SCHEMBL619494

SCHEMBL619494

O=C(CCl)NCC(O)CO

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.44
SMN1; SMN2 Q16637 2/20 0.44
LMNA P02545 2/20 0.35
MEN1 O00255 2/20 0.33
KMT2A Q03164 2/20 0.33
USP2 O75604 1/20 0.33
MAPT P10636 1/20 0.33
CYP2C19 P33261 1/20 0.33
HIF1A Q16665 1/20 0.33
NPC1 O15118 1/20 0.33
S1PR4 O95977 1/20 0.33
S1PR1 P21453 1/20 0.33
HTT P42858 1/20 0.33
RAB9A P51151 1/20 0.33
KDM4E B2RXH2 1/20 0.33
HPGD P15428 1/20 0.33
EGFR P00533 1/20 0.31
SRC P12931 1/20 0.31
CA2 P00918 1/20 0.31
ASAH1 Q13510 1/20 0.31

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
SCHEMBL620059 1.00 ALDH1A1 (0.44) ALDH1A1SMN1; SMN2LMNAMEN1KMT2A
SCHEMBL619493 1.00 ALDH1A1 (0.44) ALDH1A1SMN1; SMN2LMNAMEN1KMT2A
SCHEMBL9147732 0.88 ALDH1A1 (0.50) ALDH1A1SMN1; SMN2MEN1KMT2AUSP2
SCHEMBL29638822 0.83 LMNA (0.40) ALDH1A1LMNAMEN1KMT2AUSP2
SCHEMBL10296842 0.81 LMNA (0.38) ALDH1A1LMNAMEN1KMT2AUSP2
SCHEMBL9735094 0.81 LMNA (0.38) ALDH1A1LMNAMEN1KMT2AUSP2
SCHEMBL10296844 0.81 LMNA (0.38) ALDH1A1LMNAMEN1KMT2AUSP2
SCHEMBL11284773 0.80 ALDH1A1 (0.43) ALDH1A1SMN1; SMN2LMNAMEN1KMT2A
SCHEMBL8858994 0.78 MAPT (0.34) ALDH1A1LMNAMEN1KMT2AUSP2
SCHEMBL21779362 0.78

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250163061-A1 INHIBITORS OF MENIN-MLL INTERACTION BALA THERAPEUTICS, INC. 2025-05-22 US disclosed
EP-2683697-B1 SUBSTITUTED MORPHOLINES AS MODULATORS FOR THE CALCIUM SENSING RECEPTOR LUPIN ATLANTIS HOLDINGS SA (CH) 2017-09-06 EP disclosed
US-20170152258-A9 Substituted Pyridopyrazines as Syk Inhibitors HUTCHISON MEDIPHARMA LIMITED (CN) 2017-06-01 US disclosed
US-20160250219-A1 SUBSTITUTED MORPHOLINES AS MODULATORS FOR THE CALCIUM SENSING RECEPTOR LUPIN ATLANTIS HOLDINGS SA (CH) 2016-09-01 US disclosed
US-20160250219-A1 SUBSTITUTED MORPHOLINES AS MODULATORS FOR THE CALCIUM SENSING RECEPTOR LUPIN ATLANTIS HOLDINGS SA (CH) 2016-09-01 US disclosed
EP-2197874-B1 PYRAZIN-2-YL-PYRIDIN-2-YL-AMINE AND PYRAZIN-2-YL-PYRIMIDIN-4-YL-AMINE COMPOUNDS AND THEIR USE CANCER REC TECH LTD (GB) 2016-08-31 EP disclosed
US-9382216-B2 Substituted morpholines as modulators for the calcium sensing receptor LUPIN LIMITED (IN) 2016-07-05 US disclosed
US-9382216-B2 Substituted morpholines as modulators for the calcium sensing receptor LUPIN LIMITED (IN) 2016-07-05 US disclosed
CN-105593232-A Benzoxazoloxazinone compounds as coagulation factor Xa inhibitors NORTH CHINA PHARMACEUTICAL NEW DRUG R & D CO LTD 2016-05-18 CN disclosed
US-20160002221-A1 Substituted Pyridopyrazines as Syk Inhibitors HUTCHISON MEDIPHARMA LTD (CN) 2016-01-07 US disclosed
US-20090181967-A1 New compounds I BIOVITRUM AB (SE) 2009-07-16 US disclosed
WO-2009071658-A1 PIPERAZINES AS ANTI-OBESITY AGENTS BIOVITRUM AB (PUBL) (SE) 2009-06-11 WO disclosed
WO-2009044162-A1 PYRAZIN-2-YL-PYRIDIN-2-YL-AMINE AND PYRAZIN-2-YL-PYRIMIDIN-4-YL-AMINE COMPOUNDS AND THEIR USE CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2009-04-09 WO disclosed
WO-2008075007-A1 MORPHOLINO-SUBSTITUTED BICYCLOHETEROARYL COMPOUNDS AND THEIR USE AS ANTI CANCER AGENTS CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2008-06-26 WO disclosed
WO-2007006715-A1 CYSTEINE PROTEASE INHIBITORS MEDIVIR AB (SE) 2007-01-18 WO disclosed
WO-2007005935-A2 NOREPINEPHRINE TRANSPORTER RADIOTRACERS AND METHODS OF SYNTHESES THEREOF MOLECULAR NEUROIMAGING, LLC (US) 2007-01-11 WO disclosed
US-4512796-A Haloacetylaminomethyl dioxolane herbicide antidotes STAUFFER CHEMICAL COMPANY (US) 1985-04-23 US disclosed
US-4406686-A Haloalkylaminomethyldioxolane herbicide antidotes STAUFFER CHEMICAL COMPANY (US) 1983-09-27 US disclosed
US-4216222-A Alkyl or alkoxy-O-alkyl-S-[N-(2-alkyl, phenyl or vinyl-1,3-dioxolan-4-yl) methylaminoacetyl] dithiophosphates or phosphonates as insecticides and acaricides STAUFFER CHEMICAL COMPANY (US) 1980-08-05 US disclosed
US-4154595-A PREEMERGENCE HERBICIDES, POSTEMERGENCE HERBICIDES STAUFFER CHEMICAL COMPANY (US) 1979-05-15 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 (5 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-20250163061-A1 INHIBITORS OF MENIN-MLL INTERACTION MLLT1, MEN1, BMI1 ALDH1A1 3650/4885SMN1; SMN2 1478/4885LMNA 531/4885
US-20160250219-A1 SUBSTITUTED MORPHOLINES AS MODULATORS FOR THE CALCIUM SENSING RECEPTOR CASR, RYR1, RYR2 ALDH1A1 3779/4885SMN1; SMN2 661/4885LMNA 1391/4885
US-20090181967-A1 New compounds I GPR119, GLP1R, FABP4 ALDH1A1 2089/4885SMN1; SMN2 4598/4885LMNA 1076/4885
US-20160002221-A1 Substituted Pyridopyrazines as Syk Inhibitors SYK, BTK, LYN ALDH1A1 3626/4885SMN1; SMN2 3889/4885LMNA 4088/4885
US-20170152258-A9 Substituted Pyridopyrazines as Syk Inhibitors SYK, BTK, LYN ALDH1A1 3626/4885SMN1; SMN2 3889/4885LMNA 4088/4885

“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.