SCHEMBL317052

SCHEMBL317052

[c]1cnn(Cc2ccccc2)c1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP19A1 P11511 7/20 0.50
L3MBTL1 Q9Y468 3/20 0.47
SIGMAR1 Q99720 2/20 0.40
HTR2C P28335 1/20 0.39
RAB9A P51151 2/20 0.39
RECQL P46063 1/20 0.39
F2 P00734 1/20 0.39
PLG P00747 1/20 0.39
ELANE P08246 1/20 0.39
CTSG P08311 1/20 0.39
CMA1 P23946 1/20 0.39
CTRC Q99895 1/20 0.39
NPC1 O15118 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
ALDH1A1 P00352 1/20 0.38
CYP1A2 P05177 1/20 0.37
POLB P06746 1/20 0.37
CYP3A4 P08684 1/20 0.37
CYP2D6 P10635 1/20 0.37
MAPT P10636 1/20 0.37

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
SCHEMBL4794465 0.89 L3MBTL1 (0.50) CYP19A1L3MBTL1RAB9ANPC1ALDH1A1
SCHEMBL16050432 0.84 CYP19A1 (0.59) CYP19A1L3MBTL1ALDH1A1CYP11B1CYP11B2
SCHEMBL16050449 0.84 LTA4H (0.44) CYP19A1TSHR
SCHEMBL15653896 0.82 SIGMAR1 (0.47) CYP19A1L3MBTL1SIGMAR1NPC1SMN1; SMN2
SCHEMBL16050368 0.82 KDM4E (0.43) CYP19A1L3MBTL1ALDH1A1CYP1A2CYP3A4
SCHEMBL16050737 0.81 ALDH1A1 (0.49) SMN1; SMN2ALDH1A1CYP3A4
SCHEMBL4794171 0.80 RAB9A (0.42) CYP19A1L3MBTL1RAB9ANPC1SMN1; SMN2
SCHEMBL4795010 0.80 LMNA (0.49) CYP19A1RAB9ANPC1ALDH1A1POLB
SCHEMBL15652147 0.80 HRH3 (0.44) L3MBTL1SIGMAR1RAB9ANPC1POLB
SCHEMBL15652608 0.80 ALDH1A1 (0.49) L3MBTL1ALDH1A1CYP1A2CYP2D6CYP11B1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4352059-A1 TRICYCLIC HETEROCYCLES AS FGFR INHIBITORS Incyte Corporation (US) 2024-04-17 EP claimed
US-11939331-B2 Tricyclic heterocycles as FGFR inhibitors INCYTE CORPORATION (US) 2024-03-26 US claimed
US-20230192680-A1 NEW AGENT FOR PROMOTING PHOSPHORYLATION OF eIF2a ER STRESS RESEARCH INSTITUTE, INC. (JP) 2023-06-22 US claimed
US-20230002385-A1 TRICYCLIC HETEROCYCLES AS FGFR INHIBITORS INCYTE CORPORATION 2023-01-05 US claimed
WO-2022261160-A1 TRICYCLIC HETEROCYCLES AS FGFR INHIBITORS INCYTE CORPORATION (US) 2022-12-15 WO claimed
CN-105980386-B Pyrazolo compounds and uses thereof 基因泰克公司 2021-08-13 CN claimed
US-10959986-B2 Inhibitors of indoleamine 2,3-dioxygenase and methods of their use BRISTOL-MYERS SQUIBB COMPANY (US) 2021-03-30 US claimed
US-10815222-B2 Compounds for use in the treatment of kinetoplastid infection C.N.C.C.S. S.C.A.R.L. COLLEZIONE NAZIONALE DEI COMPOSTI CHIMICI E CENTRO SCREENING (IT) 2020-10-27 US claimed
WO-2020184578-A1 NOVEL elF2α PHOSPHORYLATION PROMOTER 小胞体ストレス研究所株式会社 2020-09-17 WO claimed
EP-3124489-B1 THIAZOLO-PYRIDINE COMPOUNDS AS HIF MODULATORS FIBROGEN INC (US) 2020-07-15 EP claimed
WO-2007070818-A1 SIX-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2007-06-21 WO claimed
WO-2007048771-A1 ARYLUREA DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY NOVARTIS AG (CH) 2007-05-03 WO claimed
EP-1742944-A1 INDOLES, 1H-INDAZOLES, 1,2-BENZISOXAZOLES, 1,2-BENZOISOTHIAZOLES, AND PREPARATION AND USES THEREOF Memory Pharmaceuticals Corporation (US) 2007-01-17 EP claimed
WO-2006001894-A1 INDOLES, 1H-INDAZOLES, 1,2-BENZISOXAZOLES, 1,2-BENZOISOTHIAZOLES, AND PREPARATION AND USES THEREOF MEMORY PHARMACEUTICAL CORPORATION (US) 2006-01-05 WO claimed
US-20050250808-A1 Indoles, 1h-indazoles, 1,2-benzisoxazoles, 1,2-benzoisothiazoles, and preparation and uses thereof MEMORY PHARMACEUTICAL CORPORATION 2005-11-10 US claimed
EP-1414837-B1 ADENOSINE A3 RECEPTOR AGONISTS CV THERAPEUTICS INC (US) 2005-10-19 EP claimed
US-20040116376-A1 Adenosine A3 receptor agonists CV THERAPEUTICS, INC. 2004-06-17 US claimed
EP-1414837-A1 ADENOSINE A3 RECEPTOR AGONISTS CV THERAPEUTICS, INC. (US) 2004-05-06 EP claimed
US-20030078232-A1 Adenosine receptor A3 agonists CV THERAPEUTICS, INC. 2003-04-24 US claimed
WO-2003014137-A1 ADENOSINE A3 RECEPTOR AGONISTS CV THERAPEUTICS, INC. (US) 2003-02-20 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 (7 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-20030078232-A1 Adenosine receptor A3 agonists ADORA3, ADORA2A, ADORA1 CYP19A1 3376/4885L3MBTL1 1597/4885SIGMAR1 1237/4885
US-10959986-B2 Inhibitors of indoleamine 2,3-dioxygenase and methods of their use IDO1, IDO2, INMT CYP19A1 588/4885L3MBTL1 3787/4885SIGMAR1 3303/4885
US-20230192680-A1 NEW AGENT FOR PROMOTING PHOSPHORYLATION OF eIF2a EIF2A, EIF2AK1, EIF2AK4 CYP19A1 3538/4885L3MBTL1 1529/4885SIGMAR1 753/4885
US-20050250808-A1 Indoles, 1h-indazoles, 1,2-benzisoxazoles, 1,2-benzoisothiazoles, and preparation and uses thereof CHRNA7, CHRNA5, CHRNA2 CYP19A1 2876/4885L3MBTL1 3107/4885SIGMAR1 454/4885
US-10815222-B2 Compounds for use in the treatment of kinetoplastid infection NISCH, TK2, FDPS CYP19A1 4450/4885L3MBTL1 2337/4885SIGMAR1 3883/4885
US-11939331-B2 Tricyclic heterocycles as FGFR inhibitors FGFR3, FGFR1, FGFR2 CYP19A1 474/4885L3MBTL1 3254/4885SIGMAR1 4689/4885
US-20230002385-A1 TRICYCLIC HETEROCYCLES AS FGFR INHIBITORS FGFR3, FGFR1, FGFR2 CYP19A1 474/4885L3MBTL1 3254/4885SIGMAR1 4689/4885

“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.