SCHEMBL1336862

SCHEMBL1336862

OC(CCl)CN(Cc1ccccc1)Cc1ccccc1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
POLB P06746 2/20 0.49
ALDH1A1 P00352 5/20 0.43
MAPT P10636 2/20 0.43
GAA P10253 1/20 0.43
MAPK1 P28482 1/20 0.43
PNP P00491 2/20 0.43
NPC1 O15118 2/20 0.42
TSHR P16473 3/20 0.40
RECQL P46063 1/20 0.40
GLA P06280 1/20 0.40
HTT P42858 1/20 0.40
RAB9A P51151 1/20 0.40
PAX8 Q06710 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
DNM1 Q05193 1/20 0.39
CNR2 P34972 1/20 0.38
CYP1A2 P05177 1/20 0.38
CYP2D6 P10635 1/20 0.38
CYP2C9 P11712 1/20 0.38
CYP2C19 P33261 1/20 0.38

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
SCHEMBL23512823 1.00 POLB (0.49) POLBALDH1A1MAPTGAAMAPK1
SCHEMBL1336860 1.00 POLB (0.49) POLBALDH1A1MAPTGAAMAPK1
SCHEMBL18970299 0.96 POLB (0.49) POLBALDH1A1MAPTGAAMAPK1
SCHEMBL4926941 0.90 ALDH1A1 (0.46) POLBALDH1A1MAPTGAAMAPK1
SCHEMBL8321789 0.88 ALDH1A1 (0.58) POLBALDH1A1MAPTGAAMAPK1
SCHEMBL26253773 0.88 ALDH1A1 (0.58) POLBALDH1A1MAPTGAAMAPK1
SCHEMBL6227253 0.88 POLB (0.54) POLBALDH1A1MAPTGAAMAPK1
SCHEMBL21936369 0.86 POLB (0.53) POLBALDH1A1MAPTGAAMAPK1
SCHEMBL28594973 0.82 PNP (0.53) POLBALDH1A1MAPTGAAMAPK1
SCHEMBL7193663 0.82 POLB (0.50) POLBALDH1A1MAPTGAAMAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260028356-A1 1,3,4,7-TETRAHYDRO-2H-PYRROLO[3',2':5,6]PYRIDO[2,3-B][1,4]OXAZEPINE BCL-2 INHIBITORS ABBVIE INC (US) 2026-01-29 US disclosed
US-20250066388-A1 1,3,4,7-TETRAHYDRO-2H-PYRROLO[3',2':5,6]PYRIDO[2,3-B][1,4]OXAZEPINE BCL-2 INHIBITORS ABBVIE INC (US) 2025-02-27 US disclosed
US-11964990-B2 1,3,4,7-tetrahydro-2H-pyrrolo[3′,2′:5,6]pyrido[2,3-b][1,4]oxazepine bcl-2 inhibitors ABBVIE INC. (US) 2024-04-23 US disclosed
US-20230234971-A1 1,3,4,7-Tetrahydro-2H-pyrrolo[3',2':5,6]pyrido[2,3-b][1,4]oxazepine Bcl-2 Inhibitors ABBVIE INC. (US) 2023-07-27 US disclosed
WO-2023141536-A1 1,3,4,7-TETRAHYDRO-2H-PYRROLO [3',2':5,6] PYRIDO[2,3-B] [1,4] OXAZEPINE BC1-2 INHIBITORS ABBVIE INC. (US) 2023-07-27 WO disclosed
EP-4073051-A1 PROCESS AND INTERMEDIATE FOR THE PREPARATION OF OXETAN-2-YLMETHANAMINE Eli Lilly and Company (US) 2022-10-19 EP disclosed
CN-114728923-A Process and intermediates for the preparation of oxetan-2-ylmethylamines 伊莱利利公司 2022-07-08 CN disclosed
CN-110035745-B Small molecule AMPK activators 匹兹堡大学联邦系统高等教育 2022-04-29 CN disclosed
WO-2021118906-A1 PROCESS AND INTERMEDIATE FOR THE PREPARATION OF OXETAN-2-YLMETHANAMINE ELI LILLY AND COMPANY (US) 2021-06-17 WO disclosed
