Benzil

Benzil

SCHEMBL4750330

CS(=O)(=O)O.O=C(C(=O)c1ccccc1)c1ccccc1

nearest known ligand 0.70

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of Benzil. 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
CES2 O00748 12/20 0.70
CES1 P23141 12/20 0.70
RAB9A P51151 1/20 0.54
TSHR P16473 2/20 0.50
KMT2A Q03164 2/20 0.48
MAPT P10636 2/20 0.48
SMN1; SMN2 Q16637 2/20 0.48
LMNA P02545 1/20 0.48
XBP1 P17861 1/20 0.48
ATM Q13315 1/20 0.48
NPSR1 Q6W5P4 1/20 0.48
KDM4E B2RXH2 1/20 0.48
MEN1 O00255 1/20 0.48
CYP3A4 P08684 1/20 0.48
HPGD P15428 1/20 0.48
ALOX15 P16050 1/20 0.48
MAPK1 P28482 1/20 0.48
TDP1 Q9NUW8 1/20 0.48
DAO P14920 1/20 0.48
NAPRT Q6XQN6 1/20 0.48

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
Benzoic Acid SCHEMBL8139336 0.85 TSHR (0.70) CES2CES1TSHRKMT2AMAPT
Benzophenone SCHEMBL27919557 0.85 ALDH1A1 (0.70) RAB9ATSHRKMT2ASMN1; SMN2LMNA
Benzil SCHEMBL5372731 0.84 CES2 (0.78) CES2CES1RAB9ATSHRKMT2A
Benzil SCHEMBL4832229 0.84 CES2 (0.88) CES2CES1RAB9ATSHRMAPT
Benzil SCHEMBL27655380 0.84 CES2 (0.88) CES2CES1RAB9ATSHRMAPT
Benzil SCHEMBL66 0.84 CES2 (1.00) CES2CES1RAB9ATSHRKMT2A
Benzil SCHEMBL28475956 0.84 CES2 (1.00) CES2CES1RAB9ATSHRKMT2A
Benzil SCHEMBL2156589 0.84 CES2 (1.00) CES2CES1RAB9ATSHRKMT2A
Benzil SCHEMBL7142843 0.84 CES2 (1.00) CES2CES1RAB9ATSHRKMT2A
Benzil SCHEMBL9517636 0.84 CES2 (1.00) CES2CES1RAB9ATSHRKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2008129530-A1 GEMCITABINE PRODUCTION PROCESS CHEMAGIS LTD. (IL) 2008-10-30 WO disclosed
US-20080262215-A1 GEMCITABINE PRODUCTION PROCESS CHEMAGIS LTD. (IL) 2008-10-23 US disclosed
WO-2007070804-A2 PROCESS FOR PREPARING GEMCITABINE AND ASSOCIATED INTERMEDIATES CHEMAGIS LTD. (IL) 2007-06-21 WO disclosed
EP-0732338-B1 2,2-Difluoro-3-carbamoyl ribose sulfonate compounds and process for the preparation of beta nucleosides LILLY CO ELI (US) 2002-05-15 EP disclosed
EP-0732338-A1 2,2-Difluoro-3-carbamoyl ribose sulfonate compounds and process for the preparation of beta nucleosides ELI LILLY AND COMPANY (US) 1996-09-18 EP disclosed
US-5521294-A 2,2-difluoro-3-carbamoyl ribose sulfonate compounds and process for the preparation of beta nucleosides ELI LILLY AND COMPANY (US) 1996-05-28 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 (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-20080262215-A1 GEMCITABINE PRODUCTION PROCESS SAMHD1, DCK, DCTD CES2 879/4885CES1 1866/4885RAB9A 2732/4885

“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.