Chloramphenicol

Chloramphenicol

SCHEMBL4262903

O=C(N[C@H](CO)[C@H](O)c1ccc([N+](=O)[O-])cc1)C(Cl)Cl.O=C(N[C@H](CO)[C@H](O)c1ccc([N+](=O)[O-])cc1)C(Cl)Cl

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 Chloramphenicol. 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
LMNA P02545 4/20 1.00
CYP3A4 P08684 3/20 1.00
TSHR P16473 2/20 1.00
SMN1; SMN2 Q16637 1/20 1.00
ALDH1A1 P00352 1/20 1.00
MARS2 Q96GW9 1/20 1.00
CYP2C19 P33261 1/20 1.00
RPLP1 P05386 1/20 0.90
RPLP0 P05388 1/20 0.90
RPS17 P08708 1/20 0.90
RPSA P08865 1/20 0.90
RPS2 P15880 1/20 0.90
RPL35A P18077 1/20 0.90
RPL7 P18124 1/20 0.90
RPL17 P18621 1/20 0.90
RPS4Y1 P22090 1/20 0.90
RPS3 P23396 1/20 0.90
RPS12 P25398 1/20 0.90
RPL13 P26373 1/20 0.90
RPL10 P27635 1/20 0.90

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
Chloramphenicol SCHEMBL28181476 1.00 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL49057 1.00 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL16111 1.00 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL29557257 1.00 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL4295048 1.00 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL537158 1.00 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL11131056 0.99 LMNA (0.97) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL41042 0.99 LMNA (0.97) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL20531030 0.99 LMNA (0.97) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL28607485 0.99 LMNA (0.97) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10550384-B2 Methods for selecting microbes from a diverse genetically modified library to detect and optimize the production of metabolites PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2020-02-04 US claimed
US-20180127746-A1 Production and Monitoring of Metabolites in Cells UNITED STATES DEPARTMENT OF ENERGY 2018-05-10 US claimed
US-11774442-B2 Molecule sensor systems ENEVOLV, INC. (US) 2023-10-03 US disclosed
US-11603528-B2 Methods for selecting microbes from a diverse genetically modified library to detect and optimize the production of metabolites PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2023-03-14 US disclosed
US-11365410-B2 Production and monitoring of metabolites in cells PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2022-06-21 US disclosed
EP-3108003-B1 DE NOVO DESIGN OF ALLOSTERIC PROTEINS HARVARD COLLEGE (US) 2022-02-09 EP disclosed
US-10920217-B2 De novo design of allosteric proteins PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2021-02-16 US disclosed
US-20200216835-A1 Methods For Selecting Microbes From A Diverse Genetically Modified Library to Detect and Optimize the Production of Metabolites U.S. DEPARTMENT OF ENERGY 2020-07-09 US disclosed
US-20200123531-A1 De Novo Design of Allosteric Proteins PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2020-04-23 US disclosed
US-10550384-B2 Methods for selecting microbes from a diverse genetically modified library to detect and optimize the production of metabolites PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2020-02-04 US disclosed
CN-110161099-A Using titanium dioxide nano-rod composite material as the construction method of the electrochemical aptamer sensor of electrochemistry tracer 河南大学 2019-08-23 CN disclosed
US-20170132358-A1 De Novo Design of Allosteric Proteins UNITED STATES DEPARTMENT OF ENERGY 2017-05-11 US disclosed
US-20160017317-A1 Methods For Selecting Microbes From A Diverse Genetically Modified Library to Detect and Optimize the Production of Metabolites ENERGY, UNITED STATES DEPARTMENT OF 2016-01-21 US disclosed
EP-2102363-A2 ASSAYS FOR FUNGAL INFECTION The University of Manchester (GB) 2009-09-23 EP disclosed
WO-2008063370-A9 ASSAYS FOR FUNGAL INFECTION UNIV MANCHESTER (GB) 2008-07-31 WO disclosed
WO-2008063370-A2 ASSAYS FOR FUNGAL INFECTION THE UNIVERSITY OF MANCHESTER (GB) 2008-05-29 WO disclosed
EP-0970065-A4 ANTIBIOTICS AND PROCESS FOR PREPARATION TRUETT WILLIAM L (US) 2001-03-07 EP disclosed
EP-0970065-A1 ANTIBIOTICS AND PROCESS FOR PREPARATION Truett, William L. (US) 2000-01-12 EP disclosed
WO-1999028308-A1 ANTIBIOTICS AND PROCESS FOR PREPARATION TRUETT WILLIAM L (US) 1999-06-10 WO disclosed
US-5693791-A PENICILLINS AND CEPHALOSPORINS LINKED TO METRONIDAZOLE TO PRODUCE ANTIBIOTICS WITH NEW PROPERTIES TRUETT WILLIAM L (US) 1997-12-02 US disclosed