Efavirenz

Efavirenz

SCHEMBL13098636

O=C1Nc2ccc(Cl)cc2[C@](C#CC2CC2)(C(F)(F)F)O1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

pol

The experimentally established mechanism targets of Efavirenz. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP46A1 Q9Y6A2 10/20 1.00
NR1I2 O75469 1/20 1.00
NR3C1 P04150 1/20 1.00
PGR P06401 1/20 1.00
ADRB1 P08588 1/20 1.00
ADORA3 P0DMS8 1/20 1.00
MAPT P10636 1/20 1.00
CNR1 P21554 1/20 1.00
SLC6A2 P23975 1/20 1.00
HTR2A P28223 1/20 1.00
HTR2C P28335 1/20 1.00
MAPK1 P28482 1/20 1.00
AGTR1 P30556 1/20 1.00
CCKBR P32239 1/20 1.00
PPARG P37231 1/20 1.00
OPRK1 P41145 1/20 1.00
SLC6A3 Q01959 1/20 1.00
PDE4D Q08499 1/20 1.00
PDE3A Q14432 1/20 1.00
NPSR1 Q6W5P4 1/20 1.00

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
Efavirenz SCHEMBL1560709 1.00 CYP46A1 (1.00) CYP46A1NR1I2NR3C1PGRADRB1
Efavirenz SCHEMBL37762 1.00 CYP46A1 (1.00) CYP46A1NR1I2NR3C1PGRADRB1
Efavirenz SCHEMBL3227745 1.00 CYP46A1 (1.00) CYP46A1NR1I2NR3C1PGRADRB1
Efavirenz SCHEMBL464769 1.00 CYP46A1 (1.00) CYP46A1NR1I2NR3C1PGRADRB1
Efavirenz SCHEMBL28518509 0.99 CYP46A1 (0.98) CYP46A1NR1I2NR3C1PGRADRB1
Efavirenz SCHEMBL28400913 0.99 CYP46A1 (0.98) CYP46A1NR1I2NR3C1PGRADRB1
Efavirenz SCHEMBL5576237 0.99 CYP46A1 (0.98) CYP46A1NR1I2NR3C1PGRADRB1
Efavirenz SCHEMBL28777926 0.99 CYP46A1 (0.98) CYP46A1NR1I2NR3C1PGRADRB1
Efavirenz SCHEMBL5028560 0.95 CYP46A1 (0.90) CYP46A1NR1I2NR3C1PGRADRB1
Efavirenz SCHEMBL28698666 0.92 CYP46A1 (0.84) CYP46A1NR1I2NR3C1PGRADRB1

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 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115819256-A Purification method of efavirenz intermediate 上海迪赛诺生物医药有限公司 2023-03-21 CN disclosed
US-20200262775-A1 Process for Friedel-Crafts Reaction, and Catalyst Therefore FUJIAN YONGJING TECHNOLOGY CO., LTD. (CN) 2020-08-20 US disclosed
US-8318930-B2 Process for preparing polymorphic forms of (S)-6-chloro-(cyclopropylethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one MATRIX LABORATORIES LIMITED (IN) 2012-11-27 US disclosed
US-8318930-B2 Process for preparing polymorphic forms of (S)-6-chloro-(cyclopropylethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one MATRIX LABORATORIES LIMITED (IN) 2012-11-27 US disclosed
US-20100274007-A1 PROCESS FOR PREPARING POLYMORPHIC FORMS OF (S)-6-CHLORO-(CYCLOPROPYLETHYNYL)-1,4-DIHYDRO-4-(TRIFLUOROMETHYL)-2H-3,1-BENZOXAZIN-2-ONE MATRIX LABORATORIES LIMITED (IN) 2010-10-28 US disclosed
US-20100274007-A1 PROCESS FOR PREPARING POLYMORPHIC FORMS OF (S)-6-CHLORO-(CYCLOPROPYLETHYNYL)-1,4-DIHYDRO-4-(TRIFLUOROMETHYL)-2H-3,1-BENZOXAZIN-2-ONE MATRIX LABORATORIES LIMITED (IN) 2010-10-28 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 (2 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-20100274007-A1 PROCESS FOR PREPARING POLYMORPHIC FORMS OF (S)-6-CHLORO-(CYCLOPROPYLETHYNYL)-1,4-DIHYDRO-4-(TRIFLUOROMETHYL)-2H-3,1-BENZOXAZIN-2-ONE CYP1A1, CYP4Z1, CYP1B1 CYP46A1 296/4885NR1I2 131/4885NR3C1 1991/4885
US-20200262775-A1 Process for Friedel-Crafts Reaction, and Catalyst Therefore HNF4A, TFEB, HACL2 CYP46A1 246/4885NR1I2 2696/4885NR3C1 1383/4885

“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.