SCHEMBL1934879

SCHEMBL1934879

O=C(Cl)c1cc(I)ccc1Cl

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 6/20 0.42
TP53 P04637 1/20 0.42
ANO1 Q5XXA6 1/20 0.39
ABL1 P00519 1/20 0.38
BCR P11274 1/20 0.38
PTPRC P08575 1/20 0.38
PTPN2 P17706 1/20 0.38
PTPN1 P18031 1/20 0.38
PTPRA P18433 1/20 0.38
PTPRB P23467 1/20 0.38
PTPRE P23469 1/20 0.38
PTPN6 P29350 1/20 0.38
CES2 O00748 1/20 0.37
CES1 P23141 1/20 0.37
KDM4E B2RXH2 1/20 0.36
NPC1 O15118 1/20 0.36
POLB P06746 1/20 0.36
MAPT P10636 1/20 0.36
RAB9A P51151 1/20 0.36
TDP1 Q9NUW8 1/20 0.36

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
SCHEMBL305505 0.83 ALDH1A1 (0.63) ALDH1A1TP53ANO1PTPRCPTPN2
SCHEMBL1164647 0.83 TSHR (0.42) ALDH1A1TP53PTPRCPTPN2PTPN1
SCHEMBL31364369 0.83 ALDH1A1 (0.63) ALDH1A1TP53ANO1PTPRCPTPN2
SCHEMBL21921083 0.81 ALDH1A1 (0.41) ALDH1A1TP53ANO1ABL1BCR
SCHEMBL1786179 0.81 ALDH1A1 (0.50) ALDH1A1TP53ANO1ABL1BCR
SCHEMBL27994220 0.81 ALDH1A1 (0.61) ALDH1A1TP53ANO1PTPRCPTPN2
SCHEMBL15471933 0.80 ALDH1A1 (0.68) ALDH1A1ANO1KDM4ENPC1POLB
SCHEMBL27454155 0.80 PTPN2 (0.39) ALDH1A1PTPRCPTPN2PTPN1PTPRA
SCHEMBL23242473 0.78 AR (0.47) ALDH1A1PTPRCPTPN2PTPN1PTPRA
SCHEMBL699001 0.77 ALDH1A1 (0.68) ALDH1A1TP53KDM4EMAPTRAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110872216-A Method and device for producing (2-chloro-5-iodophenyl) -4-fluorobenzyl ketone by reaction separation coupling 南京恒道医药科技有限公司 2020-03-10 CN claimed
CN-116332882-B Synthesis process of key intermediate of englitz 江苏阿尔法集团福瑞药业(宿迁)有限公司 2025-03-18 CN disclosed
CN-117964583-A Preparation method of Engliclazide chiral intermediate 江苏阿尔法药业股份有限公司 2024-05-03 CN disclosed
CN-117946039-A Chiral synthesis process of englitz intermediate 江苏阿尔法药业股份有限公司 2024-04-30 CN disclosed
CN-117683003-A New process for synthesizing englitjing intermediate 江苏阿尔法集团福瑞药业(宿迁)有限公司 2024-03-12 CN disclosed
US-20230218650-A1 COMPOSITIONS COMPRISING AND METHODS OF USING INHIBITORS OF SODIUM-GLUCOSE COTRANSPORTERS 1 AND 2 LEXICON PHARMACEUTICALS, INC. 2023-07-13 US disclosed
CN-116332882-A Synthesis process of key intermediate of englitz 江苏福瑞康泰药业有限公司 2023-06-27 CN disclosed
US-20210388016-A1 GLUCOPYRANOSE DERIVATIVES USEFUL AS SGLT2 INHIBITORS JANSSEN PHARMACEUTICA NV (BE) 2021-12-16 US disclosed
US-20210388015-A1 GLUCOPYRANOSE DERIVATIVES USEFUL AS SGLT2 INHIBITORS JANSSEN PHARMACEUTICA NV (BE) 2021-12-16 US disclosed
US-20210388015-A1 GLUCOPYRANOSE DERIVATIVES USEFUL AS SGLT2 INHIBITORS JANSSEN PHARMACEUTICA NV (BE) 2021-12-16 US disclosed
US-20080200454-A1 CARBON-LINKED TETRAHYDRO-PYRAZOLO-PYRIDINE MODULATORS OF CATHEPSIN S SUNESIS PHARMACEUTICALS, INC. 2008-08-21 US disclosed
US-20080139631-A1 3-(2-methyl-4-(trifluoromethyl)-5-cyano-indol-1-yl-methyl)-5-(3-(trifluoromethyl)phenyl)-1,2,4-oxadiazole or salt thereof; hypogonadism, sarcopenia, osteoporosis, wasting diseases, cancer cachexia, frailty, prostatic hyperplasia, prostate cancer, breast cancer; selective androgen receptor modulators SMITHKLINE BEECHAM CORPORATION (US) 2008-06-12 US disclosed
