SCHEMBL624730

SCHEMBL624730

OCCc1ccccc1Cl

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 4/20 0.60
HTR3E A5X5Y0 1/20 0.53
HTR3B O95264 1/20 0.53
HTR3A P46098 1/20 0.53
HTR3D Q70Z44 1/20 0.53
HTR3C Q8WXA8 1/20 0.53
IDO1 P14902 4/20 0.52
PNMT P11086 1/20 0.52
SLC6A2 P23975 1/20 0.50
SLC6A4 P31645 1/20 0.50
SLC6A3 Q01959 1/20 0.50
AOC3 Q16853 1/20 0.50
KCNH2 Q12809 1/20 0.50
PKM P14618 1/20 0.48
NPC1 O15118 1/20 0.47
RAB9A P51151 1/20 0.47
TDP1 Q9NUW8 1/20 0.44
LMNA P02545 2/20 0.44
HTT P42858 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44

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
SCHEMBL29538519 1.00 TAAR1 (0.60) TAAR1HTR3EHTR3BHTR3AHTR3D
SCHEMBL5584302 0.86 TAAR1 (0.52) TAAR1HTR3EHTR3BHTR3AHTR3D
SCHEMBL1044928 0.86 TAAR1 (0.56) TAAR1HTR3EHTR3BHTR3AHTR3D
SCHEMBL1804680 0.84 TAAR1 (0.54) TAAR1HTR3EHTR3BHTR3AHTR3D
SCHEMBL6740216 0.84 TAAR1 (0.71) TAAR1HTR3EHTR3BHTR3AHTR3D
SCHEMBL6062588 0.82 TAAR1 (0.52) TAAR1HTR3EHTR3BHTR3AHTR3D
SCHEMBL7037675 0.82 TAAR1 (0.52) TAAR1HTR3EHTR3BHTR3AHTR3D
SCHEMBL2963562 0.81 TAAR1 (0.63) TAAR1IDO1PNMTTDP1SMN1; SMN2
SCHEMBL29924786 0.81 TAAR1 (0.63) TAAR1IDO1PNMTTDP1SMN1; SMN2
SCHEMBL31203 0.81 TDP1 (0.55) TAAR1TDP1HTTHIF1ATSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119491240-A Method for preparing benzyl carboxylic acid compound by taking carbon dioxide as raw material 哈尔滨工业大学(深圳) 2025-02-21 CN claimed
CN-117821525-A Enzymatic synthesis method of halohydrin medicine chiral building block 宁波酶赛生物工程有限公司 2024-04-05 CN claimed
CN-113846082-B Halohydrin dehalogenase mutant, encoding gene, recombinant vector, recombinant genetic engineering bacteria and application thereof 华东理工大学 2023-06-23 CN claimed
CN-113333018-A Preparation method and application of supported catalyst for preparing halogenated styrene 中触媒新材料股份有限公司 2021-09-03 CN claimed
CN-110669743-A P450 monooxygenase mutant from deinococcus radiodurans and application thereof 遵义医科大学 2020-01-10 CN claimed
CN-103420747-A Synthetic method for olefin compounds SUZHOU OST ADVANCED MATERIALS CO LTD 2013-12-04 CN claimed
US-6989052-B1 Phase change ink printing process XEROX CORPORATION (US) 2006-01-24 US claimed
US-20060004123-A1 PHASE CHANGE INK PRINTING PROCESS XEROX CORPORATION 2006-01-05 US claimed
EP-0446301-B1 PREPARATION OF BIARYL COMPOUNDS EASTMAN CHEM CO (US) 1994-11-23 EP claimed
US-4820672-A REACTING MAGNESIUM OR ORGANOMAGNESIUM COMPOUNDS, HYDROGEN CHLORIDE, CHLOROALCOHOL, BETA-ALKYL SUBSTITUTED ALCOHOLS; POLY CAT OR SUPPORTS LITHIUM CORPORATION OF AMERICA (US) 1989-04-11 US claimed
US-20260035381-A1 COMPOUNDS AND COMPOSITIONS AND USES THEREOF SUMITOMO PHARMA AMERICA, INC. (US) 2026-02-05 US disclosed
EP-4680612-A1 CHEMICAL COMPOUNDS AN2 Therapeutics, Inc. (US) 2026-01-21 EP disclosed
CN-116514880-B Novel PNNO and PNNN chiral tetradentate ligand and application thereof in asymmetric hydrogenation 凯特立斯(深圳)科技有限公司 2025-06-10 CN disclosed
EP-4490150-A1 AMIDO CYCLOPROPYL DERIVATIVES AS LPA RECEPTOR INHIBITORS Chiesi Farmaceutici S.p.A. (IT) 2025-01-15 EP disclosed
WO-2025007074-A1 CHEMICAL COMPOUNDS REACTIVE BIOSCIENCES, INC. (US) 2025-01-02 WO disclosed
EP-0222414-A2 Novel organic selenium compounds NIPPON KAYAKU KABUSHIKI KAISHA (JP) 1987-05-20 EP disclosed
US-4629781-A STRONG ACIDOLYSIS CONTROLLED BY THE USE OF SOLVENT, ACID, CONCENTRATION AND HEATING GRUPPO LEPETIT S.P.A. (IT) 1986-12-16 US disclosed
EP-0198440-A2 Process for preparing optically active 2-halo-1-phenyl ethanol KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1986-10-22 EP disclosed
EP-0146053-A2 Chemical process for preparing antibiotic L 17392 (Deglucoteicoplanin) and its salts GRUPPO LEPETIT S.p.A. (IT) 1985-06-26 EP disclosed
EP-0082006-A2 Method for producing vicinal dihalogenated products and uses thereof, and process for preparing epoxides using the same CETUS CORPORATION (US) 1983-06-22 EP 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-20260035381-A1 COMPOUNDS AND COMPOSITIONS AND USES THEREOF ADH1C, HTR6, CNR1 TAAR1 97/4885HTR3E 211/4885HTR3B 88/4885

“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.