SCHEMBL2906683

SCHEMBL2906683

O=S(=O)(c1ccc(F)cc1)c1ccc(Br)cc1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 4/20 0.50
LMNA P02545 1/20 0.49
PKM P14618 1/20 0.49
EGFR P00533 2/20 0.49
ERBB2 P04626 2/20 0.49
PLCG1 P19174 1/20 0.48
TP53 P04637 2/20 0.48
MAPT P10636 2/20 0.48
HSD11B1 P28845 1/20 0.47
CA1 P00915 2/20 0.45
MMP1 P03956 2/20 0.45
MMP2 P08253 2/20 0.45
MMP9 P14780 2/20 0.45
MMP8 P22894 2/20 0.45
MMP13 P45452 2/20 0.45
CA12 O43570 1/20 0.45
CA9 Q16790 1/20 0.45
HTR2C P28335 2/20 0.44
HTR2A P28223 2/20 0.44
KCNH2 Q12809 2/20 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
SCHEMBL10588232 0.94 CA2 (0.55) CA2LMNAPKMEGFRERBB2
SCHEMBL30072318 0.87 HSD11B1 (0.55) CA2LMNAPKMHSD11B1CA1
SCHEMBL8978700 0.87 CA2 (0.62) CA2LMNAPLCG1MAPTCA1
SCHEMBL2121770 0.87 HSD11B1 (0.55) CA2LMNAPKMHSD11B1CA1
SCHEMBL250285 0.87 CA2 (0.62) CA2LMNAPLCG1MAPTCA1
SCHEMBL18187419 0.87 CA2 (0.62) CA2LMNAPLCG1MAPTCA1
SCHEMBL79787 0.87 HSD11B1 (0.55) CA2LMNAPKMHSD11B1CA1
SCHEMBL4328574 0.87 HSD11B1 (0.55) CA2LMNAPKMHSD11B1CA1
SCHEMBL2122562 0.87 CA2 (0.62) CA2LMNAPLCG1MAPTCA1
SCHEMBL9356008 0.80 CA2 (0.67) CA2LMNAPLCG1CA1MMP1

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
US-10937971-B2 Organic monomolecular white light material, manufacturing method for the same, and OLED element SHENZHEN CHINA STAR OPTOELECTRONICS TECHNOLOGY CO., LTD. (CN) 2021-03-02 US claimed
US-20200295274-A1 ORGANIC MONOMOLECULAR WHITE LIGHT MATERIAL, MANUFACTURING METHOD FOR THE SAME, AND OLED ELEMENT SHENZHEN CHINA STAR OPTOELECTRONICS TECHNOLOGY CO., LTD. (CN) 2020-09-17 US claimed
CN-108084150-B Organic supramolecular white light emitting material and preparation method thereof and OLED device 深圳市华星光电技术有限公司 2019-09-24 CN claimed
CN-108084150-A Organic supramolecular white light emitting material and preparation method thereof and OLED device 深圳市华星光电技术有限公司 2018-05-29 CN claimed
CN-115745885-B Chiral liquid crystal fluorescent material and application thereof 常州大学 2025-05-02 CN disclosed
CN-115745885-A High-efficiency chiral liquid crystal fluorescent material and application thereof 常州大学 2023-03-07 CN disclosed
US-10937971-B2 Organic monomolecular white light material, manufacturing method for the same, and OLED element SHENZHEN CHINA STAR OPTOELECTRONICS TECHNOLOGY CO., LTD. (CN) 2021-03-02 US disclosed
US-10937971-B2 Organic monomolecular white light material, manufacturing method for the same, and OLED element SHENZHEN CHINA STAR OPTOELECTRONICS TECHNOLOGY CO., LTD. (CN) 2021-03-02 US disclosed
US-20200295274-A1 ORGANIC MONOMOLECULAR WHITE LIGHT MATERIAL, MANUFACTURING METHOD FOR THE SAME, AND OLED ELEMENT SHENZHEN CHINA STAR OPTOELECTRONICS TECHNOLOGY CO., LTD. (CN) 2020-09-17 US disclosed
US-20200295274-A1 ORGANIC MONOMOLECULAR WHITE LIGHT MATERIAL, MANUFACTURING METHOD FOR THE SAME, AND OLED ELEMENT SHENZHEN CHINA STAR OPTOELECTRONICS TECHNOLOGY CO., LTD. (CN) 2020-09-17 US disclosed
CN-110240695-B Functional phenylene copolymerized conjugated TADF (TADF) polymer and preparation method and application thereof 中国科学院长春应用化学研究所 2020-08-25 CN disclosed
CN-108084150-B Organic supramolecular white light emitting material and preparation method thereof and OLED device 深圳市华星光电技术有限公司 2019-09-24 CN disclosed
EP-1937633-A1 BIPHENYLOXYACETIC ACID DERIVATIVES FOR THE TREATMENT OF RESPIRATORY DISEASE Astra Zeneca AB (SE) 2008-07-02 EP disclosed
WO-2007039741-A1 BIPHENYLOXYACETIC ACID DERIVATIVES FOR THE TREATMENT OF RESPIRATORY DISEASE ASTRAZENECA AB (SE) 2007-04-12 WO disclosed
US-6242654-B1 REACTING A PHENOLATE COMPOUND WITH AN ORGANIC FLUORINATING AGENT TO PREPARE A FLUORINE SUBSTITUTED AROMATIC COMPOUND MITSUI CHEMICALS, INC. (JP) 2001-06-05 US disclosed
EP-1013629-A1 Preparation process of fluorine subsituted aromatic compound Mitsui Chemicals, Inc. (JP) 2000-06-28 EP disclosed
US-5185454-A Reacting aryl bromide with acetylene in presence of palladium catalyst and nitrogen-containing heterocyclic base BAYER AKTIENGESELLSCHAFT (DE) 1993-02-09 US disclosed
US-5093467-A Increased molecular weight TOSOH CORPORATION (JP) 1992-03-03 US disclosed
EP-0425930-A2 Process for the preparation of symmetrical diarylacetylenes BAYER AG (DE) 1991-05-08 EP disclosed
EP-0348189-A2 Production of poly (arylene sulfide sulfone) Tosoh Corporation (JP) 1989-12-27 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 (2 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-10937971-B2 Organic monomolecular white light material, manufacturing method for the same, and OLED element NLRP3, NLRP1, OCIAD1 CA2 4085/4885LMNA 1306/4885PKM 3824/4885
US-20200295274-A1 ORGANIC MONOMOLECULAR WHITE LIGHT MATERIAL, MANUFACTURING METHOD FOR THE SAME, AND OLED ELEMENT NLRP3, NLRP1, OCIAD1 CA2 4085/4885LMNA 1306/4885PKM 3824/4885

“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.