SCHEMBL28831793

SCHEMBL28831793

CCCCn1ccnc1C(CC)S(=O)(=O)O.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.41

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.41
SMN1; SMN2 Q16637 3/20 0.41
ALDH1A1 P00352 3/20 0.41
KMT2A Q03164 2/20 0.41
POLB P06746 1/20 0.41
KDM4E B2RXH2 2/20 0.38
MAPT P10636 1/20 0.38
HTT P42858 1/20 0.38
TDP1 Q9NUW8 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.38
CYP1A2 P05177 1/20 0.38
CYP3A4 P08684 1/20 0.38
CYP2C9 P11712 1/20 0.38
PKM P14618 1/20 0.38
CYP2C19 P33261 1/20 0.38
ADORA2B P29275 1/20 0.36
NPSR1 Q6W5P4 1/20 0.36
TSHR P16473 1/20 0.35
TLR8 Q9NR97 2/20 0.34
MEN1 O00255 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
SCHEMBL28831716 0.90 ALDH1A1 (0.42) LMNASMN1; SMN2ALDH1A1KMT2AKDM4E
SCHEMBL28320356 0.88 ALDH1A1 (0.47) LMNASMN1; SMN2ALDH1A1KMT2APOLB
SCHEMBL28487074 0.85 TSHR (0.44) LMNASMN1; SMN2ALDH1A1KMT2AKDM4E
SCHEMBL31037659 0.82 TSHR (0.40) LMNASMN1; SMN2ALDH1A1KMT2APOLB
SCHEMBL1792059 0.82 ALDH1A1 (0.63) LMNASMN1; SMN2ALDH1A1KMT2APOLB
SCHEMBL29275155 0.80 SMN1; SMN2 (0.42) SMN1; SMN2ALDH1A1KMT2APOLBMAPT
SCHEMBL29859619 0.80 ALDH1A1 (0.46) LMNASMN1; SMN2ALDH1A1KMT2APOLB
SCHEMBL29859863 0.80 ALDH1A1 (0.46) LMNASMN1; SMN2ALDH1A1KMT2APOLB
SCHEMBL28722227 0.80 ALDH1A1 (0.46) LMNASMN1; SMN2ALDH1A1KMT2APOLB
Sulfuric Acid SCHEMBL29090850 0.78 ALDH1A1 (0.45) LMNASMN1; SMN2ALDH1A1KMT2APOLB

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 2 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114849786-B Imidazole sulfonic acid ionic liquid-based palladium phosphine complex catalyst for synthesizing methyl propionate through ethylene hydro-methyl esterification 中国科学院过程工程研究所 2023-09-05 CN disclosed
CN-114849786-A Imidazole sulfonic acid ionic liquid based palladium-phosphine complex catalyst for synthesizing methyl propionate by ethylene methyl hydrogen esterification 中国科学院过程工程研究所 2022-08-05 CN disclosed