SCHEMBL762075

SCHEMBL762075

CC1(C)OB(c2cccc(CC#N)c2)OC1(C)C

nearest known ligand 0.58

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
LIPG Q9Y5X9 12/20 0.58
LPL P06858 11/20 0.58
ESR2 Q92731 1/20 0.43
ENPP2 Q13822 1/20 0.41
KDM4E B2RXH2 1/20 0.40
TDP1 Q9NUW8 1/20 0.40
MMP3 P08254 1/20 0.40
TDP2 O95551 1/20 0.38
F11 P03951 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
SCHEMBL521491 0.85 LIPG (0.63) LIPGLPLESR2TDP2F11
SCHEMBL1163929 0.80 ESR2 (0.59) LIPGLPLESR2F11
SCHEMBL18332737 0.80 LIPG (0.69) LIPGLPLESR2F11
SCHEMBL1284463 0.79 LIPG (0.63) LIPGLPLESR2ENPP2F11
SCHEMBL1331631 0.79 LIPG (0.63) LIPGLPLENPP2F11
SCHEMBL3039403 0.79 LIPG (0.63) LIPGLPLESR2F11
SCHEMBL23071684 0.78 LIPG (0.70) LIPGLPLF11
SCHEMBL12215735 0.78 LIPG (0.80) LIPGLPLESR2F11
Hydrochloric Acid SCHEMBL1631610 0.78 LIPG (0.61) LIPGLPLENPP2F11
SCHEMBL30477495 0.78 LIPG (0.80) LIPGLPLESR2F11

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250388599-A1 TRICYCLIC PI3K INHIBITOR COMPOUNDS AND METHODS OF USE GENENTECH INC (US) 2025-12-25 US disclosed
US-20240199525-A1 SHP2-Targeting Small Molecules For Use As Anti-Cancer Agents WEST VIRGINIA UNIV BOARD OF GOVERNORS ON BEHALF OF WEST VIRGINIA UNIV (US) 2024-06-20 US disclosed
US-12012409-B2 Bicyclic heterocycles as FGFR inhibitors INCYTE CORPORATION (US) 2024-06-18 US disclosed
CN-116969987-A Method for preparing 1,2,3, 4-disilyl tetrahydroquinoline compound by utilizing chitosan Schiff base copper functional material 众力百捷(湖北)科技有限公司 2023-10-31 CN disclosed
US-20220348593-A1 TRICYCLIC PI3K INHIBITOR COMPOUNDS AND METHODS OF USE GENENTECH, INC. 2022-11-03 US disclosed
US-20220332718-A1 PYRAZOLO[1,5a]PYRIMIDINE DERIVATIVES AS IRAK4 MODULATORS GENENTECH, INC. (US) 2022-10-20 US disclosed
US-11390610-B2 Piperazine derivatives as MAGL inhibitors HOFFMANN-LA ROCHE INC. (US) 2022-07-19 US disclosed
US-20220169642-A1 COMPOUNDS FOR THE TREATMENT OF ONCOVIRUS INDUCED CANCER AND METHODS OF USE THEREOF CELLESTIA BIOTECH AG (CH) 2022-06-02 US disclosed
EP-3953335-A1 INHIBITORS OF NOTCH SIGNALLING PATHWAY AND USE THEREOF IN TREATMENT OF CANCERS Cellestia Biotech AG (CH) 2022-02-16 EP disclosed
US-11136326-B2 Pyrrolopyrimidine derivatives as TAM inhibitors INCYTE CORPORATION (US) 2021-10-05 US disclosed
US-8008481-B2 Indazole compounds ABBVIE INC. 2011-08-30 US disclosed
US-20100204221-A1 Pyrrolopyrimidinyl axl kinase inhibitors TOLERO PHARMACEUTICALS, INC. 2010-08-12 US disclosed
US-20100204221-A1 Pyrrolopyrimidinyl axl kinase inhibitors TOLERO PHARMACEUTICALS, INC. 2010-08-12 US disclosed
US-20100204221-A1 Pyrrolopyrimidinyl axl kinase inhibitors TOLERO PHARMACEUTICALS, INC. 2010-08-12 US disclosed
WO-2010090764-A1 PYRROLOPYRIMIDINYL AXL KINASE INHIBITORS SUPERGEN, INC. (US) 2010-08-12 WO disclosed
WO-2010090764-A1 PYRROLOPYRIMIDINYL AXL KINASE INHIBITORS SUPERGEN, INC. (US) 2010-08-12 WO disclosed
US-20090048258-A1 Amide Compound TAKEDA, PHARMACEUTICAL COMPANY LIMITED (JP) 2009-02-19 US disclosed
US-20070282101-A1 Indazole compounds ABBVIE INC. 2007-12-06 US disclosed
EP-1845081-A1 AMIDE COMPOUND Takeda Pharmaceutical Company Limited (JP) 2007-10-17 EP disclosed
US-6294573-B1 FOR THERAPY RHEUMATOID ARTHRITIS, OSTEOARTHRITIS, OSTEOPENIAS SUCH AS OSTEOPOROSIS, PERIODONTITIS, GINGIVITIS, CORNEAL, EPIDERMAL OR GASTRIC ULCERATION, AND TUMOR GROWTH AND METASTASIS OR INVASION ABBOTT LABORATORIES 2001-09-25 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 (11 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-12012409-B2 Bicyclic heterocycles as FGFR inhibitors FGFR3, FGFR2, FGFR1 LIPG 1939/4885LPL 2418/4885ESR2 1074/4885
US-20100204221-A1 Pyrrolopyrimidinyl axl kinase inhibitors AXL, FLT3, TYRO3 LIPG 2466/4885LPL 3796/4885ESR2 2850/4885
US-20220169642-A1 COMPOUNDS FOR THE TREATMENT OF ONCOVIRUS INDUCED CANCER AND METHODS OF USE THEREOF NOTCH1, NOTCH4, NOTCH2 LIPG 1717/4885LPL 4341/4885ESR2 1442/4885
US-20070282101-A1 Indazole compounds CYP3A43, CYP3A7, UGT1A1 LIPG 3363/4885LPL 3658/4885ESR2 2050/4885
US-11136326-B2 Pyrrolopyrimidine derivatives as TAM inhibitors FLT3, MERTK, MIF LIPG 1588/4885LPL 3867/4885ESR2 1114/4885
US-11390610-B2 Piperazine derivatives as MAGL inhibitors MAGI3, PYM1, MAG LIPG 2367/4885LPL 1351/4885ESR2 4722/4885
US-20220348593-A1 TRICYCLIC PI3K INHIBITOR COMPOUNDS AND METHODS OF USE PIK3CA, PIK3CD, MTOR LIPG 1634/4885LPL 3869/4885ESR2 1480/4885
US-20240199525-A1 SHP2-Targeting Small Molecules For Use As Anti-Cancer Agents PTPRO, PTPRC, PTPRCAP LIPG 2101/4885LPL 3731/4885ESR2 1428/4885
US-20220332718-A1 PYRAZOLO[1,5a]PYRIMIDINE DERIVATIVES AS IRAK4 MODULATORS IRAK1, IRAK4, IRAK2 LIPG 4695/4885LPL 4543/4885ESR2 2798/4885
US-20090048258-A1 Amide Compound DLAT, DGAT1, DGAT2 LIPG 2847/4885LPL 1611/4885ESR2 584/4885
US-20250388599-A1 TRICYCLIC PI3K INHIBITOR COMPOUNDS AND METHODS OF USE PIK3C2B, PIK3C2A, PIK3R1 LIPG 1906/4885LPL 3263/4885ESR2 425/4885

“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.