SCHEMBL982069

SCHEMBL982069

CCCCCCCCCCCCc1[c]ccc(C)c1C

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TYR P14679 2/20 0.39
ESR1 P03372 2/20 0.36
ADRA2A P08913 2/20 0.36
ADORA3 P0DMS8 2/20 0.36
TACR2 P21452 2/20 0.36
SLC6A2 P23975 2/20 0.36
SLC6A4 P31645 2/20 0.36
SLC6A3 Q01959 2/20 0.36
KCNH2 Q12809 2/20 0.36
TP53 P04637 2/20 0.36
CYP3A4 P08684 2/20 0.36
KDM4E B2RXH2 1/20 0.36
ALDH1A1 P00352 1/20 0.36
LMNA P02545 1/20 0.36
SHBG P04278 1/20 0.36
HSPD1 P10809 1/20 0.36
ADRB3 P13945 1/20 0.36
HTR2C P28335 1/20 0.36
HSPE1 P61604 1/20 0.36
HIF1A Q16665 1/20 0.36

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
SCHEMBL11422922 1.00 TYR (0.39) TYRESR1ADRA2AADORA3TACR2
SCHEMBL981210 1.00 TYR (0.39) TYRESR1ADRA2AADORA3TACR2
SCHEMBL2972954 1.00 TYR (0.39) TYRESR1ADRA2AADORA3TACR2
SCHEMBL981404 1.00 TYR (0.39) TYRESR1ADRA2AADORA3TACR2
SCHEMBL983609 1.00 TYR (0.39) TYRESR1ADRA2AADORA3TACR2
SCHEMBL817463 1.00 TYR (0.39) TYRESR1ADRA2AADORA3TACR2
SCHEMBL985513 1.00 TYR (0.39) TYRESR1ADRA2AADORA3TACR2
SCHEMBL814781 0.98 TYR (0.36) TYRESR1ADRA2AADORA3TACR2
SCHEMBL814841 0.92 SKP2 (0.35) TYRHTT
SCHEMBL983487 0.85 ESR1 (0.36) TYRESR1ADRA2AADORA3TACR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118302407-A Carbonyl compound, method for producing isocyanate compound, and isocyanate composition 旭化成株式会社 2024-07-05 CN disclosed
CN-118215651-A Method for producing isocyanate compound, method for producing urethane compound, method for recovering amine compound, and isocyanate composition 旭化成株式会社 2024-06-18 CN disclosed
WO-2023080257-A1 METHOD FOR PRODUCING ISOCYANATE COMPOUNDS, METHOD FOR PRODUCING CARBAMATE COMPOUNDS, METHOD FOR RECOVERING AMINE COMPOUNDS, AND ISOCYANATE COMPOSITION 旭化成株式会社 2023-05-11 WO disclosed
WO-2023080258-A1 CARBONYL COMPOUND, METHOD FOR PRODUCING CARBONYL COMPOUND, METHOD FOR PRODUCING ISOCYANATE COMPOUND, AND ISOCYANATE COMPOSITION 旭化成株式会社 2023-05-11 WO disclosed
EP-2275406-B1 PROCESS FOR PRODUCING ISOCYANATE ASAHI CHEMICAL IND (JP) 2018-11-28 EP disclosed
US-9233918-B2 Isocyanate production process ASAHI KASEI CHEMICALS CORPORATION (JP) 2016-01-12 US disclosed
US-9163046-B2 Process for producing substituted metallocene compounds for olefin polymerization EXXONMOBIL CHEMICAL PATENTS INC. (US) 2015-10-20 US disclosed
EP-2088138-B1 Process for producing isocyanate ASAHI KASEI CHEMICALS CORP (JP) 2013-02-27 EP disclosed
US-8362293-B2 Process for producing isocyanates ASAHI KASEI CHEMICALS CORPORATION (JP) 2013-01-29 US disclosed
US-20110092731-A1 ISOCYANATE PRODUCTION PROCESS ASAHI KASEI CHEMICALS CORPORATION (JP) 2011-04-21 US disclosed
US-5756565-A STORAGE STABLE COMPOSITION, CROSSLINKED WITH SULFUR IN BITUMINOUS MATRIX ELF ANTAR FRANCE (FR) 1998-05-26 US disclosed
EP-0554679-A1 Process for the preparation of alpha-Chloro 2,4,6-trimethylacetophenone BASF Aktiengesellschaft (DE) 1993-08-11 EP disclosed
EP-0211271-B1 PROCESS FOR THE PREPARATION OF VERATRYL CYANIDE BASF Aktiengesellschaft (DE) 1988-10-12 EP disclosed
EP-0142797-B1 METHOD FOR THE PREPARATION OF ACETONITRILES SUBSTITUTED IN POSITION 2 BY AN AROMATIC OR HETEROCYCLIC SUBSTITUENT BASF Aktiengesellschaft (DE) 1988-07-13 EP disclosed
US-4661610-A Preparation of veratryl cyanide BASF AKTIENGESELLSCHAFT (DE) 1987-04-28 US disclosed
EP-0211271-A1 Process for the preparation of veratryl cyanide BASF Aktiengesellschaft (DE) 1987-02-25 EP disclosed
EP-0142797-A2 Method for the preparation of acetonitriles substituted in position 2 by an aromatic or heterocyclic substituent BASF Aktiengesellschaft (DE) 1985-05-29 EP disclosed
EP-0019158-B1 PROCESS FOR THE PRODUCTION OF M-SUBSTITUTED N-METHYLANILINES BASF Aktiengesellschaft (DE) 1982-09-15 EP disclosed
EP-0046194-A1 Process for the preparation of o,o-disubstituted benzoic acids and their salts BASF Aktiengesellschaft (DE) 1982-02-24 EP disclosed
EP-0019158-A1 Process for the production of m-substituted N-methylanilines BASF Aktiengesellschaft (DE) 1980-11-26 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-20110092731-A1 ISOCYANATE PRODUCTION PROCESS CPS1, PHGDH, APEH TYR 582/4885ESR1 3842/4885ADRA2A 4525/4885

“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.