SCHEMBL605442

SCHEMBL605442

CC(C)(C)c1ccc(Nc2ccc(-c3ccccc3)cc2)cc1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ABCG2 Q9UNQ0 1/20 0.54
KIF11 P52732 5/20 0.50
HSD17B10 Q99714 2/20 0.48
ALDH1A1 P00352 1/20 0.48
ALOX15 P16050 1/20 0.48
TSHR P16473 1/20 0.48
ALOX12 P18054 1/20 0.48
PTGS1 P23219 1/20 0.48
SLC6A2 P23975 1/20 0.48
MAPK1 P28482 1/20 0.48
PTGS2 P35354 1/20 0.48
HTR2B P41595 1/20 0.48
TDP1 Q9NUW8 1/20 0.48
L3MBTL1 Q9Y468 1/20 0.48
SERPINE1 P05121 1/20 0.47
HPGD P15428 1/20 0.45
CNR1 P21554 1/20 0.44
CYP19A1 P11511 2/20 0.43
HSD17B2 P37059 1/20 0.43
XDH P47989 1/20 0.43

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL20209149 1.00 ABCG2 (0.54) ABCG2KIF11HSD17B10ALDH1A1ALOX15
SCHEMBL22080286 1.00 ABCG2 (0.54) ABCG2KIF11HSD17B10ALDH1A1ALOX15
SCHEMBL12367613 0.96 ALDH1A1 (0.54) ABCG2KIF11HSD17B10ALDH1A1ALOX15
SCHEMBL13133429 0.96 ALDH1A1 (0.54) ABCG2KIF11HSD17B10ALDH1A1ALOX15
SCHEMBL12357213 0.93 CNR1 (0.50) ABCG2KIF11ALDH1A1SERPINE1CNR1
SCHEMBL13321302 0.91 KIF11 (0.57) ABCG2KIF11TSHRMAPK1XDH
SCHEMBL2957181 0.91 KIF11 (0.57) ABCG2KIF11TSHRMAPK1XDH
SCHEMBL24732147 0.89 CNR1 (0.55) ABCG2KIF11HSD17B10ALDH1A1ALOX15
SCHEMBL502030 0.89 ALDH1A1 (0.62) ABCG2HSD17B10ALDH1A1ALOX15TSHR
Diphenylamine SCHEMBL29287150 0.89 ALDH1A1 (0.62) ABCG2HSD17B10ALDH1A1ALOX15TSHR

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 165 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12563964-B2 Organic light-emitting device LG CHEM, LTD. (KR) 2026-02-24 US disclosed
US-20250304595-A1 Electroactive Compounds LG CHEM, LTD. (KR) 2025-10-02 US disclosed
US-12428429-B2 Amine compound and organic light-emitting diode including same SFC CO., LTD. (KR) 2025-09-30 US disclosed
US-12384796-B2 Electroactive compounds LG CHEM, LTD. (KR) 2025-08-12 US disclosed
WO-2025120516-A1 COMPOUND AND AN ORGANIC ELECTROLUMINESCENCE DEVICE COMPRISING THE COMPOUND IDEMITSU KOSAN CO., LTD. (JP) 2025-06-12 WO disclosed
EP-4567088-A1 COMPOUND AND AN ORGANIC ELECTROLUMINESCENCE DEVICE COMPRISING THE COMPOUND Idemitsu Kosan Co.,Ltd. (JP) 2025-06-11 EP disclosed
CN-113924307-B Polycyclic compound and organic light-emitting element including the same 株式会社LG化学 2024-08-20 CN disclosed
US-12004419-B2 Electroactive compounds LG CHEM, LTD. (KR) 2024-06-04 US disclosed
WO-2024096383-A1 ORGANIC ELECTRONIC DEVICE COMPRISING PLURALITY OF LIGHT-EMITTING AUXILIARY LAYERS, AND ELECTRONIC APPARATUS THEREFOR 덕산네오룩스 주식회사 2024-05-10 WO disclosed
WO-2023213837-A1 CYCLIC COMPOUNDS FOR ORGANIC ELECTROLUMINESCENT DEVICES MERCK PATENT GMBH (DE) 2023-11-09 WO disclosed
US-20110186836-A1 GREEN LUMINESCENT MATERIALS E.I.DU PONT DE NEMOURS AND COMPANY (US) 2011-08-04 US disclosed
US-20110037381-A1 CHRYSENE DERIVATIVE MATERIALS E. I. DU PONT DE NEMOURS AND COMPANY (US) 2011-02-17 US disclosed
WO-2011019360-A1 CHRYSENE DERIVATIVE MATERIALS E. I. DU PONT DE NEMOURS AND COMPANY (US) 2011-02-17 WO disclosed
US-20110037056-A1 PHOTOACTIVE COMPOSITION AND ELECTRONIC DEVICE MADE WITH THE COMPOSITION E. I. DU PONT DE NEMOURS AND COMPANY (US) 2011-02-17 US disclosed
WO-2010068865-A2 PHOTOACTIVE COMPOSITION AND ELECTRONIC DEVICE MADE WITH THE COMPOSITION E. I. DU PONT DE NEMOURS AND COMPANY (US) 2010-06-17 WO disclosed
CN-101679209-A Be used for the  that blue-light-emitting is used DU PONT 2010-03-24 CN disclosed
US-20080303429-A1 GREEN LUMINESCENT MATERIALS E. I. DU PONT DE NEMOURS AND COMPANY 2008-12-11 US disclosed
US-20080303429-A1 GREEN LUMINESCENT MATERIALS E. I. DU PONT DE NEMOURS AND COMPANY 2008-12-11 US disclosed
WO-2008150828-A2 GREEN LUMINESCENT MATERIALS E.I. DU PONT DE NEMOURS AND COMPANY (US) 2008-12-11 WO disclosed
US-20080303425-A1 CHRYSENES FOR BLUE LUMINESCENT APPLICATIONS E. I. DU PONT DE NEMOURS AND COMPANY 2008-12-11 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (9 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20250304595-A1 Electroactive Compounds NAT1, NES, SULT1E1 ABCG2 1310/4885KIF11 3995/4885HSD17B10 1677/4885
US-20080303425-A1 CHRYSENES FOR BLUE LUMINESCENT APPLICATIONS CRY2, CRY1, CYBA ABCG2 1284/4885KIF11 3360/4885HSD17B10 3141/4885
US-20110186836-A1 GREEN LUMINESCENT MATERIALS IK, GLB1, AFF2 ABCG2 1016/4885KIF11 1165/4885HSD17B10 2908/4885
US-20110037381-A1 CHRYSENE DERIVATIVE MATERIALS RIF1, CCNL2, ARL1 ABCG2 4280/4885KIF11 2021/4885HSD17B10 2078/4885
US-12563964-B2 Organic light-emitting device CRY1, CYP1A1, CTNNA1 ABCG2 2674/4885KIF11 3497/4885HSD17B10 931/4885
US-12384796-B2 Electroactive compounds NES, NAT1, SCN1B ABCG2 1376/4885KIF11 3889/4885HSD17B10 1770/4885
US-20080303429-A1 GREEN LUMINESCENT MATERIALS IK, GLB1, AFF2 ABCG2 1016/4885KIF11 1165/4885HSD17B10 2908/4885
US-12428429-B2 Amine compound and organic light-emitting diode including same MAOA, AOC2, MAOB ABCG2 3330/4885KIF11 2772/4885HSD17B10 2998/4885
US-12004419-B2 Electroactive compounds KCNN3, KCNN2, HCN3 ABCG2 984/4885KIF11 3875/4885HSD17B10 1050/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.