SCHEMBL422198

SCHEMBL422198

CC(C)c1cc(Cl)cc(Cl)c1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.50
GABRA1 P14867 2/20 0.46
GABRB1 P18505 1/20 0.46
CNR1 P21554 1/20 0.40
CNR2 P34972 1/20 0.40
TP53 P04637 1/20 0.38
CYP3A4 P08684 1/20 0.38
GABRB2 P47870 1/20 0.37
ADRB2 P07550 1/20 0.36
FABP3 P05413 2/20 0.36
FABP4 P15090 2/20 0.36
IDO1 P14902 1/20 0.35
TDO2 P48775 1/20 0.35
TYR P14679 2/20 0.35
FABP5 Q01469 1/20 0.34
GRN P28799 1/20 0.33
SORT1 Q99523 1/20 0.33
ALDH1A1 P00352 1/20 0.33
CYP1A2 P05177 1/20 0.33
POLB P06746 1/20 0.33

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
Ammonia Solution, Strong SCHEMBL5676040 0.97 TSHR (0.47) TSHRGABRA1GABRB1CNR1CNR2
SCHEMBL11574451 0.94 GABRA1 (0.46) TSHRGABRA1GABRB1CNR1CNR2
Hydrogen Peroxide SCHEMBL11577393 0.88 GABRA1 (0.48) TSHRGABRA1GABRB1CNR1CNR2
SCHEMBL6124148 0.84 GABRA1 (0.39) TSHRGABRA1GABRB1CNR1CNR2
SCHEMBL16959948 0.82 GABRA1 (0.38) TSHRGABRA1GABRB1CNR1CNR2
SCHEMBL20844085 0.82 GABRA1 (0.38) TSHRGABRA1GABRB1CNR1CNR2
SCHEMBL9967735 0.82 GABRA1 (0.38) TSHRGABRA1GABRB1CNR1CNR2
SCHEMBL4547915 0.82 TRPM8 (0.38) TSHRGABRA1GABRB1CNR1CNR2
SCHEMBL13523275 0.82 GABRA1 (0.48) TSHRGABRA1GABRB1CNR1CNR2
SCHEMBL3791553 0.82 CYP3A4 (0.55) TSHRGABRA1GABRB1CNR1CNR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-104529789-B Synthetic process of 3,5-dichloro-alpha,alpha-dimethyl benzylamine 苏州市玮琪生物科技有限公司 2017-02-22 CN claimed
CN-104529789-A Synthetic process of 3,5-dichloro-alpha,alpha-dimethyl benzylamine SUZHOU WELL BRIDGE BIOLOG TECHNOLOGY CO LTD 2015-04-22 CN claimed
EP-0322869-B1 PROCESS FOR SEPARATING DICHLOROCUMENE ISOMER TORAY INDUSTRIES, INC. (JP) 1992-09-09 EP claimed
US-5030777-A Synthesis of 3,5-dichloroalkylbenzene and recovery of 1,3-dichlorobenzene STANDARD CHLORINE OF DELAWARE, INC. (US) 1991-07-09 US claimed
EP-0322869-A2 Process for separating dichlorocumene isomer TORAY INDUSTRIES, INC. (JP) 1989-07-05 EP claimed
EP-0090875-B1 SEPARATION OF 3,5-DICHLOROCUMENE FROM A MIXTURE OF 3,5-DICHLOROCUMENE AND 2,4-DICHLOROCUMENE THE DOW CHEMICAL COMPANY (US) 1985-07-31 EP claimed
EP-0061720-B1 PROCESS FOR THE SELECTIVE ALIPHATIC CHLORINATION OF ALKYLBENZENES THE DOW CHEMICAL COMPANY (US) 1985-03-13 EP claimed
EP-0090875-A1 Separation of 3,5-dichlorocumene from a mixture of 3,5-dichlorocumene and 2,4-dichlorocumene THE DOW CHEMICAL COMPANY (US) 1983-10-12 EP claimed
EP-0061720-A1 Process for the selective aliphatic chlorination of alkylbenzenes THE DOW CHEMICAL COMPANY (US) 1982-10-06 EP claimed
US-4348265-A Process for the selective aliphatic chlorination of alkylbenzenes THE DOW CHEMICAL COMPANY (US) 1982-09-07 US claimed
US-4329524-A Separation of 3,5-dichlorocumene from a mixture of 3,5-dichlorocumene and 2,4-dichlorocumene THE DOW CHEMICAL COMPANY (US) 1982-05-11 US claimed
US-4104315-A Process for separating an ar, ar-dihalo-ar-alkylbenzene from an isomeric mixture of ar, ar-dihalo-ar-alkylbenzenes THE DOW CHEMICAL COMPANY (US) 1978-08-01 US claimed
JP-2178240-A None JP disclosed
JP-1319444-A None JP disclosed
US-20240239772-A1 PROTEASE INHIBITORS AND METHODS OF USE THE CLEVELAND CLINIC FOUNDATION 2024-07-18 US disclosed
US-20240239772-A1 PROTEASE INHIBITORS AND METHODS OF USE THE CLEVELAND CLINIC FOUNDATION 2024-07-18 US disclosed
US-4104315-A Process for separating an ar, ar-dihalo-ar-alkylbenzene from an isomeric mixture of ar, ar-dihalo-ar-alkylbenzenes THE DOW CHEMICAL COMPANY (US) 1978-08-01 US disclosed
US-4087473-A Preferential aliphatic halogenation of ar-substituted alkylbenzenes THE DOW CHEMICAL COMPANY (US) 1978-05-02 US disclosed
US-4087473-A Preferential aliphatic halogenation of ar-substituted alkylbenzenes THE DOW CHEMICAL COMPANY (US) 1978-05-02 US disclosed
US-4059642-A Preferential alkylation or acylation of meta-disubstituted benzenes THE DOW CHEMICAL COMPANY (US) 1977-11-22 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 (1 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-20240239772-A1 PROTEASE INHIBITORS AND METHODS OF USE ACE2, ACE, TMPRSS2 TSHR 4756/4885GABRA1 3840/4885GABRB1 3878/4885

“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.