SCHEMBL982272

SCHEMBL982272

CCCc1ccccc1-c1ccccc1O

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR1A P08908 1/20 0.47
ELANE P08246 1/20 0.45
CTSG P08311 1/20 0.45
CNR1 P21554 1/20 0.44
CNR2 P34972 1/20 0.44
HSPA5 P11021 1/20 0.43
USP2 O75604 1/20 0.43
ALOX5 P09917 1/20 0.42
TAAR1 Q96RJ0 1/20 0.42
ALDH1A1 P00352 1/20 0.41
HPGD P15428 1/20 0.41
BCL2L1 Q07817 1/20 0.41
HSD17B10 Q99714 1/20 0.41
GCGR P47871 1/20 0.40
TSHR P16473 2/20 0.40
IAPP P10997 1/20 0.40
CYP2D6 P10635 1/20 0.39
HIF1A Q16665 1/20 0.39
PPARA Q07869 1/20 0.38
PDE5A O76074 1/20 0.38

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
SCHEMBL548498 0.88 ELANE (0.48) HTR1AELANECTSGBCL2L1TSHR
SCHEMBL30212610 0.88 ELANE (0.48) HTR1AELANECTSGBCL2L1TSHR
SCHEMBL6704515 0.87 PPARA (0.41) HTR1AELANECTSGALDH1A1HPGD
SCHEMBL28161120 0.86 ELANE (0.53) HTR1AELANECTSGCNR1CNR2
SCHEMBL324186 0.86 ELANE (0.47) HTR1AELANECTSGBCL2L1TSHR
SCHEMBL983845 0.86 LIPG (0.53) ELANECTSGALOX5BCL2L1HSD17B10
SCHEMBL5588855 0.86 ELANE (0.49) HTR1AELANECTSGHSPA5ALDH1A1
SCHEMBL984108 0.85 LIPG (0.56) ELANECTSGALOX5BCL2L1HSD17B10
SCHEMBL982370 0.85 LIPG (0.56) ELANECTSGALOX5BCL2L1HSD17B10
SCHEMBL983656 0.85 LIPG (0.56) ELANECTSGALOX5BCL2L1HSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4446310-A1 METHOD FOR PRODUCING BLOCKED ISOCYANATE COMPOUND AND METHOD FOR PRODUCING ISOCYANATE COMPOUND Asahi Kasei Kabushiki Kaisha (JP) 2024-10-16 EP disclosed
WO-2023106377-A1 METHOD FOR PRODUCING BLOCKED ISOCYANATE COMPOUND AND METHOD FOR PRODUCING ISOCYANATE COMPOUND 旭化成株式会社 2023-06-15 WO disclosed
CN-115779493-A Method for purifying liquid crystal monomer or liquid crystal composition by using functionalized silica gel material 苏州硒诺唯新新材料科技有限公司 2023-03-14 CN disclosed
EP-2275405-B1 PROCESS FOR PRODUCING ISOCYANATE USING DIARYL CARBONATE ASAHI CHEMICAL IND (JP) 2019-04-24 EP disclosed
EP-2275406-B1 PROCESS FOR PRODUCING ISOCYANATE ASAHI CHEMICAL IND (JP) 2018-11-28 EP disclosed
EP-2792673-B1 Carbamic acid ester derivatives for the production of isocyanate and aromatic hydroxy compounds ASAHI CHEMICAL IND (JP) 2018-07-25 EP disclosed
US-9685597-B2 Curable composition for sealing optical semiconductor DAICEL CORPORATION (JP) 2017-06-20 US disclosed
US-9637445-B2 Isocyanate production process using composition containing carbamic acid ester and aromatic hydroxy compound, and composition for transfer and storage of carbamic acid ester ASAHI KASEI CHEMICALS CORPORATION (JP) 2017-05-02 US disclosed
EP-2147909-B1 METHOD FOR PRODUCTION OF ISOCYANATE USING COMPOSITION COMPRISING CARBAMIC ACID ESTER AND AROMATIC HYDROXY COMPOUND, AND COMPOSITION FOR TRANSPORT OR STORAGE OF CARBAMIC ACID ESTER ASAHI CHEMICAL IND (JP) 2016-12-14 EP disclosed
US-20160126431-A1 CURABLE COMPOSITION FOR SEALING OPTICAL SEMICONDUCTOR DAICEL CORPORATION (JP) 2016-05-05 US disclosed
US-20100113823-A1 ISOCYANATE PRODUCTION PROCESS USING COMPOSITION CONTAINING CARBAMIC ACID ESTER AND AROMATIC HYDROXY COMPOUND, AND COMPOSITION FOR TRANSFER AND STORAGE OF CARBAMIC ACID ESTER ASAHI KASEI CHEMICALS CORPORATION (JP) 2010-05-06 US disclosed
EP-2147909-A1 METHOD FOR PRODUCTION OF ISOCYANATE USING COMPOSITION COMPRISING CARBAMIC ACID ESTER AND AROMATIC HYDROXY COMPOUND, AND COMPOSITION FOR TRANSPORT OR STORAGE OF CARBAMIC ACID ESTER Asahi Kasei Chemicals Corporation (JP) 2010-01-27 EP disclosed
US-4157324-A High ortho etherified resole resins admixed with coreactive resins MONSANTO COMPANY (US) 1979-06-05 US disclosed
US-4122235-A LAMINATE, METAL SALT CURING ACCELERATOR MONSANTO COMPANY (US) 1978-10-24 US disclosed
US-4122054-A High ortho etherified resole resins MONSANTO COMPANY (US) 1978-10-24 US disclosed
US-4120847-A High ortho etherified resole resins MONSANTO COMPANY (US) 1978-10-17 US disclosed
US-4112188-A LAMINATE, BORIC ACID, DIAMMONIUM TETRABORATE, DIAMMONIUM PENTABORATE, AND/OR DIAMMONIUM OCTABORATE AS ACCELERATORS MONSANTO COMPANY (US) 1978-09-05 US disclosed
US-4045398-A BORON COMPOUND CURING ACCELERATOR MONSANTO COMPANY (US) 1977-08-30 US disclosed
US-4043970-A IMPROVED CURE RATE IN ELECTRICAL LAMINATES MONSANTO COMPANY (US) 1977-08-23 US disclosed
US-4022942-A NOVOLAKS OR B-STAGE RESINS MONSANTO COMPANY (US) 1977-05-10 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-20100113823-A1 ISOCYANATE PRODUCTION PROCESS USING COMPOSITION CONTAINING CARBAMIC ACID ESTER AND AROMATIC HYDROXY COMPOUND, AND COMPOSITION FOR TRANSFER AND STORAGE OF CARBAMIC ACID ESTER PAH, APEH, CPS1 HTR1A 2960/4885ELANE 1749/4885CTSG 158/4885

“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.