SCHEMBL71911

SCHEMBL71911

O=C(O)C(O)(Cl)c1ccccc1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 3/20 0.62
TSHR P16473 2/20 0.48
CYP2C9 P11712 2/20 0.45
KEAP1 Q14145 1/20 0.44
NFE2L2 Q16236 1/20 0.44
CYP2D6 P10635 1/20 0.42
MAPT P10636 1/20 0.41
KMT2A Q03164 1/20 0.41
ALDH1A1 P00352 1/20 0.41
KCNN4 O15554 3/20 0.40
CYP2C19 P33261 2/20 0.40
HIF1A Q16665 1/20 0.40
HDAC3 O15379 1/20 0.39
HDAC4 P56524 1/20 0.39
HDAC1 Q13547 1/20 0.39
HDAC7 Q8WUI4 1/20 0.39
HDAC2 Q92769 1/20 0.39
HDAC10 Q969S8 1/20 0.39
HDAC11 Q96DB2 1/20 0.39
HDAC8 Q9BY41 1/20 0.39

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
SCHEMBL29614400 1.00 CYP1A2 (0.62) CYP1A2TSHRCYP2C9KEAP1NFE2L2
SCHEMBL1922803 1.00 CYP1A2 (0.62) CYP1A2TSHRCYP2C9KEAP1NFE2L2
SCHEMBL9211554 0.81 MAPT (0.54) CYP1A2TSHRCYP2D6MAPTKMT2A
SCHEMBL44516 0.79 CES1 (0.50) CYP1A2TSHRMAPTKMT2AALDH1A1
SCHEMBL4633443 0.79 CES2 (0.50) CYP1A2TSHRALDH1A1PTPN1CES1
SCHEMBL10444618 0.78 CYP1A2 (0.48) CYP1A2TSHRCYP2C9CYP2D6MAPT
SCHEMBL1244297 0.77 CYP1A2 (0.65) CYP1A2TSHRCYP2C9KEAP1NFE2L2
SCHEMBL2547243 0.77 CYP1A2 (0.65) CYP1A2TSHRCYP2C9KEAP1NFE2L2
SCHEMBL41202 0.77 CYP1A2 (1.00) CYP1A2TSHRCYP2C9KEAP1NFE2L2
SCHEMBL31506887 0.76 KCNN4 (0.62) CYP1A2TSHRMAPTKMT2AALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108410831-A Ketoacid reductase, gene, engineering bacterium and application in synthesis of chiral aromatic 2-hydroxy acid 浙江工业大学 2018-08-17 CN claimed
US-8697847-B2 Protein purification using HCIC and ion exchange chromatography MEDAREX, L.L.C. (US) 2014-04-15 US claimed
US-20120165511-A1 PROTEIN PURIFICATION USING HCIC AND ION EXCHANGE CHROMATOGRAPHY MEDAREX, INC. 2012-06-28 US claimed
US-20090105465-A1 Protein Purification Using HCIC and Ion Exchange Chromatography MEDAREX, INC. (US) 2009-04-23 US claimed
EP-1869067-A1 PROTEIN PURIFICATION USING HCIC AMD ION EXCHANGE CHROMATOGRAPHY Medarex, Inc. (US) 2007-12-26 EP claimed
WO-2006110277-A1 PROTEIN PURIFICATION USING HCIC AMD ION EXCHANGE CHROMATOGRAPHY MEDAREX, INC. (US) 2006-10-19 WO claimed
EP-4626415-A1 METHODS FOR TREATING BIOFILMS Next Science IP Holdings Pty Ltd (AU) 2025-10-08 EP disclosed
CN-117945937-B Method for preparing high-optical-purity sulbactam besylate 重庆华森制药股份有限公司 2024-07-30 CN disclosed
WO-2024118545-A1 METHODS FOR TREATING BIOFILMS Next Science IP Holdings Pty Ltd (AU) 2024-06-06 WO disclosed
CN-117945937-A Method for preparing high-optical-purity sulbactam besylate 重庆华森制药股份有限公司 2024-04-30 CN disclosed
CN-116655652-A New synthesis method of clopidogrel 宿迁盛基医药科技有限公司 2023-08-29 CN disclosed
EP-2632562-B1 METHODS FOR CAPTURING VIRUS LIKE PARTICLES FROM PLANTS USING EXPANDED BED CHROMATOGRAPHY PHILIP MORRIS PRODUCTS SA (CH) 2020-08-05 EP disclosed
CN-110172021-A A kind of separating and extracting process of (R)-o-chloromandelic acid 武汉武药制药有限公司 2019-08-27 CN disclosed
EP-1869067-A1 PROTEIN PURIFICATION USING HCIC AMD ION EXCHANGE CHROMATOGRAPHY Medarex, Inc. (US) 2007-12-26 EP disclosed
WO-2006110277-A1 PROTEIN PURIFICATION USING HCIC AMD ION EXCHANGE CHROMATOGRAPHY MEDAREX, INC. (US) 2006-10-19 WO disclosed
CN-1778936-A Process of clopidogrel HUIKE PHARMACEUTICAL CO LTD HU (CN) 2006-05-31 CN disclosed
EP-0783366-B1 CHROMATOGRAPHIC RESINS AND METHODS FOR USING SAME UNIV MASSEY (NZ) 2004-08-18 EP disclosed
EP-0773954-A1 HYDROPHOBIC CHROMATOGRAPHIC RESINS WITH IONIZABLE GROUPS MASSEY UNIVERSITY (NZ) 1997-05-21 EP disclosed
EP-0746551-A1 OPTICALLY PURE 4-ARYL-2-HYDROXYTETRONIC ACIDS THE OHIO STATE UNIVERSITY RESEARCH FOUNDATION (US) 1996-12-11 EP disclosed
WO-1996000735-A1 HYDROPHOBIC CHROMATOGRAPHIC RESINS WITH IONIZABLE GROUPS MASSEY UNIVERSITY (NZ) 1996-01-11 WO disclosed