SCHEMBL392840

SCHEMBL392840

O=C(O)c1ccc(Cl)cc1F

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.63
TSHR P16473 1/20 0.63
CASP1 P29466 1/20 0.63
ALDH1A1 P00352 2/20 0.57
TP53 P04637 1/20 0.57
CA1 P00915 1/20 0.55
CA2 P00918 1/20 0.55
GRIK1 P39086 4/20 0.53
MRGPRX4 Q96LA9 2/20 0.50
MYC P01106 1/20 0.49
F7 P08709 1/20 0.47
F3 P13726 1/20 0.47
KEAP1 Q14145 1/20 0.47
NFE2L2 Q16236 1/20 0.47
CYP11B2 P19099 1/20 0.46
KMO O15229 1/20 0.46
KDM4E B2RXH2 2/20 0.46
MEN1 O00255 1/20 0.46
KMT2A Q03164 1/20 0.46
SRD5A2 P31213 1/20 0.46

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
SCHEMBL8162477 0.85 SMN1; SMN2 (0.46) SMN1; SMN2TSHRCASP1ALDH1A1TP53
SCHEMBL283203 0.84 ALDH1A1 (0.65) SMN1; SMN2TSHRCASP1ALDH1A1TP53
SCHEMBL27442149 0.84 SMN1; SMN2 (0.48) SMN1; SMN2TSHRCASP1ALDH1A1TP53
SCHEMBL30396748 0.84 ALDH1A1 (0.65) SMN1; SMN2TSHRCASP1ALDH1A1TP53
SCHEMBL6017915 0.84 RARB (0.55) SMN1; SMN2TSHRCASP1ALDH1A1TP53
SCHEMBL7840274 0.83 CES2 (0.50) SMN1; SMN2TSHRCASP1ALDH1A1TP53
SCHEMBL645757 0.83 ALDH1A1 (0.54) SMN1; SMN2TSHRCASP1ALDH1A1TP53
SCHEMBL911253 0.81 DGAT1 (0.60) SMN1; SMN2TSHRCASP1ALDH1A1CYP11B2
SCHEMBL29392929 0.81 MAOB (0.58) SMN1; SMN2TSHRCASP1ALDH1A1CYP11B2
SCHEMBL325429 0.81 MAOB (0.58) SMN1; SMN2TSHRCASP1ALDH1A1CYP11B2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118666668-A Synthesis method of pain medicine synthesis building block 4, 5-dichloro-2-fluorobenzoic acid in clinical research 上海苏博医药科技有限公司 2024-09-20 CN claimed
CN-113880762-B Triacylamine derivatives containing 1,8-naphthalimide as well as preparation method and application thereof 河北农业大学 2023-02-21 CN claimed
CN-115043833-A Bcl-2 fluorescent probe and preparation method and application thereof 山东大学 2022-09-13 CN claimed
CN-110724050-B Refining method of 2-chloro-6-fluorobenzoic acid 浙江大洋生物科技集团股份有限公司 2022-04-22 CN claimed
CN-111689881-B Synthetic method of azosemide intermediate 苏州华道生物药业股份有限公司 2022-04-01 CN claimed
CN-113880762-A 1, 8-naphthalimide-containing triacylamine derivatives, and preparation method and application thereof 河北农业大学 2022-01-04 CN claimed
EP-3551633-B1 SUBSTITUTED PYRAZOLOAZEPIN-4-ONES AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS LEO PHARMA AS (DK) 2021-03-31 EP claimed
CN-111689881-A Synthetic method of azosemide intermediate 苏州华道生物药业股份有限公司 2020-09-22 CN claimed
CN-111518055-A Preparation method of benzothiazepine oxide, product prepared by preparation method and application of product 西安都创医药科技有限公司 2020-08-11 CN claimed
CN-110818556-A Method for producing high-purity 2-chloro-6-fluorobenzoyl chloride by using waste residues 浙江大洋生物科技集团股份有限公司 2020-02-21 CN claimed
CN-110724050-A Refining method of 2-chloro-6-fluorobenzoic acid 浙江大洋生物科技集团股份有限公司 2020-01-24 CN claimed
EP-3551633-A1 SUBSTITUTED PYRAZOLOAZEPIN-4-ONES AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS Leo Pharma A/S (DK) 2019-10-16 EP claimed
CN-106986789-B Hydroquinone compound and preparation method thereof and the application in antitumor or immunological regulation 中国人民解放军军事医学科学院生物医学分析中心 2019-07-16 CN claimed
WO-2018108230-A1 SUBSTITUTED PYRAZOLOAZEPIN-4-ONES AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS LEO PHARMA A/S (DK) 2018-06-21 WO claimed
CN-106986789-A Hydroquinone compound and preparation method thereof and the application in antitumor or immunological regulation 中国人民解放军军事医学科学院生物医学分析中心 2017-07-28 CN claimed
US-20110260051-A1 METHOD FOR DETECTING TRACER COMPOUNDS FOR HYDROCARBON PRODUCTION TOTAL S.A. (FR) 2011-10-27 US claimed
US-7205318-B2 Lactam-containing cyclic diamines and derivatives as a factor Xa inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2007-04-17 US claimed
US-20040204454-A1 Lactam-containing cyclic diamines and derivatives as factor Xa inhibitors BRISTOL-MYERS SQUIBB COMPANY 2004-10-14 US claimed
US-20260144252-A1 BROMINE- OR IODINE-PARA-SUBSTITUTED [(1,5-DIPHENYL-1H-1,2,4-TRIAZOL-3-YL)OXY]ACETIC ACID DERIVATIVES AND THEIR SALTS, AGENTS FOR PROTECTING USEFUL PLANTS OR CROP PLANTS COMPRISING THEM, METHODS FOR PRODUCING THEM AND THEIR USE AS SAFENERS BAYER AKTIENGESELLSCHAFT (DE) 2026-05-28 US disclosed
US-4243819-A Substituted amino acids ZOECON CORPORATION (US) 1981-01-06 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 (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-20260144252-A1 BROMINE- OR IODINE-PARA-SUBSTITUTED [(1,5-DIPHENYL-1H-1,2,4-TRIAZOL-3-YL)OXY]ACETIC ACID DERIVATIVES AND THEIR SALTS, AGENTS FOR PROTECTING USEFUL PLANTS OR CROP PLANTS COMPRISING THEM, METHODS FOR PRODUCING THEM AND THEIR USE AS SAFENERS CBR3, CBR1, CA3 SMN1; SMN2 3105/4885TSHR 385/4885CASP1 724/4885
US-20040204454-A1 Lactam-containing cyclic diamines and derivatives as factor Xa inhibitors PEPD, TFPI, F2 SMN1; SMN2 3010/4885TSHR 2279/4885CASP1 459/4885

“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.