SCHEMBL256802

SCHEMBL256802

CC(N)c1ccc(Br)cc1

nearest known ligand 0.56

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ ADRB2 P07550 1/20 0.56
▸ ALOX5 P09917 1/20 0.45
▸ PDE2A O00408 1/20 0.45
▸ MAOA P21397 1/20 0.45
▸ CYP2A6 P11509 1/20 0.44
▸ HTR2A P28223 1/20 0.43
▸ CYP1A2 P05177 1/20 0.41
▸ ALDH1A1 P00352 2/20 0.41
▸ ALOX15 P16050 1/20 0.41
▸ MAPK1 P28482 1/20 0.41
▸ PYCR1 P32322 1/20 0.39
▸ SMN1; SMN2 Q16637 1/20 0.37
▸ DPP4 P27487 1/20 0.36

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
SCHEMBL352653 1.00 ADRB2 (0.56) ADRB2ALOX5PDE2AMAOACYP2A6
SCHEMBL116807 1.00 ADRB2 (0.56) ADRB2ALOX5PDE2AMAOACYP2A6
Hydrochloric Acid SCHEMBL9900692 0.97 ADRB2 (0.54) ADRB2ALOX5PDE2AMAOACYP2A6
Hydrochloric Acid SCHEMBL14977817 0.97 ADRB2 (0.54) ADRB2ALOX5PDE2AMAOACYP2A6
Iodide SCHEMBL29177617 0.97 ADRB2 (0.54) ADRB2ALOX5PDE2AMAOACYP2A6
Bromide SCHEMBL25277530 0.97 ADRB2 (0.54) ADRB2ALOX5PDE2AMAOACYP2A6
Hydrochloric Acid SCHEMBL2903958 0.97 ADRB2 (0.54) ADRB2ALOX5PDE2AMAOACYP2A6
Hexane SCHEMBL11623547 0.87 ADRB2 (0.45) ADRB2ALOX5PDE2AMAOAHTR2A
SCHEMBL1314596 0.85 ADRB2 (0.72) ADRB2PDE2AALDH1A1ALOX15
SCHEMBL12280986 0.79 ALOX5 (0.42) ADRB2ALOX5MAOACYP2A6HTR2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-121718034-B Circular polarized luminescence adjustable aryl acetylene supermolecular polymer, preparation and application 中国科学技术大学 2026-05-12 — — CN claimed
CN-119081075-A Triphenylamine supermolecular polymer capable of adjusting circularly polarized light, preparation method and application 安徽理工大学 2024-12-06 — — CN claimed
CN-118956392-A Perovskite quantum dot, preparation method thereof, ink, perovskite thin film and light-emitting device 华侨大学 2024-11-15 — — CN claimed
CN-117801815-B Chiral quasi two-dimensional perovskite film capable of emitting circularly polarized light and preparation method thereof 天津大学 2024-08-09 — — CN claimed
CN-118125984-A Benzenesulfonamide compound and preparation method and application thereof 中国药科大学 2024-06-04 — — CN claimed
CN-117886718-B Preparation method of high-selectivity asymmetric urea compound and asymmetric urea compound 内蒙古工业大学 2024-05-24 — — CN claimed
CN-117886718-A Preparation method of high-selectivity asymmetric urea compound and asymmetric urea compound 内蒙古工业大学 2024-04-16 — — CN claimed
CN-117801815-A Chiral quasi two-dimensional perovskite film capable of emitting circularly polarized light and preparation method thereof 天津大学 2024-04-02 — — CN claimed
CN-117342958-A Buried interface material and flexible perovskite solar cell prepared from buried interface material 武汉理工大学 2024-01-05 — — CN claimed
US-11760750-B1 Process for preparing levoketoconazole NURAY CHEMICALS PRIVATE LIMITED (IN) 2023-09-19 — — US claimed
US-6084065-A FOR AGRICULTURAL USE ISAGRO SPA (IT) 2000-07-04 — — US claimed
EP-0652229-B1 Oligopeptides with fungicidal activity ISAGRO SPA (IT) 2000-05-24 — — EP claimed
EP-0976760-A2 Oligopeptides with fungicidal activity ISAGRO S.p.A. (IT) 2000-02-02 — — EP claimed
EP-0508307-B1 Optically active secondary amine compound; process for producing optically active secondary amine compound and process for producing optically active carboxylic acid by using said compound SUMITOMO CHEMICAL CO (JP) 1995-11-29 — — EP claimed
EP-0652229-A2 Oligopeptides with fungicidal activity ISAGRO S.p.A. (IT) 1995-05-10 — — EP claimed
EP-0508307-A2 Optically active secondary amine compound; process for producing optically active secondary amine compound and process for producing optically active carboxylic acid by using said compound SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1992-10-14 — — EP claimed
EP-0101570-B1 METHOD FOR THE RESOLUTION OF RACEMIC 2-CP-DIFLUOROMETHOXY PHENYL)-3-METHYLBUTYRIC ACID AMERICAN CYANAMID COMPANY (US) 1988-01-27 — — EP claimed
US-4454344-A Method for the resolution of racemic 2-(p-difluoromethoxyphenyl)-3-methylbutyric acid AMERICAN CYANAMID COMPANY (US) 1984-06-12 — — US claimed
EP-0101570-A1 Method for the resolution of racemic 2-CP-difluoromethoxy phenyl)-3-methylbutyric acid AMERICAN CYANAMID COMPANY (US) 1984-02-29 — — EP claimed
US-4129580-A Resolution of certain asymmetric primary amines using lasalocid HOFFMANN-LA ROCHE INC. (US) 1978-12-12 — — US claimed

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-11760750-B1 Process for preparing levoketoconazole KHK, KYAT3, PLK3 ADRB2 1631/4885ALOX5 1572/4885PDE2A 1916/4885

“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.

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