SCHEMBL1719720

SCHEMBL1719720

CCOC(=O)Nc1ccc(C)cc1

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 4/20 0.71
ALDH1A1 P00352 2/20 0.71
LMNA P02545 1/20 0.71
RECQL P46063 1/20 0.71
HSD17B10 Q99714 1/20 0.71
NPC1 O15118 4/20 0.65
RAB9A P51151 4/20 0.65
HPGD P15428 2/20 0.65
CRHBP P24387 1/20 0.65
CRHR2 Q13324 1/20 0.65
CYP1A2 P05177 2/20 0.62
CYP2C9 P11712 2/20 0.62
CYP2C19 P33261 2/20 0.62
POLB P06746 1/20 0.59
L3MBTL1 Q9Y468 1/20 0.58
TSHR P16473 1/20 0.58
KDM4E B2RXH2 1/20 0.58
MAPT P10636 1/20 0.57
CYP3A4 P08684 1/20 0.55
CYP2D6 P10635 1/20 0.55

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
SCHEMBL7565510 0.94 RAB9A (0.71) SMN1; SMN2ALDH1A1LMNARECQLHSD17B10
Urethane SCHEMBL10734196 0.91 SMN1; SMN2 (0.62) SMN1; SMN2ALDH1A1LMNARECQLHSD17B10
SCHEMBL8737482 0.91 NPC1 (0.79) SMN1; SMN2ALDH1A1LMNARECQLHSD17B10
SCHEMBL11790359 0.88 RAB9A (0.65) SMN1; SMN2ALDH1A1LMNARECQLHSD17B10
SCHEMBL7565512 0.88 RAB9A (0.70) SMN1; SMN2ALDH1A1LMNARECQLHSD17B10
SCHEMBL9146676 0.88 LMNA (0.68) SMN1; SMN2ALDH1A1LMNARECQLHSD17B10
SCHEMBL11326733 0.87 RAB9A (0.60) SMN1; SMN2ALDH1A1LMNARECQLHSD17B10
SCHEMBL10192026 0.87 SMN1; SMN2 (0.69) SMN1; SMN2ALDH1A1LMNARECQLHSD17B10
SCHEMBL19390510 0.86 SMN1; SMN2 (0.67) SMN1; SMN2ALDH1A1LMNARECQLHSD17B10
SCHEMBL352811 0.86 RAB9A (0.63) SMN1; SMN2ALDH1A1LMNARECQLHSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102498095-A Indoline derivatives TOKYO INST TECH 2012-06-13 CN claimed
US-11697636-B2 Substituted benzamides HOFFMANN-LA ROCHE INC. (US) 2023-07-11 US disclosed
US-11518766-B2 Tricyclic compound, preparation method therefor and use thereof SHANGHAI JEMINCARE PHARMACEUTICALS CO., LTD. (CN) 2022-12-06 US disclosed
EP-3998263-A1 TRICYCLIC COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF Shanghai Jemincare Pharmaceuticals Co., Ltd. (CN) 2022-05-18 EP disclosed
EP-3853305-A1 HIGH-PURITY PEG LIPIDS AND USES THEREOF ModernaTX, Inc. (US) 2021-07-28 EP disclosed
EP-3508473-B1 METHOD FOR PRODUCING CARBAMIC ACID ESTER AIST (JP) 2021-05-26 EP disclosed
EP-3720833-A1 PROPELLANT CHARGE Nederlandse Organisatie voor toegepast- natuurwetenschappelijk Onderzoek TNO (NL) 2020-10-14 EP disclosed
US-10752579-B2 Production method of carbamic acid ester NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 2020-08-25 US disclosed
WO-2020061295-A1 HIGH-PURITY PEG LIPIDS AND USES THEREOF MODERNATX, INC. (US) 2020-03-26 WO disclosed
WO-2018227012-A9 POLYMER-LIPID MATERIALS FOR DELIVERY OF NUCLEIC ACIDS MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2019-11-14 WO disclosed
US-4550150-A COLORIMETRIC DETECTION ALLIED CORPORATION (US) 1985-10-29 US disclosed
EP-0083096-A2 Production of urethane compounds Asahi Kasei Kogyo Kabushiki Kaisha (JP) 1983-07-06 EP disclosed
US-4375000-A Process for the preparation of an aryl mono-, di-, and/or polyurethane BASF AKTIENGESELLSCHAFT (DE) 1983-02-22 US disclosed
US-4294925-A FERMENTATION, AEROBIC PROCESSES HOFFMANN-LA ROCHE INC. (US) 1981-10-13 US disclosed
US-4263427-A REACTING HYDROXYL WITH ISOCYANATE TO OBTAIN ANTIBIOTICS HOFFMANN-LA ROCHE INC. (US) 1981-04-21 US disclosed
US-4186269-A REACTING AROMATIC NITRO COMPOUND, AN ALCOHOL, AND CARBON MONOXIDE IN PRESENCE OF CATALYST MITSUI TOATSU CHEMICALS, INCORPORATED (JP) 1980-01-29 US 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
US-4069240-A GROUP 8 METAL CATALYST UNIROYAL, INC. (US) 1978-01-17 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 (3 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-11518766-B2 Tricyclic compound, preparation method therefor and use thereof TFPI, TFPI2, F11 SMN1; SMN2 3397/4885ALDH1A1 3573/4885LMNA 601/4885
US-10752579-B2 Production method of carbamic acid ester CA2, CA7, CA4 SMN1; SMN2 3068/4885ALDH1A1 3215/4885LMNA 3973/4885
US-11697636-B2 Substituted benzamides TAAR1, TAAR5, NPY1R SMN1; SMN2 1965/4885ALDH1A1 440/4885LMNA 3001/4885

“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.