolamide (PEA)
* RVD-Hpα
* Stearoylethanolamide (SEA)
* O-Arachidonoyl ethanolamine (O-AEA; virodhamine)

Synthetic
cannabinoids|

| Classical cannabinoids
(dibenzopyrans)|

* A-40174
* A-41988
* A-42574
* Ajulemic acid
* AM-087
* AM-411
* AM-855
* AM-905
* AM-906
* AM-919
* AM-926
* AM-938
* AM-2389
* AM-4030
* AMG-1
* AMG-3
* AMG-36
* AMG-41
* Dexanabinol (HU-211)
* DMHP
* Dronabinol
* HHC
* HU-210
* HU-243
* JWH-051
* JWH-133
* JWH-139
* JWH-161
* JWH-229
* JWH-359
* KM-233
* L-759,633
* L-759,656
* Levonantradol (CP 50,5561)
* Menabitan
* Nabazenil
* Nabidrox (Canbisol)
* Nabilone
* Nabitan
* Naboctate
* O-224
* O-581
* O-774
* O-806
* O-823
* O-1057
* O-1125
* O-1191
* O-1238
* O-2048
* O-2113
* O-2365
* O-2372
* O-2373
* O-2383
* O-2426
* O-2484
* O-2545
* O-2694
* O-2715
* O-2716
* O-3223
* O-3226
* Parahexyl
* Pirnabine
* THC-O-acetate
* THC-O-phosphate

|

Non-classical
cannabinoids|

* Cannabicyclohexanol
* CBD-DMH
* CP 47,497
* (C6)-CP 47,497
* (C9)-CP 47,497
* CP 55,244
* CP 55,940
* HU-308
* HU-320
* HU-331
* HU-336
* HU-345
* HU-446
* HU-465
* HU-910
* HUF-101
* Nonabine
* O-1376
* O-1422
* O-1601
* O-1656
* O-1657
* O-1660
* O-1663
* O-1871
* SPA-229
* Tinabinol

Benzoylindoles|

* 1-Butyl-3-(2-methoxybenzoyl)indole
* 1-Butyl-3-(4-methoxybenzoyl)indole
* 1-Pentyl-3-(2-methoxybenzoyl)indole
* AM-630
* AM-679
* AM-694
* AM-1241
* AM-2233
* GW-405,833 (L-768,242)
* Pravadoline
* RCS-4
* WIN 54,461

Naphthoylindoles|

* AM-1220
* AM-1221
* AM-1235
* AM-2201
* AM-2232
* CHM-081
* EAM-2201
* FUB-JWH-018
* JWH-007
* JWH-015
* JWH-018
* JWH-019
* JWH-073
* JWH-081
* JWH-098
* JWH-116
* JWH-122
* JWH-149
* JWH-164
* JWH-182
* JWH-193
* JWH-198
* JWH-200
* JWH-210
* JWH-398
* JWH-424
* MAM-1220
* MAM-2201
* NE-CHMIMO

Naphthoylindazoles|

* THJ-018
* THJ-2201

Pyrrolobenzoxazines|

* WIN 55,212-2

Naphthylmethylindoles|

* JWH-175
* JWH-176
* JWH-184
* JWH-185
* JWH-192
* JWH-194
* JWH-195
* JWH-196
* JWH-197
* JWH-199

Phenylacetylindoles|

* Cannabipiperidiethanone
* JWH-167
* JWH-203
* JWH-249
* JWH-250
* JWH-251
* JWH-302
* RCS-8

Indole-3-carboxamides|

* 5F-ADBICA
* 5F-MDMB-PICA
* 5F-NNE1
* 5F-PCN
* 5F-SDB-006
* AB-FUBICA
* AB-PICA
* ADBICA
* ADB-FUBICA
* APICA
* CUMYL-BICA
* CUMYL-PICA
* CUMYL-5F-PICA
* FDU-NNE1
* MDMB-CHMICA
* MMB-CHMICA
* MMB-2201
* MN-25 (UR-12)
* NNE1
* PX-1
* Org 28312
* Org 28611
* SDB-006
* STS-135

