SCHEMBL2098491

SCHEMBL2098491

c1ccc(C2NCNC2c2ccccc2)cc1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ GBA1 P04062 1/20 0.50
▸ SLC18A3 Q16572 1/20 0.46
▸ SIGMAR1 Q99720 1/20 0.46
▸ MEN1 O00255 1/20 0.45
▸ KMT2A Q03164 1/20 0.45
▸ SMN1; SMN2 Q16637 1/20 0.43
▸ PRCP P42785 2/20 0.40
▸ TSHR P16473 1/20 0.40
▸ CHRNA7 P36544 1/20 0.39
▸ MAOA P21397 5/20 0.39
▸ MAOB P27338 5/20 0.39
▸ KDM1A O60341 4/20 0.39
▸ CYP2C19 P33261 4/20 0.39
▸ CYP2B6 P20813 3/20 0.39
▸ CYP1A2 P05177 2/20 0.39
▸ CYP2D6 P10635 2/20 0.39
▸ CYP2C9 P11712 2/20 0.39
▸ LMNA P02545 1/20 0.39
▸ CYP3A4 P08684 1/20 0.39
▸ HTR1A P08908 1/20 0.39

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
SCHEMBL23951733 1.00 GBA1 (0.50) GBA1SLC18A3SIGMAR1MEN1KMT2A
SCHEMBL15250705 1.00 GBA1 (0.50) GBA1SLC18A3SIGMAR1MEN1KMT2A
SCHEMBL5521949 1.00 GBA1 (0.50) GBA1SLC18A3SIGMAR1MEN1KMT2A
SCHEMBL8222209 0.83 SLC18A3 (0.52) GBA1SLC18A3SIGMAR1MEN1KMT2A
Bromide SCHEMBL28484405 0.81 SLC18A3 (0.50) GBA1SLC18A3SIGMAR1MEN1KMT2A
Hydrochloric Acid SCHEMBL28486863 0.81 SLC18A3 (0.50) GBA1SLC18A3SIGMAR1MEN1KMT2A
SCHEMBL28875477 0.77 POLB (0.40) GBA1MEN1KMT2A
Trimethylammonium SCHEMBL28490265 0.75 SLC18A3 (0.45) GBA1SLC18A3SIGMAR1MEN1KMT2A
SCHEMBL19270305 0.74 SMN1; SMN2 (0.40) GBA1SLC18A3SIGMAR1MEN1KMT2A
SCHEMBL12371293 0.74 GBA1 (0.57) GBA1SLC18A3SIGMAR1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2398774-A2 PROCESSES FOR PREPARING JAK INHIBITORS AND RELATED INTERMEDIATE COMPOUNDS Incyte Corporation (US) 2011-12-28 — — EP claimed
US-20100190981-A1 PROCESSES FOR PREPARING JAK INHIBITORS AND RELATED INTERMEDIATE COMPOUNDS INCYTE CORPORATION 2010-07-29 — — US claimed
WO-2010083283-A2 PROCESSES FOR PREPARING JAK INHIBITORS AND RELATED INTERMEDIATE COMPOUNDS INCYTE CORPORATION (US) 2010-07-22 — — WO claimed
US-20250340559-A1 PROCESSES FOR PREPARING JAK INHIBITORS AND RELATED INTERMEDIATE COMPOUNDS INCYTE HOLDINGS CORP (US) 2025-11-06 — — US disclosed
US-12247030-B2 Process for preparing compositions comprising an enantiomeric excess of a substituted pyrrolo[2,3-d]pyrimidine INCYTE HOLDINGS CORPORATION (US) 2025-03-11 — — US disclosed
EP-4501410-A2 PROCESSES FOR PREPARING JAK INHIBITORS AND RELATED INTERMEDIATE COMPOUNDS Incyte Holdings Corporation (US) 2025-02-05 — — EP disclosed
CN-119306753-A Methods for preparing JAK inhibitors and related intermediate compounds 因西特控股公司 2025-01-14 — — CN disclosed
EP-3272738-B1 PROCESSES FOR PREPARING JAK INHIBITORS AND RELATED INTERMEDIATE COMPOUNDS INCYTE HOLDINGS CORP (US) 2024-11-13 — — EP disclosed
CN-108395433-B Methods for preparing JAK inhibitors and related intermediate compounds 因西特控股公司 2024-10-22 — — CN disclosed