EP-3013907-B1 PARTICLE OF MODIFIED SILICA NOURYON CHEMICALS INT BV (NL) 2019-08-28 EP disclosed
EP-2388251-B1 METHOD FOR PREPARING LINEZOLID AND INTERMEDIATES THEREOF LIANHE CHEMICAL TECHNOLOGY CO LTD (CN) 2013-08-28 EP disclosed
WO-2013046211-A1 PROCESSES FOR THE PREPARATION OF 5-CHLORO-N-({(5S)-2-OXO-3-[4-(3-OXO-4-MORPHOLINYL) PHENYL]-1,3-OXAZOLIDIN-5-YL}METHYL)-2-THIOPHENE-CARBOXAMIDE AND INTERMEDIATES THEREOF SYMED LABS LIMITED (IN) 2013-04-04 WO disclosed
CN-102351807-A Dibenzyl-1,3-oxazolidine-2-ketone compound and preparation method and application thereof UNIV SICHUAN 2012-02-15 CN disclosed
EP-2388251-A1 METHOD FOR PREPARING LINEZOLID AND INTERMEDIATES THEREOF Lianhe Chemical Technology Co., Ltd. (CN) 2011-11-23 EP disclosed
US-20110275805-A1 METHOD FOR PREPARING LINEZOLID AND INTERMEDIATES THEREOF LIANHE CHEMICAL TECHNOLOGY CO., LTD. (CN) 2011-11-10 US disclosed
US-8038543-B2 Golf swing training device CAPESIUS DEAN C 2011-10-18 US disclosed
US-4659721-A GASTROINTESTINAL DISORDER, HISTAMINE H2-ANTOGONISTS LUDWIG HEUMANN & CO. GMBH (DE) 1987-04-21 US disclosed
US-4656180-A HISTAMINE-H2 RECEPTORS; ANTIULCER AGENTS LUDWIG HEUMANN & CO., GMBH (DE) 1987-04-07 US disclosed
EP-0158789-A1 Diamine derivatives, process for their preparation and medicines containing these compounds LUDWIG HEUMANN & CO GMBH (DE) 1985-10-23 EP disclosed
EP-0154721-A1 Alcanol derivatives, processes for their preparation and medicines containing these compounds LUDWIG HEUMANN & CO GMBH (DE) 1985-09-18 EP 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 (5 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-20260028356-A1 1,3,4,7-TETRAHYDRO-2H-PYRROLO[3',2':5,6]PYRIDO[2,3-B][1,4]OXAZEPINE BCL-2 INHIBITORS BCL9L, BCL2L2, BCL2L1 POLB 3669/4885ALDH1A1 1491/4885MAPT 4241/4885
US-20250066388-A1 1,3,4,7-TETRAHYDRO-2H-PYRROLO[3',2':5,6]PYRIDO[2,3-B][1,4]OXAZEPINE BCL-2 INHIBITORS BCL9L, BCL2L1, BCL2L2 POLB 2788/4885ALDH1A1 912/4885MAPT 4485/4885
US-20230234971-A1 1,3,4,7-Tetrahydro-2H-pyrrolo[3',2':5,6]pyrido[2,3-b][1,4]oxazepine Bcl-2 Inhibitors BCL9L, BCL2L1, BCL2L2 POLB 2788/4885ALDH1A1 912/4885MAPT 4485/4885
US-11964990-B2 1,3,4,7-tetrahydro-2H-pyrrolo[3′,2′:5,6]pyrido[2,3-b][1,4]oxazepine bcl-2 inhibitors BCL9L, BCL2L1, BCL9 POLB 2728/4885ALDH1A1 920/4885MAPT 4499/4885
US-20110275805-A1 METHOD FOR PREPARING LINEZOLID AND INTERMEDIATES THEREOF HDAC9, KAT5, ACMSD POLB 281/4885ALDH1A1 361/4885MAPT 2937/4885

“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.