Ampicillin

Ampicillin

SCHEMBL3467975

CC1(C)S[C@@H]2[C@H](NC(=O)C(N)c3ccccc3)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 Ampicillin. 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
KDM4E B2RXH2 10/20 1.00
RECQL P46063 4/20 1.00
HPGD P15428 4/20 1.00
TDP1 Q9NUW8 3/20 1.00
POLB P06746 2/20 1.00
MEN1 O00255 1/20 1.00
KMT2A Q03164 1/20 1.00
TEK Q02763 1/20 1.00
SLC15A2 Q16348 1/20 1.00
LMNA P02545 6/20 0.98
TSHR P16473 2/20 0.98
RARB P10826 1/20 0.84
RARG P13631 1/20 0.84
NR1H2 P55055 1/20 0.84
NR1H3 Q13133 1/20 0.84
NR1I3 Q14994 1/20 0.84
CYP3A4 P08684 5/20 0.82
HSD17B10 Q99714 2/20 0.82
GLA P06280 1/20 0.82
BLM P54132 1/20 0.82

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
Ampicillin SCHEMBL14148474 1.00 KDM4E (1.00) KDM4ERECQLHPGDTDP1POLB
Ampicillin SCHEMBL11985596 1.00 KDM4E (1.00) KDM4ERECQLHPGDTDP1POLB
Ampicillin SCHEMBL9528765 1.00 KDM4E (1.00) KDM4ERECQLHPGDTDP1POLB
Ampicillin SCHEMBL2282070 1.00 KDM4E (1.00) KDM4ERECQLHPGDTDP1POLB
Ampicillin SCHEMBL13014516 1.00 KDM4E (1.00) KDM4ERECQLHPGDTDP1POLB
Ampicillin SCHEMBL24312533 1.00 KDM4E (1.00) KDM4ERECQLHPGDTDP1POLB
Ampicillin SCHEMBL13240124 1.00 KDM4E (1.00) KDM4ERECQLHPGDTDP1POLB
Ampicillin SCHEMBL15577318 1.00 KDM4E (1.00) KDM4ERECQLHPGDTDP1POLB
Ampicillin SCHEMBL22380861 1.00 KDM4E (1.00) KDM4ERECQLHPGDTDP1POLB
Ampicillin SCHEMBL13007617 1.00 KDM4E (1.00) KDM4ERECQLHPGDTDP1POLB

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 214 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3498717-B1 COMPOSITION FOR HARDENING SOFT TISSUE CATHOLIC UNIV KOREA IND ACADEMIC COOPERATION FOUNDATION (KR) 2022-05-04 EP claimed
US-20200339601-A1 Composition for Hardening Soft Tissue THE CATHOLIC UNIVERSITY OF KOREA INDUSTRY-ACADEMIC COOPERATION FOUNDATION (KR) 2020-10-29 US claimed
US-10745417-B2 Composition for hardening soft tissue THE CATHOLIC UNIVERSITY OF KOREA INDUSTRY-ACADEMIC COOPERATION FOUNDATION (KR) 2020-08-18 US claimed
US-20190315770-A1 COMPOSITION FOR HARDENING SOFT TISSUE SONY SEMICONDUCTOR SOLUTIONS CORPORATION (JP) 2019-10-17 US claimed
EP-3498717-A1 COMPOSITION FOR HARDENING SOFT TISSUE The Catholic University of Korea Industry-Academic Cooperation Foundation (KR) 2019-06-19 EP claimed
WO-2018030840-A1 COMPOSITION FOR HARDENING SOFT TISSUE 가톨릭대학교 산학협력단 2018-02-15 WO claimed
WO-2010078258-A1 COMPOUNDS COMPRISING TWO OR MORE BIOLOGICALLY FUNCTIONAL IONS AND METHOD OF TREATING PARKINSON'S DISEASE THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ALABAMA (US) 2010-07-08 WO claimed
EP-0294789-B1 Process for preparing 6-/D(-)-Alpha-(4-ethyl-2,3-dioxo-1-piperazine-carboxamido)-phenylacetamido/pennicillanic acid KRKA TOVARNA ZDRAVIL (YU) 1994-10-12 EP claimed
EP-0317484-B1 N,N'-carboxyl-bis-(4-ethyl-2,3-dioxo)-piperazine, process for the preparation thereof and use thereof GEMA SA (ES) 1994-03-16 EP claimed
US-5015736-A Piperazine intermediates GEMA, S.A. (ES) 1991-05-14 US 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
EP-0014651-B1 TALAMPICILLIN 2-METHOXYPHENOXY ACETATE, PROCESS FOR ITS PREPARATION AND MEDICAMENTS CONTAINING IT SANOFI S.A. (FR) 1982-08-04 EP claimed
US-4293560-A BACTERICIDES, ANTIBIOTICS C M INDUSTRIES (FR) 1981-10-06 US claimed
US-4287181-A TO ENHANCE THE EFFECTIVENESS OF B-LACTAM ANTIBIOTICS PFIZER INC. (US) 1981-09-01 US claimed
US-4260598-A ADMINISTERING 6-AMINOPENICILLANIC ACID 1,1-DIOXIDE OR ESTERS THEREOF PFIZER INC. (US) 1981-04-07 US claimed
US-4256733-A Acetoxymethyl penam compounds as β-lactamase inhibitors PFIZER INC. (US) 1981-03-17 US claimed
US-4241050-A Penam 1,1-dioxides as beta-lactamase inhibitors PFIZER INC. (US) 1980-12-23 US claimed
US-4234579-A Penicillanic acid 1,1-dioxides as β-lactamase inhibitors PFIZER INC. (US) 1980-11-18 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-3941773-A CRYSTALLINE BRISTOL-MYERS COMPANY (US) 1976-03-02 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 (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-20200339601-A1 Composition for Hardening Soft Tissue PNLIP, AMY2A, RNASE1 KDM4E 2054/4885RECQL 890/4885HPGD 115/4885
US-20190315770-A1 COMPOSITION FOR HARDENING SOFT TISSUE PNLIP, AMY2A, RNASE1 KDM4E 2054/4885RECQL 890/4885HPGD 115/4885
US-10745417-B2 Composition for hardening soft tissue PNLIP, AMY2A, RNASE1 KDM4E 2054/4885RECQL 890/4885HPGD 115/4885

“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.