SCHEMBL691603

SCHEMBL691603

Clc1nc(Cl)c2cc[nH]c2n1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PRKCI P41743 3/20 0.44
AXL P30530 3/20 0.44
ADORA2A P29274 2/20 0.40
ADORA1 P30542 2/20 0.40
DYRK1A Q13627 2/20 0.40
TTBK1 Q5TCY1 4/20 0.35
TTBK2 Q6IQ55 4/20 0.35
NUDT1 P36639 2/20 0.33
HRH4 Q9H3N8 1/20 0.33
PIK3R1 P27986 1/20 0.33
PIK3CA P42336 1/20 0.33
IKBKB O14920 2/20 0.33
CHUK O15111 2/20 0.33
RHEB Q15382 1/20 0.33
TGFBR1 P36897 1/20 0.32
PDK1 Q15118 1/20 0.32
DAPK3 O43293 1/20 0.32
JAK2 O60674 1/20 0.32
PRKD3 O94806 1/20 0.32
MAP4K4 O95819 1/20 0.32

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
SCHEMBL29700716 1.00 PRKCI (0.44) PRKCIAXLADORA2AADORA1DYRK1A
SCHEMBL31507871 0.79 CHUK (0.51) PRKCIAXLADORA2AADORA1DYRK1A
SCHEMBL12574854 0.79 PRKCI (0.46) PRKCIAXLADORA2AADORA1DYRK1A
SCHEMBL31514673 0.79 PRKCI (0.41) PRKCIAXLADORA2AADORA1DYRK1A
SCHEMBL2147990 0.79 PRKCI (0.41) PRKCIAXLADORA2AADORA1DYRK1A
SCHEMBL3124523 0.79 PRKCI (0.46) PRKCIAXLADORA2AADORA1DYRK1A
SCHEMBL17731714 0.79 PRKCI (0.41) PRKCIAXLADORA2AADORA1DYRK1A
SCHEMBL760829 0.79 CHUK (0.51) PRKCIAXLADORA2AADORA1DYRK1A
SCHEMBL13666508 0.79 PRKCI (0.41) PRKCIAXLADORA2AADORA1DYRK1A
SCHEMBL15384626 0.79 PRKCI (0.41) PRKCIAXLADORA2AADORA1DYRK1A

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 1161 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118103371-B EGFR inhibitor and preparation method and application thereof SHANDONG NEW TIME PHARMACEUTICAL Co.,Ltd. (CN) 2026-05-26 CN claimed
US-20250122202-A1 EGFR INHIBITOR, PREPARATION METHOD THEREFOR AND USE THEREOF SHANDONG NEW TIME PHARMACEUTICAL CO., LTD. (CN) 2025-04-17 US claimed
US-12227478-B2 Processes for preparing (3R,4R)-1-benzyl-N,4-dimethylpiperidin-3-amine or a salt thereof and processes for preparing tofacitinib using the same YUHAN CORPORATION (KR) 2025-02-18 US claimed
EP-4403556-A1 EGFR INHIBITOR, PREPARATION METHOD THEREFOR AND USE THEREOF Shandong New Time Pharmaceutical Co., Ltd. (CN) 2024-07-24 EP claimed
CN-118103371-A EGFR inhibitor and preparation method and application thereof 山东新时代药业有限公司 2024-05-28 CN claimed
CN-113614069-B Process for preparing (3R, 4R) -1-benzyl-N, 4-dimethylpiperidin-3-amine or a salt thereof and process for preparing tofacitinib using the same 柳韩洋行 2024-05-28 CN claimed
EP-3927689-B1 PROCESSES FOR PREPARING (3R,4R)-1-BENZYL-N,4-DIMETHYLPIPERIDIN-3-AMINE OR A SALT THEREOF AND PROCESSES FOR PREPARING TOFACITINIB USING THE SAME YUHAN CORP (KR) 2024-01-24 EP claimed
CN-115838370-A EGFR inhibitor and preparation method and application thereof 山东新时代药业有限公司 2023-03-24 CN claimed
WO-2023041071-A1 EGFR INHIBITOR, PREPARATION METHOD THEREFOR AND USE THEREOF 山东新时代药业有限公司 2023-03-23 WO claimed
CN-115181100-A Sulfonamide micromolecule inhibitor with purine and pyrrolopyrimidine parent nucleus 广西大学 2022-10-14 CN claimed
CN-113614069-A Process for preparing (3R,4R) -1-benzyl-N, 4-dimethylpiperidin-3-amine or a salt thereof and process for preparing tofacitinib using the same 柳韩洋行 2021-11-05 CN claimed
WO-2020204647-A1 PROCESSES FOR PREPARING (3R,4R)-1-BENZYL-N,4-DIMETHYLPIPERIDIN-3-AMINE OR A SALT THEREOF AND PROCESSES FOR PREPARING TOFACITINIB USING THE SAME YUHAN CORPORATION (KR) 2020-10-08 WO claimed
CN-111072671-A Preparation method of 5-bromo-2-chloro-7H-pyrrolo [2,3-d ] pyrimidine 浙江理工大学 2020-04-28 CN claimed
CN-108864057-B JAK and HDAC double-target-point inhibitor containing 4-aminopyrazole structure and preparation method and application thereof 山东大学 2020-03-31 CN claimed
CN-108276414-B A kind of preparation method of citric acid tropsch imatinib 齐鲁天和惠世制药有限公司 2019-07-23 CN claimed
CN-107793417-A Pyrrolo- [2,3 d] pyrimidines and its salt, and preparation method and pharmaceutical usage 复旦大学 2018-03-13 CN claimed
WO-2016073771-A2 PYRROLOPYRIMIDINE DERIVATIVES AS MPS1/TTK KINASE INHIBITORS OHIO STATE INNOVATION FOUNDATION (US) 2016-05-12 WO claimed
US-20110288297-A1 Pyrrolo[2,3-d]Pyrimidine Derivatives; Their Intermediates and Synthesis PFIZER, INC. (US) 2011-11-24 US claimed
EP-1913000-A2 PYRROLO[2,3-D]PYRIMIDINE DERIVATIVES; THEIR INTERMEDIATES AND SYNTHESIS Pfizer Products Inc. (US) 2008-04-23 EP claimed
WO-2007012953-A2 PYRROLO[2,3-D]PYRIMIDINE DERIVATIVES; THEIR INTERMEDIATES AND SYNTHESIS PFIZER PRODUCTS INC. (US) 2007-02-01 WO claimed

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

For each of this compound's patents that has machine-readable text (3 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-20250122202-A1 EGFR INHIBITOR, PREPARATION METHOD THEREFOR AND USE THEREOF EGFR, NHERF1, AREG PRKCI 220/4885AXL 990/4885ADORA2A 3735/4885
US-12227478-B2 Processes for preparing (3R,4R)-1-benzyl-N,4-dimethylpiperidin-3-amine or a salt thereof and processes for preparing tofacitinib using the same JAK3, JAK1, JAK2 PRKCI 219/4885AXL 1570/4885ADORA2A 4237/4885
US-20110288297-A1 Pyrrolo[2,3-d]Pyrimidine Derivatives; Their Intermediates and Synthesis DPYD, CPS1, TYMS PRKCI 1239/4885AXL 1463/4885ADORA2A 3457/4885

“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.