Moxalactam

Moxalactam

SCHEMBL22205083

CO/N=C(\C(=O)N[C@@H]1C(=O)N2C(C(=O)[O-])=C(C[N+]3(C)CCCC3)CS[C@H]12)c1csc(N)n1.CO[C@@]1(NC(=O)C(C(=O)O)c2ccc(O)cc2)C(=O)N2C(C(=O)O)=C(CSc3nnnn3C)CO[C@@H]21.CO[C@@]1(NC(=O)CSC(F)F)C(=O)N2C(C(=O)O)=C(CSc3nnnn3CCO)CO[C@@H]21

nearest known ligand 0.52

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Moxalactam. 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
NR1I2 O75469 4/20 0.52
PGR P06401 2/20 0.52
PTGS1 P23219 1/20 0.51
ESR1 P03372 1/20 0.50
DRD2 P14416 1/20 0.50
ADRA2B P18089 1/20 0.50
HRH3 Q9Y5N1 1/20 0.50
TDP1 Q9NUW8 7/20 0.49
HSD17B10 Q99714 4/20 0.49
MAPT P10636 4/20 0.44
APEX1 P27695 3/20 0.44
ALDH1A1 P00352 2/20 0.44
POLB P06746 2/20 0.44
RECQL P46063 2/20 0.44
CYP2D6 P10635 1/20 0.44
KDM4E B2RXH2 1/20 0.44
BLM P54132 1/20 0.44
DAO P14920 1/20 0.42
PPARG P37231 1/20 0.42
SNCA P37840 1/20 0.42

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
Moxalactam SCHEMBL28086495 0.87 NR1I2 (0.69) NR1I2PGRPTGS1TDP1HSD17B10
Moxalactam SCHEMBL6521966 0.85 NR1I2 (0.64) NR1I2PGRPTGS1TDP1HSD17B10
Flomoxef SCHEMBL18065040 0.85 NR1I2 (0.58) NR1I2PGRPTGS1TDP1HSD17B10
Ceftriaxone SCHEMBL3389557 0.84 NR1I2 (0.64) NR1I2PGRPTGS1TDP1HSD17B10
Moxalactam SCHEMBL13723425 0.82 PTGS1 (0.64) NR1I2PGRPTGS1TDP1HSD17B10
Ceftazidime SCHEMBL715368 0.82 NR1I2 (0.58) NR1I2PGRPTGS1ESR1TDP1
SCHEMBL11463469 0.73 NR1I2 (0.86) NR1I2PGRTDP1HSD17B10MAPT
SCHEMBL11463468 0.73 NR1I2 (0.86) NR1I2PGRTDP1HSD17B10MAPT
Hydrochloric Acid SCHEMBL11481373 0.73 NR1I2 (0.85) NR1I2PGRTDP1HSD17B10MAPT
Hydrochloric Acid SCHEMBL11481370 0.73 NR1I2 (0.85) NR1I2PGRTDP1HSD17B10MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20200222434-A1 THERAPEUTIC USES OF PHARMACEUTICAL COMPOSITIONS COMPRISING CYCLIC BORONIC ACID ESTER DERIVATIVES MELINTA SUBSIDIARY CORP. 2020-07-16 US claimed

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-20200222434-A1 THERAPEUTIC USES OF PHARMACEUTICAL COMPOSITIONS COMPRISING CYCLIC BORONIC ACID ESTER DERIVATIVES BCL6B, BCL6, SLC10A2 NR1I2 3513/4885PGR 199/4885PTGS1 3640/4885

“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.