SCHEMBL629964

SCHEMBL629964

COC(=O)c1cc2cc(O)ccc2cc1O

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA12 O43570 2/20 0.66
CA1 P00915 2/20 0.66
CA2 P00918 2/20 0.66
CA7 P43166 2/20 0.66
CA9 Q16790 2/20 0.66
CA14 Q9ULX7 2/20 0.66
PDK2 Q15119 1/20 0.66
PDK4 Q16654 1/20 0.66
SRC P12931 1/20 0.54
MEN1 O00255 5/20 0.50
KMT2A Q03164 5/20 0.50
ESR1 P03372 3/20 0.50
POLA1 P09884 1/20 0.49
NPC1 O15118 2/20 0.49
CASP3 P42574 1/20 0.49
SENP8 Q96LD8 1/20 0.49
SENP7 Q9BQF6 1/20 0.49
SENP6 Q9GZR1 1/20 0.49
GAA P10253 1/20 0.49
EGFR P00533 2/20 0.48

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
SCHEMBL30382562 1.00 CA12 (0.66) CA12CA1CA2CA7CA9
SCHEMBL2735777 1.00 CA12 (0.66) CA12CA1CA2CA7CA9
SCHEMBL10479344 0.91 CA12 (0.61) CA12CA1CA2CA7CA9
SCHEMBL18952948 0.87 CA12 (0.59) CA12CA1CA2CA7CA9
SCHEMBL6294366 0.85 LCK (0.58) CA12CA1CA2CA7CA9
SCHEMBL2964316 0.85 NPC1 (0.54) CA12CA1CA2CA7CA9
SCHEMBL18775431 0.85 CA12 (0.50) CA12CA1CA2CA7CA9
SCHEMBL28671628 0.85 CA12 (0.54) CA12CA1CA2CA7CA9
SCHEMBL12641829 0.85 NPC1 (0.54) CA12CA1CA2CA7CA9
SCHEMBL6881678 0.85 CA12 (0.50) CA12CA1CA2CA7CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4668315-A1 COMPOSITION FOR FORMING PROTECTIVE FILM FOR SEMICONDUCTOR CHIP MANUFACTURE, SEMICONDUCTOR SUBSTRATE, SEMICONDUCTOR CHIP, AND METHOD FOR MANUFACTURING SEMICONDUCTOR CHIP Nissan Chemical Corporation (JP) 2025-12-24 EP disclosed
US-20250361419-A1 COMPOSITION FOR FORMING COATING FILM FOR REMOVING FOREIGN MATTERS AND SEMICONDUCTOR SUBSTRATE NISSAN CHEMICAL CORPORATION (JP) 2025-11-27 US disclosed
EP-4629280-A1 COMPOSITION FOR FORMING COATING FILM FOR FOREIGN SUBSTANCE REMOVAL, AND SEMICONDUCTOR SUBSTRATE Nissan Chemical Corporation (JP) 2025-10-08 EP disclosed
CN-110366768-B Composition for forming coating film for removing foreign matter 日产化学株式会社 2023-09-26 CN disclosed
US-20230250314-A1 COMPOSITION FOR FORMING A COATING FILM FOR REMOVING FOREIGN MATTERS NISSAN CHEMICAL CORPORATION (JP) 2023-08-10 US disclosed
CN-116034453-A Composition for forming coating film for removing foreign matter 日产化学株式会社 2023-04-28 CN disclosed
US-11319514-B2 Composition for forming a coating film for removing foreign matters NISSAN CHEMICAL CORPORATION (JP) 2022-05-03 US disclosed
US-10954194-B2 18-20 member bi-polycyclic compounds Haro Pharmaceuticals Inc. (US) 2021-03-23 US disclosed
US-10752591-B2 18-20 member bi-polycyclic compounds Haro Pharmaceuticals Inc. (US) 2020-08-25 US disclosed
US-20200140792-A1 COMPOSITION FOR FORMING A COATING FILM FOR REMOVING FOREIGN MATTERS NISSAN CHEMICAL CORPORATION (JP) 2020-05-07 US disclosed
US-5637262-A REVERSIBLE PHOTOCHROMIC DYES FOR OPHTHALMIC LENSES TRANSITIONS OPTICAL, INC. (US) 1997-06-10 US disclosed
WO-1997020239-A1 PHOTOCHROMIC SUBSTITUTED NAPHTHOPYRAN COMPOUNDS PPG INDUSTRIES, INC. (US) 1997-06-05 WO disclosed
CN-1150589-A New sulfuric acid esters of sugar alcohols HOFFMANN LA ROCHE (CH) 1997-05-28 CN disclosed
US-5578252-A Photochromic substituted naphthopyran compounds TRANSITIONS OPTICAL, INC. (US) 1996-11-26 US disclosed
EP-0710367-A4 1996-05-15 EP disclosed
EP-0710367-A1 PHOTOCHROMIC SUBSTITUTED NAPHTHOPYRAN COMPOUNDS PPG INDUSTRIES, INC. (US) 1996-05-08 EP disclosed
WO-1996011926-A1 PHOTOCHROMIC NAPHTHOXAZINE COMPOUNDS PPG INDUSTRIES, INC. (US) 1996-04-25 WO disclosed
US-5466398-A Photochromic substituted naphthopyran compounds TRANSITIONS OPTICAL, INC. (US) 1995-11-14 US disclosed
US-5405958-A Photochromic spiro(indoline)naphthoxazine compounds TRANSITIONS OPTICAL, INC. (US) 1995-04-11 US disclosed
WO-1995000867-A1 PHOTOCHROMIC SUBSTITUTED NAPHTHOPYRAN COMPOUNDS PPG INDUSTRIES, INC. (US) 1995-01-05 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 (2 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-10752591-B2 18-20 member bi-polycyclic compounds TNNI3, TNNC1, MYLK2 CA12 2828/4885CA1 3047/4885CA2 1803/4885
US-10954194-B2 18-20 member bi-polycyclic compounds BRCA1, UGT2B17, TP53 CA12 188/4885CA1 1435/4885CA2 1858/4885

“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.