WO-2008042571-A2 SUBSTITUTED INDOLE COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2008-04-10 WO disclosed
US-20080081928-A1 reacting 2-chloro-5-iodo-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide with allyl alcohol in the presence of a palladium catalyst and a tertiary amine base, to form 2-chloro-5-(3-oxopropyl)-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide; chemical intermediates for drugs ASTRAZENECA AB (SE) 2008-04-03 US disclosed
WO-2008030160-A1 PROCESS FOR PREPARING N-METHYLADAMANTYL DERIVATIVES BY A PALLADIUM CATALYSED COUPLING REACTION FOLLOWED BY REDUCTIVE AMINATION ASTRAZENECA AB (SE) 2008-03-13 WO disclosed
CN-1161336-C Quinoline carboxamides as antiviral agents �������Ŷ���Լ��������˾ 2004-08-11 CN disclosed
CN-1333753-A Quinoline carboxamides as antiviral agents UPJOHN CO (US) 2002-01-30 CN disclosed
EP-1140850-A1 QUINOLINECARBOXAMIDES AS ANTIVIRAL AGENTS PHARMACIA & UPJOHN COMPANY (US) 2001-10-10 EP disclosed
US-6248739-B1 DNA POLYMERASE INHIBITORS EFFECTIVE AGAINST HERPESVIRUSES PHARMACIA & UPJOHN COMPANY 2001-06-19 US disclosed
WO-2000040561-A1 QUINOLINECARBOXAMIDES AS ANTIVIRAL AGENTS PHARMACIA & UPJOHN COMPANY (US) 2000-07-13 WO 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 (6 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-20210388016-A1 GLUCOPYRANOSE DERIVATIVES USEFUL AS SGLT2 INHIBITORS SLC5A2, SLC5A1, UGGT1 ALDH1A1 1242/4885TP53 4884/4885ANO1 817/4885
US-20080200454-A1 CARBON-LINKED TETRAHYDRO-PYRAZOLO-PYRIDINE MODULATORS OF CATHEPSIN S CTSS, CTSK, CTSZ ALDH1A1 4404/4885TP53 1392/4885ANO1 4662/4885
US-20080139631-A1 3-(2-methyl-4-(trifluoromethyl)-5-cyano-indol-1-yl-methyl)-5-(3-(trifluoromethyl)phenyl)-1,2,4-oxadiazole or salt thereof; hypogonadism, sarcopenia, osteoporosis, wasting diseases, cancer cachexia, frailty, prostatic hyperplasia, prostate cancer, breast cancer; selective androgen receptor modulators AR, NR5A1, NR3C2 ALDH1A1 3006/4885TP53 628/4885ANO1 1134/4885
US-20210388015-A1 GLUCOPYRANOSE DERIVATIVES USEFUL AS SGLT2 INHIBITORS SLC5A2, SLC5A1, UGGT1 ALDH1A1 1242/4885TP53 4884/4885ANO1 817/4885
US-20080081928-A1 reacting 2-chloro-5-iodo-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide with allyl alcohol in the presence of a palladium catalyst and a tertiary amine base, to form 2-chloro-5-(3-oxopropyl)-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide; chemical intermediates for drugs ADH1A, ADH1C, ADH5 ALDH1A1 4/4885TP53 4421/4885ANO1 349/4885
US-20230218650-A1 COMPOSITIONS COMPRISING AND METHODS OF USING INHIBITORS OF SODIUM-GLUCOSE COTRANSPORTERS 1 AND 2 SLC5A2, SLC5A1, SLC2A2 ALDH1A1 1202/4885TP53 4619/4885ANO1 362/4885

“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.