Toluene

Toluene

SCHEMBL10187782

Cc1ccccc1.[B+3].[Cl-].[Cl-].[Cl-]

nearest known ligand 0.85

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Toluene. 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
ACHE known ✓ P22303 5/20 0.85
TSHR P16473 2/20 0.85
LMNA P02545 2/20 0.85
ALOX12 P18054 1/20 0.85
TDP1 Q9NUW8 2/20 0.50
HPGD P15428 2/20 0.48
CES2 O00748 1/20 0.43
CES1 P23141 1/20 0.43
NPSR1 Q6W5P4 1/20 0.42
RAB9A P51151 3/20 0.39
NPC1 O15118 2/20 0.39
POLB P06746 2/20 0.39
HTT P42858 1/20 0.39
MEN1 O00255 1/20 0.39
KMT2A Q03164 1/20 0.39
CYP2C19 P33261 1/20 0.39
NFKB1 P19838 1/20 0.39
NFKB2 Q00653 1/20 0.39
RELA Q04206 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39

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
Toluene SCHEMBL29256383 0.92 ACHE (0.85) ACHETSHRLMNAALOX12TDP1
Toluene SCHEMBL10447461 0.92 ACHE (0.85) ACHETSHRLMNAALOX12TDP1
Toluene SCHEMBL14954009 0.92 ACHE (0.85) ACHETSHRLMNAALOX12TDP1
Toluene SCHEMBL3410328 0.92 ACHE (0.85) ACHETSHRLMNAALOX12TDP1
Toluene SCHEMBL17825900 0.92
Toluene SCHEMBL5718701 0.92 ACHE (0.85) ACHETSHRLMNAALOX12TDP1
Toluene SCHEMBL4067546 0.92 ACHE (0.85) ACHETSHRLMNAALOX12TDP1
Toluene SCHEMBL14953879 0.92 ACHE (0.85) ACHETSHRLMNAALOX12TDP1
Toluene SCHEMBL22471986 0.92 ACHE (0.85) ACHETSHRLMNAALOX12TDP1
Toluene SCHEMBL28987173 0.92 ACHE (0.85) ACHETSHRLMNAALOX12TDP1

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
CN-114751852-B Preparation method of silodosin key intermediate 山西库邦生物医药科技有限公司 2023-09-15 CN claimed
CN-114751852-A Preparation method of key intermediate of silodosin 山西库邦生物医药科技有限公司 2022-07-15 CN claimed
CN-114751852-B Preparation method of silodosin key intermediate 山西库邦生物医药科技有限公司 2023-09-15 CN disclosed
CN-114751852-A Preparation method of key intermediate of silodosin 山西库邦生物医药科技有限公司 2022-07-15 CN disclosed
US-20120245344-A1 GPR119 AGONIST NIPPON CHEMIPHAR CO., LTD. (JP) 2012-09-27 US disclosed
EP-2474540-A1 GPR119 AGONIST Nippon Chemiphar Co., Ltd. (JP) 2012-07-11 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-20120245344-A1 GPR119 AGONIST GPR119, GPR4, GPR55 ACHE 4185/4885TSHR 205/4885LMNA 3326/4885

“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.