SCHEMBL1840317

SCHEMBL1840317

CCCCCCCCN(CCCCCCCC)c1ccccc1O

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.44
TP53 P04637 1/20 0.44
MEN1 O00255 1/20 0.42
MAPT P10636 1/20 0.42
HTT P42858 1/20 0.42
KMT2A Q03164 1/20 0.42
ATM Q13315 1/20 0.42
NAAA Q02083 1/20 0.41
LMNA P02545 1/20 0.41
KCNH2 Q12809 1/20 0.41
DRD2 P14416 2/20 0.41
OPRM1 P35372 2/20 0.41
DRD3 P35462 2/20 0.41
OPRD1 P41143 2/20 0.41
OPRK1 P41145 2/20 0.41
NPC1 O15118 1/20 0.41
JAK2 O60674 1/20 0.41
RAB9A P51151 1/20 0.41
PAX8 Q06710 1/20 0.41
SERPINE1 P05121 1/20 0.40

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
SCHEMBL1835429 1.00 ALDH1A1 (0.44) ALDH1A1TP53MEN1MAPTHTT
SCHEMBL1836466 1.00 ALDH1A1 (0.44) ALDH1A1TP53MEN1MAPTHTT
SCHEMBL1838702 1.00 ALDH1A1 (0.44) ALDH1A1TP53MEN1MAPTHTT
SCHEMBL1838513 1.00 ALDH1A1 (0.44) ALDH1A1TP53MEN1MAPTHTT
SCHEMBL1838977 1.00 ALDH1A1 (0.44) ALDH1A1TP53MEN1MAPTHTT
SCHEMBL30368111 1.00 ALDH1A1 (0.44) ALDH1A1TP53MEN1MAPTHTT
SCHEMBL1839177 1.00 ALDH1A1 (0.44) ALDH1A1TP53MEN1MAPTHTT
SCHEMBL6882362 0.98 LMNA (0.43) ALDH1A1TP53MEN1MAPTHTT
SCHEMBL1834459 0.98 LMNA (0.42) ALDH1A1TP53MEN1MAPTHTT
SCHEMBL6881608 0.96 ALDH1A1 (0.42) ALDH1A1TP53MEN1MAPTHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3959297-B1 LUBRICANT COMPOSITION AND USE AS A LUBRICANT ADDITIVE OF GUANIDINIUM-BASED IONIC LIQUIDS TOTALENERGIES ONETECH (FR) 2024-06-26 EP claimed
CN-113728080-B Lubricant composition and use of guanidinium-based ionic liquids as lubricant additives 道达尔销售服务公司 2022-10-28 CN claimed
EP-3959297-A1 LUBRICANT COMPOSITION AND USE AS A LUBRICANT ADDITIVE OF GUANIDINIUM-BASED IONIC LIQUIDS Total Marketing Services (FR) 2022-03-02 EP claimed
CN-113728080-A Lubricant composition and use of guanidinium-based ionic liquids as lubricant additives 道达尔销售服务公司 2021-11-30 CN claimed
WO-2020216655-A1 LUBRICANT COMPOSITION AND USE AS A LUBRICANT ADDITIVE OF GUANIDINIUM-BASED IONIC LIQUIDS TOTAL MARKETING SERVICES (FR) 2020-10-29 WO claimed
EP-4416251-A1 CARBODIIMIDE FOR USE AS AN ADDITIVE IN LUBRICANTS INTENDED FOR DRIVE DEVICE SYSTEMS FOR IMPROVED ELASTOMER COMPATIBILITY TotalEnergies OneTech (FR) 2024-08-21 EP disclosed
EP-3959297-B1 LUBRICANT COMPOSITION AND USE AS A LUBRICANT ADDITIVE OF GUANIDINIUM-BASED IONIC LIQUIDS TOTALENERGIES ONETECH (FR) 2024-06-26 EP disclosed
CN-118251483-A Carbodiimides as additives for improving compatibility with elastomers in lubricants intended for motorized systems 道达尔能源万泰克公司 2024-06-25 CN disclosed
US-11905485-B2 Lubricant composition and use as a lubricant additive of guanidinium-based ionic liquids TOTAL MARKETING SERVICES (FR) 2024-02-20 US disclosed
WO-2023061899-A1 CARBODIIMIDE FOR USE AS AN ADDITIVE IN LUBRICANTS INTENDED FOR DRIVE DEVICE SYSTEMS FOR IMPROVED ELASTOMER COMPATIBILITY TOTALENERGIES ONETECH (FR) 2023-04-20 WO disclosed
CN-113728080-B Lubricant composition and use of guanidinium-based ionic liquids as lubricant additives 道达尔销售服务公司 2022-10-28 CN disclosed
EP-3838892-B1 METHOD FOR PRODUCING ISOCYANATE ASAHI CHEMICAL IND (JP) 2022-10-12 EP disclosed
US-20140194644-A1 N-Substituted Carbamic Acid Ester Production Method, Isocyanate Production Method Using Such N-Substituted Carbamic Acid Ester, and Composition for Transfer and Storage of N-Substituted Carbamic Acid Ester Comprising N-Substituted Carbamic Acid Ester and Aromatic Hydroxy Compound ASAHI KASEI CHEMICALS CORPORATION (JP) 2014-07-10 US disclosed
