Tobramycin

Tobramycin

SCHEMBL7025058

CCC1(c2ccccc2)C(=O)NC(=O)NC1=O.NC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](N)[C@H]3O)[C@H](N)C[C@@H]2N)[C@H](N)C[C@@H]1O

nearest known ligand 0.63

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

rplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmHrpmIrpmJrpmJ2rpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsU

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

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
ALOX15 P16050 2/20 0.63
HPSE Q9Y251 1/20 0.63
CYP3A4 P08684 1/20 0.63
GAA P10253 1/20 0.61
GJB2 P29033 5/20 0.51
GJA1 P17302 2/20 0.51
MEN1 O00255 1/20 0.51
CYP2C9 P11712 1/20 0.51
TSHR P16473 1/20 0.51
KMT2A Q03164 1/20 0.51
ALDH1A1 P00352 1/20 0.51
KDM4E B2RXH2 1/20 0.50
MAPT P10636 1/20 0.49
LMNA P02545 1/20 0.47

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
Tobramycin SCHEMBL28251261 0.81 ALOX15 (0.84) ALOX15HPSECYP3A4GAAGJB2
Tobramycin SCHEMBL1178021 0.80 ALOX15 (0.87) ALOX15HPSECYP3A4GAAGJB2
Tobramycin SCHEMBL19678587 0.79 ALOX15 (1.00) ALOX15HPSECYP3A4GAAGJB2
Tobramycin SCHEMBL15263385 0.79 ALOX15 (1.00) ALOX15HPSECYP3A4GAAGJB2
Tobramycin SCHEMBL17145817 0.79 ALOX15 (1.00) ALOX15HPSECYP3A4GAAGJB2
Tobramycin SCHEMBL3658310 0.79 ALOX15 (1.00) ALOX15HPSECYP3A4GAAGJB2
Tobramycin SCHEMBL12930900 0.79 ALOX15 (1.00) ALOX15HPSECYP3A4GAAGJB2
Tobramycin SCHEMBL22364334 0.79 ALOX15 (1.00) ALOX15HPSECYP3A4GAAGJB2
Tobramycin SCHEMBL20953776 0.79 ALOX15 (1.00) ALOX15HPSECYP3A4GAAGJB2
Tobramycin SCHEMBL17680145 0.79 ALOX15 (1.00) ALOX15HPSECYP3A4GAAGJB2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1273917-B1 Acridinium ester labels having hydrophilic modifiers SIEMENS HEALTHCARE DIAGNOSTICS (US) 2014-05-07 EP disclosed
US-6664043-B2 Detectable chemiluminescent acridinium ester label, comprising an acridinium ester with a hydrophilic modifier BAYER CORPORATION 2003-12-16 US disclosed
US-20030045716-A1 Acridinium ester labels having hydrophilic modifiers SIEMENS HEALTHCARE DIAGNOSTICS INC. 2003-03-06 US disclosed
EP-1273917-A2 Acridinium ester labels having hydrophilic modifiers Bayer Corporation (US) 2003-01-08 EP disclosed
EP-0410645-A2 Automated analytical apparatus and method TECHNICON INSTRUMENTS CORPORATION (US) 1991-01-30 EP 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 (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-20030045716-A1 Acridinium ester labels having hydrophilic modifiers SRM, SMS, ACR ALOX15 4407/4885HPSE 275/4885CYP3A4 1434/4885

“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.