SCHEMBL69360

SCHEMBL69360

CCOC(=O)Nc1ccccc1C

nearest known ligand 0.71

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 2/20 0.71
RAB9A P51151 2/20 0.71
SMN1; SMN2 Q16637 2/20 0.67
ALDH1A1 P00352 4/20 0.66
HPGD P15428 3/20 0.66
MAPT P10636 1/20 0.61
L3MBTL1 Q9Y468 1/20 0.61
NLRP3 Q96P20 1/20 0.60
CYP1A2 P05177 1/20 0.59
CYP2C9 P11712 1/20 0.59
CYP2C19 P33261 1/20 0.59
GAA P10253 2/20 0.57
MEN1 O00255 1/20 0.56
KMT2A Q03164 1/20 0.56
LMNA P02545 1/20 0.56
DHODH Q02127 1/20 0.55
ALOX12 P18054 1/20 0.54

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
SCHEMBL30593915 1.00 NPC1 (0.71) NPC1RAB9ASMN1; SMN2ALDH1A1HPGD
Urethane SCHEMBL10734204 0.92 NPC1 (0.61) NPC1RAB9ASMN1; SMN2ALDH1A1HPGD
SCHEMBL28401182 0.90 ALDH1A1 (0.72) NPC1RAB9ASMN1; SMN2ALDH1A1HPGD
SCHEMBL26588350 0.89 NLRP3 (0.78) NPC1RAB9ASMN1; SMN2ALDH1A1HPGD
SCHEMBL17856292 0.88 NPC1 (0.65) NPC1RAB9ASMN1; SMN2ALDH1A1HPGD
SCHEMBL7921939 0.87 NPC1 (0.56) NPC1RAB9ASMN1; SMN2ALDH1A1HPGD
SCHEMBL840955 0.86 ALDH1A1 (0.59) NPC1RAB9ASMN1; SMN2ALDH1A1HPGD
SCHEMBL1955909 0.86 NLRP3 (0.80) NPC1RAB9ASMN1; SMN2ALDH1A1HPGD
SCHEMBL13506223 0.85 SMN1; SMN2 (0.68) NPC1RAB9ASMN1; SMN2ALDH1A1HPGD
SCHEMBL1601240 0.85 NPC1 (0.57) NPC1RAB9ASMN1; SMN2ALDH1A1HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4162362-A CONDESATION OF N-ARYL CARBAMIC ACID ESTER WITH FORMALDEHYDE IN THE PRESENCE OF A SULFONIC ACID ATLANTIC RICHFIELD COMPANY (US) 1979-07-24 US claimed
EP-3044190-B1 BURN RATE MODIFIER THALES AUSTRALIA LTD (AU) 2024-07-03 EP disclosed
CN-112020493-B Method for producing urethane and method for producing isocyanate 旭化成株式会社 2023-04-21 CN disclosed
EP-3720833-A1 PROPELLANT CHARGE Nederlandse Organisatie voor toegepast- natuurwetenschappelijk Onderzoek TNO (NL) 2020-10-14 EP disclosed
EP-3621952-A1 METHOD FOR THE PRODUCTION OF PHENYLGUANIDINES OR THE SALTS THEREOF AlzChem Trostberg GmbH (DE) 2020-03-18 EP disclosed
EP-3044191-B1 BURN RATE MODIFIER THALES AUSTRALIA LTD (AU) 2019-11-20 EP disclosed
US-20190210938-A1 PROPELLANT STABILIZER THALES AUSTRALIA LIMITED (AU) 2019-07-11 US disclosed
WO-2019112437-A1 PROPELLANT CHARGE NEDERLANDSE ORGANISATIE VOOR TOEGEPAST-NATUURWETENSCHAPPELIJK ONDERZOEK TNO (NL) 2019-06-13 WO disclosed
CN-109641835-A Method for producing carbamate 国立研究开发法人产业技术综合研究所 2019-04-16 CN disclosed
US-10196323-B2 Burn rate modifier THALES AUSTRALIA LIMITED (AU) 2019-02-05 US disclosed
US-4278805-A FROM AROMATIC AMINE, CARBAMATE AND ALCOHOL; METAL COMPOUND CATALYST BASF AKTIENGESELLSCHAFT (DE) 1981-07-14 US disclosed
EP-0027954-A1 Process for preparing urethanes and their use in the preparation of isocyanates BAYER AG (DE) 1981-05-06 EP disclosed
US-4266070-A CARBONYLS OF COBALT, MOLYBDENUM, TITANIUM, RHODIUM, IRON, NICKEL AND IRIDIUM AS CATALYSTS FOR THE CARBONYLATION OF PRIMARY OR SECONDARY AMINES AND ALCOHOLS TO FORM CARBAMATES HALCON RESEARCH AND DEVELOPMENT CORP. (US) 1981-05-05 US disclosed
US-4259511-A Process for separating selenium, selenium compounds, sulfur and/or sulfur compounds from polyurethanes containing these elements and/or compounds BAYER AKTIENGESELLSCHAFT (DE) 1981-03-31 US disclosed
US-4243815-A Preparation of methylene-bis(4-phenylcarbamic acid esters) BASF AKTIENGESELLSCHAFT (DE) 1981-01-06 US disclosed
US-4230877-A ACID CATALYZED CONDENSATION OF AN N-ARYL CARBAMIC ACID ESTER WITH A CARBONYL COMPOUND ATLANTIC RICHFIELD COMPANY (US) 1980-10-28 US disclosed
EP-0014406-A1 Process for the separation of selenium, selenium compounds, sulfur and/or sulfur compounds from urethanes containing these elements and/or compounds BAYER AG (DE) 1980-08-20 EP disclosed
US-4151154-A COUPLERS, SURFACTANTS UNION CARBIDE CORPORATION (US) 1979-04-24 US disclosed
US-4136080-A REINFORCED WITH A SILANE - TREATED ALUMINA HYDRATE UNION CARBIDE CORPORATION (US) 1979-01-23 US disclosed
US-4105465-A COATED WITH A SILANE CONTAINING HYDROLYZABLE GROUPS AND A POLYALKYLENE OXIDE GROUP UNION CARBIDE CORPORATION (US) 1978-08-08 US disclosed