SCHEMBL30137348

SCHEMBL30137348

O=C([O-])c1cccnc1Cl.[Na+]

nearest known ligand 0.66

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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 2/20 0.66
SMN1; SMN2 Q16637 2/20 0.66
EGFR P00533 4/20 0.50
POLB P06746 1/20 0.49
NPC1 O15118 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
CYP1A2 P05177 1/20 0.46
CYP2C9 P11712 1/20 0.46
CYP2C19 P33261 1/20 0.46
CASP3 P42574 1/20 0.46
SENP8 Q96LD8 1/20 0.46
SENP7 Q9BQF6 1/20 0.46
SENP6 Q9GZR1 1/20 0.46
ALDH1A1 P00352 2/20 0.45
HPGD P15428 2/20 0.45
KDM4E B2RXH2 2/20 0.45
GFER P55789 1/20 0.45
GAA P10253 1/20 0.44
MEN1 O00255 1/20 0.44
KMT2A Q03164 1/20 0.44

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
SCHEMBL28529875 1.00 LMNA (0.66) LMNASMN1; SMN2EGFRPOLBNPC1
Lithium Ion SCHEMBL30137319 0.96 LMNA (0.66) LMNASMN1; SMN2EGFRPOLBNPC1
Lithium Ion SCHEMBL28965991 0.96 LMNA (0.66) LMNASMN1; SMN2EGFRPOLBNPC1
Potassium Ion SCHEMBL5250400 0.96 LMNA (0.66) LMNASMN1; SMN2EGFRPOLBNPC1
SCHEMBL950218 0.81 LMNA (0.73) LMNASMN1; SMN2EGFRPOLBNPC1
SCHEMBL30639807 0.79 KDM4E (0.63) LMNASMN1; SMN2L3MBTL1ALDH1A1HPGD
SCHEMBL29799007 0.79 SMN1; SMN2 (0.70) LMNASMN1; SMN2EGFRPOLBNPC1
SCHEMBL105459 0.79 SMN1; SMN2 (0.70) LMNASMN1; SMN2EGFRPOLBNPC1
SCHEMBL17180592 0.79 LMNA (0.70) LMNASMN1; SMN2EGFRPOLBNPC1
SCHEMBL29412848 0.79 SMN1; SMN2 (1.00) LMNASMN1; SMN2EGFRPOLBNPC1

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-115611802-B Synthetic method of 3-acetyl-2-chloropyridine 北京迪泰医药科技有限公司 2023-03-14 CN disclosed
CN-115611802-A Synthetic method of 3-acetyl-2-chloropyridine 北京迪泰医药科技有限公司 2023-01-17 CN disclosed