SCHEMBL367263

SCHEMBL367263

CCCCPc1ccccc1

nearest known ligand 0.44

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
LTA4H P09960 2/20 0.38
PCSK9 Q8NBP7 1/20 0.38
PTGS2 P35354 1/20 0.36
CES2 O00748 2/20 0.35
CES1 P23141 2/20 0.35
SMN1; SMN2 Q16637 2/20 0.35
SIGMAR1 Q99720 1/20 0.35
ESR1 P03372 1/20 0.35
TP53 P04637 2/20 0.35
TDP1 Q9NUW8 1/20 0.34
TSHR P16473 1/20 0.34
DNM1 Q05193 1/20 0.34
MEN1 O00255 1/20 0.33
MAPK1 P28482 1/20 0.33
KMT2A Q03164 1/20 0.33

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
Hydrochloric Acid SCHEMBL11572419 0.98 LTA4H (0.36) LTA4HPCSK9PTGS2CES2CES1
Hydrochloric Acid SCHEMBL11572407 0.98 LTA4H (0.36) LTA4HPCSK9PTGS2CES2CES1
Butane SCHEMBL27520586 0.98 LTA4H (0.36) LTA4HPCSK9PTGS2CES2CES1
SCHEMBL27678592 0.98 LTA4H (0.36) LTA4HPCSK9PTGS2CES2CES1
Hydrochloric Acid SCHEMBL9619305 0.98 LTA4H (0.36) LTA4HPCSK9PTGS2CES2CES1
Bromide SCHEMBL25216737 0.98 LTA4H (0.36) LTA4HPCSK9PTGS2CES2CES1
SCHEMBL3445934 0.93 LTA4H (0.38) LTA4HPCSK9PTGS2CES2CES1
SCHEMBL3411655 0.92 LTA4H (0.33) LTA4HPCSK9PTGS2CES2CES1
SCHEMBL5389878 0.91 DNM1 (0.40) LTA4HPTGS2CES2CES1SMN1; SMN2
SCHEMBL5394695 0.91 DNM1 (0.40) LTA4HPTGS2CES2CES1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114805430-A Preparation method of seleno-phosphide and thiophosphite 烟台大学 2022-07-29 CN claimed
CN-114573422-A Treatment method of 3-methyl-3-butene-1-ol process waste liquid 万华化学集团股份有限公司 2022-06-03 CN claimed
CN-110041373-A The recovery method of noble metal catalyst in a kind of production procedure of centre Lei Dipawei 江苏万年长药业有限公司 2019-07-23 CN claimed
EP-3484840-A1 CATALYTIC PROCESS FOR DIENE DIMERIZATION Total Raffinage Chimie (FR) 2019-05-22 EP claimed
WO-2018011157-A1 CATALYTIC PROCESS FOR DIENE DIMERIZATION TOTAL RAFFINAGE CHIMIE (FR) 2018-01-18 WO claimed
US-7816525-B1 Process for the preparation of optically pure tetrahydropterins and derivatives, and specifically of optically pure tetrahydrofolic acid and derivatives thereof, by stereospecific hydrogenation Merck & Cie (CH) 2010-10-19 US claimed
US-20080306263-A1 Process For The Preparation Of Optically Pure Tetrahydropterins And Derivatives, And Specifically Of Optically Pure Tetrahydrofolic Acid And Derivatives Thereof, By Stereospecific Hydrogenation MULLER HANS RUDOLF 2008-12-11 US claimed
CN-1264842-C Process for the preparation of optically pure tetrahydropterin and derivatives thereof, in particular optically pure tetrahydrofolic acid and derivatives thereof, by stereoselective hydrogenation EPROVA AG (CH) 2006-07-19 CN claimed
EP-1622861-A1 METHOD OF FORMING A CARBON-HETEROATOM BOND RHODIA CHIMIE (FR) 2006-02-08 EP claimed
WO-2004101496-A1 METHOD OF FORMING A CARBON-HETEROATOM BOND RHODIA CHIMIE (FR) 2004-11-25 WO claimed
WO-2001042197-A1 METHOD FOR PREPARING A POLYAROMATIC COMPOUND RHODIA CHIMIE (FR) 2001-06-14 WO claimed
EP-0975571-A1 METHOD FOR PREPARING AROMATIC ALDEHYDES RHODIA CHIMIE (FR) 2000-02-02 EP claimed
WO-1999042424-A1 METHOD FOR PREPARING AROMATIC KETONE COMPOUNDS RHODIA CHIMIE (FR) 1999-08-26 WO claimed
WO-1998047848-A1 METHOD FOR PREPARING AROMATIC ALDEHYDES RHODIA CHIMIE (FR) 1998-10-29 WO claimed
EP-0249984-B1 PROCESS FOR PRODUCING BUTENE-1 POLYMER IDEMITSU PETROCHEMICAL CO. LTD. (JP) 1992-01-08 EP claimed
JP-1060623-A None JP disclosed
CN-115210213-B Active ester, curable resin composition, and cured product DIC株式会社 2024-12-10 CN disclosed
US-4119652-A HYDROGENATION CATALYSTS; COORDINATION COMPOUNDS OF IRIDIUM, RHODIUM OR RUTHENIUM WITH PHOSPHINE OR ARSINE LIGANDS; OPTICALLY ACTIVE MONSANTO COMPANY (US) 1978-10-10 US disclosed
US-4028481-A ACTIVATED TITANIUM TRICHLORIDE AND AN ORGANOALUMINUM COMPOUND MITSUI TOATSU CHEMICALS, INCORPORATED (JA) 1977-06-07 US disclosed
US-3968147-A COORDINATION CATALYST MONSANTO COMPANY (US) 1976-07-06 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 (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-20080306263-A1 Process For The Preparation Of Optically Pure Tetrahydropterins And Derivatives, And Specifically Of Optically Pure Tetrahydrofolic Acid And Derivatives Thereof, By Stereospecific Hydrogenation DHFR, MTHFD2, MTHFD1 LTA4H 1467/4885PCSK9 943/4885PTGS2 868/4885

“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.