SCHEMBL28765248

SCHEMBL28765248

CC(C)(C)O/N=C/C=N/Nc1cccc(F)c1

nearest known ligand 0.40

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ DEPTOR Q8TB45 1/20 0.40
▸ ALDH1A1 P00352 2/20 0.37
▸ POLB P06746 1/20 0.37
▸ GAA P10253 1/20 0.37
▸ NPSR1 Q6W5P4 1/20 0.37
▸ RAPGEF4 Q8WZA2 1/20 0.35
▸ SMN1; SMN2 Q16637 5/20 0.34
▸ MAPT P10636 4/20 0.34
▸ TP53 P04637 1/20 0.34
▸ MEN1 O00255 5/20 0.34
▸ KMT2A Q03164 5/20 0.34
▸ MMP1 P03956 3/20 0.34
▸ MMP2 P08253 3/20 0.34
▸ MMP9 P14780 3/20 0.34
▸ NPC1 O15118 3/20 0.34
▸ RAB9A P51151 3/20 0.34
▸ HPGD P15428 1/20 0.33
▸ MAOB P27338 1/20 0.33

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
SCHEMBL31482886 1.00 DEPTOR (0.40) DEPTORALDH1A1POLBGAANPSR1
SCHEMBL29711832 0.84 DEPTOR (0.43) DEPTORALDH1A1GAARAPGEF4SMN1; SMN2
SCHEMBL28765184 0.84 DEPTOR (0.43) DEPTORALDH1A1GAARAPGEF4SMN1; SMN2
SCHEMBL28765241 0.84 DEPTOR (0.43) DEPTORALDH1A1GAARAPGEF4SMN1; SMN2
SCHEMBL31482885 0.80 DEPTOR (0.40) DEPTORALDH1A1POLBGAARAPGEF4
SCHEMBL22968434 0.80 DEPTOR (0.40) DEPTORALDH1A1POLBGAARAPGEF4
SCHEMBL31482887 0.78 TSHR (0.43) DEPTORGAASMN1; SMN2MAPTTP53
SCHEMBL28765116 0.78 TSHR (0.43) DEPTORGAASMN1; SMN2MAPTTP53
SCHEMBL31482884 0.77 DEPTOR (0.40) DEPTORALDH1A1GAASMN1; SMN2MAPT
SCHEMBL28765252 0.77 DEPTOR (0.40) DEPTORALDH1A1GAASMN1; SMN2MAPT

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 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12570658-B2 Synthetic methods of making (2H-1, 2, 3-triazol-2-yl) phenyl compounds as orexin receptor modulators JANSSEN PHARMACEUTICA NV (BE) 2026-03-10 — — US disclosed
US-20220289754-A1 IMPROVED SYNTHETIC METHODS OF MAKING (2H-1, 2, 3-TRIAZOL-2-YL) PHENYL COMPOUNDS AS OREXIN RECEPTOR MODULATORS JANSSEN PHARMACEUTICA NV (BE) 2022-09-15 — — US disclosed
EP-4010325-A1 IMPROVED SYNTHETIC METHODS OF MAKING (2H-1,2,3-TRIAZOL-2-YL)PHENYL COMPOUNDS AS OREXIN RECEPTOR MODULATORS Janssen Pharmaceutica NV (BE) 2022-06-15 — — EP disclosed
CN-114555603-A Improved synthesis for the preparation of (2H-1,2, 3-triazol-2-yl) phenyl compounds as orexin receptor modulators 詹森药业有限公司 2022-05-27 — — CN 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-12570658-B2 Synthetic methods of making (2H-1, 2, 3-triazol-2-yl) phenyl compounds as orexin receptor modulators HCRTR2, HCRTR1, HRH1 DEPTOR 806/4885ALDH1A1 895/4885POLB 3865/4885
US-20220289754-A1 IMPROVED SYNTHETIC METHODS OF MAKING (2H-1, 2, 3-TRIAZOL-2-YL) PHENYL COMPOUNDS AS OREXIN RECEPTOR MODULATORS HCRTR2, HCRTR1, HTR3B DEPTOR 416/4885ALDH1A1 2699/4885POLB 3996/4885

“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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