SCHEMBL348918

SCHEMBL348918

Nc1cc(Cl)cc(Cl)c1C(=O)O

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 3/20 0.53
AKR1C4 P17516 1/20 0.45
AKR1C3 P42330 1/20 0.45
AKR1C2 P52895 1/20 0.45
AKR1C1 Q04828 1/20 0.45
GRIN1 Q05586 2/20 0.43
TPMT P51580 1/20 0.43
TSHR P16473 5/20 0.42
CASP1 P29466 2/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
SRC P12931 1/20 0.40
KDR P35968 1/20 0.40
HPGD P15428 3/20 0.40
ALOX15 P16050 2/20 0.40
KMT2A Q03164 2/20 0.40
MEN1 O00255 1/20 0.40
GRIN2D O15399 1/20 0.40
GRIN3B O60391 1/20 0.40
CYP1A2 P05177 1/20 0.40
CYP2D6 P10635 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
SCHEMBL111202 0.84 AKR1C4 (0.54) CYP3A4AKR1C4AKR1C3AKR1C2AKR1C1
SCHEMBL31460347 0.83 THRB (0.44) CYP3A4TPMTTSHRCASP1SMN1; SMN2
SCHEMBL366927 0.83 CYP3A4 (0.44) CYP3A4AKR1C4AKR1C3AKR1C2AKR1C1
Urea SCHEMBL29192961 0.82 AKR1C4 (0.48) CYP3A4AKR1C4AKR1C3AKR1C2AKR1C1
SCHEMBL1301827 0.81 AKR1C4 (0.52) CYP3A4AKR1C4AKR1C3AKR1C2AKR1C1
SCHEMBL5878784 0.81 AKR1C4 (0.52) CYP3A4AKR1C4AKR1C3AKR1C2AKR1C1
SCHEMBL28392002 0.81 AKR1C4 (0.52) CYP3A4AKR1C4AKR1C3AKR1C2AKR1C1
Hydrochloric Acid SCHEMBL2512939 0.81 AKR1C4 (0.52) CYP3A4AKR1C4AKR1C3AKR1C2AKR1C1
SCHEMBL1398113 0.79 KEAP1 (0.41) CYP3A4TSHRHPGDCYP2C19TDP1
SCHEMBL31057404 0.79 KDM4E (0.41) CYP3A4AKR1C4AKR1C3AKR1C2AKR1C1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1690040-A 3,5-dichloroaniline preparing process YANCHENG GUANGXIN CHEMICAL CO (CN) 2005-11-02 CN claimed
US-3931300-A Process for the production of dichlorobenzoic acids BASF AKTIENGESELLSCHAFT (DT) 1976-01-06 US claimed
EP-4146220-B1 HETEROCYCLIC COMPOUNDS AS TRIGGERING RECEPTOR EXPRESSED ON MYELOID CELLS 2 AGONISTS AND METHODS OF USE AMGEN INC (US) 2026-02-18 EP disclosed
US-20250388574-A1 HETEROCYCLIC COMPOUNDS AS TRIGGERING RECEPTOR EXPRESSED ON MYELOID CELLS 2 AGONISTS AND METHODS OF USE AMGEN INC (US) 2025-12-25 US disclosed
US-12503467-B2 2-oxoquinazoline derivatives as methionine adenosyltransferase 2A inhibitors IDEAYA BIOSCIENCES, INC. (US) 2025-12-23 US disclosed
US-12319691-B2 Heterocyclic compounds as triggering receptor expressed on myeloid cells 2 agonists and methods of use AMGEN INC. (US) 2025-06-03 US disclosed
US-20250171452-A1 TRYPTANTHRIN DERIVATIVES AND USES THEREOF VISCIENT BIO, INC. 2025-05-29 US disclosed
US-12252489-B2 Heterocyclic compounds as triggering receptor expressed on myeloid cells 2 agonists and methods of use AMGEN INC. (US) 2025-03-18 US disclosed
EP-4514804-A1 TRYPTANTHRIN DERIVATIVES AND USES THEREOF Viscient Bio, Inc. (US) 2025-03-05 EP disclosed
CN-119528824-A 2-Oxo quinazoline derivatives as methionine adenosyltransferase 2A inhibitors 伊迪亚生物科学有限公司 2025-02-28 CN disclosed
CN-119487031-A Tryptanthrin derivatives and uses thereof 威森特生物公司 2025-02-18 CN disclosed
EP-0206323-A1 2-Oxy-4H-3,1-benzoxazin-4-one derivatives and related compounds SYNTEX (U.S.A.) INC. (US) 1986-12-30 EP disclosed
EP-0104389-B1 QUINOLINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE IN THE CONTROL OF UNDESIRED PLANT GROWTH BASF Aktiengesellschaft (DE) 1986-07-16 EP disclosed
US-4587339-A USED TO COLOR PLASTICS, PAINTS, AND INKS SUN CHEMICAL CORPORATION (US) 1986-05-06 US disclosed
US-4582902-A AZO-METHINE NICKEL-COMPLEXED PIGMENTS; PAINTS; PLASTICS; LACQUERS; PHOTSTABILITY SUN CHEMICAL CORPORATION (US) 1986-04-15 US disclosed
US-4581450-A INTERMEDIATES FOR PIGEMENTS SUN CHEMICAL CORPORATION (US) 1986-04-08 US disclosed
US-4508899-A COLORFAST RED-ORANGE-YELLOW ORGANIC PIGMENT SUN CHEMICAL CORPORATION (US) 1985-04-02 US disclosed
EP-0104389-A2 Quinoline derivatives, process for their preparation and their use in the control of undesired plant growth BASF Aktiengesellschaft (DE) 1984-04-04 EP disclosed
US-3971741-A DISPERSION PIGMENTS BAYER AKTIENGESELLSCHAFT (DT) 1976-07-27 US disclosed
US-3931300-A Process for the production of dichlorobenzoic acids BASF AKTIENGESELLSCHAFT (DT) 1976-01-06 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 (5 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-20250171452-A1 TRYPTANTHRIN DERIVATIVES AND USES THEREOF IDO2, IDO1, TPSB2 CYP3A4 1477/4885AKR1C4 3453/4885AKR1C3 3366/4885
US-12252489-B2 Heterocyclic compounds as triggering receptor expressed on myeloid cells 2 agonists and methods of use MSR1, FPR2, CD14 CYP3A4 1451/4885AKR1C4 3816/4885AKR1C3 3315/4885
US-12319691-B2 Heterocyclic compounds as triggering receptor expressed on myeloid cells 2 agonists and methods of use MSR1, FPR2, CD14 CYP3A4 1273/4885AKR1C4 3681/4885AKR1C3 3154/4885
US-12503467-B2 2-oxoquinazoline derivatives as methionine adenosyltransferase 2A inhibitors MAT2B, MAT2A, MAT1A CYP3A4 3573/4885AKR1C4 2335/4885AKR1C3 2681/4885
US-20250388574-A1 HETEROCYCLIC COMPOUNDS AS TRIGGERING RECEPTOR EXPRESSED ON MYELOID CELLS 2 AGONISTS AND METHODS OF USE MSR1, FCER2, HAVCR2 CYP3A4 2837/4885AKR1C4 2866/4885AKR1C3 2046/4885

“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.