Momelotinib

Momelotinib

SCHEMBL2237234

N#CCNC(=O)c1ccc(-c2ccnc(Nc3ccc(N4CCOCC4)cc3)n2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACVR1JAK1JAK2

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
JAK2 known ✓ O60674 20/20 1.00
JAK1 known ✓ P23458 10/20 1.00
ACVR1 known ✓ Q04771 1/20 1.00
JAK3 P52333 16/20 1.00
HDAC1 Q13547 3/20 1.00
TYK2 P29597 2/20 1.00
BMPR1B O00238 1/20 1.00
PLK4 O00444 1/20 1.00
CIT O14578 1/20 1.00
GAK O14976 1/20 1.00
OPA1 O60313 1/20 1.00
ROCK2 O75116 1/20 1.00
STK16 O75716 1/20 1.00
PRKD3 O94806 1/20 1.00
CSNK2A2 P19784 1/20 1.00
CDK2 P24941 1/20 1.00
MARK3 P27448 1/20 1.00
BMPR1A P36894 1/20 1.00
TGFBR1 P36897 1/20 1.00
STAT3 P40763 1/20 1.00

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
Momelotinib SCHEMBL22282523 1.00 JAK2 (1.00) JAK2JAK3JAK1HDAC1TYK2
Momelotinib SCHEMBL29352115 1.00 JAK2 (1.00) JAK2JAK3JAK1HDAC1TYK2
Momelotinib SCHEMBL2863022 0.99 JAK2 (0.98) JAK2JAK3JAK1HDAC1TYK2
Momelotinib SCHEMBL29774318 0.99 JAK2 (0.98) JAK2JAK3JAK1HDAC1TYK2
Momelotinib SCHEMBL17333087 0.99 JAK2 (0.98) JAK2JAK3JAK1HDAC1TYK2
Momelotinib SCHEMBL2863013 0.99 JAK2 (0.98) JAK2JAK3JAK1HDAC1TYK2
Momelotinib SCHEMBL3619656 0.97 JAK2 (0.93) JAK2JAK3JAK1HDAC1TYK2
Momelotinib SCHEMBL30051896 0.97 JAK2 (0.93) JAK2JAK3JAK1HDAC1TYK2
Momelotinib SCHEMBL3619662 0.97 JAK2 (0.93) JAK2JAK3JAK1HDAC1TYK2
SCHEMBL2858799 0.94 JAK2 (0.89) JAK2JAK3JAK1HDAC1TYK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026043077-A1 MIXED STRAINS FOR ALLEVIATING SARCOPENIA AND COMPOSITION COMPRISING SAME 주식회사 락토메이슨 2026-02-26 WO claimed
US-RE50497-E1 (N-(cyanomethyl)-4-(2-(4-morpholinophenylamino)pyrimidin-4-yl)benzamide GLAXOSMITHKLINE LLC (US) 2025-07-22 US claimed
CN-119792300-A Pharmaceutical composition for treating kidney cancer 复旦大学附属肿瘤医院 2025-04-11 CN claimed
CN-118930560-A Bifunctional degradation agents for hematopoietic progenitor cell kinases and therapeutic uses thereof 新锐思生物制药股份有限公司 2024-11-12 CN claimed
EP-4430052-A1 BIFUNCTIONAL DEGRADERS OF HEMATOPOIETIC PROGENITOR KINASE AND THERAPEUTIC USES THEREOF Nurix Therapeutics, Inc. (US) 2024-09-18 EP claimed
CN-118510786-A Bifunctional degradation agents for hematopoietic progenitor cell kinases and therapeutic uses thereof 新锐思生物制药股份有限公司 2024-08-16 CN claimed
EP-4412621-A2 COMPOSITIONS AND METHODS FOR ENHANCED PROTEIN PRODUCTION HDT Bio Corp. (US) 2024-08-14 EP claimed
CN-115605488-B Bifunctional degradation agents for hematopoietic progenitor cell kinases and therapeutic uses thereof 新锐思生物制药股份有限公司 2024-08-09 CN claimed
US-12037342-B2 Substituted eneoxindoles and uses thereof GILEAD SCIENCES, INC. (US) 2024-07-16 US claimed
CN-113227089-B Substituted 6-azabenzimidazole compounds as HPK1 inhibitors 吉利德科学公司 2024-07-05 CN claimed
WO-2014004376-A2 METHODS FOR TREATING TYROSINE-KINASE-INHIBITOR-RESISTANT MALIGNANCIES IN PATIENTS WITH GENETIC POLYMORPHISMS OR AHI1 DYSREGULATIONS OR MUTATIONS EMPLOYING DIANHYDROGALACTITOL, DIACETYLDIANHYDROGALACTITOL, DIBROMODULCITOL, OR ANALOGS OR DERIVATIVES THEREOF DEL MAR PHARMACEUTICALS (CA) 2014-01-03 WO claimed
US-20140005180-A1 PHENYL AMINO PYRIMIDINE COMPOUNDS AND USES THEREOF GLAXOSMITHKLINE LLC 2014-01-02 US claimed
EP-2646029-A1 TREATMENT OF JAK2-MEDIATED CONDITIONS YM BioSciences Australia Pty Ltd (AU) 2013-10-09 EP claimed
WO-2013112942-A1 BIOMARKERS AND COMBINATION THERAPIES USING ONCOLYTIC VIRUS AND IMMUNOMODULATION DNA TRIX, INC. (US) 2013-08-01 WO claimed
US-8486941-B2 Phenyl amino pyrimidine compounds and uses thereof YM BIOSCIENCES AUSTRALIA PTY LTD (AU) 2013-07-16 US claimed
WO-2012149602-A1 MULTIPLE MYELOMA TREATMENT YM BIOSCIENCES AUSTRALIA PTY LTD (AU) 2012-11-08 WO claimed
WO-2012071612-A1 TREATMENT OF JAK2-MEDIATED CONDITIONS YM BIOSCIENCES AUSTRALIA PTY LTD (AU) 2012-06-07 WO claimed
US-20100197671-A1 PHENYL AMINO PYRIMIDINE COMPOUNDS AND USES THEREOF GLAXOSMITHKLINE LLC 2010-08-05 US claimed
EP-2152701-A1 PHENYL AMINO PYRIMIDINE COMPOUNDS AND USES THEREOF Cytopia Research Pty Ltd (AU) 2010-02-17 EP claimed
WO-2008109943-A1 PHENYL AMINO PYRIMIDINE COMPOUNDS AND USES THEREOF CYTOPIA RESEARCH PTY LTD (AU) 2008-09-18 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-20100197671-A1 PHENYL AMINO PYRIMIDINE COMPOUNDS AND USES THEREOF JAK2, JAK1, JAK3 JAK2 1/4885JAK1 2/4885ACVR1 3660/4885
US-12037342-B2 Substituted eneoxindoles and uses thereof HIPK1, HPGDS, HIPK3 JAK2 591/4885JAK1 556/4885ACVR1 2079/4885
US-20140005180-A1 PHENYL AMINO PYRIMIDINE COMPOUNDS AND USES THEREOF JAK2, JAK1, JAK3 JAK2 1/4885JAK1 2/4885ACVR1 3660/4885

“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.