SCHEMBL489909

SCHEMBL489909

CN1C(=O)Cc2cc(S(=O)(=O)Cl)ccc21

nearest known ligand 0.61

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
PKM P14618 5/20 0.61
GAA P10253 2/20 0.60
ALDH1A1 P00352 1/20 0.60
MEN1 O00255 1/20 0.55
KMT2A Q03164 1/20 0.55
IDO1 P14902 1/20 0.55
LMNA P02545 5/20 0.55
POLB P06746 3/20 0.55
TRIM24 O15164 1/20 0.52
THRB P10828 1/20 0.51
SCN3A Q9NY46 1/20 0.49
MAPT P10636 1/20 0.48

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
SCHEMBL8600438 0.86 TRIM24 (0.53) PKMGAAALDH1A1MEN1KMT2A
SCHEMBL1591102 0.84 GAA (0.64) PKMGAAALDH1A1MEN1KMT2A
SCHEMBL14333569 0.84 GAA (0.60) PKMGAAALDH1A1MEN1KMT2A
SCHEMBL10154069 0.81 PKM (0.66) PKMGAAALDH1A1MEN1KMT2A
SCHEMBL1925311 0.76 PKM (0.59) PKMGAAALDH1A1MEN1KMT2A
SCHEMBL434054 0.74 TRIM24 (0.54) PKMGAAALDH1A1MEN1KMT2A
SCHEMBL30222138 0.74 TRIM24 (0.54) PKMGAAALDH1A1MEN1KMT2A
SCHEMBL6532369 0.74 GAA (0.50) PKMGAAALDH1A1LMNAPOLB
SCHEMBL578369 0.73 LMNA (0.60) PKMGAAALDH1A1MEN1KMT2A
SCHEMBL8999096 0.73 TRIM24 (0.49) PKMGAAALDH1A1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3645533-B1 TDO2 AND IDO1 INHIBITORS GENENTECH INC (US) 2025-03-26 EP disclosed
WO-2023202583-A1 FXR REGULATOR AND USE THEREOF 北京大学 2023-10-26 WO disclosed
CN-116903559-A FXR modulators and uses thereof 北京大学 2023-10-20 CN disclosed
US-11603373-B2 TDO2 and IDO1 inhibitors GENENTECH, INC. (US) 2023-03-14 US disclosed
CN-114181199-A 2, 4-disubstituted pyrimidine derivative and preparation method and application thereof 成都赜灵生物医药科技有限公司 2022-03-15 CN disclosed
WO-2021260722-A1 DESIGN, SYNTHESIS OF NOVEL OXYINDOLE INHIBITORS OF DENV RNA DEPENDENT RNA POLYMERASE TRANSLATIONAL HEALTH SCIENCE AND TECHNOLOGY INSTITUTE (IN) 2021-12-30 WO disclosed
EP-3645533-A1 TDO2 AND IDO1 INHIBITORS Genentech, Inc. (US) 2020-05-06 EP disclosed
US-20200123163-A1 TDO2 and IDO1 Inhibitors GENENTECH, INC. 2020-04-23 US disclosed
WO-2019005559-A1 TDO2 AND IDO1 INHIBITORS GENENTECH, INC. (US) 2019-01-03 WO disclosed
US-9931327-B2 Derivatives of 1-phenyl-2-pyridinyl alkyl alcohols as phosphodiesterase inhibitors CHIESI FARMACEUTICI S.P.A. (IT) 2018-04-03 US disclosed
CN-100345829-C Pyrimidyl sulphone amide derivatives as chemokine receptor modulators ASTRAZENECA AB (SE) 2007-10-31 CN disclosed
US-20060025432-A1 Pyrimidyl sulphone amide derivatives as chemokine receptor modulators ASTRAZENECA AB (SE) 2006-02-02 US disclosed
CN-1681795-A Pyrimidyl sulfonamide derivatives as chemokine receptor modulators ASTRAZENECA AB (SE) 2005-10-12 CN disclosed
EP-1527051-A1 PYRIMIDYL SULPHONE AMIDE DERIVATIVES AS CHEMOKINE RECEPTOR MODULATORS Astrazeneca AB (SE) 2005-05-04 EP disclosed
WO-2004011443-A1 PYRIMIDYL SULPHONE AMIDE DERIVATIVES AS CHEMOKINE RECEPTOR MODULATORS ASTRAZENECA AB (SE) 2004-02-05 WO disclosed
EP-0623614-B1 4-Aryl-4-hydroxy-tetrahydropyrans and 3-aryl-3-hydroxy-tetrahydrofurans as 5-lipoxygenase inhibitors ZENECA LTD (GB) 1998-02-25 EP disclosed
US-5512594-A ADMINISTERING TO TREAT A MEDICAL CONDITION MEDIATED BY ONE OR MORE LEUKOTRIENES ZENECA LIMITED (GB) 1996-04-30 US disclosed
US-5478842-A Antiinflammatory agents, antiallergens, drugs for treatment of diseases mediated by leukotrienes ZENECA LIMITED (GB) 1995-12-26 US disclosed
WO-1994025453-A1 4-ARYL-4-HYDROXY-TETRAHYDROPYRANS AND 3-ARYL-3-HYDROXY-TETRAHYDROFURANS AS 5-LIPOXYGENASE INHIBITORS ZENECA LIMITED (GB) 1994-11-10 WO disclosed
EP-0623614-A1 4-Aryl-4-hydroxy-tetrahydropyrans and 3-aryl-3-hydroxy-tetrahydrofurans as 5-lipoxygenase inhibitors ZENECA LIMITED (GB) 1994-11-09 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 (3 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-11603373-B2 TDO2 and IDO1 inhibitors IDO1, TDO2, IDO2 PKM 4209/4885GAA 2380/4885ALDH1A1 855/4885
US-20060025432-A1 Pyrimidyl sulphone amide derivatives as chemokine receptor modulators ACKR3, GPR17, CCL11 PKM 1904/4885GAA 2860/4885ALDH1A1 2245/4885
US-20200123163-A1 TDO2 and IDO1 Inhibitors IDO1, TDO2, IDO2 PKM 4209/4885GAA 2380/4885ALDH1A1 855/4885

“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.