SCHEMBL927812

SCHEMBL927812

O=c1c(=O)c2ccccc12

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 7/20 0.50
▸ KDM4E B2RXH2 5/20 0.50
▸ SMN1; SMN2 Q16637 4/20 0.50
▸ MAPT P10636 4/20 0.50
▸ LMNA P02545 4/20 0.50
▸ GAA P10253 3/20 0.50
▸ HTT P42858 3/20 0.50
▸ HSD17B10 Q99714 3/20 0.50
▸ GLA P06280 2/20 0.50
▸ HPGD P15428 2/20 0.50
▸ MAOA P21397 2/20 0.50
▸ ATM Q13315 1/20 0.50
▸ CYP3A4 P08684 1/20 0.50
▸ PGAM1 P18669 1/20 0.50
▸ CASP1 P29466 1/20 0.50
▸ CASP7 P55210 1/20 0.50
▸ S100A4 P26447 2/20 0.44
▸ POLB P06746 3/20 0.43
▸ NPC1 O15118 2/20 0.42
▸ RAB9A P51151 2/20 0.42

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
SCHEMBL17987 0.96 ALDH1A1 (0.48) ALDH1A1KDM4ESMN1; SMN2MAPTLMNA
SCHEMBL29362920 0.96 ALDH1A1 (0.48) ALDH1A1KDM4ESMN1; SMN2MAPTLMNA
SCHEMBL6050558 0.96 ALDH1A1 (0.48) ALDH1A1KDM4ESMN1; SMN2MAPTLMNA
SCHEMBL32671774 0.96 ALDH1A1 (0.48) ALDH1A1KDM4ESMN1; SMN2MAPTLMNA
Water SCHEMBL592692 0.93 ALDH1A1 (0.46) ALDH1A1KDM4ESMN1; SMN2MAPTLMNA
SCHEMBL4930798 0.93 ALDH1A1 (0.46) ALDH1A1KDM4ESMN1; SMN2MAPTLMNA
SCHEMBL30139899 0.93 ALDH1A1 (0.46) ALDH1A1KDM4ESMN1; SMN2MAPTLMNA
SCHEMBL5536637 0.93 ALDH1A1 (0.46) ALDH1A1KDM4ESMN1; SMN2MAPTLMNA
SCHEMBL4921603 0.93 ALDH1A1 (0.46) ALDH1A1KDM4ESMN1; SMN2MAPTLMNA
Water SCHEMBL29662270 0.93 ALDH1A1 (0.46) ALDH1A1KDM4ESMN1; SMN2MAPTLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2532660-B1 Process for preparing chiral compounds PFIZER PROD INC (US) 2014-09-10 — — EP disclosed
US-20110003878-A1 NOVEL DERIVATIVES OF PHTHALIMIDE AS HISTONE DEACETYLASE INHIBITORS UNIVERSIDAD DE GRANADA (ES) 2011-01-06 — — US disclosed
EP-2045239-A1 NOVEL DERIVATIVES OF PHTHALIMIDE AS HISTONE DEACETYLASE INHIBITORS Universidad De Granada (ES) 2009-04-08 — — EP disclosed
US-20080165668-A1 RECORDING MEDIUM AND INFORMATION RECORDING AND REPRODUCING METHOD USING THE SAME FUJIFILM CORPORATION 2008-07-10 — — US disclosed
WO-2008003801-A1 NOVEL DERIVATIVES OF PHTHALIMIDE AS HISTONE DEACETYLASE INHIBITORS UNIVERSIDAD DE GRANADA (ES) 2008-01-10 — — WO disclosed
CN-101044028-A Optical information recording medium FUJI PHOTO FILM CO LTD (JP) 2007-09-26 — — CN disclosed
US-20060194151-A1 Recording medium and information recording and reproducing method using the same FUJI PHOTO FILM CO., LTD. 2006-08-31 — — US disclosed
US-7058001-B2 Recording medium and information recording and reproducing method using the same FUJI PHOTO FILM CO., LTD. (JP) 2006-06-06 — — US disclosed
US-20050002835-A1 Micro-engineered reactor ASTRAZENECA AB (SE) 2005-01-06 — — US disclosed
EP-1439904-A1 A MICRO-ENGINEERED CHEMICAL REACTOR AstraZeneca AB (SE) 2004-07-28 — — EP disclosed
US-20020118627-A1 Recording medium and information recording and reproducing method using the same FUJIFILM CORPORATION (JP) 2002-08-29 — — US disclosed
US-6437887-B1 Optical logic device and optical memory device FUJI PHOTO FILM CO., LTD. (JP) 2002-08-20 — — US disclosed
EP-1130585-A2 Recording medium and information recording and reproducing method using the same Fuji Photo Film Co., Ltd. (JP) 2001-09-05 — — EP disclosed
US-6203876-B1 RADIATION TRANSPARENT LAYER ON RECORDING LAYER WITH ORGANIC DYE AND OXIDIZER FUJI PHOTO FILM CO., LTD. (JP) 2001-03-20 — — US disclosed
EP-1035428-A2 Optical logic device and optical memory device Fuji Photo Film Co., Ltd. (JP) 2000-09-13 — — EP disclosed
US-5879772-A Information recording medium FUJI PHOTO FILM CO., LTD. (JP) 1999-03-09 — — US disclosed
EP-0820057-A1 Information recording medium FUJI PHOTO FILM CO., LTD. (JP) 1998-01-21 — — EP disclosed
US-5593970-A ANTITUMOR AND ANTCARCINOGENIC AGENTS; TRETMENT OF CANCEROUS BONE MARROW BEFORE REGRAFTING BIOCHEM PHARMA INC. (CA) 1997-01-14 — — US disclosed
EP-0533744-A1 HETEROCYCLIC ANTHRACYCLIONE AND ANTHRACYCLINE ANALOGS BIOCHEM PHARMA INC. (CA) 1993-03-31 — — EP disclosed
WO-1991019725-A2 HETEROCYCLIC ANTHRACYCLIONE AND ANTHRACYCLINE ANALOGS BIOCHEM PHARMA INC. (CA) 1991-12-26 — — 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 (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-20110003878-A1 NOVEL DERIVATIVES OF PHTHALIMIDE AS HISTONE DEACETYLASE INHIBITORS HDAC1, HDAC2, HDAC11 ALDH1A1 340/4885KDM4E 134/4885SMN1; SMN2 2910/4885

“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.

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