Indole-3-carboxylates|

* 5F-PB-22
* FDU-PB-22
* FUB-PB-22
* QUCHIC (BB-22)
* QUPIC (PB-22)
* NM-2201

Tetramethylcyclo-
propanoylindoles|

* 5Br-UR-144
* 5Cl-UR-144
* A-796,260
* A-834,735
* FUB-144
* UR-144
* XLR-11
* XLR-12

Indazole-3-
carboxamides|

* 4F-MDMB-BINACA
* 5Cl-APINACA
* 5F-ADB
* 5F-ADB-PINACA
* 5F-AMB
* 5F-APINACA
* 5F-CUMYL-PINACA
* 5F-EDMB-PINACA
* 5F-EMB-PINACA
* AB-CHMINACA
* AB-FUBINACA
* AB-FUBINACA 2-fluorobenzyl isomer
* AB-PINACA
* ADB-CHMINACA
* ADB-FUBINACA
* ADB-PINACA
* Adamantyl-THPINACA
* ADSB-FUB-187
* AMB-CHMINACA
* AMB-FUBINACA
* APINACA (AKB48)
* APP-FUBINACA
* CUMYL-4CN-BINACA
* CUMYL-PINACA
* CUMYL-THPINACA
* EMB-FUBINACA
* FUB-APINACA
* MDMB-4en-PINACA
* MDMB-FUBINACA
* MDMB-CHMINACA
* MN-18
* PX-2
* PX-3

Tetramethylcyclo-
propanoylindazoles|

* FAB-144

Naphthoylpyrroles|

* JWH-030
* JWH-147
* JWH-307
* JWH-369
* JWH-370

Eicosanoids|

* AM-883
* AM-1346
* ACEA
* ACPA
* Methanandamide (AM-356)
* O-585
* O-689
* O-1812
* O-1860
* O-1861

Pyrazolecarboxamides|

* 5F-AB-FUPPYCA
* AB-CHFUPYCA

Others|

* 2F-QMPSB
* 4-HTMPIPO
* 5F-PY-PICA
* 5F-PY-PINACA
* 5F-3-pyridinoylindole
* A-836,339
* A-955,840
* Abnormal cannabidiol
* AB-001
* BzODZ-EPyr
* AM-1248
* AM-1714
* AZ-11713908
* AZD-1940
* BAY 38-7271
* BAY 59-3074
* BIM-018
* CB-13
* CB-86
* CBS-0550
* CUMYL-4CN-B7AICA
* 5F-CUMYL-P7AICA
* CUMYL-PEGACLONE
* FUBIMINA
* GSK-554,418A
* GW-842,166X
* JTE 7-31
* LASSBio-881
* LBP-1
* Leelamine
* MDA-7
* MDA-19
* MEPIRAPIM
* NESS-040C5
* NMP-7
* O-889
* O-1269
* O-1270
* O-1399
* O-1602
* O-2220
* Olorinab
* PF-03550096
* PSB-SB-1202
* PTI-1
* PTI-2
* PTI-3
* QMPSB
* S-444,823
* SER-601
* Tedalinab
* URB-447
* VSN-16
* WIN 56,098

Allosteric CBR ligands|

* Org 27569
* Org 27759
* Org 29647
* RTI-371
* Pregnenolone

Endocannabinoid
enhancers
(inactivation inhibitors)|

* 4-Nonylphenylboronic acid
* AM-404
* Arachidonoyl serotonin
* Arvanil
* BIA 10-2474
* Biochanin A
* CAY-10401
* CAY-10429
* Genistein
* Guineesine
* IDFP
* JNJ 1661010
* JNJ-42165279
* JZL184
* JZL195
* Kaempferol
* LY-2183240
* MK-4409
* O-1624
* O-2093
* Oleoylethanolamide (OEA)
* Olvanil
* Palmitoylethanolamide (PEA)
* PF-04457845
* PF-622
* PF-750
* PF-3845
* PHOP
* URB-447
* URB-597
* URB-602
* URB-754
* VDM-11

Anticannabinoids
(antagonists/inverse
agonists/antibodies)|

* AM-251
* AM-281
* AM-630
* AM-1387
* AM-4113
* AM-6527
* AM-6545
* BML-190
* Brizantin (Бризантин)
* CAY-10508
* CB-25
* CB-52
* CB-86
* Dietressa (Диетресса)
* Drinabant (AVE1625)
* Hemopressin
* Ibipinabant (SLV319)
* JTE-907
* LH-21
* LY-320,135
* MDA-77
* MJ-15
* MK-9470
* NESS-0327
* NIDA-41020
* O-606
* O-1184
* O-1248
* O-1918
* O-2050
* O-2654
* Otenabant (CP-945,598)
* PF-514273
* PipISB
* PSB-SB-487
* Rimonabant (SR141716)
* Rosonabant (E-6776)
* SR-144,528
* Surinabant (SR147778)
* Taranabant (MK-0364)
* TM-38837
* VCHSR

* See also: Cannabinoid receptor modulators (cannabinoids by pharmacology)
* List of: AM cannabinoids
* JWH cannabinoids
* Designer drugs § Synthetic cannabimimetics

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