SCHEMBL938157

SCHEMBL938157

COC(=O)/C=C/CN(C)C

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HCAR2 Q8TDS4 2/20 0.52
NFE2L2 Q16236 2/20 0.52
KEAP1 Q14145 1/20 0.52
TTR P02766 1/20 0.35
APP P05067 1/20 0.35
CA12 O43570 1/20 0.34
CA1 P00915 1/20 0.34
CA2 P00918 1/20 0.34
TYR P14679 1/20 0.34
CA7 P43166 1/20 0.34
CA9 Q16790 1/20 0.34
CA14 Q9ULX7 1/20 0.34
ALDH1A1 P00352 4/20 0.34
MAPT P10636 3/20 0.34
ALOX15 P16050 2/20 0.34
HSD17B10 Q99714 2/20 0.34
KDM4E B2RXH2 2/20 0.34
MEN1 O00255 1/20 0.34
TP53 P04637 1/20 0.34
CYP1A2 P05177 1/20 0.34

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
SCHEMBL2132535 1.00 HCAR2 (0.52) HCAR2NFE2L2KEAP1TTRAPP
Hydrochloric Acid SCHEMBL2134245 0.98 HCAR2 (0.50) HCAR2NFE2L2KEAP1TTRAPP
Hydrochloric Acid SCHEMBL2134248 0.98 HCAR2 (0.50) HCAR2NFE2L2KEAP1TTRAPP
SCHEMBL2607970 0.88 HCAR2 (0.44) HCAR2NFE2L2KEAP1TTRAPP
SCHEMBL30300922 0.85 HCAR2 (0.46) HCAR2NFE2L2KEAP1TTRAPP
Hydrochloric Acid SCHEMBL2131093 0.84 HCAR2 (0.44) HCAR2NFE2L2KEAP1TTRAPP
SCHEMBL30154155 0.83 HCAR2 (0.48) HCAR2NFE2L2KEAP1TTRAPP
SCHEMBL10044352 0.80 HCAR2 (0.30) HCAR2
SCHEMBL938137 0.79 HCAR2 (0.44) HCAR2NFE2L2KEAP1TTRAPP
SCHEMBL663907 0.78 HCAR2 (0.52) HCAR2TTRCA12CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105968103-A Synthesis method of anti-tumor medicine afatinib 山东罗欣药业集团恒欣药业有限公司 2016-09-28 CN claimed
CN-100415753-C 4-dimethylamino crotonic acid and its derivatives and their preparation method WYETH CORP (US) 2008-09-03 CN claimed
CN-1803806-A Anti-tumor combination drug WYETH CORP (US) 2006-07-19 CN claimed
CN-118561729-A Synthetic method and application of nitro cyclic compound 江南大学 2024-08-30 CN disclosed
EP-3733663-B1 1-[6-[[4-(PHENYLAMINO)-6-QUINAZOLINYL]OXY]-3-AZABICYCLO[3.1.1]HEPT-3-YL]-2-PROPEN-1-ONE DERIVATIVES AND RELATED COMPOUNDS AS IRREVERSIBLE INHIBITORS OF PAN-HER TYROSINE KINASE FOR THE TREATMENT OF CANCER CHENGDU JINRUI FOUND BIOTECH CO LTD (CN) 2023-05-17 EP disclosed
US-20220177473-A1 AZAAROMATIC AMIDE DERIVATIVES FOR THE TREATMENT OF CANCER SHENZHEN FORWARD PHARMACEUTICALS CO., LTD. (CN) 2022-06-09 US disclosed
US-20210078958-A1 QUINAZOLINE DERIVATIVE AND USE THEREOF MEDSHINE DISCOVERY INC. (CN) 2021-03-18 US disclosed
US-10399933-B2 Inhibitors of indoleamine-2,3-dioxygenase for the treatment of cancer BRISTOL-MYERS SQUIBB COMPANY (US) 2019-09-03 US disclosed
US-10399932-B2 Inhibitors of indoleamine-2,3-dioxygenase for the treatment of cancer BRISTOL-MYERS SQUIBB COMPANY (US) 2019-09-03 US disclosed
