SCHEMBL1154872

SCHEMBL1154872

OCc1cccc2cccnc12

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.55
MMP2 P08253 2/20 0.55
CHRM1 P11229 1/20 0.55
COMT P21964 1/20 0.55
ADRA1A P35348 1/20 0.55
METAP2 P50579 1/20 0.55
METAP1 P53582 1/20 0.55
HDAC8 Q9BY41 1/20 0.55
KDM4E B2RXH2 6/20 0.54
LMNA P02545 4/20 0.54
MAPT P10636 3/20 0.54
HTT P42858 2/20 0.54
SMN1; SMN2 Q16637 2/20 0.54
TP53 P04637 2/20 0.54
GMNN O75496 1/20 0.54
HSP90AA1 P07900 1/20 0.54
CYP3A4 P08684 1/20 0.54
CYP2D6 P10635 1/20 0.54
MMP9 P14780 1/20 0.54
ALOX15 P16050 1/20 0.54

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
SCHEMBL30003476 1.00 TSHR (0.55) TSHRMMP2CHRM1COMTADRA1A
SCHEMBL1360579 0.98 TSHR (0.53) TSHRMMP2CHRM1COMTADRA1A
Hydrochloric Acid SCHEMBL27297244 0.98 TSHR (0.53) TSHRMMP2CHRM1COMTADRA1A
SCHEMBL11497495 0.84 HDAC6 (0.52) TSHRMMP2CHRM1COMTADRA1A
SCHEMBL30203803 0.84 HDAC6 (0.52) TSHRMMP2CHRM1COMTADRA1A
SCHEMBL7424652 0.79 KDM4E (0.54) TSHRMMP2CHRM1COMTADRA1A
SCHEMBL31261655 0.79 KDM4E (0.54) TSHRMMP2CHRM1COMTADRA1A
SCHEMBL7372603 0.79 PSMD14 (0.55) TSHRMMP2CHRM1COMTADRA1A
SCHEMBL7344355 0.79 KDM4E (0.54) TSHRMMP2CHRM1COMTADRA1A
SCHEMBL19303228 0.79 KDM4E (0.54) TSHRMMP2CHRM1COMTADRA1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117361454-A Method for preparing hydroxylamine aqueous solution by thermal decomposition of hydroxylamine phosphate 浙江锦华新材料股份有限公司 2024-01-09 CN claimed
CN-110465328-B Process for oximation of ketones 万华化学集团股份有限公司 2022-07-12 CN claimed
EP-3666852-B1 ETCHING SOLUTION HAVING SILICON OXIDE CORROSION INHIBITOR AND METHOD OF USING THE SAME VERSUM MAT US LLC (US) 2022-01-05 EP claimed
EP-3666852-A2 ETCHING SOLUTION HAVING SILICON OXIDE CORROSION INHIBITOR AND METHOD OF USING THE SAME Versum Materials US, LLC (US) 2020-06-17 EP claimed
CN-111197182-A Etching solution with silicon oxide corrosion inhibitor and method of use thereof 弗萨姆材料美国有限责任公司 2020-05-26 CN claimed
US-20200157422-A1 Etching Solution Having Silicon Oxide Corrosion Inhibitor And Method Of Using The Same VERSUM MATERIALS US, LLC (US) 2020-05-21 US claimed
US-6620823-B2 Antiinflammatory agents; rheumatic disorders BRISTOL-MYERS SQUIBB PHARME COMPANY 2003-09-16 US claimed
CN-1100414-A Preparation of pharmaceutical compound containing novel derivative of leukol SMITHKLINE BECKMAN INTERCREDIT (NL) 1995-03-22 CN claimed
EP-0628036-A4 N-SUBSTITUTED-FURYLALKENYL HYDROXAMIC ACID AND N-HYDROXYUREA COMPOUNDS HAVING LIPOXYGENASE INHIBITORY ACTIVITY. 1995-01-11 EP claimed
CN-1027368-C Process for preparing substituted quinoline derivatives SMITHKLINE BECKMAN INTERCREDIT (NL) 1995-01-11 CN claimed
EP-0628036-A1 N-SUBSTITUTED-FURYLALKENYL HYDROXAMIC ACID AND N-HYDROXYUREA COMPOUNDS HAVING LIPOXYGENASE INHIBITORY ACTIVITY ABBOTT LABORATORIES (US) 1994-12-14 EP claimed
WO-1993017006-A1 N-SUBSTITUTED-FURYLALKENYL HYDROXAMIC ACID AND N-HYDROXYUREA COMPOUNDS HAVING LIPOXYGENASE INHIBITORY ACTIVITY ABBOTT LABORATORIES (US) 1993-09-02 WO claimed
US-5169854-A N-substituted-furylalkenyl hydroxamic acid and N-hydroxyurea compounds having lipoxygenase inhibitory activity ABBOTT LABORATORIES (US) 1992-12-08 US claimed
CN-1035501-A PROCESS FOR PREPARING SUBSTITUTED QUINOLINE DERIVATIVES SMITHKLINE BECKMAN INTERCREDIT (NL) 1989-09-13 CN claimed
JP-60090202-A None JP disclosed
JP-2157282-A None JP disclosed
US-12331056-B2 SHP2 phosphatase inhibitors and methods of use thereof RELAY THERAPEUTICS, INC. (US) 2025-06-17 US disclosed
JP-S6090202-A ADSORBING POLYMER AND PRODUCTION THEREOF ASAHI CHEM IND CO LTD 1985-05-21 JP disclosed
US-3959473-A DIURETIC U.S. PHILIPS CORPORATION (US) 1976-05-25 US disclosed
US-3956420-A CPOLYOLEFIN COMPOSITION FOR ELECTRICAL INSULATIONFERROCENE, 8-SUBSTITUTED QUINOLINE DAINICHI-NIPPON CABLES, LTD. (JA) 1976-05-11 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 (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-12331056-B2 SHP2 phosphatase inhibitors and methods of use thereof PTPRCAP, PTPN22, PTPN1 TSHR 3144/4885MMP2 2370/4885CHRM1 4862/4885

“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.