SCHEMBL743611

SCHEMBL743611

O=C(NCC1CCCO1)c1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HPGD P15428 8/20 1.00
KMT2A Q03164 2/20 0.85
MEN1 O00255 1/20 0.85
ATM Q13315 1/20 0.77
ALDH1A1 P00352 3/20 0.76
GLA P06280 1/20 0.76
ALOX12 P18054 1/20 0.76
RAB9A P51151 1/20 0.73
CYP1A2 P05177 1/20 0.71
GAA P10253 1/20 0.71
CYP2C9 P11712 1/20 0.71
CYP2C19 P33261 1/20 0.71
SMN1; SMN2 Q16637 5/20 0.69
L3MBTL1 Q9Y468 1/20 0.69
NPC1 O15118 1/20 0.69
KDM4E B2RXH2 2/20 0.67
APOBEC3A P31941 1/20 0.67
APOBEC3G Q9HC16 1/20 0.67
TP53 P04637 1/20 0.67
POLB P06746 1/20 0.67

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
SCHEMBL29687327 1.00 HPGD (1.00) HPGDKMT2AMEN1ATMALDH1A1
SCHEMBL30678539 1.00 HPGD (1.00) HPGDKMT2AMEN1ATMALDH1A1
SCHEMBL30914546 0.92 HPGD (0.85) HPGDKMT2AMEN1ATMALDH1A1
SCHEMBL6570578 0.87 KMT2A (0.88) HPGDKMT2AMEN1ALDH1A1RAB9A
SCHEMBL23412465 0.86 KMT2A (0.78) HPGDKMT2AMEN1ATMALDH1A1
SCHEMBL30093073 0.86 KMT2A (0.78) HPGDKMT2AMEN1ATMALDH1A1
SCHEMBL763451 0.85 KMT2A (0.86) HPGDKMT2AMEN1ALDH1A1RAB9A
SCHEMBL11918653 0.85 KMT2A (0.86) HPGDKMT2AMEN1ALDH1A1RAB9A
SCHEMBL3034740 0.85 KMT2A (0.81) HPGDKMT2AMEN1ATMALDH1A1
SCHEMBL279957 0.85 KMT2A (0.86) HPGDKMT2AMEN1ALDH1A1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2850071-A1 ISOINDOLONE DERIVATIVES AbbVie Inc. (US) 2015-03-25 EP claimed
EP-2838881-A1 ISOINDOLONE DERIVATIVES AbbVie Inc. (US) 2015-02-25 EP claimed
EP-2797918-A1 BROMODOMAIN INHIBITORS AbbVie Inc. (US) 2014-11-05 EP claimed
WO-2013158952-A1 ISOINDOLONE DERIVATIVES ABBVIE INC. (US) 2013-10-24 WO claimed
WO-2013155695-A1 ISOINDOLONE DERIVATIVES ABBOTT LABORATORIES (US) 2013-10-24 WO claimed
WO-2013097601-A1 BROMODOMAIN INHIBITORS ABBVIE INC. (US) 2013-07-04 WO claimed
US-8242129-B2 6-phenylpyrimidinones as PIM modulators EXELIXIS, INC. (US) 2012-08-14 US claimed
US-20100135954-A1 6-Phenylpyrimidinones as PIM Modulators EXELIXIS, INC. (US) 2010-06-03 US claimed
EP-1888595-A2 SPIRO-OXINDOLE COMPOUNDS AND THEIR USES AS THERAPEUTIC AGENTS XENON PHARMACEUTICALS INC. (CA) 2008-02-20 EP claimed
JP-2006528597-A 2006-12-21 JP claimed
WO-2006110917-A2 SPIRO-OXINDOLE COMPOUNDS AND THEIR USES AS THERAPEUTIC AGENTS XENON PHARMACEUTICALS INC. (CA) 2006-10-19 WO claimed
EP-1658263-A1 NOVEL AMINOBENZOPHENONE COMPOUNDS Leo Pharma A/S (DK) 2006-05-24 EP claimed
WO-2005009940-A1 NOVEL AMINOBENZOPHENONE COMPOUNDS LEO PHARMA A/S (DK) 2005-02-03 WO claimed
US-12060339-B2 Dual modulator of mGluR5 and 5-HT2A receptor, and use thereof VIVOZON INC. (KR) 2024-08-13 US disclosed
US-20240092790-A1 DIHYDROFUROPYRIDINE DERIVATIVES AS RHO- KINASE INHIBITORS CHIESI FARMACEUTICI S.P.A. (IT) 2024-03-21 US disclosed
US-20220388967-A1 Phenyl Amino Pyrimidine Compounds and Uses Thereof SIERRA ONCOLOGY, INC. (US) 2022-12-08 US disclosed
WO-2004026816-A1 AROMATIC LIVER X-RECEPTOR MODULATORS PHARMACIA CORPORATION (US) 2004-04-01 WO disclosed
EP-0483714-B1 A method of preparing an acid additional salt of delta-aminolevulinic acid JAPAN TOBACCO INC (JP) 1995-05-03 EP disclosed
US-5284973-A Method of preparing an acid additional salt of delta-aminolevulinic acid JAPAN TOBACCO INC. (JP) 1994-02-08 US disclosed
EP-0483714-A1 A method of preparing an acid additional salt of delta-aminolevulinic acid Japan Tobacco Inc. (JP) 1992-05-06 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 (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-20100135954-A1 6-Phenylpyrimidinones as PIM Modulators PIM1, PIM2, PIM3 HPGD 2939/4885KMT2A 1421/4885MEN1 3946/4885
US-12060339-B2 Dual modulator of mGluR5 and 5-HT2A receptor, and use thereof GRM5, HTR5A, HTR2A HPGD 1388/4885KMT2A 959/4885MEN1 4816/4885
US-20240092790-A1 DIHYDROFUROPYRIDINE DERIVATIVES AS RHO- KINASE INHIBITORS ROCK1, ROCK2, RHOA HPGD 61/4885KMT2A 3061/4885MEN1 4234/4885
US-20220388967-A1 Phenyl Amino Pyrimidine Compounds and Uses Thereof JAK2, JAK1, JAK3 HPGD 1481/4885KMT2A 835/4885MEN1 4037/4885

“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.