Chloramphenicol

Chloramphenicol

SCHEMBL28607485

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

nearest known ligand 0.97

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 0.97
CYP3A4 P08684 3/20 0.97
TSHR P16473 2/20 0.97
SMN1; SMN2 Q16637 1/20 0.97
ALDH1A1 P00352 1/20 0.97
MARS2 Q96GW9 1/20 0.97
CYP2C19 P33261 1/20 0.97
RPLP1 P05386 1/20 0.88
RPLP0 P05388 1/20 0.88
RPS17 P08708 1/20 0.88
RPSA P08865 1/20 0.88
RPS2 P15880 1/20 0.88
RPL35A P18077 1/20 0.88
RPL7 P18124 1/20 0.88
RPL17 P18621 1/20 0.88
RPS4Y1 P22090 1/20 0.88
RPS3 P23396 1/20 0.88
RPS12 P25398 1/20 0.88
RPL13 P26373 1/20 0.88
RPL10 P27635 1/20 0.88

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 SCHEMBL49057 0.99 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL537158 0.99 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL29557257 0.99 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL28181476 0.99 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL4295048 0.99 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL16111 0.99 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL4262903 0.99 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL11131056 0.97 LMNA (0.97) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL41042 0.97 LMNA (0.97) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL20531030 0.97 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 1 patent. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109182566-B Method for preventing and treating bacterial soft rot of canna edulis ker 广东省农业科学院植物保护研究所 2021-07-20 CN disclosed