SCHEMBL9346702

SCHEMBL9346702

O=C(O)c1cc(=O)c(O)c[nH]1

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 3/20 0.43
KDM4E B2RXH2 3/20 0.43
SMN1; SMN2 Q16637 4/20 0.43
ALDH1A1 P00352 3/20 0.43
HPGD P15428 2/20 0.43
MAPK1 P28482 2/20 0.43
HSD17B10 Q99714 2/20 0.43
LMNA P02545 2/20 0.43
CA12 O43570 1/20 0.43
CA1 P00915 1/20 0.43
CA2 P00918 1/20 0.43
TP53 P04637 1/20 0.43
CA3 P07451 1/20 0.43
MAPT P10636 1/20 0.43
SELL P14151 1/20 0.43
SELP P16109 1/20 0.43
FUT4 P22083 1/20 0.43
CA4 P22748 1/20 0.43
CA6 P23280 1/20 0.43
DPP4 P27487 1/20 0.43

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 SCHEMBL9658601 0.98 TDP1 (0.42) TDP1KDM4ESMN1; SMN2ALDH1A1HPGD
SCHEMBL15100201 0.81 APP (0.39) HPGDGAAAPPDAOMEN1
SCHEMBL18473811 0.78 ALDH1A1 (0.45) TDP1KDM4ESMN1; SMN2ALDH1A1HPGD
SCHEMBL13467617 0.76 BRD4 (0.44) TDP1CA9APPDAOMEN1
SCHEMBL9875866 0.76 ALDH1A1 (0.47) TDP1KDM4EALDH1A1MAPK1LMNA
SCHEMBL162194 0.75
SCHEMBL20822006 0.74 SMN1; SMN2 (0.40) TDP1KDM4ESMN1; SMN2ALDH1A1HPGD
SCHEMBL10673588 0.73 DAO (0.33) TDP1KDM4EAPPDAOKMT2A
SCHEMBL14818674 0.72 SMN1; SMN2 (0.39) TDP1KDM4ESMN1; SMN2ALDH1A1HPGD
SCHEMBL15764332 0.72 CA12 (0.44) TDP1KDM4ESMN1; SMN2ALDH1A1HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5300497-A Broad spectrum antibiotics and bactericides; stable to beta-lactamase; effective against antibiotic-resistant bacteria TOYAMA CHEMICAL CO., LTD. (JP) 1994-04-05 US disclosed
US-5185330-A Penicillins/ad/ TOYAMA CHEMICAL CO., LTD. (JP) 1993-02-09 US disclosed
US-5106977-A Intermediates for a process for making 2-oxo-1-[[(substituted sulfonyl)-amino]carbonyl]azetidines E. R. SQUIBB & SONS, INC. (US) 1992-04-21 US disclosed
US-4980465-A Process for making 2-oxo-1-[[(substituted sulfonyl)-amino]carbonyl)] azetidines and intermediates used therein E. R. SQUIBB & SONS, INC. (US) 1990-12-25 US disclosed
US-4889930-A Process for making 2-oxo-1-((substituted sulfonyl)amino)carbonzyl)azetidines and intermediates used therein E. R. SQUIBB & SONS, INC. (US) 1989-12-26 US disclosed
EP-0321844-A2 Process for making 2-oxo-1-(((substituted sulfonyl)-amino)carbonyl)azetidines and intermediates used therein E.R. Squibb & Sons, Inc. (US) 1989-06-28 EP disclosed
US-4743685-A 2-oxo-1-[[(substituted sulfonyl)amino]carbonyl]azetidines E. R. SQUIBB & SONS, INC. (US) 1988-05-10 US disclosed
CN-86106980-A The alkylsulfonyl that 2-oxo-1-{[(replaces)-and amino] carbonyl } azetidine-typed 1987-04-08 CN disclosed