Tetracycline

Tetracycline

SCHEMBL4932253

CN(C)[C@@H]1C(O)=C(C(N)=O)C(=O)[C@@]2(O)C(O)=C3C(=O)c4c(O)cccc4[C@](C)(O)[C@H]3C[C@@H]12

nearest known ligand 0.70

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

rplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Tetracycline. 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
▸ MEN1 O00255 8/20 0.70
▸ KMT2A Q03164 8/20 0.70
▸ TDP1 Q9NUW8 7/20 0.70
▸ KDM4E B2RXH2 5/20 0.70
▸ MAPT P10636 5/20 0.70
▸ USP2 O75604 3/20 0.70
▸ LMNA P02545 3/20 0.70
▸ POLB P06746 3/20 0.70
▸ ALDH1A1 P00352 3/20 0.70
▸ RECQL P46063 2/20 0.70
▸ CYP3A4 P08684 1/20 0.70
▸ THRB P10828 4/20 0.69
▸ L3MBTL1 Q9Y468 1/20 0.69
▸ HSD17B10 Q99714 5/20 0.67
▸ CYP1A2 P05177 1/20 0.67
▸ ALOX15 P16050 1/20 0.67
▸ BRCA1 P38398 1/20 0.67
▸ AKR1C3 P42330 1/20 0.58
▸ GAA P10253 2/20 0.54
▸ HIF1A Q16665 2/20 0.54

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
Tetracycline SCHEMBL12856676 1.00 MEN1 (0.70) MEN1KMT2ATDP1KDM4EMAPT
Tetracycline SCHEMBL12356690 1.00 MEN1 (0.70) MEN1KMT2ATDP1KDM4EMAPT
Epitetracycline SCHEMBL19771301 1.00 MEN1 (0.70) MEN1KMT2ATDP1KDM4EMAPT
Tetracycline SCHEMBL2614976 1.00 MEN1 (0.70) MEN1KMT2ATDP1KDM4EMAPT
Tetracycline SCHEMBL16302914 1.00 MEN1 (0.70) MEN1KMT2ATDP1KDM4EMAPT
Tetracycline SCHEMBL13223984 1.00 MEN1 (0.70) MEN1KMT2ATDP1KDM4EMAPT
Tetracycline SCHEMBL6666071 1.00 MEN1 (0.70) MEN1KMT2ATDP1KDM4EMAPT
Tetracycline SCHEMBL4932271 1.00 MEN1 (0.70) MEN1KMT2ATDP1KDM4EMAPT
Tetracycline SCHEMBL21900130 1.00 MEN1 (0.70) MEN1KMT2ATDP1KDM4EMAPT
Tetracycline SCHEMBL12247641 1.00 MEN1 (0.70) MEN1KMT2ATDP1KDM4EMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6861060-B1 Personal care formulations KARMALI, RASHIDA A. 2005-03-01 — — US claimed
EP-1384479-A1 Preventing or reducing photosensitivity and/or phototoxicity reactions to antiinfective medications G.D. SEARLE & CO. (US) 2004-01-28 — — EP claimed
EP-0741570-B1 PREVENTING OR REDUCING PHOTOSENSITIVITY AND/OR PHOTOTOXICITY REACTIONS TO ANTIINFECTIVE MEDICATIONS SEARLE & CO (US) 2003-05-07 — — EP claimed
US-6172069-B1 CONTROLLING TIME OF ADMINISTERING G. D. SEARLE & COMPANY 2001-01-09 — — US claimed
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-20050089473-A1 Potassium channel mediated delivery of agents through the blood-brain barrier CEDARS-SINAI MEDICAL CENTER 2005-04-28 — — US disclosed
EP-1384479-A1 Preventing or reducing photosensitivity and/or phototoxicity reactions to antiinfective medications G.D. SEARLE & CO. (US) 2004-01-28 — — EP disclosed
EP-0741570-B1 PREVENTING OR REDUCING PHOTOSENSITIVITY AND/OR PHOTOTOXICITY REACTIONS TO ANTIINFECTIVE MEDICATIONS SEARLE & CO (US) 2003-05-07 — — EP disclosed
US-20020042394-A1 Cobalamin compounds useful as antibiotic agents and as imaging agents HOGENKAMP HENRICUS P C (US) 2002-04-11 — — US disclosed
US-5668134-A LOMEFLOXACIN HYDROCHLORIDE G. D. SEARLE & CO. (US) 1997-09-16 — — 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 MEN1 1965/4885KMT2A 4258/4885TDP1 3879/4885
US-20050089473-A1 Potassium channel mediated delivery of agents through the blood-brain barrier KCNN2, KCNN1, KCNN3 MEN1 437/4885KMT2A 572/4885TDP1 3850/4885
US-20020042394-A1 Cobalamin compounds useful as antibiotic agents and as imaging agents MMAB, BLVRB, AHCY MEN1 54/4885KMT2A 4042/4885TDP1 4061/4885

“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.

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