(R)-camphor (CHEBI:15396)

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CHEBI:15396 - (R)-camphor

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ChEBI Name	(R)-camphor

ChEBI ID	CHEBI:15396

ChEBI ASCII Name	(R)-camphor

Definition	The (R)- enantiomer of camphor.

Stars	This entity has been manually annotated by the ChEBI Team.

Secondary ChEBI IDs	CHEBI:41334, CHEBI:16, CHEBI:10758, CHEBI:18442

Supplier Information	ZINC000096095578

Download	Molfile XML SDF

more structures >>

Molfile

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Marvin 02150916253D

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Time for openFile(

Marvin 02150916253D

27 28 0 0 0 0 999 V2000

2.0380 -3.4039 1.4073 C 0 0 2 0 0 0 0 0 0 0 0 0

3.3953 -3.7159 0.8153 C 0 0 0 0 0 0 0 0 0 0 0 0

3.7674 -4.8219 0.4947 O 0 0 0 0 0 0 0 0 0 0 0 0

4.2363 -2.4638 0.7116 C 0 0 0 0 0 0 0 0 0 0 0 0

3.1852 -1.4166 1.2113 C 0 0 1 0 0 0 0 0 0 0 0 0

2.0781 -1.3940 0.1185 C 0 0 0 0 0 0 0 0 0 0 0 0

1.3005 -2.7335 0.3093 C 0 0 0 0 0 0 0 0 0 0 0 0

2.4452 -2.2135 2.3168 C 0 0 2 0 0 0 0 0 0 0 0 0

3.2789 -2.5640 3.5797 C 0 0 0 0 0 0 0 0 0 0 0 0

1.2552 -1.4664 2.8270 C 0 0 0 0 0 0 0 0 0 0 0 0

1.2436 -4.5745 2.0314 C 0 0 0 0 0 0 0 0 0 0 0 0

4.5589 -2.2772 -0.3350 H 0 0 0 0 0 0 0 0 0 0 0 0

5.1290 -2.5188 1.3707 H 0 0 0 0 0 0 0 0 0 0 0 0

3.6173 -0.4278 1.4756 H 0 0 0 0 0 0 0 0 0 0 0 0

2.5313 -1.3445 -0.8947 H 0 0 0 0 0 0 0 0 0 0 0 0

1.4027 -0.5242 0.2656 H 0 0 0 0 0 0 0 0 0 0 0 0

0.2449 -2.5600 0.6093 H 0 0 0 0 0 0 0 0 0 0 0 0

1.3272 -3.3615 -0.6069 H 0 0 0 0 0 0 0 0 0 0 0 0

2.7802 -3.3865 4.1358 H 0 0 0 0 0 0 0 0 0 0 0 0

3.3551 -1.6684 4.2330 H 0 0 0 0 0 0 0 0 0 0 0 0

4.2965 -2.8882 3.2731 H 0 0 0 0 0 0 0 0 0 0 0 0

0.3774 -1.6831 2.1811 H 0 0 0 0 0 0 0 0 0 0 0 0

1.4675 -0.3759 2.8095 H 0 0 0 0 0 0 0 0 0 0 0 0

1.0363 -1.7860 3.8685 H 0 0 0 0 0 0 0 0 0 0 0 0

0.3443 -4.7826 1.4130 H 0 0 0 0 0 0 0 0 0 0 0 0

0.9294 -4.3009 3.0615 H 0 0 0 0 0 0 0 0 0 0 0 0

1.8862 -5.4803 2.0669 H 0 0 0 0 0 0 0 0 0 0 0 0

8 10 1 0 0 0 0

8 9 1 0 0 0 0

6 7 1 0 0 0 0

5 8 1 0 0 0 0

5 6 1 0 0 0 0

4 5 1 0 0 0 0

2 4 1 0 0 0 0

2 3 2 0 0 0 0

1 11 1 0 0 0 0

1 8 1 0 0 0 0

1 7 1 0 0 0 0

1 2 1 0 0 0 0

12 4 1 0 0 0 0

13 4 1 0 0 0 0

14 5 1 0 0 0 0

15 6 1 0 0 0 0

16 6 1 0 0 0 0

17 7 1 0 0 0 0

18 7 1 0 0 0 0

19 9 1 0 0 0 0

20 9 1 0 0 0 0

21 9 1 0 0 0 0

22 10 1 0 0 0 0

23 10 1 0 0 0 0

24 10 1 0 0 0 0

25 11 1 0 0 0 0

26 11 1 0 0 0 0

27 11 1 0 0 0 0

M END): 18 ms

reading 27 atoms

ModelSet: haveSymmetry:false haveUnitcells:false haveFractionalCoord:false

1 model in this collection. Use getProperty "modelInfo" or getProperty "auxiliaryInfo" to inspect them.

Default Van der Waals type for model set to Babel

27 atoms created

ModelSet: not autobonding; use forceAutobond=true to force automatic bond creation

Script completed

Jmol script terminated

Molfile expand

Formula

C10H16O

Net Charge

Average Mass

152.23344

Monoisotopic Mass

152.12012

InChI

InChI=1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3/t7-,10+/m1/s1

InChIKey

DSSYKIVIOFKYAU-XCBNKYQSSA-N

SMILES

CC1(C)[C@@H]2CC[C@@]1(C)C(=O)C2

Roles Classification
Biological Role(s):	plant metabolite Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms. (via camphor )

View more via ChEBI Ontology

ChEBI Ontology
Outgoing	(R)-camphor (CHEBI:15396) is a camphor (CHEBI:36773) (R)-camphor (CHEBI:15396) is enantiomer of (S)-camphor (CHEBI:15397)

Incoming	(S)-camphor (CHEBI:15397) is enantiomer of (R)-camphor (CHEBI:15396)

IUPAC Name

(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

Synonyms	Sources
(+)-bornan-2-one	ChemIDplus
(+)-Camphor	KEGG COMPOUND
(1R)-(+)-camphor	NIST Chemistry WebBook
(1R,4R)-camphor	UniProt
(R)-(+)-camphor	ChemIDplus
(R)-camphor	ChemIDplus
CAMPHOR	PDBeChem
Camphor(D)	NIST Chemistry WebBook
D-Camphor	KEGG COMPOUND

Manual Xrefs	Databases
C00000819	KNApSAcK
C00808	KEGG COMPOUND
c0407	UM-BBD
CAM	PDBeChem
CPD-862	MetaCyc
D06392	KEGG DRUG
HMDB0059838	HMDB
View more database links

Registry Numbers	Types	Sources
2042745	Reaxys Registry Number	Reaxys
464-49-3	CAS Registry Number	KEGG COMPOUND
464-49-3	CAS Registry Number	NIST Chemistry WebBook
464-49-3	CAS Registry Number	ChemIDplus
76-22-2	CAS Registry Number	KEGG COMPOUND
83276	Gmelin Registry Number	Gmelin

Citations

Chernick ET, Börzsönyi G, Steiner C, Ammon M, Gessner D, Frühbeisser S, Gröhn F, Maier S, Tykwinski RR (2014)
Optically pure, monodisperse cis-oligodiacetylenes: aggregation- induced chirality enhancement.
Angewandte Chemie (International ed. in English) 53, 310-314 [PubMed:24288289]
[show Abstract]

Funk C, Croteau R (1993)
Induction and Characterization of a Cytochrome P-450-Dependent Camphor Hydroxylase in Tissue Cultures of Common Sage (Salvia officinalis).
Plant physiology 101, 1231-1237 [PubMed:12231778]
[show Abstract]

Last Modified

04 August 2014

CHEBI:15396 - (R)-camphor

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