SCHEMBL71222

SCHEMBL71222

CCOC(=O)c1cc(Br)c(C(=O)OCC)cc1Br

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.57
KDM4E B2RXH2 3/20 0.53
NPSR1 Q6W5P4 1/20 0.53
RXFP1 Q9HBX9 1/20 0.53
CA12 O43570 3/20 0.52
CA1 P00915 3/20 0.52
CA2 P00918 3/20 0.52
CA7 P43166 3/20 0.52
CA9 Q16790 3/20 0.52
CA14 Q9ULX7 3/20 0.52
ALDH1A1 P00352 4/20 0.50
KMT2A Q03164 3/20 0.50
MAPT P10636 2/20 0.50
LMNA P02545 1/20 0.50
L3MBTL1 Q9Y468 1/20 0.50
CYP4F2 P78329 1/20 0.49
CYP4A11 Q02928 1/20 0.49
HSD17B10 Q99714 2/20 0.48
MAOB P27338 1/20 0.48
GAA P10253 2/20 0.47

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
SCHEMBL12123472 0.94 TSHR (0.55) TSHRKDM4ENPSR1RXFP1CA12
SCHEMBL7570621 0.92 TSHR (0.59) TSHRKDM4ENPSR1RXFP1CA12
SCHEMBL15025214 0.92 GAA (0.53) TSHRKDM4ENPSR1RXFP1CA12
SCHEMBL30931257 0.92 TSHR (0.50) TSHRKDM4ENPSR1RXFP1CA12
SCHEMBL26520578 0.92 KMT2A (0.59) TSHRKDM4ENPSR1RXFP1CA12
SCHEMBL24633176 0.92 TSHR (0.50) TSHRKDM4ENPSR1RXFP1CA12
SCHEMBL18506192 0.92 TSHR (0.50) TSHRKDM4ENPSR1RXFP1CA12
SCHEMBL11763447 0.92 TSHR (0.59) TSHRKDM4ENPSR1RXFP1CA12
SCHEMBL4627413 0.91 TSHR (0.57) TSHRKDM4ENPSR1RXFP1CA12
SCHEMBL16018276 0.91 TSHR (0.48) TSHRKDM4ENPSR1RXFP1CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116854631-B 4-Aryl-2-pyridone compound and preparation method thereof 安徽中医药大学 2025-04-15 CN claimed
CN-119376005-A Blue light resistant polarizer and production process thereof 湖南积发时代科技有限公司 2025-01-28 CN claimed
CN-117936778-A 2, 5-Dibromo-terephthalic acid diethyl ester composite TiO2·H2Preparation method and application of O 贵州大学 2024-04-26 CN claimed
CN-116283989-B Trans-quinacridone compound and preparation method and application thereof 华南理工大学 2024-03-01 CN claimed
CN-116854631-A 4-aryl-2-pyridone compound and preparation method thereof 安徽中医药大学 2023-10-10 CN claimed
CN-116283989-A Trans-quinacridone compound and preparation method and application thereof 华南理工大学 2023-06-23 CN claimed
CN-108947933-B Force-induced color-changing diethyl terephthalate compound, preparation method and application thereof 天津师范大学 2022-12-13 CN claimed
CN-114478569-A Multi-fused-ring conjugated small molecule based on thiophene [3,2-b ] pyrrole and preparation method and application thereof 宁波诺丁汉大学 2022-05-13 CN claimed
CN-110423429-B Efficient wear-resistant brush roll material and preparation method thereof 安徽省恒昌刷业有限公司 2022-01-14 CN claimed
CN-109666033-B Conjugated small molecule based on nona-fused heterocycle and preparation method and application thereof 南京理工大学 2021-09-03 CN claimed
CN-108069982-B Asymmetric cyanomethylene indone receptor material and preparation method and application thereof 武汉理工大学 2021-03-23 CN claimed
CN-110606856-A 3-alkyl thiophene-based hepta-fused heterocyclic conjugated small molecule and preparation method and application thereof 南京理工大学 2019-12-24 CN claimed
CN-102643284-B Preparation method and application of 4,9-bisalkylene indene thieno[3,2-b]thiophene derivative and conjugated polymer thereof LANZHOU DACHENG TECHNOLOGY CO LTD 2014-11-26 CN claimed
CN-102643284-A Preparation method and application of 4,9-bisalkylene indene thieno[3,2-b]thiophene derivative and conjugated polymer thereof LANZHOU DACHENG TECHNOLOGY CO LTD 2012-08-22 CN claimed
US-12629654-B2 Concentration of chemical species through the use of photosenstive sorbent materials GENESIS SYSTEMS LLC (US) 2026-05-19 US disclosed
US-20250196095-A1 CONCENTRATION OF CHEMICAL SPECIES THROUGH THE USE OF PHOTOSENSTIVE SORBENT MATERIALS GENESIS SYSTEMS LLC 2025-06-19 US disclosed
US-20250197653-A1 MODULATING OBJECT SIGNATURES THROUGH THE USE OF PHOTOSENSTIVE SORBENT COATINGS GENESIS SYSTEMS LLC 2025-06-19 US disclosed
EP-1232225-B1 SUBSTITUTED POLY(ARYLENE VINYLENES), METHOD FOR THE PRODUCTION THEREOF AND THEIR USE IN ELECTROLUMINESCENT DEVICES COVION ORGANIC SEMICONDUCTORS (DE) 2004-12-01 EP disclosed
EP-1232225-A1 SUBSTITUTED POLY(ARYLENE VINYLENES), METHOD FOR THE PRODUCTION THEREOF AND THEIR USE IN ELECTROLUMINESCENT DEVICES Covion Organic Semiconductors GmbH (DE) 2002-08-21 EP disclosed
WO-2001034722-A1 SUBSTITUTED POLY(ARYLENE VINYLENES), METHOD FOR THE PRODUCTION THEREOF AND THEIR USE IN ELECTROLUMINESCENT DEVICES COVION ORGANIC SEMICONDUCTORS GMBH (DE) 2001-05-17 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 (1 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-12629654-B2 Concentration of chemical species through the use of photosenstive sorbent materials TRPV4, TRPA1, TRPM4 TSHR 151/4885KDM4E 1930/4885NPSR1 1196/4885

“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.