SCHEMBL2943750

SCHEMBL2943750

COC(=O)C(Cc1ccccc1)OS(=O)(=O)C(F)(F)F

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.51
KMT2A Q03164 1/20 0.51
CA12 O43570 3/20 0.46
CA9 Q16790 3/20 0.46
CA7 P43166 2/20 0.46
CA14 Q9ULX7 2/20 0.46
CA2 P00918 2/20 0.46
CTRB1 P17538 1/20 0.46
POLB P06746 2/20 0.45
PTPN1 P18031 1/20 0.44
PPARG P37231 4/20 0.44
PPARA Q07869 3/20 0.44
ATM Q13315 1/20 0.44
SRR Q9GZT4 2/20 0.43
NOS3 P29474 1/20 0.43
NOS1 P29475 1/20 0.43
NOS2 P35228 1/20 0.43
ALDH1A1 P00352 1/20 0.43
THRB P10828 1/20 0.43
CYP2C9 P11712 1/20 0.43

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
SCHEMBL16754029 1.00 MEN1 (0.51) MEN1KMT2ACA12CA9CA7
SCHEMBL7229148 0.89 CA12 (0.49) MEN1KMT2ACA12CA9CA7
SCHEMBL8142297 0.86 MEN1 (0.43) MEN1KMT2ACA12CA9CA7
SCHEMBL7726567 0.86 MEN1 (0.43) MEN1KMT2ACA12CA9CA7
SCHEMBL7728941 0.86 MEN1 (0.43) MEN1KMT2ACA12CA9CA7
SCHEMBL8711997 0.86 PPARG (0.44) KMT2ACA12CA9CA2CTRB1
SCHEMBL8711993 0.86 PPARG (0.44) KMT2ACA12CA9CA2CTRB1
SCHEMBL7307706 0.85 SRR (0.56) PPARGPPARASRR
SCHEMBL7307715 0.85 SRR (0.56) PPARGPPARASRR
SCHEMBL7321720 0.85 SRR (0.56) PPARGPPARASRR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114206854-B FXIa inhibitor and preparation method and medical application thereof 深圳信立泰药业股份有限公司 2023-02-24 CN disclosed
CN-114206854-A FXIa inhibitor and preparation method and medical application thereof 深圳信立泰药业股份有限公司 2022-03-18 CN disclosed
EP-3138839-B1 PYRIDONE OR PYRIMIDONE DERIVATIVE, PREPARATION METHOD THEREFOR AND APPLICATION THEREOF SICHUAN HAISCO PHARMACEUTICAL CO LTD (CN) 2020-10-28 EP disclosed
CN-105829298-B A kind of pyridone or pyrimidone derivatives, and its preparation method and application 四川海思科制药有限公司 2019-02-01 CN disclosed
US-10174020-B2 Pyridone or pyrimidone derivative, preparation method therefor and application thereof SICHUAN HAISCO PHARMACEUTICAL CO., LTD. (CN) 2019-01-08 US disclosed
US-10174020-B2 Pyridone or pyrimidone derivative, preparation method therefor and application thereof SICHUAN HAISCO PHARMACEUTICAL CO., LTD. (CN) 2019-01-08 US disclosed
EP-3138839-A1 PYRIDONE OR PYRIMIDONE DERIVATIVE, PREPARATION METHOD THEREFOR AND APPLICATION THEREOF Sichuan Haisco Pharmaceutical Co., Ltd. (CN) 2017-03-08 EP disclosed
EP-3138839-A1 PYRIDONE OR PYRIMIDONE DERIVATIVE, PREPARATION METHOD THEREFOR AND APPLICATION THEREOF Sichuan Haisco Pharmaceutical Co., Ltd. (CN) 2017-03-08 EP disclosed
US-20170029423-A1 PYRIDONE OR PYRIMIDONE DERIVATIVE, PREPARATION METHOD THEREFOR AND APPLICATION THEREOF SICHUAN HAISCO PHARMACEUTICAL CO., LTD. (CN) 2017-02-02 US disclosed