US-20140194650-A1 N-Substituted Carbamic Acid Ester Production Method, Isocyanate Production Method Using Such N-Substituted Carbamic Acid Ester, and Composition for Transfer and Storage of N-Substituted Carbamic Acid Ester Comprising N-Substituted Carbamic Acid Ester and Aromatic Hydroxy Compound ASAHI KASEI CHEMICALS CORPORATION (JP) 2014-07-10 US disclosed
US-8658819-B2 N-substituted carbamic acid ester production method, isocyanate production method using such N-substituted carbamic acid ester, and composition for transfer and storage of N-substituted carbamic acid ester comprising N-substituted carbamic acid ester and aromatic hydroxy compound ASAHI KASEI CHEMICALS CORPORATION (JP) 2014-02-25 US disclosed
US-20110160476-A1 N-Substituted Carbamic Acid Ester Production Method and Isocyanate Production Method Using the N-Substituted Carbamic Acid Ester ASAHI KASEI CHEMICALS CORPORATION (JP) 2011-06-30 US disclosed
CN-102105439-A Method for producing N-substituted carbamate and method for producing isocyanate using the N-substituted carbamate ASAHI KASEI CHEMICALS CORP (JP) 2011-06-22 CN disclosed
US-20110133121-A1 N-Substituted Carbamic Acid Ester Production Method, Isocyanate Production Method Using Such N-Substituted Carbamic Acid Ester, And Composition For Transfer And Storage Of N-Substituted Carbamic Acid Ester Comprising N-Substituted Carbamic Acid Ester and Aromatic Hydroxy Compound ASAHI KASEI CHEMICALS CORPORATION (JP) 2011-06-09 US disclosed
EP-2322504-A1 PROCESS FOR THE PREPARATION OF N-SUBSTITUTED CARBAMIC ACID ESTER AND PROCESS FOR THE PREPARATION OF ISOCYANATE USING THE N-SUBSTITUTED CARBAMIC ACID ESTER Asahi Kasei Chemicals Corporation (JP) 2011-05-18 EP disclosed
US-4691057-A Process for making alkali metal aryloxides ETHYL CORPORATION (US) 1987-09-01 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 (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-20110133121-A1 N-Substituted Carbamic Acid Ester Production Method, Isocyanate Production Method Using Such N-Substituted Carbamic Acid Ester, And Composition For Transfer And Storage Of N-Substituted Carbamic Acid Ester Comprising N-Substituted Carbamic Acid Ester and Aromatic Hydroxy Compound CPS1, ALKBH3, RCC1 ALDH1A1 1568/4885TP53 2326/4885MEN1 1225/4885
US-20140194650-A1 N-Substituted Carbamic Acid Ester Production Method, Isocyanate Production Method Using Such N-Substituted Carbamic Acid Ester, and Composition for Transfer and Storage of N-Substituted Carbamic Acid Ester Comprising N-Substituted Carbamic Acid Ester and Aromatic Hydroxy Compound CPS1, ALKBH3, RCC1 ALDH1A1 1568/4885TP53 2326/4885MEN1 1225/4885
US-20110160476-A1 N-Substituted Carbamic Acid Ester Production Method and Isocyanate Production Method Using the N-Substituted Carbamic Acid Ester ALKBH3, CPS1, APEH ALDH1A1 574/4885TP53 3837/4885MEN1 1966/4885
US-20140194644-A1 N-Substituted Carbamic Acid Ester Production Method, Isocyanate Production Method Using Such N-Substituted Carbamic Acid Ester, and Composition for Transfer and Storage of N-Substituted Carbamic Acid Ester Comprising N-Substituted Carbamic Acid Ester and Aromatic Hydroxy Compound CPS1, ALKBH3, RCC1 ALDH1A1 1568/4885TP53 2326/4885MEN1 1225/4885

“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.