SCHEMBL464850

SCHEMBL464850

CC1CCC(C(C)C)C(C(=O)O)C1

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EPHX1 P07099 3/20 0.70
TRPM8 Q7Z2W7 5/20 0.53
TRPA1 O75762 2/20 0.53
SLC1A2 P43004 3/20 0.42
SLC1A1 P43005 2/20 0.42
KCNA5 P22460 1/20 0.41
TRPV1 Q8NER1 3/20 0.41
CYP2C9 P11712 1/20 0.39
CYP2C19 P33261 1/20 0.39
GRM8 O00222 1/20 0.39
GRM6 O15303 1/20 0.39
LMNA P02545 1/20 0.39
APEX1 P27695 1/20 0.39
GRM5 P41594 1/20 0.39
PMP22 Q01453 1/20 0.39
GRM1 Q13255 1/20 0.39
GRM2 Q14416 1/20 0.39
GRM3 Q14832 1/20 0.39
GRM4 Q14833 1/20 0.39
KDM4E B2RXH2 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
SCHEMBL3958539 1.00 EPHX1 (0.70) EPHX1TRPM8TRPA1SLC1A2SLC1A1
SCHEMBL1150651 1.00 EPHX1 (0.70) EPHX1TRPM8TRPA1SLC1A2SLC1A1
SCHEMBL10001722 1.00 EPHX1 (0.70) EPHX1TRPM8TRPA1SLC1A2SLC1A1
SCHEMBL3958542 1.00 EPHX1 (0.70) EPHX1TRPM8TRPA1SLC1A2SLC1A1
SCHEMBL6128484 1.00 EPHX1 (0.70) EPHX1TRPM8TRPA1SLC1A2SLC1A1
SCHEMBL10034575 1.00 EPHX1 (0.70) EPHX1TRPM8TRPA1SLC1A2SLC1A1
SCHEMBL12381602 1.00 EPHX1 (0.70) EPHX1TRPM8TRPA1SLC1A2SLC1A1
SCHEMBL2637678 1.00 EPHX1 (0.70) EPHX1TRPM8TRPA1SLC1A2SLC1A1
Hydrochloric Acid SCHEMBL21331609 0.98 EPHX1 (0.68) EPHX1TRPM8TRPA1SLC1A2SLC1A1
Hydrochloric Acid SCHEMBL291654 0.98 EPHX1 (0.68) EPHX1TRPM8TRPA1SLC1A2SLC1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-121574047-A Continuous flow preparation method of menthyl formic acid 安徽丰乐香料有限责任公司 2026-02-27 CN claimed
CN-119930456-A Method for preparing N-ethyl-L-menthyl formamide by continuous flow technology 安徽科芯微流化工科技有限公司 2025-05-06 CN claimed
US-20250108023-A1 Products for Masking Bitterness The Third People's Hospital of Henan Province (CN) 2025-04-03 US claimed
CN-119345083-A Formula and preparation method of medlar fluffy hair washing cream free of irritation and capable of controlling cooling oil 宁夏贵合源生物科技发展有限公司 2025-01-24 CN claimed
CN-117945886-B Synthesis method of WS series cooling agent key intermediate menthyl formic acid 江苏宏邦化工科技有限公司 2024-12-06 CN claimed
CN-119080629-A Menthol amide cooling agent WS-5 and preparation method thereof 辽宁友之泰医药科技有限公司 2024-12-06 CN claimed
CN-115806481-B Separation and purification method of L-menthyl formic acid 安徽丰乐香料有限责任公司 2024-11-22 CN claimed
CN-118829416-A Composition (III) 西姆莱斯股份公司 2024-10-22 CN claimed
CN-117945886-A Synthesis method of WS series cooling agent key intermediate menthyl formic acid 江苏宏邦化工科技有限公司 2024-04-30 CN claimed
CN-117813077-A Composition and method for producing the same 西姆莱斯股份公司 2024-04-02 CN claimed
US-20060116277-A1 Method for the preparation of high-content NaY molecular sieves synthesized from kaolin sprayed microspheres PETROCHINA COMPANY LIMITED 2006-06-01 US claimed
EP-1656144-A2 TRP-P8 ACTIVE COMPOUNDS AND THERAPEUTIC TREATMENT METHODS Genentech, Inc. (US) 2006-05-17 EP claimed
WO-2005117811-A2 PHYSIOLOGICAL COOLING COMPOSITIONS MILLENNIUM SPECIALTY CHEMICALS (US) 2005-12-15 WO claimed
US-20050265930-A1 Physiological cooling compositions RENESSENZ LLC 2005-12-01 US claimed
WO-2005097735-A1 PHYSIOLOGICAL COOLING COMPOSITIONS CONTAINING HIGHLY PURIFIED ETHYL ESTER OF N-[[5-METHYL-2-(1-METHYLETHYL)CYCLOHEXYL)CARBONYL]GLYCINE MILLENNIUM SPECIALTY CHEMICALS (US) 2005-10-20 WO claimed
US-20050222256-A1 Physiological cooling compositions containing highly purified ethyl ester of N-[[5-methyl-2-(1-methylethyl)cyclohexyl] carbonyl]glycine PINOVA HOLDINGS, INC 2005-10-06 US claimed
US-20050159394-A1 Aryl-substituted derivatives of cycloalkyl and branched chain alkyl carboxylic acids useful as antinociceptive drugs for peripheral targets WEI EDWARD T (US) 2005-07-21 US claimed
US-20050090514-A1 Trp-p8 active compounds and therapeutic treatment methods GENENTECH, INC. 2005-04-28 US claimed
WO-2005002582-A2 TRP-P8 ACTIVE COMPOUNDS AND THERAPEUTIC TREATMENT METHODS GENENTECH, INC. (US) 2005-01-13 WO claimed
US-4157384-A Compositions having a physiological cooling effect WILKINSON SWORD LIMITED (GB) 1979-06-05 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 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-20050265930-A1 Physiological cooling compositions LDHA, HADHA, PC EPHX1 1239/4885TRPM8 119/4885TRPA1 751/4885
US-20050222256-A1 Physiological cooling compositions containing highly purified ethyl ester of N-[[5-methyl-2-(1-methylethyl)cyclohexyl] carbonyl]glycine GNMT, GLS, GPR18 EPHX1 697/4885TRPM8 528/4885TRPA1 1529/4885
US-20050090514-A1 Trp-p8 active compounds and therapeutic treatment methods TSG101, TP53, BAX EPHX1 1033/4885TRPM8 28/4885TRPA1 80/4885
US-20050159394-A1 Aryl-substituted derivatives of cycloalkyl and branched chain alkyl carboxylic acids useful as antinociceptive drugs for peripheral targets OPRL1, OPRK1, OPRD1 EPHX1 3744/4885TRPM8 588/4885TRPA1 21/4885

“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.