(+)-Menthol

(+)-Menthol

SCHEMBL9968934

CC(C)C1CC[C@@H](C)C[C@@H]1O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

TRPA1TRPM8

The experimentally established mechanism targets of (+)-Menthol. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
TRPM8 known ✓ Q7Z2W7 5/20 1.00
TRPA1 known ✓ O75762 2/20 1.00
EPHX1 P07099 3/20 0.52
ALDH1A1 P00352 1/20 0.41
KCNA5 P22460 1/20 0.39
TRPV1 Q8NER1 3/20 0.38
LMNA P02545 1/20 0.36
OPRM1 P35372 1/20 0.36

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
(+)-Menthol SCHEMBL10072505 1.00 TRPM8 (1.00) TRPM8TRPA1EPHX1ALDH1A1KCNA5
(+)-Menthol SCHEMBL15449169 1.00 TRPM8 (1.00) TRPM8TRPA1EPHX1ALDH1A1KCNA5
Isomenthol SCHEMBL677675 1.00 TRPM8 (1.00) TRPM8TRPA1EPHX1ALDH1A1KCNA5
Racementhol SCHEMBL521946 1.00 TRPM8 (1.00) TRPM8TRPA1EPHX1ALDH1A1KCNA5
(+)-Menthol SCHEMBL1709231 1.00 TRPM8 (1.00) TRPM8TRPA1EPHX1ALDH1A1KCNA5
(+) Neomenthol SCHEMBL260049 1.00 TRPM8 (1.00) TRPM8TRPA1EPHX1ALDH1A1KCNA5
(+)-Menthol SCHEMBL12646785 1.00 TRPM8 (1.00) TRPM8TRPA1EPHX1ALDH1A1KCNA5
(+)-Menthol SCHEMBL13059620 1.00 TRPM8 (1.00) TRPM8TRPA1EPHX1ALDH1A1KCNA5
Menthol SCHEMBL20771511 1.00 TRPM8 (1.00) TRPM8TRPA1EPHX1ALDH1A1KCNA5
(+)-Menthol SCHEMBL2454317 1.00 TRPM8 (1.00) TRPM8TRPA1EPHX1ALDH1A1KCNA5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4540797-A Process for resolution of chiral alcohols or phenols or chiral lactonic compounds ROUSSEL UCLAF (FR) 1985-09-10 US claimed
EP-0004493-B1 ETHERS WHOSE ORGANIC MOIETIES HAVE ASYMMETRIC ATOMS, METHODS FOR THEIR PREPARATION AND THEIR USE FOR THE RESOLUTION OF ALCOHOLS, PHENOLS OR CERTAIN COMPOUNDS WITH A LACTONE STRUCTURE ROUSSEL-UCLAF (FR) 1981-05-06 EP claimed
US-20180169641-A1 BENZO[H]QUINOLINE LIGANDS AND COMPLEXES THEREOF JOHNSON MATTHEY PUBLIC LIMITED COMPANY (GB) 2018-06-21 US disclosed
US-9988331-B2 Method for producing optically active, racemic menthol BASF SE (DE) 2018-06-05 US disclosed
WO-2014125967-A1 3,6-O-CROSSLINKED PYRANOSE COMPOUND, AND PRODUCTION METHOD FOR α-O-PYRANOSIDE 学校法人関西学院 (JP) 2014-08-21 WO disclosed
EP-2329271-B1 METHODS TO IDENTIFY MODULATORS GIVAUDAN SA (CH) 2012-06-20 EP disclosed
US-20110143376-A1 Methods to Identify Modulators GIVAUDAN SA (CH) 2011-06-16 US disclosed
US-20100303935-A1 Medicinal Composition MCGINLEY PARTNERS, LLC (US) 2010-12-02 US disclosed
WO-2010022529-A1 METHODS TO IDENTIFY MODULATORS GIVAUDAN SA (CH) 2010-03-04 WO disclosed
US-4720556-A 3-oxabicyclo-(3,1,0)-hexan-2-ones ROUSSEL UCLAF (FR) 1988-01-19 US disclosed
US-4658043-A Ethers of pantolactone ROUSSEL UCLAF (FR) 1987-04-14 US disclosed
US-4540797-A Process for resolution of chiral alcohols or phenols or chiral lactonic compounds ROUSSEL UCLAF (FR) 1985-09-10 US disclosed
US-4374257-A Novel ethers containing a lactone group and a chiral atom ROUSSEL UCLAF (FR) 1983-02-15 US disclosed
US-4265817-A Novel chiral ethers and their use in resolution of alcohols and phenols ROUSSEL UCLAF (FR) 1981-05-05 US disclosed
EP-0004493-A1 Ethers whose organic moieties have asymmetric atoms, methods for their preparation and their use for the resolution of alcohols, phenols or certain compounds with a lactone structure ROUSSEL-UCLAF (FR) 1979-10-03 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 (2 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-20180169641-A1 BENZO[H]QUINOLINE LIGANDS AND COMPLEXES THEREOF BRD4, NQO1, NQO2 TRPM8 2221/4885TRPA1 1214/4885EPHX1 1734/4885
US-20100303935-A1 Medicinal Composition MUSK, TNNC1, ACHE TRPM8 316/4885TRPA1 143/4885EPHX1 1973/4885

“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.