Homatropine

Homatropine

SCHEMBL10743457

CC(=O)O.CN1[C@@H]2CC[C@H]1C[C@@H](OC(=O)C(O)c1ccccc1)C2

nearest known ligand 0.95

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Homatropine. 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
ADRA2C known ✓ P18825 2/20 0.67
ADRA2A known ✓ P08913 1/20 0.54
ADRA2B known ✓ P18089 1/20 0.54
OPRK1 known ✓ P41145 1/20 0.54
LMNA P02545 4/20 0.95
CYP2D6 P10635 3/20 0.95
CYP2C9 P11712 1/20 0.95
HSD17B10 Q99714 1/20 0.95
CHRM2 P08172 6/20 0.92
CHRM1 P11229 6/20 0.92
CHRM3 P20309 6/20 0.92
CHRM5 P08912 5/20 0.92
CHRM4 P08173 4/20 0.92
BLM P54132 2/20 0.92
SMN1; SMN2 Q16637 1/20 0.92
TDP1 Q9NUW8 1/20 0.92
HTR2C P28335 3/20 0.67
ADRA1A P35348 2/20 0.67
HRH1 P35367 2/20 0.67
ADRA1D P25100 2/20 0.67

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
Homatropine SCHEMBL23468168 0.97 LMNA (1.00) LMNACYP2D6CYP2C9HSD17B10CHRM2
Homatropine SCHEMBL15275620 0.97 LMNA (1.00) LMNACYP2D6CYP2C9HSD17B10CHRM2
Homatropine SCHEMBL23969 0.97 LMNA (1.00) LMNACYP2D6CYP2C9HSD17B10CHRM2
Homatropine SCHEMBL9653008 0.97 LMNA (1.00) LMNACYP2D6CYP2C9HSD17B10CHRM2
Homatropine SCHEMBL23970 0.97 LMNA (1.00) LMNACYP2D6CYP2C9HSD17B10CHRM2
Homatropine SCHEMBL41951 0.96 CHRM2 (1.00) LMNACYP2D6CYP2C9HSD17B10CHRM2
Homatropine SCHEMBL41950 0.96 CHRM2 (1.00) LMNACYP2D6CYP2C9HSD17B10CHRM2
Homatropine SCHEMBL220965 0.96 LMNA (0.97) LMNACYP2D6CYP2C9HSD17B10CHRM2
Homatropine SCHEMBL220964 0.96 LMNA (0.97) LMNACYP2D6CYP2C9HSD17B10CHRM2
Homatropine SCHEMBL14672464 0.95 LMNA (0.95) LMNACYP2D6CYP2C9HSD17B10CHRM2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10351497-B2 Use of a Lewis donor solvent to purify a feedstock that contains ethanol, acetaldehyde, and impurities IFP Energies Nouvelles (FR) 2019-07-16 US disclosed
US-20190144366-A1 USE OF A LEWIS DONOR SOLVENT TO PURIFY A FEEDSTOCK THAT CONTAINS ETHANOL, ACETALDEHYDE, AND IMPURITIES IFP Energies Nouvelles (JP) 2019-05-16 US disclosed
US-10081588-B2 Production of butyl acetate from ethanol RESCURVE, LLC (US) 2018-09-25 US disclosed
CN-105073697-B Production of higher alcohols 雷斯库尔有限责任公司 2017-05-24 CN disclosed
US-20160297737-A1 Production of Butyl Acetate from Ethanol VIRIDIS CHEMICAL, LLC 2016-10-13 US disclosed
US-9018427-B2 Production of higher alcohols GREENYUG, LLC (US) 2015-04-28 US disclosed
US-20140235901-A1 Production of Higher Alcohols GREENYUG, LLC (US) 2014-08-21 US disclosed
US-4656294-A MATRIX RESINS, SEALS MITSUBISHI PETROCHEMICAL CO., LTD. (JP) 1987-04-07 US disclosed
US-4456742-A PROTECTIVE COATING FMC CORPORATION (US) 1984-06-26 US disclosed
US-4093677-A POLYAMIDE-AMINE BLOCK POLYMERS FERRUTI PAOLO 1978-06-06 US disclosed