SCHEMBL474644

SCHEMBL474644

C#Cc1cccc(NC(C)=O)c1

nearest known ligand 0.62

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
EGFR P00533 1/20 0.61
ALDH1A1 P00352 3/20 0.58
HSD17B10 Q99714 2/20 0.58
CYP1A2 P05177 1/20 0.58
RAB9A P51151 2/20 0.55
MEN1 O00255 1/20 0.55
NPC1 O15118 1/20 0.55
KMT2A Q03164 1/20 0.55
TDP1 Q9NUW8 1/20 0.55
P2RX1 P51575 1/20 0.54
POLB P06746 1/20 0.53
NR4A1 P22736 1/20 0.53
NAPRT Q6XQN6 1/20 0.52
L3MBTL1 Q9Y468 1/20 0.51
GRM5 P41594 1/20 0.51
SMN1; SMN2 Q16637 1/20 0.50
IDH1 O75874 1/20 0.50
TP53 P04637 1/20 0.49

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
SCHEMBL31046593 1.00 EGFR (0.61) EGFRALDH1A1HSD17B10CYP1A2RAB9A
Acetonitrile SCHEMBL28273231 0.94 EGFR (0.59) EGFRALDH1A1HSD17B10CYP1A2RAB9A
SCHEMBL11238391 0.91 EGFR (0.54) EGFRALDH1A1HSD17B10CYP1A2RAB9A
SCHEMBL4749975 0.85 MEN1 (0.60) EGFRALDH1A1HSD17B10RAB9AMEN1
SCHEMBL1040883 0.84 ALDH1A1 (0.59) ALDH1A1HSD17B10CYP1A2RAB9AMEN1
SCHEMBL1025225 0.84 MEN1 (0.56) EGFRALDH1A1RAB9AMEN1NPC1
SCHEMBL12049693 0.83 IDH1 (0.54) EGFRALDH1A1HSD17B10RAB9AMEN1
SCHEMBL171190 0.82 ALDH1A1 (0.66) ALDH1A1HSD17B10CYP1A2RAB9AMEN1
SCHEMBL21715154 0.82 GRM5 (0.58) ALDH1A1HSD17B10CYP1A2RAB9AMEN1
SCHEMBL30368222 0.82 ALDH1A1 (0.66) ALDH1A1HSD17B10CYP1A2RAB9AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109265325-A A kind of bis- bromo alkenes compounds of 1,2- and its preparation method and application 广东工业大学 2019-01-25 CN claimed
CN-112176418-B High-throughput compound library construction and screening method and reaction device 中宏鑫投资控股(深圳)有限公司 2024-11-29 CN disclosed
CN-114057658-B Polytriazole compound, and preparation method and application thereof 中宏鑫投资控股(深圳)有限公司 2024-08-16 CN disclosed
CN-112292386-B Tetrahydropyrane-based thiodisaccharide mimetics as galectin-3 inhibitors 百时美施贵宝公司 2024-06-11 CN disclosed
US-11970511-B2 Tetrahydropyran-based thiodisaccharide mimics as Galectin-3 inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2024-04-30 US disclosed
CN-116903585-A Oxo-pyridine derivative and application thereof in medicine 天津药物研究院有限公司 2023-10-20 CN disclosed
CN-110590485-B FSO 2 N 3 Use in the production of azido compounds 中宏鑫投资控股(深圳)有限公司 2023-04-14 CN disclosed
US-20220356182-A1 INHIBITORS OF HEPATITIS C VIRUS REPLICATION MERCK SHARP & DOHME CORP. (US) 2022-11-10 US disclosed
US-20220356182-A1 INHIBITORS OF HEPATITIS C VIRUS REPLICATION MERCK SHARP & DOHME CORP. (US) 2022-11-10 US disclosed
US-20220291202-A1 HIGH THROUGHPUT METHOD FOR CONSTRUCTING AND SCREENING COMPOUND LIBRARY AND REACTION DEVICE DEEPSYN. CO (CN) 2022-09-15 US disclosed
EP-1274424-A1 COMPOUNDS AND METHODS SMITHKLINE BEECHAM CORPORATION (US) 2003-01-15 EP disclosed
US-20020128263-A1 Phenylethynyl and styryl derivatives of imidazole and fused ring heterocycles F.HOFFMANN-LA ROCHE AG (CH) 2002-09-12 US disclosed
WO-2002046166-A1 PHENYLETHENYL OR PHENYLETHINYL DERIVATIVES AS GLUTAMATE RECEPTOR ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2002-06-13 WO disclosed
WO-2001078723-A1 COMPOUNDS AND METHODS SMITHKLINE BEECHAM CORPORATION (US) 2001-10-25 WO disclosed
EP-0834499-B1 Process for the preparation of aromatic vinyl compounds DAINIPPON INK & CHEMICALS (JP) 2001-07-25 EP disclosed
EP-0834499-A1 Process for the preparation of aromatic vinyl compounds DAINIPPON INK AND CHEMICALS, INC. (JP) 1998-04-08 EP disclosed
EP-0171209-B1 ACETYLENIC PHENOXYPROPANOL DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS FOR THE TREATMENT OF HYPERTENSION McNeilab, Inc. (US) 1989-03-01 EP disclosed
US-4652584-A Acetylenic phenoxypropanol derivatives and pharmaceutical compositions for the treatment of hypertension MCNEILAB, INC. (US) 1987-03-24 US disclosed
EP-0171209-A1 Acetylenic phenoxypropanol derivatives and pharmaceutical compositions for the treatment of hypertension McNeilab, Inc. (US) 1986-02-12 EP disclosed
US-4162265-A Aromatic enyne compounds and their synthesis THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE AIR FORCE (US) 1979-07-24 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-11970511-B2 Tetrahydropyran-based thiodisaccharide mimics as Galectin-3 inhibitors LGALS3, LGALS1, LGALS3BP EGFR 2203/4885ALDH1A1 2364/4885HSD17B10 2921/4885
US-20220356182-A1 INHIBITORS OF HEPATITIS C VIRUS REPLICATION HAVCR2, HCCS, EIF2AK2 EGFR 3021/4885ALDH1A1 2400/4885HSD17B10 1056/4885
US-20020128263-A1 Phenylethynyl and styryl derivatives of imidazole and fused ring heterocycles GRM5, GRIK5, GRM1 EGFR 401/4885ALDH1A1 2819/4885HSD17B10 1746/4885
US-20220291202-A1 HIGH THROUGHPUT METHOD FOR CONSTRUCTING AND SCREENING COMPOUND LIBRARY AND REACTION DEVICE CMA1, DHX29, DHX15 EGFR 3317/4885ALDH1A1 1746/4885HSD17B10 358/4885

“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.