SCHEMBL427243

SCHEMBL427243

O=C(O)c1ccc(Cl)cc1C(F)(F)F

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ SMN1; SMN2 Q16637 2/20 0.59
▸ TSHR P16473 1/20 0.59
▸ CASP1 P29466 1/20 0.59
▸ GRIK1 P39086 3/20 0.57
▸ TP53 P04637 2/20 0.53
▸ ALDH1A1 P00352 2/20 0.53
▸ CA1 P00915 1/20 0.52
▸ CA2 P00918 1/20 0.52
▸ RAB9A P51151 2/20 0.50
▸ CYP1A2 P05177 1/20 0.50
▸ CYP2D6 P10635 1/20 0.50
▸ CYP2C19 P33261 1/20 0.50
▸ KDM4E B2RXH2 2/20 0.49
▸ MAPT P10636 1/20 0.49
▸ CES2 O00748 1/20 0.48
▸ MRGPRX4 Q96LA9 2/20 0.47
▸ MEN1 O00255 1/20 0.47
▸ KMT2A Q03164 1/20 0.47
▸ MPO P05164 1/20 0.47
▸ MYC P01106 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
SCHEMBL28462798 0.88 RAB9A (0.50) SMN1; SMN2TSHRCASP1GRIK1TP53
SCHEMBL110827 0.86 RAB9A (0.49) SMN1; SMN2TSHRCASP1GRIK1TP53
SCHEMBL950905 0.86 ALDH1A1 (0.57) SMN1; SMN2TSHRCASP1GRIK1TP53
SCHEMBL38420096 0.86 ALDH1A1 (0.57) SMN1; SMN2TSHRCASP1GRIK1TP53
SCHEMBL7779187 0.85 RAB9A (0.50) SMN1; SMN2TSHRCASP1GRIK1TP53
SCHEMBL31591114 0.85 RAB9A (0.50) SMN1; SMN2TSHRCASP1GRIK1TP53
SCHEMBL3922426 0.85 RAB9A (0.47) SMN1; SMN2TSHRCASP1GRIK1TP53
Hydrochloric Acid SCHEMBL4377513 0.83 RAB9A (0.46) SMN1; SMN2GRIK1TP53ALDH1A1RAB9A
SCHEMBL26023312 0.82 RAB9A (0.48) SMN1; SMN2GRIK1TP53RAB9ACYP1A2
SCHEMBL12132735 0.82 ALDH1A1 (0.61) SMN1; SMN2GRIK1TP53ALDH1A1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3551633-B1 SUBSTITUTED PYRAZOLOAZEPIN-4-ONES AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS LEO PHARMA AS (DK) 2021-03-31 — — EP claimed
CN-110088108-A SUBSTITUTED PYRAZOLOAZEPIN-4-ONES AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS 利奥制药有限公司 2019-08-02 — — CN claimed
EP-3802500-B1 MELANOCORTIN SUBTYPE-2 RECEPTOR (MC2R) ANTAGONISTS AND USES THEREOF CRINETICS PHARMACEUTICALS INC (US) 2026-05-27 — — EP disclosed
EP-4714953-A1 MELANOCORTIN 2-TYPE RECEPTOR ANTAGONIST Scohia Pharma, Inc. (JP) 2026-03-25 — — EP disclosed
US-12479828-B2 Melanocortin subtype-2 receptor (MC2R) antagonists and uses thereof Crinetics Pharmaceuticals, Inc. (US) 2025-11-25 — — US disclosed
US-12479825-B2 Melanocortin subtype-2 receptor (MC2R) antagonists and uses thereof Crinetics Pharmaceuticals, Inc. (US) 2025-11-25 — — US disclosed
US-12410170-B2 2,3,5-trisubstituted pyrazolo[1,5-A]pyrimidine compounds ARCUS BIOSCIENCES, INC. (US) 2025-09-09 — — US disclosed
EP-4605364-A1 PROCESS FOR THE PREPARATION OF 4-CHLORO-2-(TRIFLUOROMETHYL)PHENYL GRIGNARD COMPOUND AND DERIVATIVES THEREOF BASF Agro B.V. (NL) 2025-08-27 — — EP disclosed
CN-120051451-A Process for preparing 4-chloro-2- (trifluoromethyl) phenyl grignard compounds and derivatives thereof 巴斯夫农业公司 2025-05-27 — — CN disclosed
US-20250011326-A1 FUSED HETEROCYCLIC DERIVATIVES AND THEIR USE IN THE TREATMENT OF HBV INFECTION Janssen Sciences Ireland Unlimited Company (IE) 2025-01-09 — — US disclosed
WO-2024237266-A1 MELANOCORTIN 2-TYPE RECEPTOR ANTAGONIST 株式会社スコヒアファーマ 2024-11-21 — — WO disclosed
US-5747424-A HEATING AN AROMATIC DIKETONE WITH A SALT OF HYDROXYLAMINE IN A SOLVENT RHONE-POULENC AGRICULTURE LTD. (GB) 1998-05-05 — — US disclosed
US-5656573-A Herbicidal 4-substituted isoxazoles RHONE-POULENC AGRICULTURE LTD. (GB) 1997-08-12 — — US disclosed
US-5650533-A Intermediates to herbicidal 4-substituted isoxazoles RHONE-POULENC AGRICULTURE LTD. (GB) 1997-07-22 — — US disclosed
EP-0487357-B1 4 Benzoyl isoxazole derivatives RHONE POULENC AGRICULTURE (GB) 1997-07-02 — — EP disclosed
CN-1061596-A 4-Benzoylisoxazole Derivatives RHONE POULENC AGRICULTURE (GB) 1992-06-03 — — CN disclosed
EP-0487357-A1 4 Benzoyl isoxazole derivatives RHONE-POULENC AGRICULTURE LTD. (GB) 1992-05-27 — — EP disclosed
EP-0097357-B1 PROCESS FOR PREPARING TRIFLUOROMETHYLBENZENE DERIVATIVES Daikin Kogyo Co., Ltd. (JP) 1986-01-08 — — EP disclosed
US-4493800-A REACTING A TRIFLUOROMETHYLHALOGENOBENZENE WITH COPPER CYANIDE DAIKIN KOGYO CO., LTD. (JP) 1985-01-15 — — US disclosed
EP-0097357-A1 Process for preparing trifluoromethylbenzene derivatives Daikin Kogyo Co., Ltd. (JP) 1984-01-04 — — 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 (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-12410170-B2 2,3,5-trisubstituted pyrazolo[1,5-A]pyrimidine compounds PIK3CA, PIK3CG, PIK3CD SMN1; SMN2 3842/4885TSHR 3567/4885CASP1 682/4885
US-12479825-B2 Melanocortin subtype-2 receptor (MC2R) antagonists and uses thereof MC3R, MC1R, MC2R SMN1; SMN2 2938/4885TSHR 102/4885CASP1 4853/4885
US-20250011326-A1 FUSED HETEROCYCLIC DERIVATIVES AND THEIR USE IN THE TREATMENT OF HBV INFECTION HAVCR2, HCCS, HDGF SMN1; SMN2 4515/4885TSHR 3425/4885CASP1 1799/4885
US-12479828-B2 Melanocortin subtype-2 receptor (MC2R) antagonists and uses thereof MC3R, MC1R, MC2R SMN1; SMN2 2938/4885TSHR 102/4885CASP1 4853/4885

“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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