Ticarcillin

Ticarcillin

SCHEMBL10738085

CC1(C)S[C@@H]2C(NC(=O)C(C(=O)O)c3ccsc3)C(=O)N2[C@H]1C(=O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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 1.00
▸ SMN1; SMN2 Q16637 1/20 0.72
▸ KDM4E B2RXH2 8/20 0.62
▸ RECQL P46063 4/20 0.62
▸ TDP1 Q9NUW8 3/20 0.62
▸ POLB P06746 2/20 0.62
▸ MEN1 O00255 2/20 0.62
▸ KMT2A Q03164 2/20 0.62
▸ HPGD P15428 2/20 0.62
▸ TEK Q02763 1/20 0.62
▸ SLC15A2 Q16348 1/20 0.62
▸ LMNA P02545 4/20 0.61
▸ TSHR P16473 1/20 0.61
▸ RARB P10826 1/20 0.60
▸ RARG P13631 1/20 0.60
▸ NR1H2 P55055 1/20 0.60
▸ NR1H3 Q13133 1/20 0.60
▸ NR1I3 Q14994 1/20 0.60
▸ 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 SCHEMBL10738099 1.00 PTGS1 (1.00) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL34025 1.00 PTGS1 (1.00) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL5047437 1.00 PTGS1 (1.00) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL28757995 0.99 PTGS1 (0.98) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL9929365 0.99 PTGS1 (0.98) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL193733 0.99 PTGS1 (0.98) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL4935398 0.99 PTGS1 (0.98) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL4228859 0.99 PTGS1 (0.98) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL4935408 0.99 PTGS1 (0.98) PTGS1SMN1; SMN2KDM4ERECQLTDP1
Ticarcillin SCHEMBL27742456 0.99 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 29 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0074783-B1 BETA-LACTAMASE INHIBITING 2-BETA-SUBSTITUTED-2-ALPHA-METHYL-(5R) PENAM-3-ALPHA-CARBOXYLIC ACID 1,1-DIOXIDES AND INTERMEDIATES THEREFOR PFIZER INC. (US) 1985-07-31 — — EP claimed
EP-0083977-A1 6-Alpha-hydroxymethylpenicillanic acid sulfone as a beta-lactamase inhibitor PFIZER INC. (US) 1983-07-20 — — EP claimed
EP-0074783-A1 Beta-lactamase inhibiting 2-beta-substituted-2-alpha-methyl-(5R) penam-3-alpha-carboxylic acid 1,1-dioxides and intermediates therefor PFIZER INC. (US) 1983-03-23 — — EP claimed
EP-0008917-B1 PENAM-3-CARBOXYLIC ACID 1,1-DIOXIDES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS PFIZER INC. (US) 1982-11-24 — — EP claimed
US-4287181-A TO ENHANCE THE EFFECTIVENESS OF B-LACTAM ANTIBIOTICS PFIZER INC. (US) 1981-09-01 — — US claimed
US-4256733-A Acetoxymethyl penam compounds as β-lactamase inhibitors PFIZER INC. (US) 1981-03-17 — — US claimed
EP-0008917-A1 Penam-3-carboxylic acid 1,1-dioxides, process for their preparation and pharmaceutical compositions PFIZER INC. (US) 1980-03-19 — — EP claimed
US-4656263-A 6-β-substituted penicillanic acid compound free of the 6-α-epimer PFIZER INC. (US) 1987-04-07 — — US disclosed
EP-0095341-B1 PENICILLANIC ACID DIOXIDE PRODRUG PFIZER INC. (US) 1986-02-26 — — EP disclosed
EP-0074783-B1 BETA-LACTAMASE INHIBITING 2-BETA-SUBSTITUTED-2-ALPHA-METHYL-(5R) PENAM-3-ALPHA-CARBOXYLIC ACID 1,1-DIOXIDES AND INTERMEDIATES THEREFOR PFIZER INC. (US) 1985-07-31 — — EP disclosed
US-4518530-A 6-β-Substituted penicillanic acids as β-lactamase inhibitors PFIZER INC. (US) 1985-05-21 — — US disclosed
US-4517126-A Penicillanic acid derivative PFIZER INC. (US) 1985-05-14 — — US disclosed
EP-0055933-B1 6-(2-ARYL-2-(1,1-DIOXOPENICILLANOYLOXY-METHOXYCARBONYL)ACETAMIDO) PENICILLANIC ACIDS PFIZER INC. (US) 1984-11-28 — — EP disclosed
US-4323499-A 6-(2-Aryl-2-(1,1-dioxopenicillanoyloxy-methoxycarbonyl)acetamido penicillanic acids PFIZER INC. (US) 1982-04-06 — — US disclosed
US-4287181-A TO ENHANCE THE EFFECTIVENESS OF B-LACTAM ANTIBIOTICS PFIZER INC. (US) 1981-09-01 — — US disclosed
US-4256733-A Acetoxymethyl penam compounds as β-lactamase inhibitors PFIZER INC. (US) 1981-03-17 — — US disclosed
US-4241050-A Penam 1,1-dioxides as beta-lactamase inhibitors PFIZER INC. (US) 1980-12-23 — — US disclosed
US-4234579-A Penicillanic acid 1,1-dioxides as β-lactamase inhibitors PFIZER INC. (US) 1980-11-18 — — US disclosed
EP-0008917-A1 Penam-3-carboxylic acid 1,1-dioxides, process for their preparation and pharmaceutical compositions PFIZER INC. (US) 1980-03-19 — — EP disclosed
US-4066664-A Intermediates for preparing α-carboxy-α-(3-thienyl)penicillin and cephalosporin derivatives RECHERCHE ET INDUSTRIE THERAPEUTIQUES (BE) 1978-01-03 — — US disclosed
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