SCHEMBL7943831

SCHEMBL7943831

OCC(O)(CO)c1ccccc1

nearest known ligand 0.58

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CYP2C19 P33261 3/20 0.58
CYP1A2 P05177 2/20 0.58
CYP2C9 P11712 1/20 0.58
KDM4E B2RXH2 2/20 0.41
MAPK1 P28482 2/20 0.40
TSHR P16473 4/20 0.39
ALDH1A1 P00352 4/20 0.39
KCNN4 O15554 2/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
HIF1A Q16665 1/20 0.38
CYP2D6 P10635 1/20 0.38
HSD17B10 Q99714 1/20 0.38
LMNA P02545 1/20 0.38
TAAR1 Q96RJ0 1/20 0.37
ALOX15 P16050 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
SCHEMBL13946505 0.85 CYP2C19 (0.50) CYP2C19CYP1A2CYP2C9KDM4EALDH1A1
SCHEMBL7974570 0.85 CYP1A2 (0.50) CYP2C19CYP1A2CYP2C9KDM4EMAPK1
SCHEMBL13950244 0.85 CYP1A2 (0.50) CYP2C19CYP1A2CYP2C9KDM4ETSHR
SCHEMBL6481609 0.85 CYP2C19 (0.50) CYP2C19CYP1A2CYP2C9KDM4EALDH1A1
SCHEMBL6481604 0.85 CYP2C19 (0.50) CYP2C19CYP1A2CYP2C9KDM4EALDH1A1
SCHEMBL28576999 0.85 CYP2C19 (0.50) CYP2C19CYP1A2CYP2C9KDM4EMAPK1
SCHEMBL28577000 0.85 CYP2C19 (0.50) CYP2C19CYP1A2CYP2C9KDM4EMAPK1
SCHEMBL10813669 0.85 CYP2C19 (0.50) CYP2C19CYP1A2CYP2C9KDM4EMAPK1
SCHEMBL10553210 0.85 ALDH1A1 (0.52) CYP2C19CYP1A2CYP2C9KDM4ETSHR
SCHEMBL10550998 0.85 ALDH1A1 (0.52) CYP2C19CYP1A2CYP2C9KDM4ETSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115433204-B Synthesis method and application of spiro-expandable monomer with multi-benzene ring structure 深圳市安伯斯科技有限公司 2024-01-19 CN claimed
CN-116660543-A Diagnostic and prognostic markers for nonalcoholic fatty liver disease and uses thereof 中国人民解放军陆军军医大学第一附属医院 2023-08-29 CN claimed
CN-115433204-A Synthetic method and application of spiro-expansible monomer with multi-benzene ring structure 深圳市安伯斯科技有限公司 2022-12-06 CN claimed
US-4540650-A Photoresists suitable for forming relief structures of highly heat-resistant polymers MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) 1985-09-10 US claimed
CN-115433204-B Synthesis method and application of spiro-expandable monomer with multi-benzene ring structure 深圳市安伯斯科技有限公司 2024-01-19 CN disclosed
CN-115433204-B Synthesis method and application of spiro-expandable monomer with multi-benzene ring structure 深圳市安伯斯科技有限公司 2024-01-19 CN disclosed
CN-112174960-B Toll-like receptor modulating 4, 6-diamino-pyrido [3,2-D ] pyrimidine compounds 吉利德科学公司 2023-10-10 CN disclosed
CN-113024547-B Bicyclic heterocycles as FGFR4 inhibitors 因赛特控股公司 2023-07-21 CN disclosed
CN-115433204-A Synthetic method and application of spiro-expansible monomer with multi-benzene ring structure 深圳市安伯斯科技有限公司 2022-12-06 CN disclosed
CN-115433204-A Synthetic method and application of spiro-expansible monomer with multi-benzene ring structure 深圳市安伯斯科技有限公司 2022-12-06 CN disclosed
CN-109641885-B Heterocyclic compounds as immunomodulators 因赛特公司 2022-09-30 CN disclosed
US-11345690-B2 Methods of synthesizing a difluorolactam analog CAYMAN CHEMICAL COMPANY, INC. (US) 2022-05-31 US disclosed
EP-0403132-A2 Monocarbamate diols, polymers derived from them, and NLO-active materials therefrom MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1990-12-19 EP disclosed
US-4831109-A Copolymerizable UV stabilizers MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1989-05-16 US disclosed
US-4691059-A Copolymerizable UV stabilizers MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1987-09-01 US disclosed
EP-0213925-A2 Copolymerizable UV stabilizers MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1987-03-11 EP disclosed
EP-0103225-B1 PHOTORESIST FOR CREATING RELIEF STRUCTURES ON HIGH-TEMPERATURE RESISTANT POLYMERS MERCK PATENT GmbH (DE) 1987-02-04 EP disclosed
US-4540650-A Photoresists suitable for forming relief structures of highly heat-resistant polymers MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) 1985-09-10 US disclosed
EP-0103225-A2 Photoresist for creating relief structures on high-temperature resistant polymers MERCK PATENT GmbH (DE) 1984-03-21 EP disclosed
EP-0099525-A2 Photoresist MERCK PATENT GmbH (DE) 1984-02-01 EP 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 (1 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-11345690-B2 Methods of synthesizing a difluorolactam analog PTGER4, PTGER1, PTGIR CYP2C19 505/4885CYP1A2 961/4885CYP2C9 511/4885

“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.