SCHEMBL133189

SCHEMBL133189

c1ccc(-c2ccccc2P(C2CCCCC2)C2CCCCC2)cc1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 7/20 0.41
MEN1 O00255 3/20 0.41
KMT2A Q03164 3/20 0.41
NPSR1 Q6W5P4 2/20 0.41
LMNA P02545 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
GAA P10253 1/20 0.38
TDP1 Q9NUW8 1/20 0.36
ROCK2 O75116 1/20 0.35
HRH1 P35367 1/20 0.34
HTT P42858 1/20 0.34
HSD17B10 Q99714 2/20 0.33
ADORA3 P0DMS8 1/20 0.33
ADORA2A P29274 1/20 0.33
ADORA2B P29275 1/20 0.33
ADORA1 P30542 1/20 0.33
HPGD P15428 1/20 0.33
BCL2L1 Q07817 1/20 0.33
CYP2A6 P11509 1/20 0.33
BCHE P06276 1/20 0.33

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
SCHEMBL1159030 1.00 ALDH1A1 (0.41) ALDH1A1MEN1KMT2ANPSR1LMNA
SCHEMBL29353025 1.00 ALDH1A1 (0.41) ALDH1A1MEN1KMT2ANPSR1LMNA
SCHEMBL1931350 0.98 ALDH1A1 (0.40) ALDH1A1MEN1KMT2ANPSR1LMNA
SCHEMBL5840557 0.98 ALDH1A1 (0.40) ALDH1A1MEN1KMT2ANPSR1LMNA
Hydrochloric Acid SCHEMBL29639278 0.98 ALDH1A1 (0.40) ALDH1A1MEN1KMT2ANPSR1LMNA
SCHEMBL33526641 0.98 ALDH1A1 (0.40) ALDH1A1MEN1KMT2ANPSR1LMNA
SCHEMBL16694717 0.98 GAA (0.39) ALDH1A1MEN1KMT2ANPSR1LMNA
SCHEMBL27516331 0.95 ALDH1A1 (0.41) ALDH1A1MEN1KMT2ANPSR1LMNA
SCHEMBL19469297 0.95 ALDH1A1 (0.38) ALDH1A1MEN1KMT2ANPSR1LMNA
Dimethylamine SCHEMBL645332 0.93 ALDH1A1 (0.40) ALDH1A1MEN1KMT2ANPSR1LMNA

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

Appears in 6774 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122036529-A Preparation method of enantiomerically enriched amino alcohol compound 苏州亚科科技股份有限公司 2026-05-15 CN claimed
EP-4725945-A1 PREPARATION METHOD FOR FORMAMIDE COMPOUNDS Shanghai Senhui Medicine Co., Ltd. (CN) 2026-04-15 EP claimed
US-20250206723-A1 METHODS AND PROCESSES FOR THE PREPARATION OF MCT4 INHIBITORS Vettore, LLC 2025-06-26 US claimed
EP-2427468-B2 PREPARATION OF A METAL COMPLEX JOHNSON MATTHEY PLC (GB) 2025-06-04 EP claimed
WO-2024251227-A1 PREPARATION METHOD FOR FORMAMIDE COMPOUNDS 上海森辉医药有限公司 2024-12-12 WO claimed
US-12162829-B2 Gas phase process for acrylate production from ethylene and carbon dioxide CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) 2024-12-10 US claimed
US-20240322260-A1 SECONDARY BATTERY AND ELECTRICAL APPARATUS CONTAINING THE SAME CONTEMPORARY AMPEREX TECHNOLOGY (HONG KONG) LIMITED (CN) 2024-09-26 US claimed
CN-111417627-B Hydrogenation of Imines Using RU Complexes 弗门尼舍有限公司 2024-07-12 CN claimed
CN-118047707-A Direct cross coupling method of sulfoxide ylide and aryl fluorosulfonate 南京工业大学 2024-05-17 CN claimed
CN-117924171-A Phenanthrone derivative and synthesis method thereof 华南理工大学 2024-04-26 CN claimed
CN-1517354-A Copper complex and its use ˹���ػ�ѧ��Ʒ�ɷ����޹�˾ 2004-08-04 CN claimed
EP-1437356-A1 Copper complexes and the use thereof Bayer Chemicals AG (DE) 2004-07-14 EP claimed
WO-2004055003-A1 2-SUBSTITUTED QUINAZOLIN-4-YLAMINE ANALOGUES AS CAPSAICIN RECEPTOR MODULATORS NEUROGEN CORPORATION (US) 2004-07-01 WO claimed
US-6706895-B1 CHEMICAL INTERMEDIATES FOR BIFENAZATE UNIROYAL CHEMICAL COMPANY, INC. 2004-03-16 US claimed
US-20040024237-A1 Synthesis of aminoarylboronic esters and substituted anilines from arenes via catalytic C-H activation/borylation/amination and uses thereof BOARD OF TRUSTEES OF MICHIGAN STATE UNIVERSITY (US) 2004-02-05 US claimed
US-6686495-B2 IN PRESENCE OF PALLADIUM CATALYST; USEFUL IN PRODUCING CHEMICAL INTERMEDIATES FOR PHARMACEUTICALS, OPTICAL BRIGHTENING AGENTS AND AGROCHEMICALS OMG AG & CO KG (DE) 2004-02-03 US claimed
US-6664396-B1 Reacting N,N'-unsubstituted quinacridone compound with haloaryl compound in presence of metal or metal compound to arylate N and N' positions and form corresponding N,N'-diarylquinacridone compound EASTMAN KODAK COMPANY 2003-12-16 US claimed
US-20030060624-A1 Process for the preparation of 1,3-substituted indenes and aryl-fused azapolycyclic componunds PFIZER INC. 2003-03-27 US claimed
US-20020107426-A1 Process for the preparation of mono-, bi- or poly- functional biaryls UMICORE AG & CO. KG (DE) 2002-08-08 US claimed
EP-1199292-A1 Process for the production of mono-, bi- or polyfunctional biaryls OMG AG & Co. KG (DE) 2002-04-24 EP claimed