Sugi Predict

Sugi Predict / Compounds / SCHEMBL776706

SCHEMBL776706

SCHEMBL776706

O=S(=O)(c1ccccc1)c1ccccc1F

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HTR6 P50406 5/20 0.57
▸ HSD11B1 P28845 1/20 0.57
▸ KMT2A Q03164 1/20 0.55
▸ CNR2 P34972 1/20 0.51
▸ HTR2C P28335 1/20 0.50
▸ HTR2B P41595 1/20 0.50
▸ ABCC9 O60706 1/20 0.49
▸ ABCC8 Q09428 1/20 0.49
▸ KCNJ11 Q14654 1/20 0.49
▸ KCNJ8 Q15842 1/20 0.49
▸ HTR2A P28223 3/20 0.49
▸ CNR1 P21554 2/20 0.48
▸ AKR1B1 P15121 1/20 0.47
▸ TSHR P16473 1/20 0.47
▸ HTT P42858 1/20 0.47
▸ CA12 O43570 1/20 0.47
▸ CA1 P00915 1/20 0.47
▸ CA2 P00918 1/20 0.47
▸ CA7 P43166 1/20 0.47
▸ CA13 Q8N1Q1 1/20 0.47

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
SCHEMBL2474755 0.87 HTR2A (0.59) HSD11B1KMT2ACNR2HTR2CHTR2B
SCHEMBL30333632 0.85 AKR1B1 (0.53) HSD11B1KMT2ACNR2HTR2CHTR2B
SCHEMBL2124755 0.85 AKR1B1 (0.53) HSD11B1KMT2ACNR2HTR2CHTR2B
SCHEMBL250919 0.85 AKR1B1 (0.53) HSD11B1KMT2ACNR2HTR2CHTR2B
SCHEMBL545481 0.85 HTR6 (0.52) HTR6HSD11B1KMT2ACNR2HTR2C
SCHEMBL8866512 0.84 HTR6 (0.59) HTR6HSD11B1KMT2ACNR2HTR2C
SCHEMBL3446333 0.84 CNR1 (0.58) HSD11B1KMT2ACNR2HTR2CHTR2B
SCHEMBL31108984 0.83 MEN1 (0.56) HSD11B1KMT2ACNR2HTR2CHTR2B
SCHEMBL8080841 0.83 HTR6 (0.72) HTR6KMT2ATSHRHTTCA12
SCHEMBL7935381 0.82 HTR2A (0.58) HTR6HSD11B1HTR2CHTR2BHTR2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12100809-B2 Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery MITSUBISHI CHEMICAL CORPORATION (JP) 2024-09-24 — — US disclosed
WO-2023163533-A1 ORGANIC MOLECULE FOR OPTOELECTRONIC DEVICE 삼성디스플레이주식회사 2023-08-31 — — WO disclosed
US-20220149436-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2022-05-12 — — US disclosed
US-11283107-B2 Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery MITSUBISHI CHEMICAL CORPORATION (JP) 2022-03-22 — — US disclosed
EP-3621141-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2020-03-11 — — EP disclosed
US-20190229372-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2019-07-25 — — US disclosed
US-10333172-B2 Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery MITSUBISHI CHEMICAL CORPORATION (JP) 2019-06-25 — — US disclosed
US-10290901-B2 — — 2019-05-14 — — US disclosed
US-20180282483-A1 Polyarylene ether sulfone (PAES) Polymers and Methods for Making the Same SOLVAY SPECIALTY POLYMERS USA, LLC (US) 2018-10-04 — — US disclosed
US-9868825-B2 Polyarylene ether sulfone (PAES) polymers SOLVAY SPECIALTY POLYMERS USA, LLC (US) 2018-01-16 — — US disclosed
CN-1169759-C Process for producing substituted aromatic compound ������ѧ��ʽ���� 2004-10-06 — — CN disclosed
WO-2004014981-A2 POLYPHENYLENE-TYPE POLYMERS, PREPARATION METHOD THEREOF, MEMBRANES AND FUEL CELL DEVICE COMPRISING SAID MEMBRANES COMMISSARIAT A L'ENERGIE ATOMIQUE (FR) 2004-02-19 — — WO disclosed
EP-1275630-A1 PROCESS FOR PRODUCING SUBSTITUTED AROMATIC COMPOUND Mitsui Chemicals, Inc. (JP) 2003-01-15 — — EP disclosed
CN-1380880-A Process for producing substituted aromatic compound MITSUI CHEMICALS INC (JP) 2002-11-20 — — CN disclosed
US-20020161227-A1 PROCESS FOR PREPARATION OF SUBSTITUTED AROMATIC COMPOUND MITSUI CHEMICALS, INC. (JP) 2002-10-31 — — US disclosed
US-6469224-B1 REACTING A PHOSPHAZENIUM COMPOUND WITH A HALOGENATED AROMATIC COMPOUNDS, ESPECIALLY CHLORINATED AROMATIC COMPOUNDS MITSUI CHEMICALS, INC. (JP) 2002-10-22 — — US disclosed
EP-0373633-B1 Polyetheric copolymers, process for preparing the same, compositions containing the same, their molded products, and their use IDEMITSU KOSAN CO (JP) 1996-02-28 — — EP disclosed
US-5115077-A Condensation polymerization of a dihalogen benzonitrile and a 4,4*-biphenol and a benzophenone in the presence of an alkali metal catalyst IDEMITSU KOSAN COMPANY LIMITED (JP) 1992-05-19 — — US disclosed
EP-0394933-A2 Polyphenylene sulfide resin composition TORAY INDUSTRIES, INC. (JP) 1990-10-31 — — EP disclosed
EP-0373633-A2 Polyetheric copolymers, process for preparing the same, compositions containing the same, their molded products, and their use IDEMITSU KOSAN COMPANY LIMITED (JP) 1990-06-20 — — 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-20020161227-A1 PROCESS FOR PREPARATION OF SUBSTITUTED AROMATIC COMPOUND H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, AFF1, PAH HTR6 2298/4885HSD11B1 2412/4885KMT2A 1767/4885

“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.