SCHEMBL842866

SCHEMBL842866

CC(C)(C)N[SiH](c1ccccc1)c1ccccc1

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPK1 P28482 1/20 0.37
ATM Q13315 1/20 0.33
CACNA1F O60840 1/20 0.32
CHRM2 P08172 1/20 0.32
CHRM1 P11229 1/20 0.32
ADRA2B P18089 1/20 0.32
CHRM3 P20309 1/20 0.32
ADRA1A P35348 1/20 0.32
HRH1 P35367 1/20 0.32
OPRK1 P41145 1/20 0.32
CACNA1D Q01668 1/20 0.32
SLC6A3 Q01959 1/20 0.32
KCNH2 Q12809 1/20 0.32
CACNA1S Q13698 1/20 0.32
CACNA1C Q13936 1/20 0.32
SCN5A Q14524 1/20 0.32
SLC6A4 P31645 1/20 0.32
LMNA P02545 1/20 0.32
CYP2D6 P10635 1/20 0.32
KCNN4 O15554 1/20 0.32

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
Hydrochloric Acid SCHEMBL5085782 0.98 MAPK1 (0.36) MAPK1ATMCACNA1FCHRM2CHRM1
Trifluoromethanesulfonic Acid SCHEMBL5090051 0.82 HSD11B1 (0.34) CYP2D6TSHRALDH1A1
SCHEMBL20218966 0.76 ATM (0.31) MAPK1ATMCACNA1FCHRM2CHRM1
SCHEMBL6902987 0.72 LMNA (0.35) CACNA1FCHRM2CHRM1ADRA2BCHRM3
SCHEMBL2268375 0.70 TSHR (0.41) MAPK1ATMCHRM2ADRA1AHRH1
SCHEMBL27966762 0.70 TDP1 (0.42) ATMCHRM2ADRA1ALMNACYP2D6
SCHEMBL4835275 0.70 MAPK1 (0.33) MAPK1TSHRALDH1A1ALOX15
SCHEMBL12273825 0.69 TDP1 (0.35) MAPK1LMNACYP2D6TSHRALDH1A1
SCHEMBL8710885 0.68 KCNN4 (0.41) MAPK1ATMCACNA1FCHRM2CHRM1
SCHEMBL28114301 0.67 TSHR (0.32) LMNAKCNN4TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260138946-A1 PROCESS AND INTERMEDIATES FOR THE PREPARATION OF UPADACITINIB CURIA SPAIN S A U (ES) 2026-05-21 US disclosed
US-20260062395-A1 PROCESS AND INTERMEDIATES FOR THE PREPARATION OF VILOXAZINE AND OTHER 2-SUBSTITUTED MORPHOLINE DERIVATIVES CURIA SPAIN S A U (ES) 2026-03-05 US disclosed
US-12552746-B2 Process and intermediates for the preparation of upadacitinib CURIA SPAIN, S.A.U. (ES) 2026-02-17 US disclosed
EP-4317141-A1 PROCESS AND INTERMEDIATES FOR THE PREPARATION OF VILOXAZINE AND OTHER 2-SUBSTITUTED MORPHOLINE DERIVATIVES Curia Spain S.A.U. (ES) 2024-02-07 EP disclosed
US-20230139156-A1 PROCESS AND INTERMEDIATES FOR THE PREPARATION OF UPADACITINIB CURIA SPAIN, S.A.U. (ES) 2023-05-04 US disclosed
EP-4077276-A1 PROCESS AND INTERMEDIATES FOR THE PREPARATION OF UPADACITINIB Curia Spain S.A.U. (ES) 2022-10-26 EP disclosed
CN-115151529-A Process and intermediates for the preparation of Wu Pati ni 库里亚西班牙公司 2022-10-04 CN disclosed
US-11312708-B2 Process and intermediates for the preparation of benzo[b]thiophene compounds CRYSTAL PHARMA, S.A.U. (ES) 2022-04-26 US disclosed
WO-2021123288-A1 PROCESS AND INTERMEDIATES FOR THE PREPARATION OF UPADACITINIB CRYSTAL PHARMA, S.A.U. (ES) 2021-06-24 WO disclosed
US-20200172523-A1 PROCESS AND INTERMEDIATES FOR THE PREPARATION OF BENZO[B]THIOPHENE COMPOUNDS CURIA SPAIN, S.A.U. (ES) 2020-06-04 US disclosed
US-20070051922-A1 Polymer light-emitting material and polymer light-emitting device SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2007-03-08 US disclosed
EP-0610038-B1 Preparation of alkylsilyl nitrile SIVENTO INC (US) 2001-08-29 EP disclosed
CN-1042336-C Preparation of trialkylsilyl nitrile HULS AMERICA INC (US) 1999-03-03 CN disclosed
EP-0544757-B1 NOVEL POLYAMINE CONJUGATED OLIGONUCLEOTIDES ISIS PHARMACEUTICALS INC (US) 1997-10-08 EP disclosed
CN-1101913-A Preparation of trialkylsilyl nitrile HULS AMERICA INC (US) 1995-04-26 CN disclosed
EP-0610038-A1 Preparation of alkylsilyl nitrile HÜLS AMERICA INC. (US) 1994-08-10 EP disclosed
EP-0544757-A4 NOVEL POLYAMINE CONJUGATED OLIGONUCLEOTIDES ISIS PHARMACEUTICALS INC (US) 1994-07-06 EP disclosed
US-5258534-A Preparation of trialkylsilyl nitrile HULS AMERICA, INC. (US) 1993-11-02 US disclosed
EP-0544757-A1 NOVEL POLYAMINE CONJUGATED OLIGONUCLEOTIDES. ISIS PHARMACEUTICALS INC (US) 1993-06-09 EP disclosed
WO-1992002531-A1 NOVEL POLYAMINE CONJUGATED OLIGONUCLEOTIDES ISIS PHARMACEUTICALS, INC. (US) 1992-02-20 WO 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-20260138946-A1 PROCESS AND INTERMEDIATES FOR THE PREPARATION OF UPADACITINIB JAK1, JAK3, JAK2 MAPK1 48/4885ATM 841/4885CACNA1F 3672/4885
US-20200172523-A1 PROCESS AND INTERMEDIATES FOR THE PREPARATION OF BENZO[B]THIOPHENE COMPOUNDS CYP4X1, CYP2B6, CYP2C19 MAPK1 949/4885ATM 4530/4885CACNA1F 436/4885
US-20230139156-A1 PROCESS AND INTERMEDIATES FOR THE PREPARATION OF UPADACITINIB CDK19, CDK11B, CDK9 MAPK1 166/4885ATM 1359/4885CACNA1F 4754/4885
US-12552746-B2 Process and intermediates for the preparation of upadacitinib JAK1, JAK3, MET MAPK1 37/4885ATM 720/4885CACNA1F 3790/4885
US-11312708-B2 Process and intermediates for the preparation of benzo[b]thiophene compounds CYP4X1, CYP2B6, CYP2C19 MAPK1 949/4885ATM 4530/4885CACNA1F 436/4885
US-20260062395-A1 PROCESS AND INTERMEDIATES FOR THE PREPARATION OF VILOXAZINE AND OTHER 2-SUBSTITUTED MORPHOLINE DERIVATIVES OGFRL1, SALL4, OGFR MAPK1 3355/4885ATM 3485/4885CACNA1F 23/4885

“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.