Avutometinib

Avutometinib

SCHEMBL960093

CNS(=O)(=O)Nc1nccc(Cc2c(C)c3ccc(Oc4ncccn4)cc3oc2=O)c1F

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MAP2K1MAP2K2

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

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
MAP2K1 known ✓ Q02750 17/20 1.00
MAP2K2 known ✓ P36507 1/20 1.00
RAF1 P04049 16/20 1.00
CYP2C9 P11712 3/20 1.00
BRAF P15056 1/20 1.00
MAP2K5 Q13163 1/20 1.00
CYP3A4 P08684 2/20 0.80
ALDH1A1 P00352 2/20 0.44
KDM4E B2RXH2 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
HSD17B10 Q99714 1/20 0.44
ALDH1A2 O94788 1/20 0.44
ALDH1B1 P30837 1/20 0.44
ALDH1A3 P47895 1/20 0.44
STS P08842 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
Avutometinib SCHEMBL29358292 1.00 MAP2K1 (1.00) MAP2K1RAF1CYP2C9BRAFMAP2K2
Avutometinib SCHEMBL29360048 1.00 MAP2K1 (1.00) MAP2K1RAF1CYP2C9BRAFMAP2K2
Avutometinib SCHEMBL29515377 1.00 MAP2K1 (1.00) MAP2K1RAF1CYP2C9BRAFMAP2K2
Avutometinib SCHEMBL963844 0.99 MAP2K1 (0.98) MAP2K1RAF1CYP2C9BRAFMAP2K2
Avutometinib SCHEMBL959675 0.99 MAP2K1 (0.98) MAP2K1RAF1CYP2C9BRAFMAP2K2
Avutometinib SCHEMBL963841 0.99 MAP2K1 (0.98) MAP2K1RAF1CYP2C9BRAFMAP2K2
Avutometinib SCHEMBL959677 0.99 MAP2K1 (0.98) MAP2K1RAF1CYP2C9BRAFMAP2K2
SCHEMBL24876938 0.94 MAP2K1 (0.89) MAP2K1RAF1CYP2C9BRAFMAP2K2
SCHEMBL958779 0.93 MAP2K1 (0.88) MAP2K1RAF1CYP2C9BRAFMAP2K2
SCHEMBL959279 0.93 MAP2K1 (0.86) MAP2K1RAF1CYP2C9BRAFMAP2K2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-RE50313-E1 Musculoskeletal stem cell and medium for inducing differentiation of musculoskeletal stem cell CELLATOZ THERAPEUTICS, INC. (KR) 2025-02-25 US claimed
EP-3702445-B1 NOVEL MUSCULOSKELETAL STEM CELL CELLATOZ THERAPEUTICS INC (KR) 2022-12-07 EP claimed
EP-3702445-A2 NOVEL MUSCULOSKELETAL STEM CELL Cellatoz Therapeutics, Inc. (KR) 2020-09-02 EP claimed
EP-3643777-A1 NOVEL MUSCULOSKELETAL STEM CELL AND MEDIUM FOR INDUCING DIFFERENTIATION OF MUSCULOSKELETAL STEM CELL Cellatoz Therapeutics, Inc. (KR) 2020-04-29 EP claimed
US-10576106-B2 Musculoskeletal stem cell and medium for inducing differentiation of musculoskeletal stem cell CELLATOZ THERAPEUTICS, INC. (KR) 2020-03-03 US claimed
US-20190247441-A1 NOVEL MUSCULOSKELETAL STEM CELL AND MEDIUM FOR INDUCING DIFFERENTIATION OF MUSCULOSKELETAL STEM CELL CELLATOZ THERAPEUTICS, INC. (KR) 2019-08-15 US claimed
EP-2172198-B1 p27 PROTEIN INDUCER CHUGAI PHARMACEUTICAL CO LTD (JP) 2014-04-16 EP claimed
US-8569378-B2 p27 protein inducer Sakai, Toshiyuki (JP) 2013-10-29 US claimed
EP-1982982-B1 NOVEL COUMARIN DERIVATIVE HAVING ANTITUMOR ACTIVITY CHUGAI PHARMACEUTICAL CO LTD (JP) 2012-09-26 EP claimed
US-7897792-B2 Coumarin derivative having antitumor activity CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2011-03-01 US claimed
US-20110009398-A1 p27 Protein Inducer CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2011-01-13 US claimed
EP-2172198-A1 p27 PROTEIN INDUCER Chugai Seiyaku Kabushiki Kaisha (JP) 2010-04-07 EP claimed
US-20100004233-A1 NOVEL COUMARIN DERIVATIVE HAVING ANTITUMOR ACTIVITY CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2010-01-07 US claimed
EP-1982982-A1 NOVEL COUMARIN DERIVATIVE HAVING ANTITUMOR ACTIVITY CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2008-10-22 EP claimed
US-12605450-B2 C3-carbon linked glutarimide Degronimers for target protein degradation C4 THERAPEUTICS, INC. (US) 2026-04-21 US disclosed
US-12605387-B2 Treatment of cancers using PI3 kinase isoform modulators SECURA BIO, INC. (US) 2026-04-21 US disclosed
EP-4717317-A2 N/O-LINKED DEGRONS AND DEGRONIMERS FOR PROTEIN DEGRADATION C4 Therapeutics, Inc. (US) 2026-04-01 EP disclosed
US-20100004233-A1 NOVEL COUMARIN DERIVATIVE HAVING ANTITUMOR ACTIVITY CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2010-01-07 US disclosed
EP-1982982-A1 NOVEL COUMARIN DERIVATIVE HAVING ANTITUMOR ACTIVITY CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2008-10-22 EP disclosed
EP-1982982-A1 NOVEL COUMARIN DERIVATIVE HAVING ANTITUMOR ACTIVITY CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2008-10-22 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 (4 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-20110009398-A1 p27 Protein Inducer CDKN1A, CDK2, SKP2 MAP2K1 1179/4885MAP2K2 990/4885RAF1 1656/4885
US-12605450-B2 C3-carbon linked glutarimide Degronimers for target protein degradation NEDD4, UBE3A, UBE3C MAP2K1 2217/4885MAP2K2 2209/4885RAF1 2086/4885
US-12605387-B2 Treatment of cancers using PI3 kinase isoform modulators PIK3R5, PIK3R4, PIK3CD MAP2K1 73/4885MAP2K2 74/4885RAF1 56/4885
US-20100004233-A1 NOVEL COUMARIN DERIVATIVE HAVING ANTITUMOR ACTIVITY H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, SULT1A1, SULT1E1 MAP2K1 3163/4885MAP2K2 2806/4885RAF1 438/4885

“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.