Baricitinib

Baricitinib

SCHEMBL871150

CCS(=O)(=O)N1CC(CC#N)(n2cc(-c3ncnc4[nH]ccc34)cn2)C1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

JAK1JAK2

The experimentally established mechanism targets of Baricitinib. 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
JAK1 known ✓ P23458 20/20 1.00
JAK2 known ✓ O60674 19/20 1.00
JAK3 P52333 15/20 1.00
TYK2 P29597 3/20 1.00
CIT O14578 1/20 1.00
GAK O14976 1/20 1.00
ROCK2 O75116 1/20 1.00
ULK1 O75385 1/20 1.00
PRKCB P05771 1/20 1.00
RET P07949 1/20 1.00
PRKCA P17252 1/20 1.00
PRKACA P17612 1/20 1.00
MARK3 P27448 1/20 1.00
STAT3 P40763 1/20 1.00
CLK1 P49759 1/20 1.00
CSNK1G2 P78368 1/20 1.00
PRKCD Q05655 1/20 1.00
MAP3K1 Q13233 1/20 1.00
ROCK1 Q13464 1/20 1.00
TNK1 Q13470 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
Baricitinib SCHEMBL29349824 1.00 JAK1 (1.00) JAK1JAK2JAK3TYK2CIT
Baricitinib SCHEMBL20135561 0.99 JAK1 (0.98) JAK1JAK2JAK3TYK2CIT
Baricitinib SCHEMBL20135563 0.99 JAK1 (0.98) JAK1JAK2JAK3TYK2CIT
Baricitinib SCHEMBL20135659 0.97 JAK1 (0.95) JAK1JAK2JAK3TYK2CIT
Baricitinib SCHEMBL20135562 0.97 JAK1 (0.95) JAK1JAK2JAK3TYK2CIT
Baricitinib SCHEMBL20135649 0.96 JAK1 (0.93) JAK1JAK2JAK3TYK2CIT
Baricitinib SCHEMBL20135651 0.96 JAK1 (0.93) JAK1JAK2JAK3TYK2CIT
Baricitinib SCHEMBL871037 0.96 JAK1 (0.92) JAK1JAK2JAK3TYK2CIT
Baricitinib SCHEMBL1396340 0.96 JAK1 (0.92) JAK1JAK2JAK3TYK2CIT
SCHEMBL872210 0.95 JAK1 (0.90) JAK1JAK2JAK3TYK2CIT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117462554-A Application of barytinib in preparation of chronic non-bacterial mastitis treatment drugs 浙江大学医学院附属第一医院 2024-01-30 CN claimed
US-20200093825-A1 JANUS KINASE INHIBITORS FOR TREATMENT OF DRY EYE AND OTHER EYE RELATED DISEASES INCYTE CORPORATION 2020-03-26 US claimed
EP-3321267-A1 CRYSTALLINE FORMS OF 2-[1-ETHYLSULFONYL-3-[7H-PYRROLO[2,3-D]PYRIMIDIN-4-YL)PYRAZOL-1-YL]AZETIDIN-3-YL]ACETONITRILE SALTS AND PREPARATION THEREOF Zentiva K.S. (CZ) 2018-05-16 EP claimed
EP-2288610-B1 AZETIDINE AND CYCLOBUTANE DERIVATIVES AS JAK INHIBITORS INCYTE HOLDINGS CORP (US) 2016-08-31 EP claimed
EP-3042655-A1 JANUS KINASE INHIBITORS FOR TREATMENT OF DRY EYE AND OTHER EYE RELATED DISEASES Incyte Holdings Corporation (US) 2016-07-13 EP claimed
US-20140377221-A1 BIOMARKERS AND COMBINATION THERAPIES USING ONCOLYTIC VIRUS AND IMMUNOMODULATION BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2014-12-25 US claimed
EP-2806883-A1 BIOMARKERS AND COMBINATION THERAPIES USING ONCOLYTIC VIRUS AND IMMUNOMODULATION Dnatrix Inc. (US) 2014-12-03 EP claimed