US-20210253584-A1 Processes for Preparing Jak Inhibitors and Related Intermediate Compounds INCYTE HOLDINGS CORPORATION 2021-08-19 — — US disclosed
US-10975085-B2 Process for preparing a composition comprising an enantiomeric excess of greater than or equal to 90% of the (R)-enantiomer of a compound of formula III INCYTE HOLDINGS CORPORATION (US) 2021-04-13 — — US disclosed
WO-2005080298-A1 CATALYTIC ASYMMETRIC SYNTHESIS OF OPTICALLY ACTIVE α-HALO-CARBONYL COMPOUNDS CHEMINOVA A/S (DK) 2005-09-01 — — WO disclosed
EP-0004748-B1 ELECTROSTATOGRAPHIC DEVELOPER MIXTURE AND IMAGING PROCESS XEROX CORPORATION (US) 1984-03-14 — — EP disclosed
US-4395471-A BUTYL METHACRYLATE-STYRENE COPOLYMER AND A COPPER PHTHALOCYANINE, AND A AZOBENZIDENE XEROX CORPORATION (US) 1983-07-26 — — US disclosed
EP-0046398-A2 Electrostatographic developer composition XEROX CORPORATION (US) 1982-02-24 — — EP disclosed
US-4312932-A RESIN PARTICLES CONTAINING UP TO FOUR PIGMENTS AND SINGLE CARRIER XEROX CORPORATION (US) 1982-01-26 — — US disclosed
US-4172721-A USING MONLAYER OF PARTICLES COMPRISING A RESIN CARRIER CONTAINING COLOR-PHOTOSENSITIVE MATERIAL AND A SOLID-FORM DYE MATERIAL XEROX CORPORATION (US) 1979-10-30 — — US disclosed
EP-0004748-A2 Electrostatographic developer mixture and imaging process XEROX CORPORATION (US) 1979-10-17 — — EP disclosed
US-4052207-A XEROGRAPHY, YELLOW MONOAZO DYE XEROX CORPORATION (US) 1977-10-04 — — US disclosed
US-4035310-A STYRENE-VINYL, STYRENE-ACRYLATE COPOLYMERS XEROX CORPORATION (US) 1977-07-12 — — 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 (5 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-12247030-B2 Process for preparing compositions comprising an enantiomeric excess of a substituted pyrrolo[2,3-d]pyrimidine DPYD, TYMS, TYMP GBA1 3329/4885SLC18A3 3633/4885SIGMAR1 4082/4885
US-10975085-B2 Process for preparing a composition comprising an enantiomeric excess of greater than or equal to 90% of the (R)-enantiomer of a compound of formula III JAK1, JAK3, JAK2 GBA1 4055/4885SLC18A3 4881/4885SIGMAR1 2072/4885
US-20210253584-A1 Processes for Preparing Jak Inhibitors and Related Intermediate Compounds JAK3, JAK1, JAK2 GBA1 4400/4885SLC18A3 4878/4885SIGMAR1 3460/4885
US-20100190981-A1 PROCESSES FOR PREPARING JAK INHIBITORS AND RELATED INTERMEDIATE COMPOUNDS JAK3, JAK1, JAK2 GBA1 4400/4885SLC18A3 4878/4885SIGMAR1 3460/4885
US-20250340559-A1 PROCESSES FOR PREPARING JAK INHIBITORS AND RELATED INTERMEDIATE COMPOUNDS JAK3, JAK1, JAK2 GBA1 4400/4885SLC18A3 4878/4885SIGMAR1 3460/4885

“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.

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