SCHEMBL4020110

SCHEMBL4020110

COC(=O)c1ccc(OC2CCCCO2)cc1

nearest known ligand 0.58

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 2/20 0.51
HPGD P15428 2/20 0.51
RAB9A P51151 1/20 0.51
KMT2A Q03164 4/20 0.48
MEN1 O00255 3/20 0.48
CA1 P00915 1/20 0.47
CA2 P00918 1/20 0.47
ALDH1A1 P00352 4/20 0.47
MAPT P10636 1/20 0.44
SMN1; SMN2 Q16637 4/20 0.44
EPHX2 P34913 1/20 0.44
LMNA P02545 1/20 0.43
L3MBTL1 Q9Y468 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
SCHEMBL16073032 0.95 ACR (0.48) NPC1HPGDRAB9AKMT2AMEN1
SCHEMBL14422348 0.86 ALDH1A1 (0.51) NPC1HPGDRAB9AKMT2AMEN1
SCHEMBL2281345 0.85 SMN1; SMN2 (0.60) NPC1HPGDRAB9AKMT2AMEN1
SCHEMBL1186911 0.85 MEN1 (0.52) NPC1RAB9AKMT2AMEN1SMN1; SMN2
SCHEMBL15654561 0.85 RAB9A (0.53) NPC1HPGDRAB9AKMT2AMEN1
SCHEMBL25621200 0.84 HPGD (0.47) NPC1HPGDRAB9AALDH1A1SMN1; SMN2
SCHEMBL225085 0.84 KMT2A (0.65) NPC1RAB9AKMT2AMEN1CA1
SCHEMBL13169521 0.83 STS (0.54) NPC1RAB9AKMT2AMEN1ALDH1A1
SCHEMBL26452181 0.82 PARP10 (0.58) HPGDKMT2AMEN1CA1CA2
SCHEMBL2980200 0.82 KMT2A (0.67) NPC1HPGDRAB9AKMT2AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3621958-B1 PHOTOCHROMIC INDENO FUSED PHENANTHRENOPYRAN COMPOUNDS TRANSITIONS OPTICAL LTD (IE) 2024-07-10 EP disclosed
CN-111620764-B Selective ether bond cleavage method of aryl alkyl ether 荆楚理工学院 2023-05-05 CN disclosed
EP-3268375-B1 PHOTOCHROMIC THIENOCHROMENE COMPOUNDS TRANSITIONS OPTICAL INC (US) 2022-06-15 EP disclosed
EP-3071576-B9 PHOTOCHROMIC INDENO-FUSED RING PYRAN COMPOUNDS TRANSITIONS OPTICAL INC (US) 2021-12-22 EP disclosed
EP-3071576-B1 PHOTOCHROMIC INDENO-FUSED RING PYRAN COMPOUNDS TRANSITIONS OPTICAL INC (US) 2021-08-18 EP disclosed
CN-111620764-A Selective ether bond breaking method of aryl alkyl ether 荆楚理工学院 2020-09-04 CN disclosed
US-20200048216-A1 Photochromic Indeno Fused Phenanthrenopyran Compounds TRANSITIONS OPTICAL, LTD. (IE) 2020-02-13 US disclosed
EP-3071550-B1 METHOD OF PREPARING FUSED RING INDENO COMPOUNDS TRANSITIONS OPTICAL INC (US) 2019-03-13 EP disclosed
US-20180051037-A1 Photochromic Thienochromene Compounds TRANSITIONS OPTICAL, INC. 2018-02-22 US disclosed
US-20180051037-A1 Photochromic Thienochromene Compounds TRANSITIONS OPTICAL, INC. 2018-02-22 US disclosed
EP-0524250-A1 RESIST MATERIAL FOR USE IN THICK FILM RESISTS E.I. DU PONT DE NEMOURS AND COMPANY (US) 1993-01-27 EP disclosed
US-5145764-A Acrylic ester polymer E. I. DU PONT DE NEMOURS AND COMPANY (US) 1992-09-08 US disclosed
US-5120633-A Polymers with acid-labile ester/ether pendant groups and acid-generating photoinitiators; positives; printed circuits; resolution E. I. DU PONT DE NEMOURS AND COMPANY (US) 1992-06-09 US disclosed
US-5077174-A Aqueous development, stripping E. I. DU PONT DE NEMOURS AND COMPANY (US) 1991-12-31 US disclosed
WO-1991015808-A1 RESIST MATERIAL FOR USE IN THICK FILM RESISTS E.I. DU PONT DE NEMOURS AND COMPANY (US) 1991-10-17 WO disclosed
WO-1991015807-A1 RESIST MATERIAL WITH CARBAZOLE DIAZONIUM SALT ACID GENERATOR AND PROCESS FOR USE E.I. DU PONT DE NEMOURS AND COMPANY (US) 1991-10-17 WO disclosed
WO-1991015810-A1 RESIST MATERIAL AND PROCESS FOR USE E.I. DU PONT DE NEMOURS AND COMPANY (US) 1991-10-17 WO disclosed
WO-1991015809-A1 POSITIVE WORKING RESIST COMPOSITIONS AND THEIR UTILITY IN DRY FILM PHOTORESISTS E.I. DU PONT DE NEMOURS AND COMPANY (US) 1991-10-17 WO disclosed
US-4985332-A Resist material with carbazole diazonium salt acid generator and process for use E. I. DU PONT DE NEMOURS AND COMPANY (US) 1991-01-15 US disclosed
US-4824993-A SYNTHETIC PROSTAGLANDINS, ANTISECRETORY AGENTS GLAXO GROUP LIMITED (GB) 1989-04-25 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 (2 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-20200048216-A1 Photochromic Indeno Fused Phenanthrenopyran Compounds ALDH1A2, RB1, INCENP NPC1 3498/4885HPGD 183/4885RAB9A 3935/4885
US-20180051037-A1 Photochromic Thienochromene Compounds CRY1, CRY2, TERT NPC1 3319/4885HPGD 125/4885RAB9A 1990/4885

“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.