US-20170029423-A1 PYRIDONE OR PYRIMIDONE DERIVATIVE, PREPARATION METHOD THEREFOR AND APPLICATION THEREOF SICHUAN HAISCO PHARMACEUTICAL CO., LTD. (CN) 2017-02-02 US disclosed
US-20060052348-A1 Oxazolo-naphthyl acids WYETH (US) 2006-03-09 US disclosed
WO-2006023866-A2 THIAZOLO-NAPHTHYL ACIDS AS INHIBITORS OF PLASMINOGEN ACTIVATOR INHIBITOR-1 WYETH (US) 2006-03-02 WO disclosed
WO-2006023865-A1 OXAZOLO-NAPHTHYL ACIDS AS PLAMINOGEN ACTIVATOR INHIBTOR TYPE-1 (PAI-1) MODULATORS USEFUL IN THE TREATMENT OF THROMBOSIS AND CARDIOVASCULAR DISEASES WYETH (US) 2006-03-02 WO disclosed
WO-2006023864-A1 PYRROLO-NAPHTHYL ACIDS AS PAI-1 INHIBITORS WYETH (US) 2006-03-02 WO disclosed
US-20060020003-A1 Biphenyloxy-acids WYETH (US) 2006-01-26 US disclosed
WO-2005030702-A1 BIPHENYLOXY-ACIDS WYETH (US) 2005-04-07 WO disclosed
EP-1397341-A1 6-(ARYL-AMIDO OR ARYL-AMIDOMETHYL)-NAPHTHALEN-2-YLOXY-ACIDIC DERIVATIVES AS INHIBITORS OF PLASMINOGEN ACTIVATOR INHIBITOR TYPE-1 (PAI-1) Wyeth (US) 2004-03-17 EP disclosed
US-6589970-B2 This invention provides novel compounds, pharmaceutical compositions and methods of treating thrombotic disorders in mammals, the compounds having the formula: WYETH 2003-07-08 US disclosed
US-20030045560-A1 6-(Aryl-amido or aryl-amidomethyl)-naphthalen-2-yloxy-acidic derivatives as inhibitors of plasminogen activator inhibitor type-1 (PAI-1) WYETH 2003-03-06 US disclosed
WO-2003000649-A1 6-(ARYL-AMIDO OR ARYL-AMIDOMETHYL)-NAPHTHALEN-2-YLOXY-ACIDIC DERIVATIVES AS INHIBITORS OF PLASMINOGEN ACTIVATOR INHIBITOR TYPE-1 (PAI-1) WYETH (US) 2003-01-03 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 (5 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-20060052348-A1 Oxazolo-naphthyl acids SERPINE1, SERPINB1, SERPINC1 MEN1 2828/4885KMT2A 4416/4885CA12 2569/4885
US-20060020003-A1 Biphenyloxy-acids AHR, ARNT, NR1H4 MEN1 3931/4885KMT2A 894/4885CA12 3136/4885
US-10174020-B2 Pyridone or pyrimidone derivative, preparation method therefor and application thereof TYMP, DHFR, TYMS MEN1 882/4885KMT2A 3474/4885CA12 4874/4885
US-20170029423-A1 PYRIDONE OR PYRIMIDONE DERIVATIVE, PREPARATION METHOD THEREFOR AND APPLICATION THEREOF TYMP, DHFR, TYMS MEN1 882/4885KMT2A 3474/4885CA12 4874/4885
US-20030045560-A1 6-(Aryl-amido or aryl-amidomethyl)-naphthalen-2-yloxy-acidic derivatives as inhibitors of plasminogen activator inhibitor type-1 (PAI-1) SERPINC1, F11, SERPINE1 MEN1 2764/4885KMT2A 3476/4885CA12 2555/4885

“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.