Ammonia Solution, Strong

Ammonia Solution, Strong

SCHEMBL7534616

N.O=C(O)c1ccccc1Cl

nearest known ligand 0.95

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 5/20 0.95
▸ CES2 O00748 1/20 0.65
▸ CES1 P23141 1/20 0.65
▸ TSHR P16473 2/20 0.64
▸ ALOX15 P16050 1/20 0.62
▸ POLB P06746 2/20 0.58
▸ ERCC5 P28715 1/20 0.53
▸ FEN1 P39748 1/20 0.53
▸ HPGD P15428 4/20 0.52
▸ SMN1; SMN2 Q16637 2/20 0.52
▸ KDM4E B2RXH2 2/20 0.52
▸ CA12 O43570 1/20 0.52
▸ CA1 P00915 1/20 0.52
▸ CA2 P00918 1/20 0.52
▸ HMGB1 P09429 1/20 0.52
▸ CA4 P22748 1/20 0.52
▸ CA6 P23280 1/20 0.52
▸ CA7 P43166 1/20 0.52
▸ CA9 Q16790 1/20 0.52
▸ NAPRT Q6XQN6 1/20 0.52

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
SCHEMBL8482425 0.97 ALDH1A1 (1.00) ALDH1A1CES2CES1TSHRALOX15
SCHEMBL29369803 0.97 ALDH1A1 (1.00) ALDH1A1CES2CES1TSHRALOX15
SCHEMBL29004189 0.97 ALDH1A1 (1.00) ALDH1A1CES2CES1TSHRALOX15
SCHEMBL29518925 0.97 ALDH1A1 (1.00) ALDH1A1CES2CES1TSHRALOX15
SCHEMBL367 0.97 ALDH1A1 (1.00) ALDH1A1CES2CES1TSHRALOX15
SCHEMBL431318 0.95 ALDH1A1 (0.95) ALDH1A1CES2CES1TSHRALOX15
Hydrochloric Acid SCHEMBL784866 0.95 ALDH1A1 (0.95) ALDH1A1CES2CES1TSHRALOX15
SCHEMBL6915177 0.95 ALDH1A1 (0.95) ALDH1A1CES2CES1TSHRALOX15
SCHEMBL8747321 0.95 ALDH1A1 (0.95) ALDH1A1CES2CES1TSHRALOX15
SCHEMBL6913277 0.95 ALDH1A1 (0.95) ALDH1A1CES2CES1TSHRALOX15

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4724443-A1 PYRAZOLO-PYRIMIDINONE COMPOUNDS FOR USE IN METHODS OF INHIBITING WEE1 A KINASE Acrivon Therapeutics, Inc. (US) 2026-04-15 — — EP disclosed
EP-3710422-B1 PROCESS FOR THE PREPARATION OF ENANTIOMERICALLY AND DIASTEREOMERICALLY ENRICHED CYCLOBUTANE AMINES AND AMIDES SYNGENTA CROP PROTECTION AG (CH) 2026-01-07 — — EP disclosed
WO-2024254490-A1 PYRAZOLO-PYRIMIDINONE COMPOUNDS FOR USE IN METHODS OF INHIBITING WEE1 A KINASE ACRIVON THERAPEUTICS, INC. (US) 2024-12-12 — — WO disclosed
CN-221108213-U O-chlorobenzonitrile production equipment 莘县正升化工有限公司 2024-06-11 — — CN disclosed
CN-110423207-B Synthesis method of o-chlorobenzonitrile 三门峡环宇生化科技有限公司 2022-08-12 — — CN disclosed
CN-110467543-B Preparation method of o-chlorobenzonitrile 三门峡环宇生化科技有限公司 2022-06-07 — — CN disclosed
CN-215440106-U Spices and essence effluent disposal system 江苏善鼎环保科技有限公司 2022-01-07 — — CN disclosed
US-11053188-B2 Process for the preparation of enantiomerically and diastereomerically enriched cyclobutane amines and amides SYNGENTA PARTICIPATIONS AG (CH) 2021-07-06 — — US disclosed
US-20200407311-A1 PROCESS FOR THE PREPARATION OF ENANTIOMERICALLY AND DIASTEREOMERICALLY ENRICHED CYCLOBUTANE AMINES AND AMIDES SYNGENTA PARTICIPATIONS AG (CH) 2020-12-31 — — US disclosed
CN-110437101-A A kind of pair of 6-chlorophenyl nitrile, the preparation method to chlorobenzamide SANMENXIA HUANYU BIOCHEMICAL TECH CO LTD 2019-11-12 — — CN disclosed
CN-110396056-A A method of preparing m-chlorobenzene nitrile SANMENXIA HUANYU BIOCHEMICAL TECH CO LTD 2019-11-01 — — CN disclosed
CN-101316810-A Ionic liquids BIONIQS LTD (GB) 2008-12-03 — — CN disclosed
EP-0770103-B1 LOW VOC REFINISH COATING COMPOSITION DU PONT (US) 2002-03-27 — — EP disclosed
EP-0770103-A1 LOW VOC REFINISH COATING COMPOSITION E.I. DU PONT DE NEMOURS AND COMPANY (US) 1997-05-02 — — EP disclosed
WO-1996001864-A1 LOW VOC REFINISH COATING COMPOSITION E.I. DU PONT DE NEMOURS AND COMPANY (US) 1996-01-25 — — WO disclosed
WO-1993000377-A1 LOW VOLATILE ORGANIC CONTENT CLEAR EPOXY ACRYLIC COATING COMPOSITION FOR BASECOAT CLEAR COAT FINISH E.I. DU PONT DE NEMOURS AND COMPANY (US) 1993-01-07 — — WO disclosed
US-5084542-A Clear colorless resistant coatings with improved weatherability E. I. DU PONT DE NEMOURS AND COMPANY (US) 1992-01-28 — — US disclosed
WO-1991018937-A1 EPOXY/ISOCYANATE CROSSLINKED COATINGS CONTAINING 1,3-DISUBSTITUTED IMIDAZOLE-2-THIONE CATALYSTS E.I. DU PONT DE NEMOURS AND COMPANY (US) 1991-12-12 — — WO 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-20200407311-A1 PROCESS FOR THE PREPARATION OF ENANTIOMERICALLY AND DIASTEREOMERICALLY ENRICHED CYCLOBUTANE AMINES AND AMIDES TBCB, ADORA2B, ADRA2B ALDH1A1 955/4885CES2 600/4885CES1 1136/4885
US-11053188-B2 Process for the preparation of enantiomerically and diastereomerically enriched cyclobutane amines and amides TBCB, ADORA2B, CCNB3 ALDH1A1 979/4885CES2 601/4885CES1 1268/4885

“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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