SCHEMBL247900

SCHEMBL247900

N#Cc1cc(Br)ccc1O

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALOX15 P16050 2/20 0.50
HPGD P15428 2/20 0.43
CES2 O00748 1/20 0.43
GALR3 O60755 1/20 0.43
CYP1A2 P05177 1/20 0.43
CYP2C9 P11712 1/20 0.43
CASP1 P29466 1/20 0.43
CYP2C19 P33261 1/20 0.43
ERN1 O75460 1/20 0.42
MAOA P21397 1/20 0.41
MAOB P27338 1/20 0.41
XDH P47989 1/20 0.41
HTT P42858 4/20 0.40
LMNA P02545 3/20 0.40
ALDH1A1 P00352 2/20 0.40
ESR1 P03372 2/20 0.40
ESR2 Q92731 2/20 0.40
MEN1 O00255 3/20 0.40
KMT2A Q03164 3/20 0.40
KDM4E B2RXH2 1/20 0.40

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
SCHEMBL30689811 1.00 ALOX15 (0.50) ALOX15HPGDCES2GALR3CYP1A2
SCHEMBL584543 0.82 MAOB (0.46) ALOX15HPGDCES2GALR3CYP1A2
SCHEMBL30044070 0.82 MAOB (0.46) ALOX15HPGDCES2GALR3CYP1A2
Ammonia Solution, Strong SCHEMBL20295047 0.80 MAOB (0.44) ALOX15HPGDCES2GALR3CYP1A2
SCHEMBL1395661 0.78 MAOB (0.61) MAOAMAOBALDH1A1KDM4ESLC1A5
SCHEMBL30475151 0.78 MAOB (0.61) MAOAMAOBALDH1A1KDM4ESLC1A5
SCHEMBL22122429 0.78 CHEK1 (0.43) ALOX15HPGDCES2GALR3CYP1A2
SCHEMBL5160436 0.77 ALOX15 (0.50) ALOX15HPGDCES2GALR3CYP1A2
SCHEMBL15074082 0.77 ALOX15 (0.50) ALOX15HPGDCES2GALR3CYP1A2
SCHEMBL19062226 0.76 MAOB (0.44) MAOAMAOBLMNAESR1ESR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110078668-B Phenyl imidazole XOR inhibitor, preparation and application 华南理工大学 2023-03-24 CN claimed
CN-109212110-B Gas chromatography-mass spectrometry combined method for measuring three trace monohalogenated hydroxyl benzonitrile in river water 丁立平 2021-05-11 CN claimed
CN-106146447-A A kind of method preparing 4 amido imide coumarin derivatives 上海应用技术学院 2016-11-23 CN claimed
EP-4722216-A1 PYRROLOPYRIMIDINE DERIVATIVE AND USE THEREOF IN MEDICINE Kangbaida (Sichuan) Biotechnology Co., Ltd. (CN) 2026-04-08 EP disclosed
US-20250382312-A1 BORON CONTAINING PYRAZOLE COMPOUNDS, COMPOSITIONS COMPRISING THEM, METHODS AND USES THEREOF BORAH INC (US) 2025-12-18 US disclosed
US-12404286-B2 Boron containing pyrazole compounds, compositions comprising them, methods and uses thereof BORAH, INC. (US) 2025-09-02 US disclosed
CN-115894459-B 2-Benzofuran carboxylic acid derivative and preparation method and application thereof 中国药科大学 2025-05-27 CN disclosed
CN-119894900-A Pyrrolo pyrimidine derivative and application thereof in medicine 康百达(四川)生物医药科技有限公司 2025-04-25 CN disclosed
US-12269814-B2 Process for preparing a compound useful to treat mycoses PULMOCIDE LIMITED (GB) 2025-04-08 US disclosed
WO-2025056068-A1 BICYCLIC COMPOUND, AND PREPARATION METHOD THEREFOR AND PHARMACEUTICAL USE THEREOF 上海济煜医药科技有限公司 2025-03-20 WO disclosed
US-12252496-B2 Organic compound, light-emitting element, light-emitting device, electronic device, and lighting device SEMICONDUCTOR ENERGY LABORATORY CO., LTD. (JP) 2025-03-18 US disclosed
US-6395919-B1 Calcilytic compounds SMITHKLINE BEECHAM CORPORATION 2002-05-28 US disclosed
CN-1346269-A Calcilytic compounds SMITHKLINE BEECHAM CORP (US) 2002-04-24 CN disclosed
EP-1070048-A4 CALCILYTIC COMPOUNDS SMITHKLINE BEECHAM CORP (US) 2001-11-07 EP disclosed
EP-1070048-A1 CALCILYTIC COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2001-01-24 EP disclosed
WO-1999051569-A1 CALCILYTIC COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 1999-10-14 WO disclosed
US-5270308-A Hypotensives TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1993-12-14 US disclosed
CN-1060467-A 1,3-benzoxazine derivatives, its production method and purposes TAKEDA CHEMICAL INDUSTRIES LTD (JP) 1992-04-22 CN disclosed
EP-0477789-A1 1,3-Benzoxazine derivatives, their production and use Takeda Chemical Industries, Ltd. (JP) 1992-04-01 EP disclosed
US-3966920-A O,S-Dialkyl-O-(2-cyanophenyl)-thionothiolphosphoric acid esters and insecticidal and acaricidal compositions and method BAYER AKTIENGESELLSCHAFT (DT) 1976-06-29 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-12252496-B2 Organic compound, light-emitting element, light-emitting device, electronic device, and lighting device TPMT, POU5F1, CCND1 ALOX15 328/4885HPGD 1056/4885CES2 2512/4885
US-20250382312-A1 BORON CONTAINING PYRAZOLE COMPOUNDS, COMPOSITIONS COMPRISING THEM, METHODS AND USES THEREOF JAK3, JAK1, JAK2 ALOX15 1124/4885HPGD 3338/4885CES2 4765/4885
US-12404286-B2 Boron containing pyrazole compounds, compositions comprising them, methods and uses thereof JAK3, JAK1, JAK2 ALOX15 1124/4885HPGD 3338/4885CES2 4765/4885
US-12269814-B2 Process for preparing a compound useful to treat mycoses C1R, CBR1, CBR3 ALOX15 2400/4885HPGD 1735/4885CES2 1330/4885

“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.