US-10196365-B2 Quinazoline derivative, preparation method therefor, and pharmaceutical composition and application thereof ARROMAX PHARMATECH CO., LTD. (CN) 2019-02-05 US disclosed
US-10167254-B2 IDO inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2019-01-01 US disclosed
EP-1585479-A2 SYNTHESIS OF 4AMINO-2-BUTENOYL CHLORIDES AND THEIR USE IN THE PREPARATION OF 3-CYANO QUINOLINES Wyeth (US) 2005-10-19 EP disclosed
CN-1538842-A Anti-tumor combination drug 2004-10-20 CN disclosed
US-20040162442-A1 Synthesis of 4-(amino)-2-butenoyl chlorides and their use in the preparation of 3-cyano quinolines WYETH (US) 2004-08-19 US disclosed
WO-2004066919-A2 SYNTHESIS OF 4AMINO-2-BUTENOYL CHLORIDES AND THEIR USE IN THE PREPARATION OF 3-CYANO QUINOLINES WYETH (US) 2004-08-12 WO disclosed
EP-1414438-A1 ANTINEOPLASTIC COMBINATIONS Wyeth (US) 2004-05-06 EP disclosed
US-6617333-B2 Rapamycin 42-ester with 3-hydroxy-2-(hydroxymethyl)-2-methyl propionic acid (CCI-779) and 4-dimethylamino-but-2-enoic acid(4-(3-chloro-4-fluoro-phenylamino)-3-cyano-7-ethoxy-quinol in-6-yl)amide (EKB-569); synergistic; antitumor agents WYETH 2003-09-09 US disclosed
WO-2003020266-A1 ANTINEOPLASTIC COMBINATIONS WYETH (US) 2003-03-13 WO disclosed
WO-2003020266-A1 ANTINEOPLASTIC COMBINATIONS WYETH (US) 2003-03-13 WO disclosed
US-20030050222-A1 Antineoplastic combinations WYETH 2003-03-13 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 (8 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-10167254-B2 IDO inhibitors IDO1, IDO2, INMT HCAR2 1414/4885NFE2L2 527/4885KEAP1 309/4885
US-20030050222-A1 Antineoplastic combinations MCL1, BCL9, ERAL1 HCAR2 2248/4885NFE2L2 921/4885KEAP1 566/4885
US-20220177473-A1 AZAAROMATIC AMIDE DERIVATIVES FOR THE TREATMENT OF CANCER ERBB4, EGFR, ERBB2 HCAR2 207/4885NFE2L2 453/4885KEAP1 2290/4885
US-10399932-B2 Inhibitors of indoleamine-2,3-dioxygenase for the treatment of cancer IDO1, IDO2, INMT HCAR2 790/4885NFE2L2 155/4885KEAP1 225/4885
US-20210078958-A1 QUINAZOLINE DERIVATIVE AND USE THEREOF ABL1, ERBB2, FLT3 HCAR2 1131/4885NFE2L2 744/4885KEAP1 278/4885
US-20040162442-A1 Synthesis of 4-(amino)-2-butenoyl chlorides and their use in the preparation of 3-cyano quinolines HBS1L, ATXN2L, ASNS HCAR2 2952/4885NFE2L2 1233/4885KEAP1 1540/4885
US-10399933-B2 Inhibitors of indoleamine-2,3-dioxygenase for the treatment of cancer IDO1, IDO2, INMT HCAR2 790/4885NFE2L2 155/4885KEAP1 225/4885
US-10196365-B2 Quinazoline derivative, preparation method therefor, and pharmaceutical composition and application thereof WEE1, WEE2, EGFR HCAR2 3127/4885NFE2L2 1772/4885KEAP1 1900/4885

“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.