SCHEMBL290143

SCHEMBL290143

OB(O)c1ccc(-c2ccccc2)s1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HSD17B1 P14061 3/20 0.48
HSD17B2 P37059 3/20 0.48
CYP2E1 P05181 1/20 0.48
CYP3A4 P08684 1/20 0.48
CYP2A6 P11509 1/20 0.48
CYP2C9 P11712 1/20 0.48
CYP2B6 P20813 1/20 0.48
CYP2C19 P33261 1/20 0.48
RAB9A P51151 3/20 0.46
MEN1 O00255 1/20 0.46
POLB P06746 1/20 0.46
KMT2A Q03164 1/20 0.46
TSHR P16473 1/20 0.45
NQO2 P16083 3/20 0.44
HDAC1 Q13547 1/20 0.44
MGLL Q99685 3/20 0.42
NPC1 O15118 2/20 0.42
KDM4E B2RXH2 1/20 0.42
ALDH1A1 P00352 1/20 0.42
HPGD P15428 1/20 0.42

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
SCHEMBL12107122 0.96 HSD17B1 (0.50) HSD17B1HSD17B2CYP2E1CYP3A4CYP2A6
SCHEMBL28527720 0.83 HSD17B1 (0.62) HSD17B1HSD17B2CYP3A4CYP2C19
SCHEMBL28529085 0.81 HSD17B1 (0.47) HSD17B1HSD17B2CYP3A4CYP2C19MEN1
SCHEMBL3479599 0.81 TSHR (0.56) TSHRMGLL
2-Thiophenenecarboxaldehyde SCHEMBL28159808 0.80 DPP4 (0.41) HSD17B1HSD17B2CYP2E1CYP3A4CYP2A6
SCHEMBL28606077 0.79 HDAC3 (0.47) HSD17B1HSD17B2CYP2E1CYP3A4CYP2A6
SCHEMBL2558370 0.79 HSD17B1 (0.42) HSD17B1HSD17B2TSHRCA2
SCHEMBL2556281 0.79 HSD17B1 (0.49) HSD17B1HSD17B2CYP3A4CYP2C9CYP2C19
SCHEMBL2556652 0.79 TSHR (0.52) HSD17B1RAB9AMEN1POLBKMT2A
SCHEMBL28527091 0.79 CYP2A6 (0.56) CYP2E1CYP3A4CYP2A6CYP2C9CYP2B6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12102715-B1 ROS-responsive liposomes for specific targeting VERILY LIFE SCIENCES LLC (US) 2024-10-01 US claimed
US-11179335-B1 ROS-responsive liposomes for specific targeting VERILY LIFE SCIENCES LLC (US) 2021-11-23 US claimed
US-10517823-B1 ROS—responsive liposomes for specific targeting VERILY LIFE SCIENCES LLC (US) 2019-12-31 US claimed
CN-113788790-B Aromatic heterocyclic amide derivative and application thereof 华东理工大学 2025-02-18 CN disclosed
US-20240360156-A1 HETEROCYCLIC COMPOUND AND USE THEREOF TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2024-10-31 US disclosed
US-12102715-B1 ROS-responsive liposomes for specific targeting VERILY LIFE SCIENCES LLC (US) 2024-10-01 US disclosed
WO-2024003151-A1 CHEMICAL SYNTHESIS PLATFORM THE UNIVERSITY COURT OF THE UNIVERSITY OF GLASGOW (GB) 2024-01-04 WO disclosed
CN-110997648-B Condensed ring compound 东曹株式会社 2023-12-19 CN disclosed
US-20220340893-A1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES NUEVOLUTION A/S (DK) 2022-10-27 US disclosed
US-20220202772-A1 COMPOSITIONS AND METHODS FOR INHIBITING RIBOSOME INACTIVATING PROTEINS RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY 2022-06-30 US disclosed
US-11318097-B1 ROS-responsive multilamellar liposomal vesicles for targeting inflammatory macrophages VERILY LIFE SCIENCES LLC (US) 2022-05-03 US disclosed
WO-2007062370-A2 CALCILYTIC COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2007-05-31 WO disclosed
EP-1784400-A1 HISTAMINE H3 RECEPTOR AGENTS, PREPARATION AND THERAPEUTIC USES ELI LILLY AND COMPANY (US) 2007-05-16 EP disclosed
EP-1723116-A2 TETRAHYDROQUINOLINONES AND THEIR USE AS ANTAGONISTS OF METABOTROPIC GLUTAMATE RECEPTORS Merz Pharma GmbH & Co. KGaA (DE) 2006-11-22 EP disclosed
US-20060122256-A1 Biaryloxymethylarenecarboxylic acids as glycogen synthase activators GILLESPIE PAUL 2006-06-08 US disclosed
WO-2006053748-A1 SUBSTITUTED [(PHENYLETHANOYL)AMINO] BENZAMIDES AND THE USE THEREOF IN THE TREATMENT OF INFLAMMATORY AND CARDIO-VASCULAR DISEASES BAYER HEALTHCARE AG (DE) 2006-05-26 WO disclosed
WO-2006023462-A1 HISTAMINE H3 RECEPTOR AGENTS, PREPARATION AND THERAPEUTIC USES ELI LILLY AND COMPANY (US) 2006-03-02 WO disclosed
WO-2005082856-A2 TETRAHYDROQUINOLINONES AND THEIR USE AS ANTAGONISTS OF METABOTROPIC GLUTAMATE RECEPTORS MERZ PHARMA GMBH & CO. KGAA (DE) 2005-09-09 WO disclosed
US-20050197361-A1 Specific binding is extremely high; low toxicity; high degree of activity; 2-(5-m-Tolyl-thiazol-2-yl )-7,8-dihydro-6H-quinolin-5-one, acute and/or chronic neurological disorders MERZ PHARMA GMBH & CO. KGAA (DE) 2005-09-08 US disclosed
JP-2004059457-A METHOD FOR PRODUCING (THIOPHENE/PHENYLENE)COOLIGOMERS SUMITOMO SEIKA CHEM CO LTD 2004-02-26 JP 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-20220202772-A1 COMPOSITIONS AND METHODS FOR INHIBITING RIBOSOME INACTIVATING PROTEINS RACK1, RRBP1, RPL30 HSD17B1 4125/4885HSD17B2 4194/4885CYP2E1 4309/4885
US-20240360156-A1 HETEROCYCLIC COMPOUND AND USE THEREOF GRIN1, GRIN2C, GRIN2A HSD17B1 441/4885HSD17B2 447/4885CYP2E1 2026/4885
US-20060122256-A1 Biaryloxymethylarenecarboxylic acids as glycogen synthase activators GYS2, GYS1, GSK3A HSD17B1 19/4885HSD17B2 18/4885CYP2E1 370/4885
US-20050197361-A1 Specific binding is extremely high; low toxicity; high degree of activity; 2-(5-m-Tolyl-thiazol-2-yl )-7,8-dihydro-6H-quinolin-5-one, acute and/or chronic neurological disorders GRM5, GRIK5, GRIN2C HSD17B1 3585/4885HSD17B2 3613/4885CYP2E1 1541/4885

“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.