SCHEMBL9627646

SCHEMBL9627646

CC(C)C1=CC(=O)c2ccccc2C1=O

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTPN1 P18031 1/20 0.70
CDC25B P30305 5/20 0.60
CDC25A P30304 4/20 0.60
MEN1 O00255 3/20 0.57
KMT2A Q03164 3/20 0.57
ALDH1A1 P00352 3/20 0.57
LMNA P02545 3/20 0.57
MAPT P10636 3/20 0.57
MAPK1 P28482 3/20 0.57
IDO1 P14902 2/20 0.57
HIF1A Q16665 2/20 0.57
CYP1A2 P05177 2/20 0.57
CYP2C9 P11712 2/20 0.57
CYP2C19 P33261 2/20 0.57
GAA P10253 2/20 0.57
HPGD P15428 2/20 0.57
ATM Q13315 2/20 0.57
SMN1; SMN2 Q16637 2/20 0.57
PLIN1 O60240 1/20 0.57
NR1I2 O75469 1/20 0.57

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
SCHEMBL30038980 1.00 PTPN1 (0.70) PTPN1CDC25BCDC25AMEN1KMT2A
SCHEMBL19459046 0.89 PTPN1 (0.80) PTPN1CDC25BCDC25AMEN1KMT2A
SCHEMBL5810766 0.87 PTPN1 (0.59) PTPN1CDC25BCDC25AMEN1KMT2A
SCHEMBL5817375 0.83 PTPN1 (0.55) PTPN1CDC25BCDC25AMEN1KMT2A
SCHEMBL10899337 0.83 PTPN1 (0.55) PTPN1CDC25BCDC25AMEN1KMT2A
SCHEMBL17969793 0.83 CDC25B (0.60) PTPN1CDC25BCDC25AMEN1KMT2A
SCHEMBL11828689 0.81 CDC25B (0.89) PTPN1CDC25BCDC25AMEN1KMT2A
SCHEMBL31619928 0.81 CDC25B (0.89) PTPN1CDC25BCDC25AMEN1KMT2A
SCHEMBL9628284 0.80 PTPN1 (0.52) PTPN1CDC25BCDC25AMEN1KMT2A
Ammonia Solution, Strong SCHEMBL28549609 0.79 PTPN1 (0.50) PTPN1CDC25BCDC25AMEN1KMT2A

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023149432-A1 COMPOSITION CONTAINING FLUORINE-CONTAINING MONOMER, METHOD FOR STABILIZING FLUORINE-CONTAINING MONOMER, METHOD FOR MANUFACTURING FLUORINE-CONTAINING POLYMER, AND METHOD FOR MANUFACTURING FLUORINE-CONTAINING MONOMER ダイキン工業株式会社 2023-08-10 WO disclosed
US-11541120-B2 Phosphonium-based ionic drug conjugates ANTHOS PARTNERS, LP (US) 2023-01-03 US disclosed
US-20200353087-A1 PHOSPHONIUM-BASED IONIC DRUG CONJUGATES ANTHOS PARTNERS, LP 2020-11-12 US disclosed
US-10266526-B2 Substituted 1,2,3-triazoles as SMYD inhibitors for treating cancer Epizyme, Inc. (US) 2019-04-23 US disclosed
CN-108530394-A A kind of synthesis vitamin K3The method of epoxides 中国科学院成都有机化学有限公司 2018-09-14 CN disclosed
US-20170355695-A1 SMYD Inhibitors Epizyme, Inc. (US) 2017-12-14 US disclosed
US-20170355695-A1 SMYD Inhibitors Epizyme, Inc. (US) 2017-12-14 US disclosed
EP-2257515-B1 1,4-NAPHTHOQUINONE DERIVATIVES AND THERAPEUTIC USE THEREOF CENTRE NAT RECH SCIENT (FR) 2017-05-17 EP disclosed
US-7253207-B2 Quinones as disease therapies CELLGATE, INC. (US) 2007-08-07 US disclosed
US-7253207-B2 Quinones as disease therapies CELLGATE, INC. (US) 2007-08-07 US disclosed
US-5155132-A Nonsteroidal antiinflammatory agents; treating psoriasis SYNTEX (U.S.A.) INC. (US) 1992-10-13 US disclosed
US-5134161-A Enzyme inhibitors for skin disorders, antiinflammatory agents SYNTEX (U.S.A.) INC. (US) 1992-07-28 US disclosed
US-5089657-A Topical antiinflammatory agents SYNTEX (U.S.A.) INC. (US) 1992-02-18 US disclosed
US-4786652-A TOPICAL ADMINISTRATION SYNTEX (U.S.A.) INC. (US) 1988-11-22 US disclosed
EP-0282006-A1 Naphtalene anti-psoriatic agents SYNTEX (U.S.A.) INC. (US) 1988-09-14 EP disclosed
EP-0282056-A2 Naphthalene anti-psoriatic agents SYNTEX (U.S.A.) INC. (US) 1988-09-14 EP disclosed
US-4758587-A Naphthalene anti-psoriatic agents SYNTEX (U.S.A.) INC. (US) 1988-07-19 US disclosed
US-4251623-A Imaging process involving thermal decomposition of Te(II) coordination complexes EASTMAN KODAK COMPANY (US) 1981-02-17 US 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 (4 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-20200353087-A1 PHOSPHONIUM-BASED IONIC DRUG CONJUGATES SLC8B1, PHOSPHO1, PBDC1 PTPN1 3200/4885CDC25B 3503/4885CDC25A 3230/4885
US-10266526-B2 Substituted 1,2,3-triazoles as SMYD inhibitors for treating cancer SMYD3, SMYD2, SNRPD3 PTPN1 2006/4885CDC25B 1373/4885CDC25A 2032/4885
US-20170355695-A1 SMYD Inhibitors SMYD3, SMYD2, SMURF2 PTPN1 2209/4885CDC25B 1117/4885CDC25A 1756/4885
US-11541120-B2 Phosphonium-based ionic drug conjugates SLC8B1, PHOSPHO1, PBDC1 PTPN1 3200/4885CDC25B 3503/4885CDC25A 3230/4885

“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.