WO-2013173506-A2 METHOD OF TREATING MUSCULAR DEGRADATION RIGEL PHARMACEUTICALS, INC. (US) 2013-11-21 WO claimed
US-20130310340-A1 METHOD OF TREATING MUSCULAR DEGRADATION RIGEL PHARMACEUTICALS, INC. (US) 2013-11-21 US claimed
WO-2013112942-A1 BIOMARKERS AND COMBINATION THERAPIES USING ONCOLYTIC VIRUS AND IMMUNOMODULATION DNA TRIX, INC. (US) 2013-08-01 WO claimed
US-8420629-B2 Azetidine and cyclobutane derivatives as JAK inhibitors INCYTE CORPORATION (US) 2013-04-16 US claimed
US-8158616-B2 Azetidine and cyclobutane derivatives as JAK inhibitors INCYTE CORPORATION (US) 2012-04-17 US claimed
US-20120077798-A1 AZETIDINE AND CYCLOBUTANE DERIVATIVES AS JAK INHIBITORS INCYTE CORPORATION 2012-03-29 US claimed
EP-2288610-A1 AZETIDINE AND CYCLOBUTANE DERIVATIVES AS JAK INHIBITORS Incyte Corporation (US) 2011-03-02 EP claimed
US-20100113416-A1 JANUS KINASE INHIBITORS FOR TREATMENT OF DRY EYE AND OTHER EYE RELATED DISEASES INCYTE CORPORATION 2010-05-06 US claimed
WO-2009114512-A1 AZETIDINE AND CYCLOBUTANE DERIVATIVES AS JAK INHIBITORS INCYTE CORPORATION (US) 2009-09-17 WO claimed
US-20090233903-A1 AZETIDINE AND CYCLOBUTANE DERIVATIVES AS JAK INHIBITORS INCYTE CORPORATION (US) 2009-09-17 US claimed
US-20260097028-A1 Methods of Treating Myeloproliferative Neoplasms KARTOS THERAPEUTICS INC (US) 2026-04-09 US disclosed
WO-2009114512-A1 AZETIDINE AND CYCLOBUTANE DERIVATIVES AS JAK INHIBITORS INCYTE CORPORATION (US) 2009-09-17 WO disclosed
US-20090233903-A1 AZETIDINE AND CYCLOBUTANE DERIVATIVES AS JAK INHIBITORS INCYTE CORPORATION (US) 2009-09-17 US 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 (6 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-20130310340-A1 METHOD OF TREATING MUSCULAR DEGRADATION PYGM, CKMT1A; CKMT1B, SMN1; SMN2 JAK1 4796/4885JAK2 4729/4885JAK3 4792/4885
US-20100113416-A1 JANUS KINASE INHIBITORS FOR TREATMENT OF DRY EYE AND OTHER EYE RELATED DISEASES JAK1, JAK3, JAK2 JAK1 1/4885JAK2 3/4885JAK3 2/4885
US-20260097028-A1 Methods of Treating Myeloproliferative Neoplasms JAK2, TP53, CDKN1A JAK1 8/4885JAK2 1/4885JAK3 91/4885
US-20200093825-A1 JANUS KINASE INHIBITORS FOR TREATMENT OF DRY EYE AND OTHER EYE RELATED DISEASES JAK1, JAK3, JAK2 JAK1 1/4885JAK2 3/4885JAK3 2/4885
US-20090233903-A1 AZETIDINE AND CYCLOBUTANE DERIVATIVES AS JAK INHIBITORS JAK1, JAK2, JAK3 JAK1 1/4885JAK2 2/4885JAK3 3/4885
US-20120077798-A1 AZETIDINE AND CYCLOBUTANE DERIVATIVES AS JAK INHIBITORS JAK1, JAK2, JAK3 JAK1 1/4885JAK2 2/4885JAK3 3/4885

“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.