Temuterkib

Temuterkib

SCHEMBL17837273

Cn1nccc1Nc1nccc(-c2cc3c(s2)C(C)(C)N(CCN2CCOCC2)C3=O)n1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MAPK1MAPK3

The experimentally established mechanism targets of Temuterkib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
MAPK1 known ✓ P28482 17/20 1.00
MAPK3 known ✓ P27361 2/20 1.00
ABL1 P00519 1/20 0.40
BCR P11274 1/20 0.40
MAP3K14 Q99558 1/20 0.39
MKNK1 Q9BUB5 1/20 0.39
MAPK6 Q16659 2/20 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
SCHEMBL17837306 0.97 MAPK1 (0.94) MAPK1MAPK3ABL1BCRMAP3K14
Temuterkib SCHEMBL28928408 0.95 MAPK1 (0.91) MAPK1MAPK3ABL1BCRMAP3K14
SCHEMBL17837212 0.93 MAPK1 (0.86) MAPK1MAPK3MAP3K14MAPK6
SCHEMBL17837242 0.92 MAPK1 (0.85) MAPK1MAPK3ABL1BCRMKNK1
Temuterkib SCHEMBL28654935 0.91 MAPK1 (0.83) MAPK1MAPK3ABL1BCRMAP3K14
SCHEMBL17856228 0.91 MAPK1 (0.83) MAPK1MAPK3MAP3K14MAPK6
SCHEMBL17837246 0.91 MAPK1 (0.83) MAPK1MAPK3MAPK6
SCHEMBL17837275 0.90 MAPK1 (0.81) MAPK1MAPK3MAP3K14MAPK6
SCHEMBL17871041 0.90 MAPK1 (0.81) MAPK1MAPK3ABL1BCRMAP3K14
SCHEMBL17837241 0.90 MAPK1 (0.81) MAPK1MAPK3ABL1BCRMAP3K14

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026090321-A1 TREATMENT OF CANCER WITH A KRAS INHIBITOR ALTEROME THERAPEUTICS, INC. (US) 2026-04-30 WO claimed
EP-4728051-A1 STANDARDISING PLURIPOTENT STEM CELLS United Kingdom Research and Innovation (GB) 2026-04-22 EP claimed
US-20250332160-A1 COMPOSITION CONTAINING ARIPIPRAZOLE AS ACTIVE INGREDIENT FOR ENHANCING ANTICANCER EFFECT OF ERK INHIBITOR KOREA INSTITUTE OF RADIOLOGICAL & MEDICAL SCIENCES (KR) 2025-10-30 US claimed
EP-4629995-A1 COMBINATION THERAPY FOR THE TREATMENT OF GLYOBLASTOMA The University of Florida Research Foundation, Inc. (US) 2025-10-15 EP claimed
US-20250228826-A1 COMBINATION OF A GREMLIN-1 ANTAGONIST WITH AN INHIBITOR OF RAS-RAF-MEK-ERK SIGNALLING UCB Biopharma SRL (BE) 2025-07-17 US claimed
CN-119790069-A Combinations of Gremlin-1 antagonists and inhibitors of Ras-Raf-MEK-ERK signaling UCB生物制药有限责任公司 2025-04-08 CN claimed
WO-2025067459-A2 THERAPIES FOR THE TREATMENT OF CANCER D3 BIO (WUXI) CO., LTD. (CN) 2025-04-03 WO claimed
EP-4523691-A1 COMPOSITION CONTAINING ARIPIPRAZOLE AS ACTIVE INGREDIENT FOR ENHANCING ANTICANCER EFFECT OF ERK INHIBITOR Korea Institute of Radiological & Medical Sciences (KR) 2025-03-19 EP claimed
EP-4504777-A1 COMBINATION OF A GREMLIN-1 ANTAGONIST WITH AN INHIBITOR OF RAS-RAF-MEK-ERK SIGNALLING UCB Biopharma SRL (BE) 2025-02-12 EP claimed
WO-2025027223-A1 DYRK2 INHIBITORS FOR TREATING TUMOURS WITH THE HYPERACTIVE MAPK/ERK PATHWAY Universidad de Córdoba (ES) 2025-02-06 WO claimed
WO-2020197917-A1 SALTS OF 5,6-DIHYDRO-4H-THIENO[2,3-C]PYRROL-4-ONE COMPOUND AS ERK INHIBITORS ELI LILLY AND COMPANY (US) 2020-10-01 WO claimed
EP-3237423-B1 THIENO[2,3-C]PYRROL-4-ONE DERIVATIVES AS ERK INHIBITORS LILLY CO ELI (US) 2019-06-05 EP claimed
EP-3478292-A1 COMBINATION OF ERK1/2 INHIBITOR COMPOUND WITH GEMCITABINE OR WITH GEMCITABINE AND NAB-PACLITAXEL FOR USE IN TREATMENT OF PANCREATIC CANCER Eli Lilly and Company (US) 2019-05-08 EP claimed
WO-2018005234-A1 COMBINATION OF ERK1/2 INHIBITOR COMPOUND WITH GEMCITABINE OR WITH GEMCITABINE AND NAB-PACLITAXEL FOR USE IN TREATMENT OF PANCREATIC CANCER ELI LILLY AND COMPANY (US) 2018-01-04 WO claimed
EP-3237423-A1 THIENO[2,3-C]PYRROL-4-ONE DERIVATIVES AS ERK INHIBITORS Eli Lilly and Company (US) 2017-11-01 EP claimed
US-20160375030-A1 ERK INHIBITORS ELI LILLY AND COMPANY 2016-12-29 US claimed
US-9526733-B1 ERK inhibitors ELI LILLY AND COMPANY (US) 2016-12-27 US claimed
US-9469652-B2 ERK inhibitors ELI LILLY AND COMPANY (US) 2016-10-18 US claimed
WO-2016106029-A1 THIENO[2,3-C]PYRROL-4-ONE DERIVATIVES AS ERK INHIBITORS ELI LILLY AND COMPANY (US) 2016-06-30 WO claimed
US-20160176896-A1 ERK INHIBITORS ELI LILLY AND COMPANY 2016-06-23 US 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-20160375030-A1 ERK INHIBITORS MAPK4, MAPK1, MAPK3 MAPK1 2/4885MAPK3 3/4885ABL1 109/4885
US-20160176896-A1 ERK INHIBITORS MAPK4, MAPK1, MAPK3 MAPK1 2/4885MAPK3 3/4885ABL1 109/4885
US-20250228826-A1 COMBINATION OF A GREMLIN-1 ANTAGONIST WITH AN INHIBITOR OF RAS-RAF-MEK-ERK SIGNALLING KRAS, NRAS, BRAF MAPK1 6/4885MAPK3 15/4885ABL1 2276/4885

“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.