Amikacin

Amikacin

SCHEMBL15515828

NCC[C@H](O)C(=O)NC1C[C@H](N)[C@@H](O[C@H]2O[C@H](CN)[C@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](N)[C@H]1O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

rplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Amikacin. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 3/20 1.00
▸ ALOX15 P16050 3/20 0.98
▸ RAD52 P43351 1/20 0.98
▸ GJB2 P29033 2/20 0.66
▸ GJA1 P17302 1/20 0.66
▸ MEN1 O00255 1/20 0.66
▸ CYP2C9 P11712 1/20 0.66
▸ TSHR P16473 1/20 0.66
▸ KMT2A Q03164 1/20 0.66
▸ ALDH1A1 P00352 1/20 0.66
▸ MAPT P10636 1/20 0.63
▸ KDM4E B2RXH2 1/20 0.59
▸ HPSE Q9Y251 1/20 0.53
▸ CYP3A4 P08684 1/20 0.53
▸ GAA P10253 1/20 0.52

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
Amikacin SCHEMBL15515830 1.00 LMNA (1.00) LMNAALOX15RAD52GJB2GJA1
Amikacin SCHEMBL20516499 1.00 LMNA (1.00) LMNAALOX15RAD52GJB2GJA1
Amikacin SCHEMBL2637141 1.00 LMNA (1.00) LMNAALOX15RAD52GJB2GJA1
Amikacin SCHEMBL15263372 1.00 LMNA (1.00) LMNAALOX15RAD52GJB2GJA1
Amikacin SCHEMBL23308753 1.00 LMNA (1.00) LMNAALOX15RAD52GJB2GJA1
Amikacin SCHEMBL20522644 1.00 LMNA (1.00) LMNAALOX15RAD52GJB2GJA1
Amikacin SCHEMBL24437395 1.00 LMNA (1.00) LMNAALOX15RAD52GJB2GJA1
Amikacin SCHEMBL13260939 1.00 LMNA (1.00) LMNAALOX15RAD52GJB2GJA1
Amikacin SCHEMBL20516498 1.00 LMNA (1.00) LMNAALOX15RAD52GJB2GJA1
Amikacin SCHEMBL15263403 1.00 LMNA (1.00) LMNAALOX15RAD52GJB2GJA1

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
EP-4633677-A1 VIROPORINS BLOCKERS/INHIBITORS AS ANTI-INFLUENZA AGENTS Yissum Research Development Company of the Hebrew University of Jerusalem Ltd. (IL) 2025-10-22 — — EP disclosed
US-20240299379-A1 COMPOSITIONS OF CLOFAZIMINE AND AMIKACIN FOR PULMONARY ADMINISTRATION IN THE TREATMENT OF RESPIRATORY DISEASES BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM 2024-09-12 — — US disclosed
WO-2024127407-A1 VIROPORINS BLOCKERS/INHIBITORS AS ANTI-INFLUENZA AGENTS YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM LTD. (IL) 2024-06-20 — — WO disclosed
WO-2022256464-A1 COMPOSITIONS OF CLOFAZIMINE AND AMIKACIN FOR PULMONARY ADMINISTRATION IN THE TREATMENT OF RESPIRATORY DISEASES BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2022-12-08 — — WO disclosed
WO-2018182515-A1 METHODS OF MODIFYING FUNGI AND USES THEREOF AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2018-10-04 — — WO disclosed
US-9539222-B2 Methods to inhibit intracellular growth of bacteria and to treat bacteria-mediated diseases AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2017-01-10 — — US disclosed
US-20150209308-A1 METHODS TO INHIBIT INTRACELLULAR GROWTH OF BACTERIA AND TO TREAT BACTERIA-MEDIATED DISEASES AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH 2015-07-30 — — US disclosed
WO-2014039011-A1 METHODS TO INHIBIT INTRACELLULAR GROWTH OF BACTERIA AND TO TREAT BACTERIA-MEDIATED DISEASES AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2014-03-13 — — WO disclosed
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