SCHEMBL1302289

SCHEMBL1302289

CCN(Cc1ccccc1)C(C)O

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.52
SIGMAR1 Q99720 1/20 0.49
CNR2 P34972 1/20 0.47
LMNA P02545 1/20 0.47
BCHE P06276 1/20 0.47
ADRA2B P18089 2/20 0.46
HTR2A P28223 2/20 0.46
KCNH2 Q12809 2/20 0.46
PGR P06401 1/20 0.46
ADRA2A P08913 1/20 0.46
HRH1 P35367 1/20 0.46
ALDH1A1 P00352 2/20 0.45
TP53 P04637 1/20 0.44
MGLL Q99685 1/20 0.44
MEN1 O00255 1/20 0.44
KMT2A Q03164 1/20 0.44
NPC1 O15118 2/20 0.44
RAB9A P51151 2/20 0.44
TRPA1 O75762 1/20 0.44
ADRA2C P18825 1/20 0.44

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
SCHEMBL1593286 0.90 TSHR (0.50) TSHRSIGMAR1LMNAADRA2BHTR2A
Hydrochloric Acid SCHEMBL16447410 0.88 TSHR (0.48) TSHRSIGMAR1LMNAADRA2BHTR2A
SCHEMBL3403185 0.85 BCHE (0.49) TSHRSIGMAR1LMNABCHEADRA2B
SCHEMBL8757082 0.84 TSHR (0.46) TSHRSIGMAR1LMNAADRA2BHTR2A
SCHEMBL12124877 0.83 TSHR (0.50) TSHRSIGMAR1CNR2LMNABCHE
SCHEMBL9380682 0.82 LMNA (0.46) TSHRSIGMAR1CNR2LMNABCHE
SCHEMBL9816880 0.81 BCHE (0.51) TSHRSIGMAR1LMNABCHEADRA2B
(Chloromethyl)Benzene SCHEMBL124016 0.81 TSHR (0.49) TSHRSIGMAR1LMNAADRA2BHTR2A
SCHEMBL9816883 0.81 BCHE (0.51) TSHRSIGMAR1LMNABCHEADRA2B
SCHEMBL454605 0.81 LMNA (0.49) TSHRSIGMAR1CNR2LMNABCHE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113754859-A Amine-containing thioxanthone polyurethane modified epoxy acrylate LED photocuring resin 明光科迪新材料有限公司 2021-12-07 CN claimed
CN-113736092-A Hyperbranched LED resin modified by amine-containing thioxanthone photoinitiating group 吉力水性新材料科技(珠海)有限公司 2021-12-03 CN claimed
CN-113717370-A 2 nd-generation hyperbranched LED resin modified by amine-containing thioxanthone photoinitiating group 吉力水性新材料科技(珠海)有限公司 2021-11-30 CN claimed
CN-113717393-A 3 rd generation dendritic LED resin modified by amine-containing thioxanthone photoinitiating group 吉力水性新材料科技(珠海)有限公司 2021-11-30 CN claimed
US-12258316-B2 Biphenyl compounds useful as muscarinic receptor antagonists THERAVANCE BIOPHARMA R&D IP, LLC (US) 2025-03-25 US disclosed
US-20220306579-A1 BIPHENYL COMPOUNDS USEFUL AS MUSCARINIC RECEPTOR ANTAGONISTS THERAVANCE BIOPHARMA R&D IP, LLC (US) 2022-09-29 US disclosed
US-11247969-B2 Biphenyl compounds useful as muscarinic receptor antagonists THERAVANCE BIOPHARMA R&D IP, LLC (US) 2022-02-15 US disclosed
CN-113754859-A Amine-containing thioxanthone polyurethane modified epoxy acrylate LED photocuring resin 明光科迪新材料有限公司 2021-12-07 CN disclosed
CN-113736092-A Hyperbranched LED resin modified by amine-containing thioxanthone photoinitiating group 吉力水性新材料科技(珠海)有限公司 2021-12-03 CN disclosed
CN-113717370-A 2 nd-generation hyperbranched LED resin modified by amine-containing thioxanthone photoinitiating group 吉力水性新材料科技(珠海)有限公司 2021-11-30 CN disclosed
CN-113717393-A 3 rd generation dendritic LED resin modified by amine-containing thioxanthone photoinitiating group 吉力水性新材料科技(珠海)有限公司 2021-11-30 CN disclosed
US-20200290966-A1 BIPHENYL COMPOUNDS USEFUL AS MUSCARINIC RECEPTOR ANTAGONISTS THERAVANCE BIOPHARMA R&D IP, LLC (US) 2020-09-17 US disclosed
EP-0177122-B1 ACRYLAMIDE DERIVATIVES Nippon Paint Co., Ltd. (JP) 1992-04-01 EP disclosed
US-4935413-A ELASTICITY, ADHESION AND DISPERSIBILITY NIPPON PAINT CO., LTD. (JP) 1990-06-19 US disclosed
US-4902727-A Compounds having a polymerizable acylurethane structure, and their production and process of using NIPPON PAINT CO., LTD. (JP) 1990-02-20 US disclosed
EP-0204497-A1 Polymerisation process employing compounds having polymerisable acylurethane structures Nippon Paint Co., Ltd. (JP) 1986-12-10 EP disclosed
EP-0177122-A2 Acrylamide derivatives Nippon Paint Co., Ltd. (JP) 1986-04-09 EP disclosed
US-4110286-A Stable polyurethane latices, emulsifiable prepolymers therefor and methods of making the same ALCOLAC INC. (US) 1978-08-29 US disclosed
US-4063887-A HYDROXYAMINE COMPOUND CELANESE CORPORATION (US) 1977-12-20 US disclosed
US-4009201-A PARTIALLY OR FULLY QUATERNIZED POLYAMINE ESTERS OF ACRYLIC ACIDS ALCOLAC INC. (US) 1977-02-22 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 (4 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-11247969-B2 Biphenyl compounds useful as muscarinic receptor antagonists CHRM2, CHRM1, CHRM3 TSHR 68/4885SIGMAR1 374/4885CNR2 49/4885
US-20220306579-A1 BIPHENYL COMPOUNDS USEFUL AS MUSCARINIC RECEPTOR ANTAGONISTS CHRM2, CHRM1, CHRM3 TSHR 68/4885SIGMAR1 374/4885CNR2 49/4885
US-12258316-B2 Biphenyl compounds useful as muscarinic receptor antagonists CHRM2, CHRM1, CHRM3 TSHR 68/4885SIGMAR1 374/4885CNR2 49/4885
US-20200290966-A1 BIPHENYL COMPOUNDS USEFUL AS MUSCARINIC RECEPTOR ANTAGONISTS CHRM2, CHRM1, CHRM3 TSHR 68/4885SIGMAR1 374/4885CNR2 49/4885

“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.