Ticarcillin

Ticarcillin

SCHEMBL4935408

CC1(C)SC2C(NC(=O)C(C(=O)O)c3ccsc3)C(=O)N2C1C(=O)O.[Na].[Na]

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Ticarcillin. 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
▸ PTGS1 P23219 3/20 0.98
▸ SMN1; SMN2 Q16637 1/20 0.71
▸ KDM4E B2RXH2 7/20 0.61
▸ RECQL P46063 4/20 0.61
▸ TDP1 Q9NUW8 3/20 0.61
▸ POLB P06746 2/20 0.61
▸ MEN1 O00255 2/20 0.61
▸ KMT2A Q03164 2/20 0.61
▸ HPGD P15428 1/20 0.61
▸ TEK Q02763 1/20 0.61
▸ SLC15A2 Q16348 1/20 0.61
▸ LMNA P02545 4/20 0.60
▸ TSHR P16473 1/20 0.60
▸ RARB P10826 1/20 0.59
▸ RARG P13631 1/20 0.59
▸ NR1H2 P55055 1/20 0.59
▸ NR1H3 Q13133 1/20 0.59
▸ NR1I3 Q14994 1/20 0.59
▸ HRH1 P35367 1/20 0.53
▸ SLC22A8 Q8TCC7 1/20 0.53

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
Ticarcillin SCHEMBL10738085 0.99 PTGS1 (1.00) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL5047437 0.99 PTGS1 (1.00) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL10738099 0.99 PTGS1 (1.00) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL34025 0.99 PTGS1 (1.00) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL193733 0.98 PTGS1 (0.98) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL28757995 0.98 PTGS1 (0.98) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL9929365 0.98 PTGS1 (0.98) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL4935398 0.98 PTGS1 (0.98) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL4228859 0.98 PTGS1 (0.98) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL27742456 0.98 PTGS1 (0.98) PTGS1SMN1; SMN2KDM4ERECQLTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20080139545-A1 FORMULATION TO TREAT EAR INFECTION CHOE WON-TAEK 2008-06-12 — — US disclosed
US-20060134226-A1 Compositions useful to treat ocular neovascular diseases and macular degeneration NU-TEIN CO., LTD. 2006-06-22 — — US disclosed
US-20060122282-A1 METHOD FOR TREATING SKIN DISORDERS WITH XANTHOPHYLLS NU-TEIN CO., INC. 2006-06-08 — — US disclosed
US-20050089473-A1 Potassium channel mediated delivery of agents through the blood-brain barrier CEDARS-SINAI MEDICAL CENTER 2005-04-28 — — 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 (3 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-20060134226-A1 Compositions useful to treat ocular neovascular diseases and macular degeneration CFD, VEGFA, CFH PTGS1 668/4885SMN1; SMN2 2277/4885KDM4E 2934/4885
US-20050089473-A1 Potassium channel mediated delivery of agents through the blood-brain barrier KCNN2, KCNN1, KCNN3 PTGS1 1076/4885SMN1; SMN2 759/4885KDM4E 1674/4885
US-20060122282-A1 METHOD FOR TREATING SKIN DISORDERS WITH XANTHOPHYLLS COL1A1, COL2A1, KRT18 PTGS1 908/4885SMN1; SMN2 4229/4885KDM4E 2315/4885

“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.

Send feedback